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A Pandya

Showing results (191-200 of 217) with videos related to

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Human Molecular Genetics|December 14, 2001
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafnessX Z Liu, X J Xia, J Adams, et al.
Journal of the American Chemical Society|May 10, 2012
Rendering protein-based particles transiently insoluble for therapeutic applicationsJing Xu, Jin Wang, J Christopher Luft, et al.
Journal of Natural Products|April 20, 2018
Absolute Configuration and Pharmacology of the Poison Frog Alkaloid PhantasmidineRichard W Fitch, Barry B Snider, Quan Zhou, et al.
Chemical Biology & Drug Design|September 12, 2015
Targeting Bacterial Cell Wall Peptidoglycan Synthesis by Inhibition of Glycosyltransferase ActivityMichael F Mesleh, Premraj Rajaratnam, Mary Conrad, et al.
Human Molecular Genetics|February 3, 2000
A polymorphic L1 retroposon insertion in the centromere of the human Y chromosomeF R Santos, A Pandya, M Kayser, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communitiesM H Lee, D Gordon, J Ott, et al.
Human Heredity|May 9, 2000
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutationsS H Blanton, A Pandya, B L Landa, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 3, 2009
A global survey of the role of ultraviolet radiation and hormonal influences in the development of melasmaJ P Ortonne, I Arellano, M Berneburg, et al.
Human Molecular Genetics|November 1, 1996
Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal malesM A Jobling, V Samara, A Pandya, et al.
Journal of Medical Genetics|August 6, 2002
A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qterS H Blanton, C Y Liang, M W Cai, et al.
Pageof 22

Showing results (191-200 of 217) with videos related to

Sort By:
Pageof 22
Human Molecular Genetics|December 14, 2001
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafnessX Z Liu, X J Xia, J Adams, et al.
Journal of the American Chemical Society|May 10, 2012
Rendering protein-based particles transiently insoluble for therapeutic applicationsJing Xu, Jin Wang, J Christopher Luft, et al.
Journal of Natural Products|April 20, 2018
Absolute Configuration and Pharmacology of the Poison Frog Alkaloid PhantasmidineRichard W Fitch, Barry B Snider, Quan Zhou, et al.
Chemical Biology & Drug Design|September 12, 2015
Targeting Bacterial Cell Wall Peptidoglycan Synthesis by Inhibition of Glycosyltransferase ActivityMichael F Mesleh, Premraj Rajaratnam, Mary Conrad, et al.
Human Molecular Genetics|February 3, 2000
A polymorphic L1 retroposon insertion in the centromere of the human Y chromosomeF R Santos, A Pandya, M Kayser, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communitiesM H Lee, D Gordon, J Ott, et al.
Human Heredity|May 9, 2000
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutationsS H Blanton, A Pandya, B L Landa, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 3, 2009
A global survey of the role of ultraviolet radiation and hormonal influences in the development of melasmaJ P Ortonne, I Arellano, M Berneburg, et al.
Human Molecular Genetics|November 1, 1996
Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal malesM A Jobling, V Samara, A Pandya, et al.
Journal of Medical Genetics|August 6, 2002
A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qterS H Blanton, C Y Liang, M W Cai, et al.
Pageof 22