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Pediatric Research|August 27, 2009
Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American populationKevin G Broadbelt, Melissa A Barger, David S Paterson, et al.Nature Communications|February 7, 2024
Hormonal steroids induce multidrug resistance and stress response genes in Neisseria gonorrhoeae by binding to MtrRGrace M Hooks, Julio C Ayala, Concerta L Holley, et al.Toxicological Sciences : an Official Journal of the Society of Toxicology|October 1, 2010
Functional genetic variants in the 3'-untranslated region of sulfotransferase isoform 1A1 (SULT1A1) and their effect on enzymatic activityXinfeng Yu, Ishwori B Dhakal, Marjorie Beggs, et al.Proceedings of the National Academy of Sciences of the United States of America|November 23, 2021
Claudin-2 and claudin-12 form independent, complementary pores required to maintain calcium homeostasisMegan R Beggs, Kennedi Young, Wanling Pan, et al.Mutation Research|May 4, 2004
Changes in expression level of genes as a function of time of day in the liver of ratsVarsha G Desai, Carrie L Moland, William S Branham, et al.Skeletal Muscle|February 10, 2015
X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 geneG Diane Shelton, Branden E Rider, Georgina Child, et al.Preventive Veterinary Medicine|November 28, 2025
Prevalence and associated plasmid resistant genome of ESBL and AmpC producing commensal E. coli isolated from lactating cows and pre-weaned calves on dairy farms in Western AustraliaMichele Tree, Frances Brigg, Anne L Barnes, et al.Journal of Cachexia, Sarcopenia and Muscle|May 10, 2024
Integrated multi-omics approach reveals the role of striated muscle preferentially expressed protein kinase in skeletal muscle including its relationship with myospryn complexQifei Li, Jasmine Lin, Shiyu Luo, et al.Proceedings of the National Academy of Sciences of the United States of America|September 15, 2021
Tetraspanin 6 is a regulator of carcinogenesis in colorectal cancerRegina Andrijes, Rahul K Hejmadi, Matthew Pugh, et al.European Journal of Medical Genetics|July 1, 2018
Expanding the phenotypic spectrum associated with OPHN1 variantsTalia S Schwartz, Monica H Wojcik, Renee C Pelletier, et al.Pageof 148