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A Pandya

Showing results (201-210 of 217) with videos related to

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American Journal of Human Genetics|July 14, 2001
Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectivelyK Lu, M H Lee, S Hazard, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|May 21, 2023
Effect of the UNOS policy change on rates of rejection, infection, and hospital readmission following heart transplantationAjay S Vaidya, Emily S Lee, Eric S Kawaguchi, et al.
American Journal of Human Genetics|May 1, 1997
Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysisT Zerjal, B Dashnyam, A Pandya, et al.
Critical Care Medicine|January 30, 2026
Recommendations for Advanced Practice Provider Postgraduate Training Programs in the United States: A Work Product of the Advanced Practice Provider Postgraduate Training Task Force of the Society of Critical Care MedicineDiane McLaughlin, Melissa Ricker, Aimee Abide, et al.
Journal of Medical Genetics|June 27, 2001
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafnessT Ben-Yosef, M Wattenhofer, S Riazuddin, et al.
American Journal of Human Genetics|October 16, 1999
Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphismM E Hurles, R Veitia, E Arroyo, et al.
The Journal of Organic Chemistry|May 23, 2013
Synthesis of stereochemically and skeletally diverse fused ring systems from functionalized C-glycosidesBaudouin Gerard, Maurice D Lee, Sivaraman Dandapani, et al.
International Journal of Legal Medicine|January 1, 1997
Evaluation of Y-chromosomal STRs: a multicenter studyM Kayser, A Caglià, D Corach, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Human Genetics|July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsA L DeStefano, L A Cupples, K S Arnos, et al.
Pageof 22

Showing results (201-210 of 217) with videos related to

Sort By:
Pageof 22
American Journal of Human Genetics|July 14, 2001
Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectivelyK Lu, M H Lee, S Hazard, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|May 21, 2023
Effect of the UNOS policy change on rates of rejection, infection, and hospital readmission following heart transplantationAjay S Vaidya, Emily S Lee, Eric S Kawaguchi, et al.
American Journal of Human Genetics|May 1, 1997
Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysisT Zerjal, B Dashnyam, A Pandya, et al.
Critical Care Medicine|January 30, 2026
Recommendations for Advanced Practice Provider Postgraduate Training Programs in the United States: A Work Product of the Advanced Practice Provider Postgraduate Training Task Force of the Society of Critical Care MedicineDiane McLaughlin, Melissa Ricker, Aimee Abide, et al.
Journal of Medical Genetics|June 27, 2001
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafnessT Ben-Yosef, M Wattenhofer, S Riazuddin, et al.
American Journal of Human Genetics|October 16, 1999
Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphismM E Hurles, R Veitia, E Arroyo, et al.
The Journal of Organic Chemistry|May 23, 2013
Synthesis of stereochemically and skeletally diverse fused ring systems from functionalized C-glycosidesBaudouin Gerard, Maurice D Lee, Sivaraman Dandapani, et al.
International Journal of Legal Medicine|January 1, 1997
Evaluation of Y-chromosomal STRs: a multicenter studyM Kayser, A Caglià, D Corach, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Human Genetics|July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsA L DeStefano, L A Cupples, K S Arnos, et al.
Pageof 22