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Biorxiv : the Preprint Server for Biology
|
December 9, 2024
An updated reference genome sequence and annotation reveals gene losses and gains underlying naked mole-rat biology
Dustin J Sokolowski, Mihai Miclăuş, Alexander Nater, et al.
Cancer Research
|
March 17, 2019
Intratumoral Genetic and Functional Heterogeneity in Pediatric Glioblastoma
Mary Hoffman, Aaron H Gillmor, Daniel J Kunz, et al.
Genome Medicine
|
October 27, 2016
Molecular profiling of advanced solid tumors and patient outcomes with genotype-matched clinical trials: the Princess Margaret IMPACT/COMPACT trial
Tracy L Stockley, Amit M Oza, Hal K Berman, et al.
Nature
|
June 29, 2017
Recurrent and functional regulatory mutations in breast cancer
Esther Rheinbay, Prasanna Parasuraman, Jonna Grimsby, et al.
European Journal of Human Genetics : EJHG
|
January 29, 2026
Non-invasive screening in hereditary cancer: a randomized controlled trial to test cell-free DNA-based early detection in the CHARM consortium
Kirsten M Farncombe, Julia A Sobotka, Melyssa Aronson, et al.
Journal for Immunotherapy of Cancer
|
March 15, 2019
An interim report on the investigator-initiated phase 2 study of pembrolizumab immunological response evaluation (INSPIRE)
Derek L Clouthier, Scott C Lien, S Y Cindy Yang, et al.
Viruses
|
August 26, 2023
Characterizing Risk Factors for Hospitalization and Clinical Characteristics in a Cohort of COVID-19 Patients Enrolled in the GENCOV Study
Gregory Morgan, Selina Casalino, Sunakshi Chowdhary, et al.
BMJ Open
|
October 22, 2020
Understanding and responding to COVID-19 in Wales: protocol for a privacy-protecting data platform for enhanced epidemiology and evaluation of interventions
Jane Lyons, Ashley Akbari, Fatemeh Torabi, et al.
Human Mutation
|
July 16, 2015
Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome
Viviana Cordeddu, Jiani C Yin, Cecilia Gunnarsson, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 22, 2017
The Role of Minimal Residual Disease Testing in Myeloma Treatment Selection and Drug Development: Current Value and Future Applications
Kenneth C Anderson, Daniel Auclair, Gary J Kelloff, et al.
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of 61
Search research articles
Search
Showing results (551-560 of 602) with videos related to
Sort By:
Page
of 61
Biorxiv : the Preprint Server for Biology
|
December 9, 2024
An updated reference genome sequence and annotation reveals gene losses and gains underlying naked mole-rat biology
Dustin J Sokolowski, Mihai Miclăuş, Alexander Nater, et al.
Cancer Research
|
March 17, 2019
Intratumoral Genetic and Functional Heterogeneity in Pediatric Glioblastoma
Mary Hoffman, Aaron H Gillmor, Daniel J Kunz, et al.
Genome Medicine
|
October 27, 2016
Molecular profiling of advanced solid tumors and patient outcomes with genotype-matched clinical trials: the Princess Margaret IMPACT/COMPACT trial
Tracy L Stockley, Amit M Oza, Hal K Berman, et al.
Nature
|
June 29, 2017
Recurrent and functional regulatory mutations in breast cancer
Esther Rheinbay, Prasanna Parasuraman, Jonna Grimsby, et al.
European Journal of Human Genetics : EJHG
|
January 29, 2026
Non-invasive screening in hereditary cancer: a randomized controlled trial to test cell-free DNA-based early detection in the CHARM consortium
Kirsten M Farncombe, Julia A Sobotka, Melyssa Aronson, et al.
Journal for Immunotherapy of Cancer
|
March 15, 2019
An interim report on the investigator-initiated phase 2 study of pembrolizumab immunological response evaluation (INSPIRE)
Derek L Clouthier, Scott C Lien, S Y Cindy Yang, et al.
Viruses
|
August 26, 2023
Characterizing Risk Factors for Hospitalization and Clinical Characteristics in a Cohort of COVID-19 Patients Enrolled in the GENCOV Study
Gregory Morgan, Selina Casalino, Sunakshi Chowdhary, et al.
BMJ Open
|
October 22, 2020
Understanding and responding to COVID-19 in Wales: protocol for a privacy-protecting data platform for enhanced epidemiology and evaluation of interventions
Jane Lyons, Ashley Akbari, Fatemeh Torabi, et al.
Human Mutation
|
July 16, 2015
Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome
Viviana Cordeddu, Jiani C Yin, Cecilia Gunnarsson, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 22, 2017
The Role of Minimal Residual Disease Testing in Myeloma Treatment Selection and Drug Development: Current Value and Future Applications
Kenneth C Anderson, Daniel Auclair, Gary J Kelloff, et al.
Page
of 61