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Ingrid Hausser

Showing results (81-90 of 112) with videos related to

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Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|July 19, 2021
Reduced Acrolein Detoxification in akr1a1a Zebrafish Mutants Causes Impaired Insulin Receptor Signaling and Microvascular AlterationsHaozhe Qi, Felix Schmöhl, Xiaogang Li, et al.
American Journal of Human Genetics|August 10, 2010
Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin diseaseVinzenz Oji, Katja-Martina Eckl, Karin Aufenvenne, et al.
Redox Biology|December 19, 2022
Loss of glyoxalase 2 alters the glucose metabolism in zebrafishChristoph Tobias Tabler, Elisabeth Lodd, Katrin Bennewitz, et al.
Human Mutation|February 11, 2011
New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutationsBert Callewaert, Marjolijn Renard, Vishwanathan Hucthagowder, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 2, 2019
Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene EditingJose Bonafont, Ángeles Mencía, Marta García, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|December 7, 2023
Impaired Detoxification of Trans, Trans-2,4-Decadienal, an Oxidation Product from Omega-6 Fatty Acids, Alters Insulin Signaling, Gluconeogenesis and Promotes Microvascular DiseaseXin Qian, Stephan Klatt, Katrin Bennewitz, et al.
American Journal of Human Genetics|November 28, 2016
Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin FragilityYinghong He, Kristin Maier, Juna Leppert, et al.
American Journal of Human Genetics|September 28, 2011
Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesionDiana C Blaydon, Daniela Nitoiu, Katja-Martina Eckl, et al.
The Journal of Clinical Investigation|April 3, 2008
A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapyAnja Fritsch, Stefan Loeckermann, Johannes S Kern, et al.
Journal of Human Genetics|April 25, 2019
SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancyBjörn Fischer-Zirnsak, Rainer Koenig, Franz Alisch, et al.
Pageof 12

Showing results (81-90 of 112) with videos related to

Sort By:
Pageof 12
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|July 19, 2021
Reduced Acrolein Detoxification in akr1a1a Zebrafish Mutants Causes Impaired Insulin Receptor Signaling and Microvascular AlterationsHaozhe Qi, Felix Schmöhl, Xiaogang Li, et al.
American Journal of Human Genetics|August 10, 2010
Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin diseaseVinzenz Oji, Katja-Martina Eckl, Karin Aufenvenne, et al.
Redox Biology|December 19, 2022
Loss of glyoxalase 2 alters the glucose metabolism in zebrafishChristoph Tobias Tabler, Elisabeth Lodd, Katrin Bennewitz, et al.
Human Mutation|February 11, 2011
New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutationsBert Callewaert, Marjolijn Renard, Vishwanathan Hucthagowder, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 2, 2019
Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene EditingJose Bonafont, Ángeles Mencía, Marta García, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|December 7, 2023
Impaired Detoxification of Trans, Trans-2,4-Decadienal, an Oxidation Product from Omega-6 Fatty Acids, Alters Insulin Signaling, Gluconeogenesis and Promotes Microvascular DiseaseXin Qian, Stephan Klatt, Katrin Bennewitz, et al.
American Journal of Human Genetics|November 28, 2016
Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin FragilityYinghong He, Kristin Maier, Juna Leppert, et al.
American Journal of Human Genetics|September 28, 2011
Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesionDiana C Blaydon, Daniela Nitoiu, Katja-Martina Eckl, et al.
The Journal of Clinical Investigation|April 3, 2008
A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapyAnja Fritsch, Stefan Loeckermann, Johannes S Kern, et al.
Journal of Human Genetics|April 25, 2019
SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancyBjörn Fischer-Zirnsak, Rainer Koenig, Franz Alisch, et al.
Pageof 12