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Clinical and Translational Gastroenterology|March 8, 2018
Food allergen triggers are increased in children with the TSLP risk allele and eosinophilic esophagitisLisa M Fahey, Prasanna M Chandramouleeswaran, Shaobo Guan, et al.
Blood|February 11, 2021
RUNX-1 haploinsufficiency causes a marked deficiency of megakaryocyte-biased hematopoietic progenitor cellsBrian Estevez, Sara Borst, Danuta Jarocha, et al.
American Journal of Medical Genetics. Part A|May 7, 2021
A new syndrome of moyamoya disease, kidney dysplasia, aminotransferase elevation, and skin disease associated with de novo variants in RNF213Alanna Strong, Gina O'Grady, Evelyn Shih, et al.
Plos One|June 4, 2010
Common variation in ISL1 confers genetic susceptibility for human congenital heart diseaseKristen N Stevens, Hakon Hakonarson, Cecilia E Kim, et al.
Science Immunology|October 24, 2020
A distinct GM-CSF+ T helper cell subset requires T-bet to adopt a TH1 phenotype and promote neuroinflammationJavad Rasouli, Giacomo Casella, Satoshi Yoshimura, et al.
Journal of Pediatric Urology|May 8, 2025
Genetic analysis of two bladder exstrophy populations of South Asian and North American originJohn K Weaver, Dana A Weiss, Austin Thompson, et al.
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.
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