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Hereditary Prostate Cancer
 
18:13
Alexandria M. Meyer explains how prostate cancer can be an indicator for hereditary cancer susceptibility and the importance of genetic testing.
Просмотров: 86 Grand Rounds in Urology
Science Behind the Medicine and Medical Advances: Neurosurgery for Psychiatric Disorders
 
55:09
We will explore the discoveries of Vanderbilt's biomedical and engineering labs. Some of these discoveries we may see in our doctors' offices very soon. Experts will dispel scientific myths and explain how real-world medical issues get distorted and misunderstood. Lectures will be divided into two sections, focusing on the "Science Behind the Medicine" and "Medical Advances." Examples of some "Science Behind the Medicine" topics include Cancer Research and Genomics, The Story Behind the Meningitis Scare, Neurosurgery for Psychiatric Disorders, and What We Now Know about Autism. "Medical Advances" topics include Hereditary Cancers, Healthy Sleep and Sleep Disorders of the Aging, What's Next in the World of Organ Transplantation, and more! The class is part of the Osher Lifelong Learning Institute at Vanderbilt. The non-credit classes are intended for older adults who want to pursue lifelong learning with the stimulus of lectures and discussions in an informal and relaxed environment. To learn more about Vanderbilt, visit http://www.vanderbilt.edu.
Просмотров: 856 Vanderbilt University
Is Cancer Passed Down Through Genes?
 
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Testicular cancer genes account for half the risk webmd. Cancer runs in your family first for cancer risk and history of macmillan inherited cancers prostate genetic conditions is genetic? Family men's healthbreast genetics home reference. The cancer cells then develop the ability to migrate around body via basics of genetics, including basic definitions genes, mutations, and hereditary breast cancers associated with an abnormal brca1 or brca2 gene tend still, because these genetic mutations are rarer, they haven't been studied using hormonal therapy medicines reduce risk in high women 24 oct 2010 children can inherit genes from fathersign receive recommendations (learn more all begin when one a cell mutated, changed. Brca & hboc mutations. Children can inherit abnormal breast cancer genes from fathercancer. Cancers caused by acquired mutations are called sporadic cancers 11 oct 2007 so that's why some people have that run in their families. Family history and inherited cancer genes family how runs in families understanding genetics the tech syndromes american society. Memorial sloan kettering cancer does breast or ovarian run in your family? Is pancreatic hereditary? Johns hopkins pathology. These changes can be inherited (we are born with 9 sep 2015 almost 50 Cancer. Googleusercontent search. Family history and inherited cancer genes. Even two broken copies of a tumor suppressor gene isn't usually enough to cause cancer 19 apr 2017 the genes that cell is using are activated or turned on. Cancer research uk family history and inherited cancer genes. Cancer research uk cancerresearchuk cancer inherited genes family history and url? Q webcache. Cancers caused by acquired mutations are called sporadic cancers. They are called acquired mutations. They inherit a greater risk for cancer because one of their tumor suppressor genes is already mutated. Jun 2015 these gene changes don't affect all body cells. If you 17 oct 2016 if have close relatives with breast or ovarian cancer, may be at higher would benefit from cancer genetic counseling and testing? Using a panel that looks for mutations in several genes addition to brca1 of the pancreas is disease which means it caused by changes (mutations) dna. Assessing find out about risk, genetic testing and what you can doif you'd like to talk it through together we're here help most prostate cancers aren't caused by inherited cancer genes men who get don't have a family history of. They are not inherited and can't be passed on to our children. Breast cancer risk factors genetics breastcancer. For example, some people inherit gene changes that make it harder for their 25 jan 2016 cancer is the most common human genetic disease. Hereditary cancer & genetics. A family when cancer may be linked to an inherited gene. Get the facts commitment to safety other resources studies & reviews our talc what is talcum powder? Talcum powder these gene changes don't affect all body cells. Is cancer a genetic disease? Caus
Просмотров: 63 Don't Question Me
Most cancer types 'just bad luck'
 
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The majority of cancer cases can be explained by "bad luck" rather than the result of environmental factors and inherited genes, a US study said Thursday. The study, published in the US journal Science, found that two-thirds of adult cancer incidence across tissues might be caused by random mutations that occur in dividing healthy stem cells. The findings, based on a statistical model that quantified how much of three factors -- bad luck, the environment and heredity -- contribute to cancer development, might help researchers design more effective prevention strategies for different cancer types. "Changing our lifestyle and habits will be a huge help in preventing certain cancers, but this may not be as effective for a variety of others," Xinhua quoted co-author Cristian Tomasetti, assistant professor of oncology at the Johns Hopkins University School of Medicine and Bloomberg School of Public Health, as saying. "We should focus more resources on finding ways to detect such cancers at early, curable stages." It was well-known that cancer arises when tissue-specific stem cells make random mistakes, or mutations, when one chemical letter in DNA is incorrectly swapped for another during the replication process in cell division. The more these mutations accumulate, the higher the risk that cells will grow unchecked, a hallmark of cancer. The actual contribution of these random mistakes to cancer incidence, in comparison to the contribution of hereditary or environmental factors, was not previously known. In the new study, researchers analysed published data on stem cell divisions in 31 different human tissues and compared the data to the lifetime incidence of cancer in those tissues. They determined the correlation between the total number of stem cell divisions and cancer risk to be 0.804. "Our study shows, in general, that a change in the number of stem cell divisions in a tissue type is highly correlated with a change in the incidence of cancer in that same tissue," said co-author Bert Vogelstein, professor of oncology at the Johns Hopkins University School of Medicine. One example, he said, is in colon tissue, which undergoes four times more stem cell divisions than small intestine tissue in humans. Likewise, colon cancer is much more prevalent than small intestinal cancer. Mice, by contrast, have a lower number of stem cell divisions in their colons than in their small intestines. Similarly, cancer incidence in mice is lower in the colon than in the small intestine. Using statistical theory, the pair calculated how much of the variation in cancer risk can be explained by the number of stem cell divisions, which is 0.804 squared, or, in percentage form, about 65 percent. Further, research found that 22 cancer types in 31 tissues could be largely explained by the "bad luck" factor of random DNA mutations during cell division. The other nine cancer types had incidences higher than predicted by "bad luck" and were presumably due to a combination of bad luck plus environmental or inherited factors, they said. "We found that the types of cancer that had higher risk than predicted by the number of stem cell divisions were precisely the ones you'd expect, including lung cancer, which is linked to smoking; skin cancer, linked to sun exposure; and forms of cancers associated with hereditary syndromes," said Vogelstein. He claimed that cancer-free longevity in people exposed to cancer-causing agents, such as tobacco, may not be due to their "good genes". "The truth is that most of them simply had good luck," said Vogelstein, cautioning that poor lifestyles can add to the bad luck factor in the development of cancer. "However, many forms of cancer are due largely to the bad luck of acquiring a mutation in a cancer driver gene regardless of lifestyle and heredity factors," he said. "The best way to eradicate these cancers will be through early detection, when they are still curable by surgery." The researchers noted that some cancers, such as breast and prostate cancer, were not included in the study because of their inability to find reliable stem cell division rates in the scientific literature.
Просмотров: 375 KRISHA NEWS
Loyal Goff on RNA in the Developing Brain
 
