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Ingrid Hausser

Showing results (101-110 of 112) with videos related to

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The Journal of Investigative Dermatology|September 18, 2020
QR-313, an Antisense Oligonucleotide, Shows Therapeutic Efficacy for Treatment of Dominant and Recessive Dystrophic Epidermolysis Bullosa: A Preclinical StudyOlivier Bornert, Marieke Hogervorst, Pauline Nauroy, et al.
Cellular and Molecular Life Sciences : CMLS|December 16, 2024
Golgi pH elevation due to loss of V-ATPase subunit V0a2 function correlates with tissue-specific glycosylation changes and globozoospermiaJohannes Kopp, Denise Jahn, Guido Vogt, et al.
Human Mutation|July 27, 2019
Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4Nadja Ballin, Alrun Hotz, Emmanuelle Bourrat, et al.
Diabetes|October 17, 2024
Exploring Structural and Molecular Features of Sciatic Nerve Lesions in Diabetic Neuropathy: Unveiling Pathogenic Pathways and TargetsDaniel Schwarz, Maxime Le Marois, Volker Sturm, et al.
Plos Genetics|March 22, 2018
Impaired proteoglycan glycosylation, elevated TGF-β signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplasticaWing Lee Chan, Magdalena Steiner, Tomasz Witkos, et al.
Nature Genetics|January 17, 2012
PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humansAnaïs Grall, Eric Guaguère, Sandrine Planchais, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|October 5, 2017
S1 guidelines for the diagnosis and treatment of ichthyoses - updateVinzenz Oji, Marie-Luise Preil, Barbara Kleinow, et al.
Gastroenterology|July 31, 2019
ECM1 Prevents Activation of Transforming Growth Factor β, Hepatic Stellate Cells, and Fibrogenesis in MiceWeiguo Fan, Tianhui Liu, Wen Chen, et al.
Journal of the American Academy of Dermatology|July 21, 2010
Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009Vinzenz Oji, Gianluca Tadini, Masashi Akiyama, et al.
Neurology|October 31, 2014
Familial occurrence and heritable connective tissue disorders in cervical artery dissectionStéphanie Debette, Barbara Goeggel Simonetti, Sabrina Schilling, et al.
Pageof 12

Showing results (101-110 of 112) with videos related to

Sort By:
Pageof 12
The Journal of Investigative Dermatology|September 18, 2020
QR-313, an Antisense Oligonucleotide, Shows Therapeutic Efficacy for Treatment of Dominant and Recessive Dystrophic Epidermolysis Bullosa: A Preclinical StudyOlivier Bornert, Marieke Hogervorst, Pauline Nauroy, et al.
Cellular and Molecular Life Sciences : CMLS|December 16, 2024
Golgi pH elevation due to loss of V-ATPase subunit V0a2 function correlates with tissue-specific glycosylation changes and globozoospermiaJohannes Kopp, Denise Jahn, Guido Vogt, et al.
Human Mutation|July 27, 2019
Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4Nadja Ballin, Alrun Hotz, Emmanuelle Bourrat, et al.
Diabetes|October 17, 2024
Exploring Structural and Molecular Features of Sciatic Nerve Lesions in Diabetic Neuropathy: Unveiling Pathogenic Pathways and TargetsDaniel Schwarz, Maxime Le Marois, Volker Sturm, et al.
Plos Genetics|March 22, 2018
Impaired proteoglycan glycosylation, elevated TGF-β signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplasticaWing Lee Chan, Magdalena Steiner, Tomasz Witkos, et al.
Nature Genetics|January 17, 2012
PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humansAnaïs Grall, Eric Guaguère, Sandrine Planchais, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|October 5, 2017
S1 guidelines for the diagnosis and treatment of ichthyoses - updateVinzenz Oji, Marie-Luise Preil, Barbara Kleinow, et al.
Gastroenterology|July 31, 2019
ECM1 Prevents Activation of Transforming Growth Factor β, Hepatic Stellate Cells, and Fibrogenesis in MiceWeiguo Fan, Tianhui Liu, Wen Chen, et al.
Journal of the American Academy of Dermatology|July 21, 2010
Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009Vinzenz Oji, Gianluca Tadini, Masashi Akiyama, et al.
Neurology|October 31, 2014
Familial occurrence and heritable connective tissue disorders in cervical artery dissectionStéphanie Debette, Barbara Goeggel Simonetti, Sabrina Schilling, et al.
Pageof 12