Gesine Huber
Tuebingen, BW, Germany
Last Updated: 09/26/2026
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Found 13 publications
Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel-associated retinopathy.
Journal: The Journal of clinical investigation
Published: July 10, 2017
AAV-Mediated Gene Supplementation Therapy in Achromatopsia Type 2: Preclinical Data on Therapeutic Time Window and Long-Term Effects.
Journal: Frontiers in neuroscience
Published: February 28, 2017
Targeted ablation of the Pde6h gene in mice reveals cross-species differences in cone and rod phototransduction protein isoform inventory.
Journal: The Journal of biological chemistry
Published: September 18, 2014
Substance abuse and pregnancy from an obstetric point of view
Journal: Zeitschrift fur Geburtshilfe und Neonatologie
Published: August 16, 2014
Targeted ablation of CRB1 and CRB2 in retinal progenitor cells mimics Leber congenital amaurosis.
Journal: PLoS genetics
Published: September 10, 2013
Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene.
Journal: Human molecular genetics
Published: September 25, 2012
Endothelial SRF/MRTF ablation causes vascular disease phenotypes in murine retinae.
Journal: The Journal of clinical investigation
Published: April 06, 2012
Relevance of exocytotic glutamate release from retinal glia.
Journal: Neuron
Published: March 07, 2012
Novel uses of afterbirth tissues in regenerative medicine
Journal: Zeitschrift fur Geburtshilfe und Neonatologie
Published: February 15, 2012
Gene therapy restores missing cone-mediated vision in the CNGA3-/- mouse model of achromatopsia.
Journal: Advances in experimental medicine and biology
Published: December 21, 2011
In vivo assessment of rodent retinal structure using spectral domain optical coherence tomography.
Journal: Advances in experimental medicine and biology
Published: December 21, 2011
Last Updated: 09/26/2026