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Investigative Ophthalmology & Visual Science
|
July 1, 1996
Photoreceptor function in heterozygotes with insertion or deletion mutations in the RDS gene
S G Jacobson, A V Cideciyan, C M Kemp, et al.
Neuroreport
|
April 17, 2001
Melatonin delays photoreceptor degeneration in the rds/rds mouse
F Q Liang, T S Aleman, ZaixinYang, et al.
Investigative Ophthalmology & Visual Science
|
December 1, 1992
X-linked retinitis pigmentosa: functional phenotype of an RP2 genotype
S G Jacobson, A J Roman, A V Cideciyan, et al.
Molecular Vision
|
September 17, 1996
A homozygous PDE6B mutation in a family with autosomal recessive retinitis pigmentosa
M Danciger, V Heilbron, Y Q Gao, et al.
Vision Research
|
November 1, 1996
The enhanced S cone syndrome: an analysis of receptoral and post-receptoral changes
V C Greenstein, Q Zaidi, D C Hood, et al.
Investigative Ophthalmology & Visual Science
|
April 1, 1994
Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa
S G Jacobson, C M Kemp, A V Cideciyan, et al.
Experimental Eye Research
|
November 1, 1996
Preferential rod and cone photoreceptor abnormalities in heterozygotes with point mutations in the RDS gene
S G Jacobson, A V Cideciyan, A M Maguire, et al.
Ophthalmic Genetics
|
March 1, 1996
Analysis of phosducin as a candidate gene for retinopathies
F Ara-Iwata, S G Jacobson, J D Gass, et al.
Investigative Ophthalmology & Visual Science
|
January 1, 1993
Autoantibodies against retinal bipolar cells in cutaneous melanoma-associated retinopathy
A H Milam, J C Saari, S G Jacobson, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
May 1, 1992
Ultrastructure of connecting cilia in different forms of retinitis pigmentosa
S D Barrong, M H Chaitin, S J Fliesler, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 139) with videos related to
Sort By:
Page
of 14
Investigative Ophthalmology & Visual Science
|
July 1, 1996
Photoreceptor function in heterozygotes with insertion or deletion mutations in the RDS gene
S G Jacobson, A V Cideciyan, C M Kemp, et al.
Neuroreport
|
April 17, 2001
Melatonin delays photoreceptor degeneration in the rds/rds mouse
F Q Liang, T S Aleman, ZaixinYang, et al.
Investigative Ophthalmology & Visual Science
|
December 1, 1992
X-linked retinitis pigmentosa: functional phenotype of an RP2 genotype
S G Jacobson, A J Roman, A V Cideciyan, et al.
Molecular Vision
|
September 17, 1996
A homozygous PDE6B mutation in a family with autosomal recessive retinitis pigmentosa
M Danciger, V Heilbron, Y Q Gao, et al.
Vision Research
|
November 1, 1996
The enhanced S cone syndrome: an analysis of receptoral and post-receptoral changes
V C Greenstein, Q Zaidi, D C Hood, et al.
Investigative Ophthalmology & Visual Science
|
April 1, 1994
Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa
S G Jacobson, C M Kemp, A V Cideciyan, et al.
Experimental Eye Research
|
November 1, 1996
Preferential rod and cone photoreceptor abnormalities in heterozygotes with point mutations in the RDS gene
S G Jacobson, A V Cideciyan, A M Maguire, et al.
Ophthalmic Genetics
|
March 1, 1996
Analysis of phosducin as a candidate gene for retinopathies
F Ara-Iwata, S G Jacobson, J D Gass, et al.
Investigative Ophthalmology & Visual Science
|
January 1, 1993
Autoantibodies against retinal bipolar cells in cutaneous melanoma-associated retinopathy
A H Milam, J C Saari, S G Jacobson, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
May 1, 1992
Ultrastructure of connecting cilia in different forms of retinitis pigmentosa
S D Barrong, M H Chaitin, S J Fliesler, et al.
Page
of 14