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Blood|May 6, 2008
Idiopathic CD4+ lymphocytopenia: natural history and prognostic factorsDimitrios I Zonios, Judith Falloon, John E Bennett, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|September 24, 2017
Incidence, determinants and outcomes of pregnancy-associated hepatitis B flares: A regional hospital-based cohort studyTatyana Kushner, Pamela A Shaw, Ankush Kalra, et al.
The Review of Scientific Instruments|September 22, 2023
A vacuum-compatible cylindrical inertial rotation sensor with picoradian sensitivityM P Ross, J van Dongen, Y Huang, et al.
American Journal of Human Genetics|July 24, 2018
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function AllelesZeynep Coban-Akdemir, Janson J White, Xiaofei Song, et al.
Nature Genetics|March 13, 2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyPetter Strømme, Marie E Mangelsdorf, Marie A Shaw, et al.
Plos Genetics|October 3, 2013
Fusion of large-scale genomic knowledge and frequency data computationally prioritizes variants in epilepsyIan M Campbell, Mitchell Rao, Sean D Arredondo, et al.
Msphere|December 16, 2017
Persistence of Supplemented Bifidobacterium longum subsp. infantis EVC001 in Breastfed InfantsSteven A Frese, Andra A Hutton, Lindsey N Contreras, et al.
Cell Reports. Medicine|November 9, 2022
Nucleocapsid-specific antibody function is associated with therapeutic benefits from COVID-19 convalescent plasma therapyJonathan D Herman, Chuangqi Wang, John Stephen Burke, et al.
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