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Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 15, 2006
Association of the progesterone receptor gene with breast cancer risk: a single-nucleotide polymorphism tagging approachKaren A Pooley, Catherine S Healey, Paula L Smith, et al.Orphanet Journal of Rare Diseases|May 18, 2013
A combination of mutations in AKR1D1 and SKIV2L in a family with severe infantile liver diseaseNeil V Morgan, Jane L Hartley, Kenneth D R Setchell, et al.Annals of Surgery|February 1, 2018
Whole Genome Methylation Analysis of Nondysplastic Barrett Esophagus that Progresses to Invasive CancerMark P Dilworth, Tom Nieto, Jo D Stockton, et al.Journal of the National Cancer Institute|June 17, 2004
Polymorphisms associated with circulating sex hormone levels in postmenopausal womenAlison M Dunning, Mitch Dowsett, Catherine S Healey, et al.Cancer Research Communications|August 11, 2023
MHC Class II is Induced by IFNγ and Follows Three Distinct Patterns of Expression in Colorectal Cancer OrganoidsOliver J Pickles, Kasun Wanigasooriya, Anetta Ptasinska, et al.Frontiers in Oncology|July 21, 2022
Patient Derived Organoids Confirm That PI3K/AKT Signalling Is an Escape Pathway for Radioresistance and a Target for Therapy in Rectal CancerKasun Wanigasooriya, Joao D Barros-Silva, Louise Tee, et al.The Journal of Clinical Investigation|May 30, 2009
Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystoniaManju A Kurian, Juan Zhen, Shu-Yuan Cheng, et al.Acta Neuropathologica Communications|December 6, 2014
Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndromeArthur B McKie, Atif Alsaedi, Julie Vogt, et al.Gastroenterology|February 24, 2010
Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy)Jane Louise Hartley, Nicholas C Zachos, Ban Dawood, et al.Human Genetics|August 10, 2006
Clinical and molecular genetic features of ARC syndromePaul Gissen, Louise Tee, Colin A Johnson, et al.Pageof 3