Showing results (61-70 of 86) with videos related to

Sort By:
Pageof 9
Pharmacogenomics|September 13, 2023
Integrating pharmacogenomic testing into paired germline and somatic genomic testing in patients with cancerNathan D Seligson, Jill M Kolesar, Benish Alam, et al.
Annals of Surgical Oncology|September 7, 2018
Natural Killer Cell IFNγ Secretion is Profoundly Suppressed Following Colorectal Cancer SurgeryLeonard Angka, Andre B Martel, Marisa Kilgour, et al.
Academic Pediatrics|July 13, 2023
Equity Concerns Across Pediatric Research Recruitment: An Analysis of Research Staff InterviewsElliott Mark Weiss, Kathryn M Porter, Tara R Sullivan, et al.
American Journal of Medical Genetics. Part A|June 7, 2016
A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hairKaren W Gripp, Kimberly A Aldinger, James T Bennett, et al.
Journal of Clinical and Translational Science|June 27, 2017
The Northwest Participant and Clinical Interactions Network: Increasing opportunities for patients to participate in research across the Northwestern United StatesLaura-Mae Baldwin, Laurie Hassell, Cindi Laukes, et al.
American Journal of Human Genetics|June 4, 2019
Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca<sup>2+</sup>-Activated K<sup>+</sup> Channel SK3 Cause Zimmermann-Laband SyndromeChristiane K Bauer, Pauline E Schneeberger, Fanny Kortüm, et al.
Blood|June 4, 2015
CD8+ T cells are predominantly protective and required for effective steroid therapy in murine models of immune thrombocytopeniaLi Ma, Elisa Simpson, June Li, et al.
Lung|October 9, 2020
Postoperative Adverse Events are Associated with Oncologic Recurrence Following Curative-intent Resection for Lung CancerStephen Gowing, Laura Baker, Alexandre Tran, et al.
Lung|November 16, 2020
Correction to: Postoperative Adverse Events are Associated with Oncologic Recurrence Following Curative‑intent Resection for Lung CancerStephen Gowing, Laura Baker, Alexandre Tran, et al.
European Journal of Human Genetics : EJHG|January 10, 2019
Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomaliesMax Krall, Stephanie Htun, Rhonda E Schnur, et al.
Pageof 9