Sandra Beck

Affiliations: 
Max Planck Institute for Biological Cybernetics, Tübingen, Baden-Württemberg, Germany 
Website:
http://www.kyb.tuebingen.mpg.de/~sbeck
Google:
"Sandra Beck"
Mean distance: 13.9 (cluster 29)
 
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Publications

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Sothilingam V, Garcia Garrido M, Jiao K, et al. (2015) Retinitis pigmentosa: impact of different Pde6a point mutations on the disease phenotype. Human Molecular Genetics
Garcia Garrido M, Mühlfriedel RL, Beck SC, et al. (2015) Scale Adjustments to Facilitate Two-Dimensional Measurements in OCT Images. Plos One. 10: e0131154
Kohl S, Zobor D, Chiang WC, et al. (2015) Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia. Nature Genetics. 47: 757-65
Antes R, Salomon-Zimri S, Beck SC, et al. (2015) VEGF Mediates ApoE4-Induced Neovascularization and Synaptic Pathology in the Choroid and Retina. Current Alzheimer Research. 12: 323-34
Katiyar R, Weissgerber P, Roth E, et al. (2015) Influence of the β2-Subunit of L-Type Voltage-Gated Cav Channels on the Structural and Functional Development of Photoreceptor Ribbon Synapses. Investigative Ophthalmology & Visual Science. 56: 2312-24
Brennenstuhl C, Tanimoto N, Burkard M, et al. (2015) Targeted ablation of the Pde6h gene in mice reveals cross-species differences in cone and rod phototransduction protein isoform inventory. The Journal of Biological Chemistry. 290: 10242-55
Weinl C, Wasylyk C, Garcia Garrido M, et al. (2014) Elk3 deficiency causes transient impairment in post-natal retinal vascular development and formation of tortuous arteries in adult murine retinae. Plos One. 9: e107048
Pirio Richardson S, Beck S, Bliem B, et al. (2014) Abnormal dorsal premotor-motor inhibition in writer's cramp. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 797-803
Michalakis S, Koch S, Sothilingam V, et al. (2014) Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosa. Advances in Experimental Medicine and Biology. 801: 733-9
Alves CH, Pellissier LP, Vos RM, et al. (2014) Targeted ablation of Crb2 in photoreceptor cells induces retinitis pigmentosa. Human Molecular Genetics. 23: 3384-401
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