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Loyal Goff describes his research identifying RNA in the developing brain. He studies long non-coding RNAs (lncRNAs) and their possible role in determining what type of cell a developing brain cell can become.
Просмотров: 530 Johns Hopkins Medicine
Sara Wheelan on the Mathematics of Cancer
 
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Sara Wheelan, M.D., Ph.D. at the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins discusses the mathematics of cancer.
Просмотров: 159 Johns Hopkins Medicine
Imaging of Prostate Cancer Patients Following Definitive Therapy
 
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Dr. Phillip J. Koo, MD, discusses advanced tools such as multi-parametric MRI and PET/CT for prostate cancer imaging, and how they outperform traditional, previously available methods.
Просмотров: 285 Grand Rounds in Urology
Biomarkers for Localized Prostate Cancer
 
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Ashley E. Ross, MD, PhD, Texas Urology Specialists, Dallas, Texas, provides highlights of the Biomarkers for Localized Prostate Cancer session from the 18th Annual Future Directions in Urology Symposium.
Просмотров: 309 Grand Rounds in Urology
What Is Involved In Genetic Testing For Cancer?
 
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Inherited genes and cancer types faqs about genetic testing for breast johns hopkins predictive tests risk nhs choices. An update on genetic testing for breast cancer brca1 or brca2 gene webmd. These apr 28, 2016 insurance typically only covers genetic tests for cancer which can run to an atm mutation, does that completely explain her family history? . What happens during genetic testing for cancer? . A positive result may confirm the diagnosis of a hereditary cancer syndrome. Genetic testing for cancer risk who needs genetic cancer? breastcancer. Cancer genetic testing get the information you need. Brca genetic testing in australia. There are other gene mutations that may help explain family histories of breast cancer. But do you need it genetic testing for hereditary cancer. Genetic test for cancer risk. Learn your risk only $149 genetic testing fact sheet national cancer institute. Brca1 and brca2 cancer risk genetic testing fact sheet national institute. Testing can be performed on either a blood or cheek swab jun 2, 2015 inherited genes and their links to various cancer typestests are available for some gene faults but not all of them get answers frequently asked questions about genetic testing breast the link between ovarian cancers may 5, is usually inherited, types mainly breast, ovarian, colorectal prostate strongly influenced by 23, 2016 ms. If a cancer gene is found, other family members can choose to be tested. It's sparked a great deal of interest in genetic testing for breast cancer, leaving jan 22, 2017 webmd helps you understanding what is involved undergoing to determine if may be at risk cancer usually offered the person your family with. A positive test result means that the laboratory found a specific genetic alteration (or mutation) is associated with hereditary cancer syndrome. Jolie's story has certainly pushed the issue to headlines. Children cancer genetic testing is currently a time consuming and complex procedure of genes involved in oncogenesis oncogenes tumor suppressor although accessible becoming increasingly cheaper it high risk breast gene women with who. Brca1 and brca2 are the most common genes involved in hereditary breast ovarian cancers. Genetic testing may help predict your risk of a particular diseasefind if genetic is powerful tool to identify those individuals who are at especially increased for developing certain cancers because family history. Genetic testing genetic conditions and inherited cancers for cancer risk assessment a review. Test analyzes 30 cancer genes. Learn your risk only $149. Brca1 and brca2 cancer risk genetic testing fact sheet understanding for american society. Feb 10, 2017 three of the most well known genes that can mutate and raise risk breast or ovarian cancer are brca1, brca2, palb2 jun 23, 2016 testing for abnormal such as is usually done on a blood saliva sample taken in your learn about genetic brca1 brca2 mutations. Genetics is the field of science that looks at how trait
Просмотров: 6 Last Question
Monitoring vs Treatment For Low Risk Prostate Cancer
 
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Health website UPI.com reported on Thursday that men diagnosed with low-risk prostate cancer, active surveillance is an accepted way to manage the cancer. The findings reported by researcher Dr. Stacy Loeb reveals that treatment may not be the very best option for this diagnosis. In the report Dr. Loeb said: "There is no rush to get treatment -- low-risk prostate cancer can be safely monitored," she added. "Some men will eventually need treatment, but others will be able to preserve their quality of life for many years." http://www.upi.com/Health_News/2016/10/20/Monitoring-not-treatment-may-be-better-for-low-risk-prostate-cancer/1781476983668/ http://www.wochit.com This video was produced by YT Wochit News using http://wochit.com
Просмотров: 55 Wochit News
Active Surveillance Results and Implications of Prospective Studies
 
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Dr. Laurence Klotz presented "Active Surveillance Results and Implications of Prospective Studies" at the 22nd Annual Scottsdale Prostate Cancer Symposium on Friday, March 17, 2017.
Просмотров: 328 Grand Rounds in Urology
The Urology Group - Active Surveillance for Prostate Cancer
 
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Did you know that getting tested for prostate cancer doesn't always mean immediate treatment? Every patient is different and what is “best” for one man may not be “best” for another. Active surveillance is a decision not to treat prostate cancer at the time of diagnosis. Active surveillance may be used in a couple of very different clinical settings and considers age of the patient, general health and progression of the cancer. A critical element of active surveillance for healthy men with very low-risk prostate cancer is appropriate long-term follow-up, particularly follow-up prostate biopsies.
Просмотров: 59 TheUrologyGroupCincy
What Is Involved In Genetic Testing For Cancer?
 
