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Bernd Wissinger

Showing results (121-130 of 196) with videos related to

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Ophthalmology|April 27, 2010
OPA1 mutations associated with dominant optic atrophy influence optic nerve head sizePiero Barboni, Michele Carbonelli, Giacomo Savini, et al.
Nature Genetics|July 20, 2004
Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophyAndreas R Janecke, Debra A Thompson, Gerd Utermann, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophiesVeronique B D Kitiratschky, Tanja Grau, Antje Bernd, et al.
The Journal of Biological Chemistry|March 6, 2015
Targeted ablation of the Pde6h gene in mice reveals cross-species differences in cone and rod phototransduction protein isoform inventoryChristina Brennenstuhl, Naoyuki Tanimoto, Markus Burkard, et al.
Human Molecular Genetics|April 23, 2021
A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defectSusanne Kohl, Pablo Llavona, Alexandra Sauer, et al.
Brain : a Journal of Neurology|February 23, 2007
A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophyMarcel V Alavi, Stefanie Bette, Simone Schimpf, et al.
Progress in Retinal and Eye Research|December 19, 2020
Dominant optic atrophy: Culprit mitochondria in the optic nerveGuy Lenaers, Albert Neutzner, Yannick Le Dantec, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 4, 2017
AAV8 Can Induce Innate and Adaptive Immune Response in the Primate EyeFelix F Reichel, Daniyar L Dauletbekov, Reinhild Klein, et al.
Archives of Neurology|September 15, 2010
Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutationsRaffaele Lodi, Caterina Tonon, Maria Lucia Valentino, et al.
Plos One|April 25, 2015
Blue cone monochromacy: visual function and efficacy outcome measures for clinical trialsXunda Luo, Artur V Cideciyan, Alessandro Iannaccone, et al.
Pageof 20

Showing results (121-130 of 196) with videos related to

Sort By:
Pageof 20
Ophthalmology|April 27, 2010
OPA1 mutations associated with dominant optic atrophy influence optic nerve head sizePiero Barboni, Michele Carbonelli, Giacomo Savini, et al.
Nature Genetics|July 20, 2004
Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophyAndreas R Janecke, Debra A Thompson, Gerd Utermann, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophiesVeronique B D Kitiratschky, Tanja Grau, Antje Bernd, et al.
The Journal of Biological Chemistry|March 6, 2015
Targeted ablation of the Pde6h gene in mice reveals cross-species differences in cone and rod phototransduction protein isoform inventoryChristina Brennenstuhl, Naoyuki Tanimoto, Markus Burkard, et al.
Human Molecular Genetics|April 23, 2021
A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defectSusanne Kohl, Pablo Llavona, Alexandra Sauer, et al.
Brain : a Journal of Neurology|February 23, 2007
A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophyMarcel V Alavi, Stefanie Bette, Simone Schimpf, et al.
Progress in Retinal and Eye Research|December 19, 2020
Dominant optic atrophy: Culprit mitochondria in the optic nerveGuy Lenaers, Albert Neutzner, Yannick Le Dantec, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 4, 2017
AAV8 Can Induce Innate and Adaptive Immune Response in the Primate EyeFelix F Reichel, Daniyar L Dauletbekov, Reinhild Klein, et al.
Archives of Neurology|September 15, 2010
Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutationsRaffaele Lodi, Caterina Tonon, Maria Lucia Valentino, et al.
Plos One|April 25, 2015
Blue cone monochromacy: visual function and efficacy outcome measures for clinical trialsXunda Luo, Artur V Cideciyan, Alessandro Iannaccone, et al.
Pageof 20