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Carcinogenesis|June 10, 2010
Genetic variation at chromosome 8q24 in osteosarcoma cases and controlsLisa Mirabello, Sonja I Berndt, Guillermo F Seratti, et al.
The Journal of Trauma|November 11, 2009
A ten-year review of enterocutaneous fistulas after laparotomy for traumaPeter E Fischer, Timothy C Fabian, Louis J Magnotti, et al.
Frontiers in Physiology|July 24, 2023
Chronic intermittent hypoxia promotes glomerular hyperfiltration and potentiates hypoxia-evoked decreases in renal perfusion and PO2Kiefer W Kious, Kalie A Savage, Stephanie C E Twohey, et al.
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.
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