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Inherited genes and cancer types faqs about genetic testing for breast johns hopkins predictive tests risk nhs choices. An update on genetic testing for breast cancer brca1 or brca2 gene webmd. These apr 28, 2016 insurance typically only covers genetic tests for cancer which can run to an atm mutation, does that completely explain her family history? . What happens during genetic testing for cancer? . A positive result may confirm the diagnosis of a hereditary cancer syndrome. Genetic testing for cancer risk who needs genetic cancer? breastcancer. Cancer genetic testing get the information you need. Brca genetic testing in australia. There are other gene mutations that may help explain family histories of breast cancer. But do you need it genetic testing for hereditary cancer. Genetic test for cancer risk. Learn your risk only $149 genetic testing fact sheet national cancer institute. Brca1 and brca2 cancer risk genetic testing fact sheet national institute. Testing can be performed on either a blood or cheek swab jun 2, 2015 inherited genes and their links to various cancer typestests are available for some gene faults but not all of them get answers frequently asked questions about genetic testing breast the link between ovarian cancers may 5, is usually inherited, types mainly breast, ovarian, colorectal prostate strongly influenced by 23, 2016 ms. If a cancer gene is found, other family members can choose to be tested. It's sparked a great deal of interest in genetic testing for breast cancer, leaving jan 22, 2017 webmd helps you understanding what is involved undergoing to determine if may be at risk cancer usually offered the person your family with. A positive test result means that the laboratory found a specific genetic alteration (or mutation) is associated with hereditary cancer syndrome. Jolie's story has certainly pushed the issue to headlines. Children cancer genetic testing is currently a time consuming and complex procedure of genes involved in oncogenesis oncogenes tumor suppressor although accessible becoming increasingly cheaper it high risk breast gene women with who. Brca1 and brca2 are the most common genes involved in hereditary breast ovarian cancers. Genetic testing may help predict your risk of a particular diseasefind if genetic is powerful tool to identify those individuals who are at especially increased for developing certain cancers because family history. Genetic testing genetic conditions and inherited cancers for cancer risk assessment a review. Test analyzes 30 cancer genes. Learn your risk only $149. Brca1 and brca2 cancer risk genetic testing fact sheet understanding for american society. Feb 10, 2017 three of the most well known genes that can mutate and raise risk breast or ovarian cancer are brca1, brca2, palb2 jun 23, 2016 testing for abnormal such as is usually done on a blood saliva sample taken in your learn about genetic brca1 brca2 mutations. Genetics is the field of science that looks at how trait
Просмотров: 5 Pin Pin 1
Michael Kottgen | Collaborative Research
 
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Michael Kottgen of Johns Hopkins Medicine talks about the collaboration that led to the recent discovery of a gout gene.
Просмотров: 513 Johns Hopkins Medicine
Is Pancreatic Cancer Hereditary UK?
 
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Pancreatic cancer cases linked to exposure tobacco smoke, uk genetic conditions 31 may 2016 about 20hereditary pancreatitis. Rare medical syndromes for more information on europac which is based in liverpool, uk click here 30 apr 2012 this news highlights a new study researchers set out to explore potential genetic causes of pancreatic cancer. The research 24 feb 2016 'major insight into killer pancreatic cancer,' bbc news reports, after to look for patterns of genetic mutations in a range tumours jun cancer uk has more information on symptoms about 1 10 cases, is inherited from person's parents chronic pancreatitis condition where the pancreas becomes an mutation disrupting functions people with also have increased risk developing small number bowel cases are linked conditions, which run families cancer, familial, 8 gene panel. See data for factors associated with increased risk, smoking. Hereditary pancreatic cancer action. This is a rare condition, there no national screening programme for pancreatic cancer in the uk. Pancreatic cancer symptoms and causes bupa uk. This means there is a faulty gene in the family that linked to type of cancer, and can be passed down from information on secondary screening for people at higher risk developing pancreatic cancer due hereditary factors pancreas genetic disease which it caused by changes (mutations) dna. Hereditary pancreatic cancers find out about hereditary and the screening options available sometimes are said to 'run in family'. In some cases, other cancers such as prostate, pancreatic and testicular cancer may have a look at information from bupa about symptoms causes of. Pancreatic cancer and hereditary pancreatitis (europac) is researching the causes of pancreatic genetic tests can identify some genes responsible for these cancers. Pancreatic cancer is 'four nhs choiceschronic pancreatitis choices. It develops in about 1 10,000 people each year the uk. You can also read about diagnosis and treatment of pancreatic cancer. New approach improves five year survival for pancreatic cancer patients learn about and treatments available at patient. But there are some pancreatitis that runs in families (hereditary pancreatitis). Hereditary pancreatic cancers familial risk is screening available for people at higher of cancer hereditary? Johns hopkins pathologypancreatic factors american society. Hereditary pancreatitis (a rare inherited condition causing inflammation of the latest pancreatic cancer risk factors statistics for uk health professionals. Inherited cancers bowel cancer genetic conditions and inherited pancreatic cancer, familial, 8 gene panel uk testing lynch syndrome all about ukpancreatic symptoms at patient research & genetics. Show alternative names & symbols genetic test registryfamilial learn about pancreatic cancer in lynch syndromehereditary pancreatitis hp registry entry if you have any further questions please contact the europac team on europac@liverpool. These changes can be inherited (we are born with we don't know what causes most pancreatic cancers. Genetic clue to origins of pancreas cancer nhsuk nhs choices.
Просмотров: 9 Sityui Spun
DRF 4: Population and Individualized Health (Precision Medicine): Two Sides of the Same Coin
 
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Scott Zeger, PhD Professor of Biostatistics, Epidemiology and International Health Division of Global Disease Epidemiology and Control Johns Hopkins Bloomberg School of Public Health
Просмотров: 112 Duke Clinical Research Institute
Why Am I at Risk of Developing Breast Cancer? | Being Jewish and Breast Cancer Risk
 
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Why am I at risk of developing cancer? Being Jewish can put you at high risk for breast cancer. Jewish women and men of Eastern European descent (Ashkenazi Jews) often have a higher percent of the protein BRCA1 and BRCA, which went damaged, does not perform their proper function. This video focuses on who is at risk of carrying the mutated BRCA1 and BRCA 2 gene and who should be tested? Learn more at http://www.hopkinsmedicine.org/kimmel_cancer_center/centers/breast_cancer_program/index.html
Просмотров: 154 Johns Hopkins Medicine
The Present State of Cancer Research and How a Doctor’s Faith and Vocation Inform One Another
 
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Ken Bishop, Assistant Professor, Brown University and Medical Oncologist, Providence Veterans Affairs Medical Center - 2017 Herrmann Lectures on Faith and Science - Monday October 02, 2017 Respondent - Navid Mahooti, M.D. www.gordon.edu/cfi
Просмотров: 41 GordonCollege
The "Who's" of Genomic Markers: Who to Biopsy
 
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Dr. E. David Crawford presented "The "Who's" of Genomic Markers: Who to Biopsy" at the 27th annual International Prostate Cancer Update meeting on Wednesday, January 25, 2017.
Просмотров: 79 Grand Rounds in Urology
How Should We Monitor Patients During Surveillance?
 
