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Nature Communications|April 17, 2021
Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune diseaseStephen Watt, Louella Vasquez, Klaudia Walter, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 17, 2023
Incorporating Alternative Polygenic Risk Scores into the BOADICEA Breast Cancer Risk Prediction ModelNasim Mavaddat, Lorenzo Ficorella, Tim Carver, et al.
Genome Biology|January 28, 2017
Genome-wide analysis of differential transcriptional and epigenetic variability across human immune cell typesSimone Ecker, Lu Chen, Vera Pancaldi, et al.
Blood Advances|September 28, 2021
G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1Kate Downes, Xuefei Zhao, Nicholas S Gleadall, et al.
Haematologica|April 18, 2020
Identification of a homozygous recessive variant in <i>PTGS1</i> resulting in a congenital aspirin-like defect in platelet functionMelissa V Chan, Melissa A Hayman, Suthesh Sivapalaratnam, et al.
Blood|January 9, 2017
Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopeniaSuthesh Sivapalaratnam, Sarah K Westbury, Jonathan C Stephens, et al.
Genome Biology|September 6, 2017
Chromosome contacts in activated T cells identify autoimmune disease candidate genesOliver S Burren, Arcadio Rubio García, Biola-Maria Javierre, et al.
Haematologica|July 25, 2020
Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlasLuigi Grassi, Osagie G Izuogu, Natasha A N Jorge, et al.
Cell Reports|November 17, 2016
eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic DataCharles E Breeze, Dirk S Paul, Jenny van Dongen, et al.
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