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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
January 19, 2013
[Effects of transcorneal electrical stimulation in patients with Stargardt's disease]
T Röck, A Schatz, L Naycheva, et al.
Cell Death & Disease
|
December 6, 2014
DNA methylation and differential gene regulation in photoreceptor cell death
P Farinelli, A Perera, B Arango-Gonzalez, et al.
Ophthalmic Research
|
January 1, 1997
The development of subretinal microphotodiodes for replacement of degenerated photoreceptors
E Zrenner, K D Miliczek, V P Gabel, et al.
Nature Genetics
|
November 5, 1997
Mutations in RPE65 cause Leber's congenital amaurosis
F Marlhens, C Bareil, J M Griffoin, et al.
Genomics
|
August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11
B Wissinger, H Jägle, S Kohl, et al.
American Journal of Human Genetics
|
June 1, 1992
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencing
J A van den Hurk, T J van de Pol, C M Molloy, et al.
Investigative Ophthalmology & Visual Science
|
November 30, 2000
Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration
D A Thompson, P Gyürüs, L L Fleischer, et al.
Nature Genetics
|
August 31, 2001
New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis
M W Seeliger, C Grimm, F Ståhlberg, et al.
Nature Genetics
|
July 14, 1998
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
T M Strom, G Nyakatura, E Apfelstedt-Sylla, et al.
Nano Letters
|
November 19, 2024
Solid-State Nanopores for Spatially Resolved Chemical Neuromodulation
F Vacca, F Galluzzi, M Blanco-Formoso, et al.
Page
of 29
Search research articles
Search
Showing results (271-280 of 284) with videos related to
Sort By:
Page
of 29
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
January 19, 2013
[Effects of transcorneal electrical stimulation in patients with Stargardt's disease]
T Röck, A Schatz, L Naycheva, et al.
Cell Death & Disease
|
December 6, 2014
DNA methylation and differential gene regulation in photoreceptor cell death
P Farinelli, A Perera, B Arango-Gonzalez, et al.
Ophthalmic Research
|
January 1, 1997
The development of subretinal microphotodiodes for replacement of degenerated photoreceptors
E Zrenner, K D Miliczek, V P Gabel, et al.
Nature Genetics
|
November 5, 1997
Mutations in RPE65 cause Leber's congenital amaurosis
F Marlhens, C Bareil, J M Griffoin, et al.
Genomics
|
August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11
B Wissinger, H Jägle, S Kohl, et al.
American Journal of Human Genetics
|
June 1, 1992
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencing
J A van den Hurk, T J van de Pol, C M Molloy, et al.
Investigative Ophthalmology & Visual Science
|
November 30, 2000
Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration
D A Thompson, P Gyürüs, L L Fleischer, et al.
Nature Genetics
|
August 31, 2001
New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis
M W Seeliger, C Grimm, F Ståhlberg, et al.
Nature Genetics
|
July 14, 1998
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
T M Strom, G Nyakatura, E Apfelstedt-Sylla, et al.
Nano Letters
|
November 19, 2024
Solid-State Nanopores for Spatially Resolved Chemical Neuromodulation
F Vacca, F Galluzzi, M Blanco-Formoso, et al.
Page
of 29