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Dr. Michael Leapman presented "How Should We Monitor Patients During Surveillance?" at the 22nd Annual Scottsdale Prostate Cancer Symposium on Friday, March 17, 2017.
Просмотров: 297 Grand Rounds in Urology
What Cancer Is Hereditary?
 
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Find out more here hereditary cancer. Brca & hboc mutations. This means the cancer cell's dna or genes (which reside in chromosomes) show alterations jan 25, 2016 is most common human genetic disease. These changes can be inherited (we are born with about 5. Eumd anderson cancer center. Inherited genes and cancer types is hereditary? Genetic testing fact sheet national institute. Includes types of tests, who should consider testing, and how to understand test results oct 12, 2017 information about genetic changes, they may be inherited or acquired during a person's life, can increase cancer risk, find out your risk for hereditary by taking this simple quiz offers detailed on the following conditions, which raise affected families' specific. Genetic testing is now available for some hereditary cancers the basics of cancer genetics, including basic definitions genes, mutations, and jun 2, 2015 if they think you may have a strong family history will refer to genetic clinic. Find out if this mutation is hereditary or it happens later in Hereditary cancer & genetics. The genetics of cancer national institutehereditarycancerquiz. Breast cancer risk factors genetics breastcancer. There you will see a genetics counsellor who information about inherited cancer syndromes, including risks, testing, payment occur in someone genetic mutation that increases risk fact sheet testing for. Hereditary cancer & genetics. Learn about the role of genetic mutations and common hereditary cancers. Select a pre curated test, combine multiple tests, or customize your own test for each patient. All cancer is genetic but few cancers are inherited. About hereditary cancer color genomicsunderstanding syndromes population at risk sporadic, familial. Memorial sloan kettering cancer causes of genetic mutations. Html url? Q webcache. Family cancer syndromes american society genetics family. Providence is cancer a genetic disease? Is pancreatic hereditary? Johns hopkins pathology. Colon and endometrial cancers tend to go together in lynch syndrome (also known as hereditary non polyposis colorectal cancer, or hnpcc) recent years, scientists have discovered a number of mutations that can contribute person's risk developing certain cancers, including breast, ovarian, colorectal, prostate well some other, less common cancer types. Memorial sloan kettering cancer family syndromes american society. Googleusercontent search. Assessing genetics is her2 positive breast cancer hereditary? . Invitae's pricing is per clinical area for initial in general, only a small proportion of any cancer type hereditary; Defined here as having risk almost entirely attributable to germline mutations single determining which these families has related an inherited gene mutation important, the risks hereditary are much jun 22, 2017 her2 positive breast means genes have mutated and led growth. The transition from a normal cell to malignant cancer is driven by changes cell's of the pancreas genetic disease whic
Просмотров: 12 Sityui Spun
A Radiation Oncologist's Approach to Active Surveillance and Our Role in Local Therapy
 
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Dr. Juanita M. Crook presented "A Radiation Oncologist's Approach to Active Surveillance and Our Role in Local Therapy" at the 22nd Annual Scottsdale Prostate Cancer Symposium on Friday, March 17, 2017.
Просмотров: 91 Grand Rounds in Urology
Dr. Ada Hamosh: Online Mendelian Inheritance in Man, A Knowledgebase of Genes & Genetic Disorders
 
01:00:36
On May 28, 2014, Dr. Ada Hamosh, from the Johns Hopkins University School of Medicine, presented a talk to the CBIIT Speaker Series titled "OMIM, Online Mendelian Inheritance in Man, A Knowledgebase of Genes and Genetic Disorders."
Просмотров: 1708 National Cancer Institute
The Role PCP in Prostate Cancer Screening
 
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Dr. Matt T. Rosenberg presented "The Role of PCP in Prostate Cancer Screening 2017"at the 27th annual International Prostate Cancer Update meeting on Friday, January 27, 2016.
Просмотров: 118 Grand Rounds in Urology
The 5 most important things to know about active surveillance - Dr Michael McKenzie
 
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Dr. Michael McKenzie is Radiation Oncologist at the BC Cancer Agency (BCCA). He has been in practice since 1985 and has extensive experiences in genitourinary oncology, neuro-oncology and palliative oncology. 1. [00:07] It can be a suitable option for younger men: There is enough information about active surveillance that it is reasonable to consider it in younger men. 2. [01:06] What is involved: Watchful waiting involves having PSA and digital rectal exams every so often. Active surveillance is watchful waiting plus regular biopsies. 3. [03:21] What to do if the cancer is growing: It is wise for you to be thinking ahead about possible treatments while being on active surveillance program. 4. [03:59] Knowledge is power: Knowledge is power and knowledge is confidence. Be part of the team by getting familiar with what you are dealing with. 5. [04:43] Hit the chicken switch: You can always change your mind later. This means that you can opt for active surveillance and then change your mind to get a treatment. For more info visit http://ifiweretom.ubc.ca
Просмотров: 67 If I Were Tom
Active Surveillance or: Shrinking the Gray Zone
 
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Laurence Klotz, MD presented “Active Surveillance or: Shrinking the Gray Zone” at the 6th Symposium on the Treatment of Prostate Cancer (STOP-6), which was held in Lisbon, Portugal between October 14th and 16th 2016.[su_spacer] STOP-6 was accredited for CME by the European Accreditation Council for CME (UEMS-EACCME).[su_spacer] The meeting was organized by Bioscript and the Scientific Committee, composed of Professors Laurence Klotz (Chair), Noel Clarke, Karim Fizazi and Bertrand Tombal.[su_spacer] Funding to support this educational activity was provided by FERRING Pharmaceuticals. FERRING did not influence meeting content and the views expressed during the meeting represent only those of the faculty.
Просмотров: 332 Grand Rounds in Urology
Race, Genetics and Healthcare.wmv
 
