Search research articles
Contact Us
Filters
Showing results (61-70 of 96) with videos related to
Page
of 10
Sort By:
Genomics
|
February 1, 1996
Characterization and sequence analysis of the human homeobox-containing gene GBX2
X 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 degeneration
Q 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 60
G A Fishman, S Grover, S G Jacobson, et al.
Novartis Foundation Symposium
|
January 31, 2004
From disease genes to cellular pathways: a progress report
J Yu, A J Mears, S Yoshida, et al.
Nature Genetics
|
November 6, 2001
Nrl is required for rod photoreceptor development
A 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 Xp21.1
R 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 function
A 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 medicine
Rajashree 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(+) channel
B 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 families
R Fujita, M Buraczynska, L Gieser, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 96) with videos related to
Sort By:
Page
of 10
Genomics
|
February 1, 1996
Characterization and sequence analysis of the human homeobox-containing gene GBX2
X 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 degeneration
Q 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 60
G A Fishman, S Grover, S G Jacobson, et al.
Novartis Foundation Symposium
|
January 31, 2004
From disease genes to cellular pathways: a progress report
J Yu, A J Mears, S Yoshida, et al.
Nature Genetics
|
November 6, 2001
Nrl is required for rod photoreceptor development
A 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 Xp21.1
R 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 function
A 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 medicine
Rajashree 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(+) channel
B 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 families
R Fujita, M Buraczynska, L Gieser, et al.
Page
of 10