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JNCI Cancer Spectrum|July 26, 2021
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor StudyJung Kim, Matthew Gianferante, Danielle M Karyadi, et al.
Nature Genetics|April 2, 2014
Rare missense variants in POT1 predispose to familial cutaneous malignant melanomaJianxin Shi, Xiaohong R Yang, Bari Ballew, et al.
Angiogenesis|September 1, 2018
Understanding the evolving phenotype of vascular complications in telomere biology disordersCecilia Higgs, Yanick J Crow, Denise M Adams, et al.
Blood|September 24, 2024
Clonal landscape and clinical outcomes of telomere biology disorders: somatic rescue and cancer mutationsFernanda Gutierrez-Rodrigues, Emma M Groarke, Natthakan Thongon, et al.
The Journal of Clinical Investigation|December 30, 2025
Mutant p53 promotes clonal hematopoiesis through generating a chronic inflammatory microenvironmentSisi Chen, Sergio Barajas, Sasidhar Vemula, et al.
JAMA Oncology|March 20, 2020
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With OsteosarcomaLisa Mirabello, Bin Zhu, Roelof Koster, et al.
Nature Genetics|June 4, 2013
Genome-wide association study identifies two susceptibility loci for osteosarcomaSharon A Savage, Lisa Mirabello, Zhaoming Wang, et al.
Cancer Discovery|June 19, 2015
A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with OsteosarcomaLisa Mirabello, Roelof Koster, Branden S Moriarity, et al.
Nature|May 2, 2003
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune diseaseHironori Ueda, Joanna M M Howson, Laura Esposito, et al.
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