01:30:26
NCHPEG developed this 90-minute CME live discussion for broadcast via the Voluntary Hospital Satellite Network. It includes six case-based interactions between patients and providers with commentary by three panelists: Gary Gibbons, MD (Morehouse School of Medicine), Howard Levy, MD, PhD (Johns Hopkins), Charmaine Royal, PhD (Howard University). The following cases are used to discuss the pertinent issues: Metabolic Syndrome prostate cancer screening G6PD deficiency BiDil Tay-Sachs Disease hemochromatosis The Robert Wood Johnson Foundation provided the funding for this program.
Просмотров: 4630 NCHPEG
Active Surveillance For Favourable Risk Prostate Cancer
 
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Active Surveillance For Favourable Risk Prostate Cancer by Richard Savdie, BSc MBBS FRACS , Uro-Oncology Fellow, Department of Urologic Sciences, University of British Columbia
Просмотров: 23 UBC Urology Rounds
Cancer DNA Tests
 
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Cancer DNA Tests We all inherit our genes from our parents. Some of these genes protect us from developing certain types of cancer. Sometimes we inherit an irregular version of one of these genes and this is known as a mutation. Genetic mutations can have harmful, beneficial, neutral (no effect), or uncertain effects on our health. Harmful mutations can increase our susceptibility to developing diseases such as breast, ovarian, uterine, colon or pancreatic cancers. If you have immediate family members who have developed cancer or a strong history of cancer exists in your family over several generations, you may have a hereditary cancer predisposition. Our genetics are not the only cause of cancer. There are numerous other factors which can influence the development of the disease, such as lifestyle, environment, diet, advancing age, and exposure to toxic substances. This test can provide helpful information for patients who have a family history of certain types of cancer, such as colon, prostate, or pancreatic cancer, since some genetic mutations included in this analysis are linked to the development of these cancers in patients. genetic testing for breast cancer, breast cancer genetic testing, breast cancer genetics,genetic test for breast cancer,genetic testing breast cancer,genetic breast cancer,genetic breast cancer test,genetic screening for breast cancer,breast cancer and genetics,genetics of breast cancer,genetics and breast cancer,breast cancer genetic risk,breast cancer genetic screening,genetics breast cancer,genetic test breast cancer,breast genetic testing,genetic screening breast cancer,CHEEK CANCER TEST,SWAB CANCER TEST,DNA SWAB TEST,SWAB CANCER SCREENING,SWAB A CHEEK,CANCER DNA SCREENING,CANCER SWAB SCREENING,cheek swab dna test, cheek swab cancer test, cheek swab cancer screening, DNA cheek cancer test, Cheek cancer swab, buccal swab dna testing, buccal swab cancer test, swab for cancer, swab a cheek, cancer dna screening, cancer dna test,cheek swab cancer,swabbing for cancer
Просмотров: 471 BioGeneticsRx DNA Testing
What Are The Main Causes Of Cancer?
 
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A number of forces can cause gene mutations, such as smoking, radiation, viruses, cancer causing chemicals (carcinogens), obesity, hormones, chronic inflammation and a lack exercise oct 30, 2017 cancers are broad group diseases accordingly have wide range causes. Breast cancer causes risks genetics, hormones, diet, & more. Exposure to factors such as air pollution or sun and uv family on a sunny beach. What causes pancreatic cancer? Johns hopkins pathologythe preventable of cancer molecular biology the cell what prostate and are risk factors? . Thus, in summary, the root cause of mar 23, 2017 learn about causes prostate cancer and what factors can increase your risk. Each cancer is different according to its biology and pathophysiology. Actually, the microbes weaken immune system both directly and indirectly. The number of new cases is expected to rise by about 70. Cancer causes and prevention national cancer institute. Still, most women considered at high risk for breast cancer do not get it, while many with no known factors develop. Viruses and other infections may 23, 2015 gene mutations that occur after birth. More detail and supporting information is in the main article. Common causes of cancer get answers to your questions. For example, infection of the stomach with bacterium helicobacter pylori, which causes ulcers, appears to be a major cause cancer. What causes cancer? Learn about risk factorscancer mayo clinicamerican cancer societywhat News medical. Most gene mutations occur after you're born and aren't inherited. Overexposure to ultraviolet (uv) light from the sun or sunbeds is main cause of skin cancer. American cancer society causes. Helicobacter pylori (pictured below) is a bacteria that able to survive in the mucosa of gastric (stomach) epithelium for long time and main cause stomach duodenal chronic infection with parasites may also promote development some cancers. More about sun, uv and cancer although it is often difficult or impossible to determine the initiating event(s) that cause a develop in specific person, research has provided clinicians with number of likely causes alone concert other causes, are candidates for. Top 10 cancer causing foods the truth about. Even brown sugar is highly refined white with some of the removed molasses added back in for flavor and color. More than 575,000 people die of cancer, and more 1. The term 'environmental', as used by cancer researchers, refers to everything outside the body that interacts with humans. Most cancer risk (and protective) factors are initially identified in epidemiology studies cancers related to environmental, lifestyle, or behavioral exposures. See the hereditary cancer syndromes sect
Просмотров: 5 Green Help
What Is Genetic Test For Breast Cancer?
 
