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Proceedings of the National Academy of Sciences of the United States of America|March 30, 2022
CSF-1 maintains pathogenic but not homeostatic myeloid cells in the central nervous system during autoimmune neuroinflammationDaniel Hwang, Maryam S Seyedsadr, Larissa Lumi Watanabe Ishikawa, et al.
Journal of Neurodevelopmental Disorders|April 29, 2023
Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disordersJoseph T Glessner, Munir E Khan, Xiao Chang, et al.
FEBS Letters|May 7, 2021
Serum levels of the IgA isotype switch factor TGF-β1 are elevated in patients with COVID-19Er-Yi Wang, Hao Chen, Bao-Qing Sun, et al.
Human Molecular Genetics|June 5, 2015
A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radiusAlessandra Chesi, Jonathan A Mitchell, Heidi J Kalkwarf, et al.
The Journal of Clinical Endocrinology and Metabolism|November 24, 2012
Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide studyTie-Lin Yang, Yan Guo, Hui Shen, et al.
American Journal of Medical Genetics. Part A|December 8, 2011
Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairmentLauren J Francey, Laura K Conlin, Hanna E Kadesch, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|February 26, 2014
Sex differences in the effect of puberty on hippocampal morphologyTheodore D Satterthwaite, Simon Vandekar, Daniel H Wolf, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|March 20, 2024
Causal effect of serum 25 hydroxyvitamin D concentration on cardioembolic stroke: Evidence from two-sample Mendelian randomizationDanial Habibi, Farshad Teymoori, Navid Ebrahimi, et al.
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