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Brain Research Bulletin|March 28, 2006
Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol-O-methyl transferase (COMT) in multiple sclerosisLotti Tajouri, Virginie Martin, Claudia Gasparini, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 19, 2023
The Chromatin Regulator Mll1 Supports T Follicular Helper Cell Differentiation by Controlling Expression of Bcl6, LEF-1, and TCF-1Simon Bélanger, Sonya Haupt, Caterina E Faliti, et al.
The New England Journal of Medicine|March 31, 2025
Lepodisiran - A Long-Duration Small Interfering RNA Targeting Lipoprotein(a)Steven E Nissen, Wei Ni, Xi Shen, et al.
Translational Stroke Research|July 1, 2022
Assessment of Irreversible Tissue Injury in Extensive Ischemic Stroke-Potential of Quantitative Cerebral PerfusionWolfgang Haupt, Lukas Meyer, Maximilian Wagner, et al.
Human Molecular Genetics|November 22, 2002
Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndromeSiddharth K Prakash, Trena A Cormier, Alanna E McCall, et al.
Neurology|December 25, 2002
Severe neurologic complications after hematopoietic stem cell transplantation in childrenM Faraci, E Lanino, G Dini, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 20, 2007
Interaction of a plant virus-encoded protein with the major nucleolar protein fibrillarin is required for systemic virus infectionSang Hyon Kim, Stuart Macfarlane, Natalia O Kalinina, et al.
BMC Research Notes|July 29, 2010
Analysis of the MTHFR C677T variant with migraine phenotypesAnnie Liu, Saraswathy Menon, Natalie J Colson, et al.
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