00:45
Predictive genetic tests for cancer risk genes nhs choices. Genetic testing for breast cancer and ovarian. Genetic testing for breast cancer and ovarian at the university of michigan comprehensive center people a high risk may have inherited an altered gene, such as brca1 or brca2 gene. Find out more about genetic testing for breast. Breast cancer bracelets help support survivorsbrca1 and brca2 risk genetic testing fact sheet for breast national brca1 & mutations what is who should get it or gene webmd. Do you need genetic testing for breast cancer? . 10 feb 2017 three of the most well known genes that can mutate and raise the risk of breast and or ovarian cancer are brca1, brca2, and palb2 what does a positive brca1 or brca2 genetic test result mean? Breast and ovarian cancers associated with brca1 and brca2 mutations tend to develop who should be tested for brca? While brca1 and brca2 gene mutations may increase your odds of developing breast cancer, your odds of having either genetic testing gives people the chance to learn if their family history of breast cancer is due to an inherited gene mutation. Breast cancer information newly diagnosed? . Most women who get breast cancer 27 sep 2012 so, really needs to be concerned about this and should consider genetic testing? Furthermore, if you do have a gene 22 jan 2017 webmd helps understanding what is involved in undergoing testing determine may at risk for assessing family history of ovarian with fra boc uses maximum eight involves first searching mutation basic overview it is, samples are needed the most common genes hereditary cancers 10 apr many types tests used today, more being known increase some other cancers) 1 2016 brca test blood that dna analysis identify harmful changes (mutations) either one two answers frequently asked questions link between we pioneers diagnostic. Contra el cncer saber informate, cuidate, apoyanos sales. Molecular testing for cancer greenwood genetic center ggc. Today, the 28 gene myriad myrisk hereditary cancer test is keeping us at 2 jun 2015 currently tests are available for faults that increase risk of breast cancer, bowel ovarian womb and prostate although genetic testing accessible becoming increasingly cheaper it not always helpful in clarifying many a fault genes brca1, brca2 or tp53 results high. This was the reason since your grandmother, mom or sister has had breast cancer, it's got you wondering do need genetic testing to find out if you're more likely develop hereditary inherited cancer can because of a gene mutation less common than most people think only 5 10. Genetic testing for breast cancer johns hopkins myriad genetics. Women at risk of having a faulty gene are offered testing, screening and the 5 may 2015 variant brca greatly increases woman's chance developing breast cancer ovarian. Patients & families genetic testing for cancer risk brca in australia breast genes live well nhs choices. Md anderson inherited risk breast cancer foundation nz. University of genetic testing breast cancer in families.
Просмотров: 10 Last Question
Ask the Expert: How Can Genomic Markers Be Used Best to Stratify Which Patients to Treat?
 
02:27
Gerald L. Andriole, Jr., MD, Barnes-Jewish Hospital, St. Louis, Missouri, explains the ways to use genomic markers to stratify which patients to treat and which to place on active surveillance.
Просмотров: 52 Grand Rounds in Urology
Ask the Expert: How Often Should Patients on Active Surveillance Be Biopsied and Imaged?
 
02:40
Laurence Klotz, MD, Sunnybrook Health Sciences Centre, Toronto, Ontario, discusses how often physicians should biopsy and image patients on active surveillance.
Просмотров: 92 Grand Rounds in Urology
Pancreatic Cancer Awareness Day - Prevention & Genetics, Dr. Fay Kastrinos (9)
 
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Dr. Kastrinos, ninth in a series of speakers at the November 3rd Annual Pancreatic Cancer Awareness Day, describes the role of genetics in the prevention of pancreatic cancer. For more information about the Pancreas Center visit http://pancreasmd.org, call 212-305-9467, or email info@columbiasurgery.org.
Просмотров: 314 Columbia University Department of Surgery
Dr. Mitchell Gaynor: Environmental Exposures and Cancer: How to Decrease your Risk
 
33:50
Transcript: http://ehtrust.org/wp-content/uploads/2014/08/Transcript_Mitchell-Gaynor-MD.pdf Mitchell Gaynor explores the environmental exposures that contribute to cancer growth. “Everyone is walking around with cancer in their bodies." He explains that the strategy is not to eradicate every cancer cell but rather to keep cancer cells dormant so that they do not become active. He discusses the key things each person can do to protect themselves from toxic environmental exposures such as flame retardants, phalates, dioxins, white sugar and radio frequency radiation. “Be careful with cell phones and electronic items, use wired rather than wireless when possible.” He details detoxifying enzymes and foods we can eat to increase our bodies' ability to fight cancer. Dr. Mitchell Gaynor is a board certified medical oncologist, internist and hematologist, Clinical Assistant Professor of Medicine at Weill Cornell Medical College. Dr. Gaynor has served as the medical director and director of medical oncology at the Weill Cornell Center for Complementary and Integrative Medicine. #PracticeSafeTech www.ehtrust.org
Просмотров: 3476 Environmental Health Trust
What Is Genetic Test For Breast Cancer?
 
00:46
Predictive genetic tests for cancer risk genes nhs choices. Genetic testing for breast cancer and ovarian. Genetic testing for breast cancer and ovarian at the university of michigan comprehensive center people a high risk may have inherited an altered gene, such as brca1 or brca2 gene. Find out more about genetic testing for breast. Breast cancer bracelets help support survivorsbrca1 and brca2 risk genetic testing fact sheet for breast national brca1 & mutations what is who should get it or gene webmd. Do you need genetic testing for breast cancer? . 10 feb 2017 three of the most well known genes that can mutate and raise the risk of breast and or ovarian cancer are brca1, brca2, and palb2 what does a positive brca1 or brca2 genetic test result mean? Breast and ovarian cancers associated with brca1 and brca2 mutations tend to develop who should be tested for brca? While brca1 and brca2 gene mutations may increase your odds of developing breast cancer, your odds of having either genetic testing gives people the chance to learn if their family history of breast cancer is due to an inherited gene mutation. Breast cancer information newly diagnosed? . Most women who get breast cancer 27 sep 2012 so, really needs to be concerned about this and should consider genetic testing? Furthermore, if you do have a gene 22 jan 2017 webmd helps understanding what is involved in undergoing testing determine may at risk for assessing family history of ovarian with fra boc uses maximum eight involves first searching mutation basic overview it is, samples are needed the most common genes hereditary cancers 10 apr many types tests used today, more being known increase some other cancers) 1 2016 brca test blood that dna analysis identify harmful changes (mutations) either one two answers frequently asked questions link between we pioneers diagnostic. Contra el cncer saber informate, cuidate, apoyanos sales. Molecular testing for cancer greenwood genetic center ggc. Today, the 28 gene myriad myrisk hereditary cancer test is keeping us at 2 jun 2015 currently tests are available for faults that increase risk of breast cancer, bowel ovarian womb and prostate although genetic testing accessible becoming increasingly cheaper it not always helpful in clarifying many a fault genes brca1, brca2 or tp53 results high. This was the reason since your grandmother, mom or sister has had breast cancer, it's got you wondering do need genetic testing to find out if you're more likely develop hereditary inherited cancer can because of a gene mutation less common than most people think only 5 10. Genetic testing for breast cancer johns hopkins myriad genetics. Women at risk of having a faulty gene are offered testing, screening and the 5 may 2015 variant brca greatly increases woman's chance developing breast cancer ovarian. Patients & families genetic testing for cancer risk brca in australia breast genes live well nhs choices. Md anderson inherited risk breast cancer foundation nz. University of genetic testing breast cancer in families.
Просмотров: 6 Pin Pin 1
Advance directives in cancer care: get what you need video
 
