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European Journal of Human Genetics : EJHG
|
November 6, 2009
Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects
Vinciane Wouters, Nisha Limaye, Melanie Uebelhoer, et al.
Iscience
|
December 5, 2022
PERIOD 2 regulates low-dose radioprotection via PER2/pGSK3β/β-catenin/Per2 loop
Aris T Alexandrou, Yixin Duan, Shanxiu Xu, et al.
Pharmacogenetics and Genomics
|
February 15, 2013
Nomenclature for alleles of the thiopurine methyltransferase gene
Malin L Appell, Jonathan Berg, John Duley, et al.
European Journal of Human Genetics : EJHG
|
December 6, 2022
Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing
Lynne J Hocking, Claire Andrews, Christine Armstrong, et al.
Breast Cancer Research and Treatment
|
July 9, 2014
TBCRC 018: phase II study of iniparib in combination with irinotecan to treat progressive triple negative breast cancer brain metastases
Carey Anders, Allison M Deal, Vandana Abramson, et al.
Familial Cancer
|
June 19, 2008
Predicting breast cancer risk: implications of a "weak" family history
Elaine Anderson, Jonathan Berg, Roger Black, et al.
The Lancet. Gastroenterology & Hepatology
|
July 9, 2026
Aspirin for cancer prevention in individuals with Lynch syndrome: first results from the CaPP3 multicentre, randomised, double-blind, non-inferiority trial
John Burn, Gillian M Borthwick, Faye Elliott, et al.
Human Molecular Genetics
|
November 11, 2011
Gene-gene interactions in breast cancer susceptibility
Clare Turnbull, Sheila Seal, Anthony Renwick, et al.
Nature Genetics
|
August 9, 2011
Germline mutations in RAD51D confer susceptibility to ovarian cancer
Chey Loveday, Clare Turnbull, Emma Ramsay, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 28, 2024
The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the Clinical Validity of 111 Gene-Disease Relationships
Eleanor Broeren, Vanessa Gitau, Alicia Byrne, et al.
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of 8
Search research articles
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Showing results (61-70 of 75) with videos related to
Sort By:
Page
of 8
European Journal of Human Genetics : EJHG
|
November 6, 2009
Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects
Vinciane Wouters, Nisha Limaye, Melanie Uebelhoer, et al.
Iscience
|
December 5, 2022
PERIOD 2 regulates low-dose radioprotection via PER2/pGSK3β/β-catenin/Per2 loop
Aris T Alexandrou, Yixin Duan, Shanxiu Xu, et al.
Pharmacogenetics and Genomics
|
February 15, 2013
Nomenclature for alleles of the thiopurine methyltransferase gene
Malin L Appell, Jonathan Berg, John Duley, et al.
European Journal of Human Genetics : EJHG
|
December 6, 2022
Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing
Lynne J Hocking, Claire Andrews, Christine Armstrong, et al.
Breast Cancer Research and Treatment
|
July 9, 2014
TBCRC 018: phase II study of iniparib in combination with irinotecan to treat progressive triple negative breast cancer brain metastases
Carey Anders, Allison M Deal, Vandana Abramson, et al.
Familial Cancer
|
June 19, 2008
Predicting breast cancer risk: implications of a "weak" family history
Elaine Anderson, Jonathan Berg, Roger Black, et al.
The Lancet. Gastroenterology & Hepatology
|
July 9, 2026
Aspirin for cancer prevention in individuals with Lynch syndrome: first results from the CaPP3 multicentre, randomised, double-blind, non-inferiority trial
John Burn, Gillian M Borthwick, Faye Elliott, et al.
Human Molecular Genetics
|
November 11, 2011
Gene-gene interactions in breast cancer susceptibility
Clare Turnbull, Sheila Seal, Anthony Renwick, et al.
Nature Genetics
|
August 9, 2011
Germline mutations in RAD51D confer susceptibility to ovarian cancer
Chey Loveday, Clare Turnbull, Emma Ramsay, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 28, 2024
The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the Clinical Validity of 111 Gene-Disease Relationships
Eleanor Broeren, Vanessa Gitau, Alicia Byrne, et al.
Page
of 8