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Clinical Genetics|April 1, 1993
Deletion analysis maps ocular albinism proximal to the steroid sulphatase locusP M Bouloux, J Kirk, P Munroe, et al.
Diabetes Care|June 1, 1989
Effects of combined insulin-sulfonylurea therapy in type II patientsM S Lewitt, V K Yu, G C Rennie, et al.
The Journal of Steroid Biochemistry and Molecular Biology|July 25, 2017
Calcitriol-mediated reduction in IFN-γ output in T cell large granular lymphocytic leukemia requires vitamin D receptor upregulationPaige M Kulling, Kristine C Olson, Thomas L Olson, et al.
Journal of Molecular and Cellular Cardiology|March 1, 1988
Hypertrophic and functional response to experimental chronic aortic regurgitationN M Magid, M S Young, D C Wallerson, et al.
Case Reports in Genetics|October 29, 2025
RAPSN-Associated Congenital Myasthenic Syndrome due to Biallelic Single Nucleotide Variants at the Same PositionLaura Keehan, Jennefer N Carter, Elijah Kravets, et al.
Research Square|August 26, 2024
EditABLE: A Simple Web Application for Designing Genome Editing ExperimentsDemetrios S Maxim, David Wei Wu, Najani Shanee Johnson, et al.
The Journal of Biological Chemistry|November 24, 1999
Xanthine phosphoribosyltransferase from Leishmania donovani. Molecular cloning, biochemical characterization, and genetic analysisA Jardim, S E Bergeson, S Shih, et al.
The Quarterly Journal of Medicine|January 1, 1981
The congenital "magnesium-losing kidney". Report of two patientsR A Evans, J N Carter, C R George, et al.
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