Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

B Wissinger

Showing results (51-60 of 61) with videos related to

Pageof 7
Sort By:
Human Molecular Genetics|August 25, 2000
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21S Kohl, B Baumann, M Broghammer, et al.
International Journal of Molecular Medicine|February 15, 2001
Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneityC M Pusch, J Maurer, J Ramser, et al.
Nature Genetics|October 4, 2000
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28C Alexander, M Votruba, U E Pesch, et al.
Genomics|August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11B Wissinger, H Jägle, S Kohl, et al.
Cellular and Molecular Life Sciences : CMLS|May 15, 2010
Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 miceK Schaeferhoff, S Michalakis, N Tanimoto, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chainI Wittig, P Augstein, G K Brown, et al.
Nature Genetics|November 4, 2000
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat proteinC M Pusch, C Zeitz, O Brandau, et al.
Cell Death & Disease|December 14, 2011
A new vicious cycle involving glutamate excitotoxicity, oxidative stress and mitochondrial dynamicsD Nguyen, M V Alavi, K-Y Kim, et al.
American Journal of Human Genetics|June 5, 2001
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) geneA I den Hollander, J R Heckenlively, L I van den Born, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|August 25, 2000
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21S Kohl, B Baumann, M Broghammer, et al.
International Journal of Molecular Medicine|February 15, 2001
Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneityC M Pusch, J Maurer, J Ramser, et al.
Nature Genetics|October 4, 2000
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28C Alexander, M Votruba, U E Pesch, et al.
Genomics|August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11B Wissinger, H Jägle, S Kohl, et al.
Cellular and Molecular Life Sciences : CMLS|May 15, 2010
Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 miceK Schaeferhoff, S Michalakis, N Tanimoto, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chainI Wittig, P Augstein, G K Brown, et al.
Nature Genetics|November 4, 2000
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat proteinC M Pusch, C Zeitz, O Brandau, et al.
Cell Death & Disease|December 14, 2011
A new vicious cycle involving glutamate excitotoxicity, oxidative stress and mitochondrial dynamicsD Nguyen, M V Alavi, K-Y Kim, et al.
American Journal of Human Genetics|June 5, 2001
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) geneA I den Hollander, J R Heckenlively, L I van den Born, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Pageof 7