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Pediatric Neurology|January 27, 2016
Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-UpAshley M Burris, Bari J Ballew, Joshua B Kentosh, et al.
JAMA Oncology|August 4, 2017
Prevalence of Cancer at Baseline Screening in the National Cancer Institute Li-Fraumeni Syndrome CohortPhuong L Mai, Payal P Khincha, Jennifer T Loud, et al.
The Journal of Experimental Medicine|April 29, 2021
Altered selection on a single self-ligand promotes susceptibility to organ-specific T cell infiltrationDavid E J Klawon, Dana C Gilmore, John D Leonard, et al.
Genes & Development|September 20, 2014
Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1Hande Kocak, Bari J Ballew, Kamlesh Bisht, et al.
Journal of the National Cancer Institute|March 11, 2026
Rare cancers research: Current state of knowledge and emerging opportunities for prevention and interceptionKajal Biswas, Sagar Ghosh, Payal P Khincha, et al.
The Journal of Clinical Investigation|June 3, 2025
Polygenic modifiers impact penetrance and expressivity in telomere biology disordersMichael Poeschla, Uma P Arora, Amanda Walne, et al.
Plos One|July 22, 2015
Pesticide Use and Relative Leukocyte Telomere Length in the Agricultural Health StudyGabriella Andreotti, Jane A Hoppin, Lifang Hou, et al.
BMC Cancer|May 31, 2011
A comprehensive candidate gene approach identifies genetic variation associated with osteosarcomaLisa Mirabello, Kai Yu, Sonja I Berndt, et al.
Molecular Genetics & Genomic Medicine|July 29, 2016
The limitations of qPCR telomere length measurement in diagnosing dyskeratosis congenitaShahinaz M Gadalla, Payal P Khincha, Hormuzd A Katki, et al.
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