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Human Molecular Genetics|September 27, 2018
Dominant negative GPR161 rare variants are risk factors of human spina bifidaSung-Eun Kim, Yunping Lei, Sun-Hee Hwang, et al.Substance Abuse|February 22, 2021
Personal and professional attitudes associated with nurses' motivation to work with patients with opioid use and opioid use-related problemsKhadejah F Mahmoud, Deborah S Finnell, Susan M Sereika, et al.Science China. Life Sciences|October 20, 2024
Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca<sup>2+</sup> overloadHongyu Li, Qingwen Ma, Yan Xue, et al.Journal of Human Genetics|July 12, 2002
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian populationPatrizia De Marco, Maria Grazia Calevo, Anna Moroni, et al.Clinical Science (London, England : 1979)|January 6, 2019
Rare mutations of <i>ADAM17</i> from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signalingYifang Xie, Anyun Ma, Boshi Wang, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 23, 2013
The transcobalamin receptor knockout mouse: a model for vitamin B12 deficiency in the central nervous systemShao-Chiang Lai, Yasumi Nakayama, Jeffrey M Sequeira, et al.Journal of Immunology (Baltimore, Md. : 1950)|August 21, 2008
PP2A dephosphorylates Elf-1 and determines the expression of CD3zeta and FcRgamma in human systemic lupus erythematosus T cellsYuang-Taung Juang, Ying Wang, Guisen Jiang, et al.Advances in Integrative Medicine|August 25, 2020
The effects of vitamin D on acute viral respiratory infections: A rapid reviewRyan Bradley, Janet Schloss, Danielle Brown, et al.Frontiers in Cell and Developmental Biology|May 7, 2021
Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and ChromatinopathiesChiara Parodi, Elisabetta Di Fede, Angela Peron, et al.Stem Cell Research & Therapy|September 22, 2023
Transcriptomic analysis of stem cells from chorionic villi uncovers the impact of chromosomes 2, 6 and 22 in the clinical manifestations of Down syndromeSalvatore Vaiasicca, Gianmarco Melone, David W James, et al.Pageof 59