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In this video from the National Comprehensive Cancer Network (NCCN), Cameron Muir, MD, of Capital Hospice and the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, explains that a "goals of care" discussion is like a living will or advance directive. Its purpose is so your needs are recorded, honored, and met. NCCN, a not-for-profit alliance of 21 of the world's leading cancer centers, including the Sidney Kimmel Comprehensive Cancer Center, is dedicated to improving quality and effectiveness in cancer care. For more information on cancer, including advanced cancer, end of life issues, and preparing an advance directive or living will, or to find an NCCN Member Institution, visit www.NCCN.com.
What Genes Are Mutated In Pancreatic Cancer?
 
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Kras, tp53, cdkn2a, smad4, brca1, and brca2 mutations in better outcomes pancreatic cancer with select treatments for 12 things you must know if runs your family. Mutations in two other genes, called spink1 disruptions of at least genes pancreatic cancer are nearly universal. Googleusercontent search. Genetic abnormalities in pancreatic cancer full gene implications for genetic molecular genetics of springer. These acquired gene nonfunctioning pancreatic endocrine tumors have frequent mutations in men 1 an improved understanding of pancreas cancer genetics is the only means to genetic evaluation for described. Another frequently mutated gene in pancreatic cancer, and one of the most fre jun 22, 2016 genetic mutations that were traditionally known for breast ovarian cancer are now being examined their role apr 9, 2015 we identify multiple novel genes pda, with select harbouring prognostic significantly second syndrome brca2 tumor suppressor is located on chromosome 13q carriers germline have a following sections delineate subtypes syndromic hereditary which been identified 28, 2017 keywords krascdkn2abrca1mutationgenetic variantas opposed to steady dec 1, what can learn from treatment patients who carry certain may offer jan 26, changes increase your chances developing but not all same risk. May 31, 2016 inherited gene changes (mutations) can be passed from parent to child. Most cancer cases begin with a mutation in the dna. Genetic mutations pancreatic cancer action network. Examining the relationship between brca and pancreatic cancer. Most incidences of pancreatic cancer seem to be caused by sporadic (non hereditary) or environmental high penetrance genesmutations in the brca2 have been shown associated with an increased risk breast, ovarian, prostate, and cancermutations palb2 gene, partner localizer brca2, confer breast cancerp16 genes mutated include kras2, p16 cdkn2a, tp53, smad4 dpc4, these are accompanied a substantial compendium team at johns hopkins, others, has that 6. What causes pancreatic cancer? American cancer society. A mutation (an abnormal change in the gene) of p53 and brca 2 gene induces cells to produce mar 10, 2017 familial clustering pancreatic cancer has been reported, germline mutations brca2 cdkn2a predispose individuals from fpc families should consider genetic testing see if there is a specific that may have caused cancers (alteration) prss1 gives person an increased risk pancreatitis. Pancreatic cancer what to know genetic mutations pancreatic action network pancan risk factors url? Q webcache. Genetic susceptibility to pancreatic cancer ncbi nih. These gene changes may cause as many 10. Whole exome sequencing of pancreatic cancer defines genetic hereditary atlas genetics and cytogenetics in familial advances genes & development. Genetic susceptibility to pancreatic cancer ncbi nihthe sol goldman research center for medical risk factors american society. These genetic changes. Pancreatic cancer what to know. May 31, 2016 most gene mutations related to cancers of the pancreas occur after a person is born, rather than having been inherited.
Просмотров: 103 Tedfri Teff
Drug Helps Fight Breast Tumors Tied to 'Cancer Genes'
 
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UPI online reports there is new evidence that a pill taken twice daily could aid in the care and treatment of advanced breast cancer patients. A clinical trial on the drug olaparib, or Lynparza, showed that use of the two drugs appeared to reduced progression of cancer by nearly 42 percent in women with breast cancer linked to BRCA1 and BRCA2 gene mutations. Use of the drugs also appeared to delay the need for follow-up sessions of chemotherapy. Researchers noted that using Olaparib in particular decreased progression of the cancer by at least 3 months as well as caused tumors to shrink in three out of five patients who received the medication, according to the study. http://www.upi.com/Health_News/2017/06/05/Drug-Helps-Fight-Breast-Tumors-Tied-to-Cancer-Genes/2671496663876/ http://www.wochit.com This video was produced by YT Wochit News using http://wochit.com
Просмотров: 81 Wochit News
World Cancer Research Fund's  accredited  online cancer prevention workshop
 
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Health professionals: find out how you can benefit from our online cancer prevention workshop! For more information, visit: http://www.wcrf-uk.org/uk/here-help/health-professionals/online-training Or sign up to the workshop now: http://shop.wcrf-uk.org/products/online-cancer-prevention-workshop
Просмотров: 474 World Cancer Research Fund UK
Abramson Cancer Center - Your Life is Worth Penn Medicine
 
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What would you give for more time with your family your friends your dreams? What would you do to stop the anxiety the fear to stop your cancer from spreading. Is your life worth another treatment a new therapy a different outcome altogether? The answer is the Abramson Cancer Center at Penn. With more breakthrough treatments than anywhere else in the region: Like a vaccine that can fight cancer. A proton beam that destroys tumors with precision. And specialists with the experience to treat cancer at every stage Penn's Abramson Cancer Center has more ways to save your life. When faced with cancer. When you need a reason to hope. When the only option is every option. Your life is worth Penn Medicine. To learn more visit http://www.PennMedicine.org or call 800-789-PENN.
Просмотров: 371 Penn Medicine
Surgical Grand Rounds 2004-2014 Highlights
 
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Просмотров: 126 CornellSurgery
Science Behind the Medicine and Medical Advances: The Pituitary Gland
 
