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Human Molecular Genetics|September 24, 2011
Retrotransposon activation contributes to fragile X premutation rCGG-mediated neurodegenerationHuiping Tan, Abrar Qurashi, Mickael Poidevin, et al.Genome Research|December 6, 2002
Haplotype and linkage disequilibrium architecture for human cancer-associated genesPenelope E Bonnen, Peggy J Wang, Marek Kimmel, et al.Genomics|August 6, 2002
The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autismTakanori Yamagata, Swaroop Aradhya, Masato Mori, et al.Naunyn-Schmiedeberg'S Archives of Pharmacology|May 19, 2005
[3H]LY334370, a novel radioligand for the 5-HT1F receptor. II. Autoradiographic localization in rat, guinea pig, monkey and human brainVirginia L Lucaites, Joseph H Krushinski, John M Schaus, et al.Behavioral Neuroscience|June 3, 2008
Social behavior in Fmr1 knockout mice carrying a human FMR1 transgeneCorinne M Spencer, Deanna F Graham, Lisa A Yuva-Paylor, et al.Instructional Course Lectures|February 5, 2020
The Opioid Epidemic: Risk Evaluation and Management Strategies for Prescribing OpioidsRobert R Slater, Jennifer Uong, Ranjan Gupta, et al.The Journal of Biological Chemistry|July 12, 2017
Human serine racemase structure/activity relationship studies provide mechanistic insight and point to position 84 as a hot spot for β-elimination functionDavid L Nelson, Greg A Applegate, Matthew L Beio, et al.Current Opinion in Allergy and Clinical Immunology|November 13, 2003
Tracking gene expression in primary immunodeficienciesHaiying Qin, Masafumi Yamada, Lan Tian, et al.American Journal of Human Genetics|May 22, 2026
Polymorphic CGG repeats in gene regulation and diseaseYijing Zhao, Dale Annear, Emily G Allen, et al.Blood|May 15, 2004
Multiple patients with revertant mosaicism in a single Wiskott-Aldrich syndrome familyTaizo Wada, Shepherd H Schurman, G Jayashree Jagadeesh, et al.Pageof 15