Kirsten A. Wunderlich

Ludwig-Maximilians-Universität München — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

14h-index622citations32works13.02yr avg
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Research Topics

Retinal Development and Disorders(20), Retinal Diseases and Treatments(4), Cellular transport and secretion(4), CRISPR and Genetic Engineering(4), Protist diversity and phylogeny(4)

Publications32 total

The glucocorticoid receptor as a master regulator of the Müller cell response to diabetic conditions in mice
Journal of Neuroinflammation·2024· 13 citedOpen Access
The glucocorticoid receptor as a master regulator of Müller cell gliosis in the diabetic retina
2023Open Access
EVs in the retina: Shining light on extracellular vesicles
Trillium Extracellular Vesicles·2023
Retinal regions shape human and murine Müller cell proteome profile and functionality
Glia·2022· 15 citedOpen Access
Release of VAMP5‐positive extracellular vesicles by retinal Müller glia in vivo
Journal of Extracellular Vesicles·2022· 23 citedOpen Access
Expression and subcellular localization of <i>USH1C</i> /harmonin in human retina provides insights into pathomechanisms and therapy
Human Molecular Genetics·2022· 16 citedOpen Access
Release of VAMP5-positive extracellular vesicles by retinal Müller glia <i>in vivo</i>
2022· 1 citedOpen Access
Early disruption of photoreceptor cell architecture and loss of vision in a humanized pig model of usher syndromes
EMBO Molecular Medicine·2022· 40 citedOpen Access
Expression and subcellular localization of <i>USH1C</i> /harmonin in the human retina provide insights into pathomechanisms and therapy
2021· 1 citedOpen Access
Expression and subcellular localization of USH1C/harmonin in the human retina
Investigative Ophthalmology & Visual Science·2021Open Access
Early Disruption of Photoreceptor Cell Architecture and Loss of Vision in a Humanized Pig Model of Usher Syndrome
2021· 4 cited
Functional characterization of the first missense variant in <i>CEP78</i> , a founder allele associated with cone‐rod dystrophy, hearing loss, and reduced male fertility
Human Mutation·2020· 22 citedOpen Access
Cell-Type-Specific Complement Expression in the Healthy and Diseased Retina
Cell Reports·2019· 94 citedOpen Access
Generation and phenotypic characterization of a transgenic pig for the Usher syndrome type 1C
2019
CiliaCarta: An integrated and validated compendium of ciliary genes
PLoS ONE·2019· 169 citedOpen Access
CiliaCarta: an integrated and validated compendium of ciliary genes
2017· 14 citedOpen Access
Deep Sequencing of the Human Retinae Reveals the Expression of Odorant Receptors
Frontiers in Cellular Neuroscience·2017· 24 citedOpen Access
The USH1G scaffold protein SANS is part of the cytoplasmic dynein transport module in the photoreceptor inner segments
Investigative Ophthalmology & Visual Science·2016Open Access
Novel Findings about the Role of Glial Cells in Retinal Function, Disease, and Therapy
Universitätsbibliothek Tübingen·2016Open Access
A FRAP-Based Method for Monitoring Molecular Transport in Ciliary Photoreceptor Cells In Vivo
Methods in molecular biology·2016
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Frequent Co-authors

Uwe Wolfrum(13), Antje Grosche(10), Lew Kaplan(8), Kerstin Nagel‐Wolfrum(7), Stefanie M. Hauck(6), Anna M. Pfaller(5), Jessica Schäfer(4), Marius Ueffing(3), Karsten Boldt(3), Bernhard H. F. Weber(3), Sophia Grotz(3), G. Dhom(3), Andrea Fischer(3), Anna Döring(3), Helen May‐Simera(3), Eckhard Wolf(3), M. Dominik Fischer(3), Nikolai Klymiuk(3), Thomas Pannicke(3), Eberhart Zrenner(3)