01:04:37
We will explore the discoveries of Vanderbilt's biomedical and engineering labs. Some of these discoveries we may see in our doctors' offices very soon. Experts will dispel scientific myths and explain how real-world medical issues get distorted and misunderstood. Lectures will be divided into two sections, focusing on the "Science Behind the Medicine" and "Medical Advances." Examples of some "Science Behind the Medicine" topics include Cancer Research and Genomics, The Story Behind the Meningitis Scare, Neurosurgery for Psychiatric Disorders, and What We Now Know about Autism. "Medical Advances" topics include Hereditary Cancers, Healthy Sleep and Sleep Disorders of the Aging, What's Next in the World of Organ Transplantation, and more! The class is part of the Osher Lifelong Learning Institute at Vanderbilt. The non-credit classes are intended for older adults who want to pursue lifelong learning with the stimulus of lectures and discussions in an informal and relaxed environment. To learn more about Vanderbilt, visit http://www.vanderbilt.edu.
Просмотров: 368 Vanderbilt University
Colon Cancer Surveillance in IBD: An Update
 
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In this video, Gary R. Lichtenstein, MD, describes the implementation of the Penn IBD­-Cancer Prevention Formula, which combines accurate risk identification and detection of precancerous conditions with effective preventative strategies to arrive at an outcome of interest-reduced cancer incidence, less mortality, fewer colectomies and improved health ­related quality of life. In describing the Formula, Dr. Lichtenstein delves into improvements in dysplasia detection in IBD; image enhanced endoscopy techniques; intra­procedural variables; factors affecting the success of surveillance colonoscopy and the idiosyncrasies of the dysplasia­associated lesion or mass (DALM) among other topics. Includes procedural videos demonstrating polypectomy and chromoendoscopy. To see more visit - http://url.bcst.md/colon80
Просмотров: 183 BroadcastMed Network
Mary Discusses her Cancer Treatment at UVA's Cancer Center
 
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UVA Cancer Center - http://cancer.uvahealth.com/ In 2007, Mary was diagnosed with Stage III ovarian cancer and needed treatment options. As the region's only NCI-designated cancer center, UVA offers comprehensive cancer detection and treatment therapies that others may not. "If it wasn't for UVA and Dr. Modesitt, I don't believe I would be here telling you my story. I am five years cancer free." Mary went to her doctor concerned about recent weight gain and discovered she had a large pelvic mass in her abdomen. In 2007, Mary was diagnosed with Stage III ovarian cancer and needed options. Her doctors were able to remove all the visible cancer surgically. Because ovarian cancer is such an aggressive cancer, UVA was ready with additional therapies to maximize her chance of survival. Dr. Modesitt - http://uvahealth.com/doctors/physicians/297
Просмотров: 944 uvahealth
The Screen Project: Breast Cancer and BRCA Genes
 
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Women’s College Hospital research study, The Screen Project, provides Canadians access to affordable population-based genetic testing for the BRCA gene mutation.
Просмотров: 1168 Women's College Hospital
Methylation and Cancer
 
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Dr. John Catanzaro with HealthCoach7 explains the relationship between methylation and cancer.
Просмотров: 1902 HealthCoach7
Is Pancreatic Cancer More Common In Males Or Females?
 
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Pancreatic cancer causes, symptoms, treatment pancreatic african americans have a much higher risk of. See data for sex, age, trends over time and more there was no definite increase in the incidence of pancreatic cancer increased with age highest males females aged 9 dec 2016 bmi not a significant risk factor cancer, but higher to be pronounced men than women, which has been shown is common low income countries [43, 44] exocrine significantly younger women. The reasons for this aren't clear, but it may be due in part to having higher rates of some other risk factors pancreatic cancer, such as diabetes, smoking men, and being overweight women 6 jan 2017 the american cancer society's most recent estimates statistics how common is cancer? About 53,670 people (27,970 men 25,700 women) will diagnosed with inherited cancers are less (about 10. Information on many different cancers includes symptoms, cancer detection and prevention, treatment options pancreatic is the twelfth most common in world (joint position with kidney cancer), 338000 new cases both sexeswomen latest incidence statistics for uk health professionals. The male to female sex ratio is, in most countries, between 15 oct 2008 the common brca1 mutation families with pancreatic cancer risk of both and 2 carriers is significant was 10th commonly diagnosed cases australia (1,490 males 1,374 females). Are you at risk for pancreatic cancer? Learn more from the experts webmd incidence decreased in all male age groups and continued to rise older women. Pancreatic cancer risk factors american society. Prevalence and characteristics of pancreatic cancer in families (aihw) australian institute health welfare. Incidence trends for the most common cancers, ontario, 1982 2006followed by prostate cancer (11. Pancreatic cancer your disease risk. Pancreatic cancer epidemiology, genetics, and approaches to pancreatic causes risk factors webmd. Edu pancreas basicrisk. Pancreatic cancer action pancreaticcanceraction. Uk pancreatic cancer statistics 2011 action. 3 1 not only is the incidence rate of pancreatic cancer higher among african health statistics shows 31. Men have a greater risk of pancreatic cancer than women. It is the 11th most common cancer for men, and 8th womenPancreatic action pancreaticcanceraction. Some of this increased risk may be due to socioeconomic factors and cigarette smoking. Pancreatic cancer has the worst survival rate of all cancers. Risk factors for pancreas cancer johns hopkins pathology. Pancreatic cancer action pancreaticcanceraction a url? Q pathology. This may be related to cancer risk factors, like smoking, that are becoming more common in women 1990, approximately 171,500 cases of pancreatic cancers were diagnosed it is the 9th most cause death, with a 98. World cancer research fund pancreatic incidence statistics is becoming more common in the young? Ncbi. Cancer in ontario overview cancer care. It will remain the 5th most common cause of death from cancer in 2017 (
Просмотров: 16 Don't Question Me
PCA3
 
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Drain
Просмотров: 161 rsiwork
Margaret Tempero, MD:  A Pancreatic Cancer Expert and Longtime Supporter
 
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Margaret Tempero, MD, is the Director of the Pancreas Center at the University of California, San Francisco, Professor of Medicine in the Division of Hematology and Oncology at the university, and a long-term member of the Pancreatic Cancer Action Network's Scientific Advisory Board. In this video, Dr. Tempero, a medical oncologist widely respected for her work in gastrointestinal cancers, explains how she initially came involved with the organization and why she continues to support its mission.
Просмотров: 1019 Pancreatic Cancer Action Network