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Circulation|December 19, 2014
Dual-specificity phosphatase 3 deficiency or inhibition limits platelet activation and arterial thrombosisLucia Musumeci, Marijke J Kuijpers, Karen Gilio, et al.
BMC Medical Genomics|October 26, 2018
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, et al.
Molecular Genetics & Genomic Medicine|January 25, 2017
CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosisGordon K C Leung, Dingge Ying, Christopher C Y Mak, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 19, 2019
Rare SUZ12 variants commonly cause an overgrowth phenotypeSharri S Cyrus, Ana S A Cohen, Ruky Agbahovbe, et al.
ACS Medicinal Chemistry Letters|March 11, 2014
Discovery of ML314, a Brain Penetrant Non-Peptidic β-Arrestin Biased Agonist of the Neurotensin NTR1 ReceptorSatyamaheshwar Peddibhotla, Michael P Hedrick, Paul Hershberger, et al.
Nature Communications|April 29, 2026
The mannose receptor on sinusoidal lining cells mediates two-step bacterial clearance in the human spleenNeama Alnabati, Francesco Flandi, Tareq Al Saoudi, et al.
Epidemiology and Psychiatric Sciences|August 25, 2020
Seasonality of suicide: a multi-country multi-community observational studyJ Yu, D Yang, Y Kim, et al.
Blood|March 12, 2025
Large-scale dependency and drug screens characterize the therapeutic vulnerabilities of Multiple Myeloma with 1qRomanos Sklavenitis-Pistofidis, Elizabeth D Lightbody, Mairead Reidy, et al.
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