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Katharina Dannhausen

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Methods in Molecular Biology (Clifton, N.J.)|March 23, 2018
Microglia Analysis in Retinal Degeneration Mouse ModelsKatharina Dannhausen, Khalid Rashid, Thomas Langmann
Methods in Molecular Biology (Clifton, N.J.)|October 17, 2018
Testing for Known Retinal Degeneration Mutants in Mouse StrainsKhalid Rashid, Katharina Dannhausen, Thomas Langmann
Disease Models & Mechanisms|July 26, 2018
Immunomodulation with minocycline rescues retinal degeneration in juvenile neuronal ceroid lipofuscinosis mice highly susceptible to light damageKatharina Dannhausen, Christoph Möhle, Thomas Langmann
Biochemistry and Biophysics Reports|December 8, 2017
Crocin, a plant-derived carotenoid, modulates microglial reactivityMücella Arikan Yorgun, Khalid Rashid, Alexander Aslanidis, et al.
Biochemical and Biophysical Research Communications|July 2, 2015
Acid sphingomyelinase (aSMase) deficiency leads to abnormal microglia behavior and disturbed retinal functionKatharina Dannhausen, Marcus Karlstetter, Albert Caramoy, et al.
Scientific Reports|February 19, 2016
Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7Kristof Van Schil, Marcus Karlstetter, Alexander Aslanidis, et al.
Human Molecular Genetics|May 17, 2014
Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degenerationMarcus Karlstetter, Nasrin Sorusch, Albert Caramoy, et al.
Scientific Reports|April 15, 2018
Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retinaSusanne C Beck, Marcus Karlstetter, Marina Garcia Garrido, et al.
Journal of Neuroinflammation|January 15, 2017
Age-related macular degeneration associated polymorphism rs10490924 in ARMS2 results in deficiency of a complement activatorSven Micklisch, Yuchen Lin, Saskia Jacob, et al.
American Journal of Human Genetics|August 4, 2016
Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in UbiquitinationFrauke Coppieters, Giulia Ascari, Katharina Dannhausen, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|March 23, 2018
Microglia Analysis in Retinal Degeneration Mouse ModelsKatharina Dannhausen, Khalid Rashid, Thomas Langmann
Methods in Molecular Biology (Clifton, N.J.)|October 17, 2018
Testing for Known Retinal Degeneration Mutants in Mouse StrainsKhalid Rashid, Katharina Dannhausen, Thomas Langmann
Disease Models & Mechanisms|July 26, 2018
Immunomodulation with minocycline rescues retinal degeneration in juvenile neuronal ceroid lipofuscinosis mice highly susceptible to light damageKatharina Dannhausen, Christoph Möhle, Thomas Langmann
Biochemistry and Biophysics Reports|December 8, 2017
Crocin, a plant-derived carotenoid, modulates microglial reactivityMücella Arikan Yorgun, Khalid Rashid, Alexander Aslanidis, et al.
Biochemical and Biophysical Research Communications|July 2, 2015
Acid sphingomyelinase (aSMase) deficiency leads to abnormal microglia behavior and disturbed retinal functionKatharina Dannhausen, Marcus Karlstetter, Albert Caramoy, et al.
Scientific Reports|February 19, 2016
Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7Kristof Van Schil, Marcus Karlstetter, Alexander Aslanidis, et al.
Human Molecular Genetics|May 17, 2014
Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degenerationMarcus Karlstetter, Nasrin Sorusch, Albert Caramoy, et al.
Scientific Reports|April 15, 2018
Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retinaSusanne C Beck, Marcus Karlstetter, Marina Garcia Garrido, et al.
Journal of Neuroinflammation|January 15, 2017
Age-related macular degeneration associated polymorphism rs10490924 in ARMS2 results in deficiency of a complement activatorSven Micklisch, Yuchen Lin, Saskia Jacob, et al.
American Journal of Human Genetics|August 4, 2016
Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in UbiquitinationFrauke Coppieters, Giulia Ascari, Katharina Dannhausen, et al.
Pageof 2