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Human Mutation|July 31, 2025
Genetic Screening of a Nonsyndromic Amelogenesis Imperfecta Patient Cohort Using a Custom smMIP Reagent for Selective Enrichment of Target LociUmmey Hany, Christopher M Watson, Lu Liu, et al.Nature Ecology & Evolution|May 6, 2026
Growing nickel supply from the tropics threatens priority conservation areasJayden Hyman, Laura J Sonter, Eve McDonald-Madden, et al.American Journal of Respiratory and Critical Care Medicine|November 9, 2010
Effects of interleukin-13 blockade on allergen-induced airway responses in mild atopic asthmaGail M Gauvreau, Louis-Philippe Boulet, Donald W Cockcroft, et al.Plos One|April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain developmentChristine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, et al.Journal of Medicinal Chemistry|July 2, 2010
Design and synthesis of novel tricyclic benzoxazines as potent 5-HT(1A/B/D) receptor antagonists leading to the discovery of 6-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}-4H-imidazo[5,1-c][1,4]benzoxazine-3-carboxamide (GSK588045)Steven M Bromidge, Roberto Arban, Barbara Bertani, et al.Arthritis & Rheumatology (Hoboken, N.J.)|November 4, 2024
Characterization of Genetic Landscape and Novel Inflammatory Biomarkers in Patients With Adult-Onset Still's DiseaseJoanne Topping, Leon Chang, Fatima Nadat, et al.Analytical Chemistry|October 7, 2014
Simultaneous measurement of tabun, sarin, soman, cyclosarin, VR, VX, and VM adducts to tyrosine in blood products by isotope dilution UHPLC-MS/MSBrian S Crow, Brooke G Pantazides, Jennifer Quiñones-González, et al.Journal of Medical Genetics|March 8, 2024
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disabilityClaire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, et al.Science (New York, N.Y.)|June 2, 2022
The minimum land area requiring conservation attention to safeguard biodiversityJames R Allan, Hugh P Possingham, Scott C Atkinson, et al.Journal of Medical Genetics|November 18, 2023
Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfectaUmmey Hany, Christopher M Watson, Lu Liu, et al.Pageof 195