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Investigative Ophthalmology & Visual Science
|
July 1, 1994
RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function
C M Kemp, S G Jacobson, A V Cideciyan, et al.
Human Molecular Genetics
|
August 1, 1994
Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p
J A Knowles, Y Shugart, P Banerjee, et al.
Nature Genetics
|
November 4, 2000
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa
A Gal, Y Li, D A Thompson, et al.
Neuron
|
August 5, 1999
Retinal rod photoreceptor-specific gene mutation perturbs cone pathway development
E Banin, A V Cideciyan, T S Alemán, et al.
Genomics
|
November 1, 1995
Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa
M Danciger, J Blaney, Y Q Gao, et al.
Human Molecular Genetics
|
July 13, 1999
A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus
X Guillonneau, N I Piriev, M Danciger, et al.
Nature Genetics
|
September 1, 1995
Night blindness in Sorsby's fundus dystrophy reversed by vitamin A
S G Jacobson, A V Cideciyan, G Regunath, et al.
Human Mutation
|
December 29, 1999
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans
D J Orten, M D Weston, P M Kelley, 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.
Investigative Ophthalmology & Visual Science
|
November 6, 1998
Relation of optical coherence tomography to microanatomy in normal and rd chickens
Y Huang, A V Cideciyan, G I Papastergiou, et al.
Page
of 14
Search research articles
Search
Showing results (71-80 of 139) with videos related to
Sort By:
Page
of 14
Investigative Ophthalmology & Visual Science
|
July 1, 1994
RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function
C M Kemp, S G Jacobson, A V Cideciyan, et al.
Human Molecular Genetics
|
August 1, 1994
Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p
J A Knowles, Y Shugart, P Banerjee, et al.
Nature Genetics
|
November 4, 2000
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa
A Gal, Y Li, D A Thompson, et al.
Neuron
|
August 5, 1999
Retinal rod photoreceptor-specific gene mutation perturbs cone pathway development
E Banin, A V Cideciyan, T S Alemán, et al.
Genomics
|
November 1, 1995
Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa
M Danciger, J Blaney, Y Q Gao, et al.
Human Molecular Genetics
|
July 13, 1999
A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus
X Guillonneau, N I Piriev, M Danciger, et al.
Nature Genetics
|
September 1, 1995
Night blindness in Sorsby's fundus dystrophy reversed by vitamin A
S G Jacobson, A V Cideciyan, G Regunath, et al.
Human Mutation
|
December 29, 1999
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans
D J Orten, M D Weston, P M Kelley, 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.
Investigative Ophthalmology & Visual Science
|
November 6, 1998
Relation of optical coherence tomography to microanatomy in normal and rd chickens
Y Huang, A V Cideciyan, G I Papastergiou, et al.
Page
of 14