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Regulatory Toxicology and Pharmacology : RTP|January 2, 2023
Re-evaluating the need for chronic toxicity studies with therapeutic monoclonal antibodies, using a weight of evidence approachHsiao-Tzu Chien, Helen Prior, Laura Andrews, et al.
American Journal of Human Genetics|December 24, 2013
Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm developmentMyriam Peyrard-Janvid, Elizabeth J Leslie, Youssef A Kousa, et al.
Psychiatry Research|July 31, 2020
Hallucinations and other psychotic experiences across diagnoses: A comparison of phenomenological featuresMaya J L Schutte, Mascha M J Linszen, Theresa M Marschall, et al.
Nature Genetics|July 19, 2011
Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndromeWalter H A Kahr, Jesse Hinckley, Ling Li, et al.
Scientific Reports|August 19, 2017
Shared peptide binding of HLA Class I and II alleles associate with cutaneous nevirapine hypersensitivity and identify novel risk allelesRebecca Pavlos, Elizabeth J McKinnon, David A Ostrov, et al.
The Journal of Allergy and Clinical Immunology|February 19, 2019
HLA-A*32:01 is strongly associated with vancomycin-induced drug reaction with eosinophilia and systemic symptomsKatherine C Konvinse, Jason A Trubiano, Rebecca Pavlos, et al.
Lancet (London, England)|September 21, 2015
Alcohol consumption and cardiovascular disease, cancer, injury, admission to hospital, and mortality: a prospective cohort studyAndrew Smyth, Koon K Teo, Sumathy Rangarajan, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 24, 2023
Cutting Edge: Polycomb Repressive Complex 1 Subunit Cbx4 Positively Regulates Effector Responses in CD8 T CellsGuilherme A Melo, Tianhao Xu, Carolina Calôba, et al.
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