Showing results (221-230 of 482) with videos related to
Sort By:
Pageof 49
Journal of Molecular Biology|May 11, 2019
PhyreRisk: A Dynamic Web Application to Bridge Genomics, Proteomics and 3D Structural Data to Guide Interpretation of Human Genetic VariantsTochukwu C Ofoegbu, Alessia David, Lawrence A Kelley, et al.Cancer Research|July 5, 2002
Identification of cyclin D1 and other novel targets for the von Hippel-Lindau tumor suppressor gene by expression array analysis and investigation of cyclin D1 genotype as a modifier in von Hippel-Lindau diseaseMalgorzata Zatyka, Nancy Fernandes da Silva, Steven C Clifford, et al.Nature Genetics|September 19, 2018
Promoter capture Hi-C-based identification of recurrent noncoding mutations in colorectal cancerGiulia Orlando, Philip J Law, Alex J Cornish, et al.Scientific Reports|July 25, 2015
Implementation of genome-wide complex trait analysis to quantify the heritability in multiple myelomaJonathan S Mitchell, David C Johnson, Kevin Litchfield, et al.Clinical Dysmorphology|September 8, 2006
A form of autosomal dominant spondyloepiphyseal dysplasia is caused by a glycine to alanine substitution in the COL2A1 geneGabrielle S Sellick, Kristein P Hoornaert, Geert R Mortier, et al.Haematologica|March 17, 2004
The diagnostic value of CD123 in B-cell disorders with hairy or villous lymphocytesIlaria Del Giudice, Estella Matutes, Ricardo Morilla, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|August 1, 2020
Pathway Analysis of Renal Cell Carcinoma Genome-Wide Association Studies Identifies Novel AssociationsMark P Purdue, Lei Song, Ghislaine Scélo, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 13, 2011
Mutational status of the TP53 gene as a predictor of response and survival in patients with chronic lymphocytic leukemia: results from the LRF CLL4 trialDavid Gonzalez, Pilar Martinez, Rachel Wade, et al.NPJ Precision Oncology|May 6, 2026
Germline haploinsufficiency of MUTYH causes mutational signature SBS18 in multiple tumour types and specifically raises colorectal cancer riskKitty Sherwood, Juan Fernandez-Tajes, Güler Gül, et al.Neuro-Oncology|November 20, 2012
Association between glioma susceptibility loci and tumour pathology defines specific molecular etiologiesAnna Luisa Di Stefano, Victor Enciso-Mora, Yannick Marie, et al.Pageof 49