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The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences
|
January 30, 2024
Meeting Summary of The NYO3 5th NO-Age/AD Meeting and the 1st Norway-UK Joint Meeting on Aging and Dementia: Recent Progress on the Mechanisms and Interventional Strategies
He-Ling Wang, Richard Siow, Tomas Schmauck-Medina, et al.
Nature Aging
|
May 14, 2026
Reduced ULK1 links impaired autophagy and mitophagy to Alzheimer's disease pathology
Jun-Ping Pan, Ping-Jie Wang, Jianying Zhang, et al.
Neurology
|
April 29, 2021
APOSTEL 2.0 Recommendations for Reporting Quantitative Optical Coherence Tomography Studies
Aykut Aytulun, Andrés Cruz-Herranz, Orhan Aktas, et al.
Hereditary Cancer in Clinical Practice
|
March 13, 2019
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
Toni T Seppälä, Aysel Ahadova, Mev Dominguez-Valentin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants
Hongyan Li, Christoph Engel, Miguel de la Hoya, et al.
CNS Drugs
|
September 18, 2021
Natalizumab Versus Fingolimod in Patients with Relapsing-Remitting Multiple Sclerosis: A Subgroup Analysis From Three International Cohorts
Sifat Sharmin, Mathilde Lefort, Johanna Balslev Andersen, et al.
Communications Biology
|
October 6, 2022
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
Christopher Hakkaart, John F Pearson, Louise Marquart, et al.
Journal of the National Cancer Institute
|
July 28, 2021
Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores
Daniel R Barnes, Valentina Silvestri, Goska Leslie, et al.
Hereditary Cancer in Clinical Practice
|
October 1, 2022
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
Pål Møller, Toni Seppälä, James G Dowty, et al.
Human Mutation
|
May 28, 2019
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
Michael T Parsons, Emma Tudini, Hongyan Li, et al.
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Search research articles
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Showing results (171-180 of 181) with videos related to
Sort By:
Page
of 19
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences
|
January 30, 2024
Meeting Summary of The NYO3 5th NO-Age/AD Meeting and the 1st Norway-UK Joint Meeting on Aging and Dementia: Recent Progress on the Mechanisms and Interventional Strategies
He-Ling Wang, Richard Siow, Tomas Schmauck-Medina, et al.
Nature Aging
|
May 14, 2026
Reduced ULK1 links impaired autophagy and mitophagy to Alzheimer's disease pathology
Jun-Ping Pan, Ping-Jie Wang, Jianying Zhang, et al.
Neurology
|
April 29, 2021
APOSTEL 2.0 Recommendations for Reporting Quantitative Optical Coherence Tomography Studies
Aykut Aytulun, Andrés Cruz-Herranz, Orhan Aktas, et al.
Hereditary Cancer in Clinical Practice
|
March 13, 2019
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
Toni T Seppälä, Aysel Ahadova, Mev Dominguez-Valentin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants
Hongyan Li, Christoph Engel, Miguel de la Hoya, et al.
CNS Drugs
|
September 18, 2021
Natalizumab Versus Fingolimod in Patients with Relapsing-Remitting Multiple Sclerosis: A Subgroup Analysis From Three International Cohorts
Sifat Sharmin, Mathilde Lefort, Johanna Balslev Andersen, et al.
Communications Biology
|
October 6, 2022
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
Christopher Hakkaart, John F Pearson, Louise Marquart, et al.
Journal of the National Cancer Institute
|
July 28, 2021
Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores
Daniel R Barnes, Valentina Silvestri, Goska Leslie, et al.
Hereditary Cancer in Clinical Practice
|
October 1, 2022
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
Pål Møller, Toni Seppälä, James G Dowty, et al.
Human Mutation
|
May 28, 2019
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
Michael T Parsons, Emma Tudini, Hongyan Li, et al.
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of 19