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A Swaroop

Showing results (61-70 of 96) with videos related to

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Genomics|February 1, 1996
Characterization and sequence analysis of the human homeobox-containing gene GBX2X Lin, A Swaroop, F M Vaccarino, et al.
Genomics|November 5, 1997
Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degenerationQ Farjo, A Jackson, S Pieke-Dahl, et al.
Ophthalmology|December 17, 1998
X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60G A Fishman, S Grover, S G Jacobson, et al.
Novartis Foundation Symposium|January 31, 2004
From disease genes to cellular pathways: a progress reportJ Yu, A J Mears, S Yoshida, et al.
Nature Genetics|November 6, 2001
Nrl is required for rod photoreceptor developmentA J Mears, M Kondo, P K Swain, et al.
Molecular Vision|December 5, 1995
A polymorphic trinucleotide repeat at DXS8170 in the critical region of X-linked retinitis pigmentosa locus RP3 at Xp21.1R Fujita, M Blumberg, D Anderson, et al.
Human Molecular Genetics|February 5, 1999
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor functionA Swaroop, Q L Wang, W Wu, et al.
Journal of Materials Chemistry. B|February 17, 2026
Designing of porous scaffolds for tissue engineering and regenerative medicineRajashree Sahoo, A Swaroop Sanket, Ananya Pattnaik, et al.
American Journal of Physiology. Cell Physiology|August 16, 2000
Cloning and functional expression of human retinal kir2.4, a pH-sensitive inwardly rectifying K(+) channelB A Hughes, G Kumar, Y Yuan, et al.
American Journal of Human Genetics|October 27, 1997
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, et al.
Pageof 10

Showing results (61-70 of 96) with videos related to

Sort By:
Pageof 10
Genomics|February 1, 1996
Characterization and sequence analysis of the human homeobox-containing gene GBX2X Lin, A Swaroop, F M Vaccarino, et al.
Genomics|November 5, 1997
Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degenerationQ Farjo, A Jackson, S Pieke-Dahl, et al.
Ophthalmology|December 17, 1998
X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60G A Fishman, S Grover, S G Jacobson, et al.
Novartis Foundation Symposium|January 31, 2004
From disease genes to cellular pathways: a progress reportJ Yu, A J Mears, S Yoshida, et al.
Nature Genetics|November 6, 2001
Nrl is required for rod photoreceptor developmentA J Mears, M Kondo, P K Swain, et al.
Molecular Vision|December 5, 1995
A polymorphic trinucleotide repeat at DXS8170 in the critical region of X-linked retinitis pigmentosa locus RP3 at Xp21.1R Fujita, M Blumberg, D Anderson, et al.
Human Molecular Genetics|February 5, 1999
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor functionA Swaroop, Q L Wang, W Wu, et al.
Journal of Materials Chemistry. B|February 17, 2026
Designing of porous scaffolds for tissue engineering and regenerative medicineRajashree Sahoo, A Swaroop Sanket, Ananya Pattnaik, et al.
American Journal of Physiology. Cell Physiology|August 16, 2000
Cloning and functional expression of human retinal kir2.4, a pH-sensitive inwardly rectifying K(+) channelB A Hughes, G Kumar, Y Yuan, et al.
American Journal of Human Genetics|October 27, 1997
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, et al.
Pageof 10