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Ingrid Hausser

Showing results (21-30 of 112) with videos related to

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Archives of Gynecology and Obstetrics|May 13, 2008
Restrictive dermopathy: a rare laminopathyMarc Thill, Thuy Duong Nguyen, Manfred Wehnert, et al.
Frontiers in Cell and Developmental Biology|July 25, 2022
Comparative Morphological, Metabolic and Transcriptome Analyses in <i>elmo1</i> <sup></sup> , <i>elmo2</i> <sup></sup> , and <i>elmo3</i> <sup></sup> Zebrafish Mutants Identified a Functional Non-Redundancy of the Elmo ProteinsMike Boger, Katrin Bennewitz, David Philipp Wohlfart, et al.
Molecular Microbiology|January 8, 2013
ClpV recycles VipA/VipB tubules and prevents non-productive tubule formation to ensure efficient type VI protein secretionNicole Kapitein, Gabriele Bönemann, Aleksandra Pietrosiuk, et al.
The Journal of Pediatrics|July 9, 2004
Variable clinical expression of an identical mutation in the ATP7A gene for Menkes disease/occipital horn syndrome in three affected males in a single familyBettina Borm, Lisbeth Birk Møller, Ingrid Hausser, et al.
The Journal of Investigative Dermatology|October 10, 2008
Ichthyosis, follicular atrophoderma, and hypotrichosis caused by mutations in ST14 is associated with impaired profilaggrin processingThomas Alef, Serena Torres, Ingrid Hausser, et al.
The Journal of Investigative Dermatology|February 23, 2016
Collagen VII Half-Life at the Dermal-Epidermal Junction Zone: Implications for Mechanisms and Therapy of GenodermatosesTobias Kühl, Markus Mezger, Ingrid Hausser, et al.
Molecular Genetics & Genomic Medicine|February 15, 2018
Familial aortic disease and a large duplication in chromosome 16p13.1Philipp Erhart, Tobias Brandt, Beate K Straub, et al.
Annals of Neurology|September 3, 2002
Exclusion mapping of the genetic predisposition for cervical artery dissections by linkage analysisCaspar Grond-Ginsbach, Bernhard Klima, Ralf Weber, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 24, 2018
Constitutional absence of epithelial integrin α3 impacts the composition of the cellular microenvironment of ILNEB keratinocytesYinghong He, Kerstin Thriene, Melanie Boerries, et al.
Human Mutation|October 31, 2008
COL5A1 signal peptide mutations interfere with protein secretion and cause classic Ehlers-Danlos syndromeSofie Symoens, Fransiska Malfait, Marjolijn Renard, et al.
Pageof 12

Showing results (21-30 of 112) with videos related to

Sort By:
Pageof 12
Archives of Gynecology and Obstetrics|May 13, 2008
Restrictive dermopathy: a rare laminopathyMarc Thill, Thuy Duong Nguyen, Manfred Wehnert, et al.
Frontiers in Cell and Developmental Biology|July 25, 2022
Comparative Morphological, Metabolic and Transcriptome Analyses in <i>elmo1</i> <sup></sup> , <i>elmo2</i> <sup></sup> , and <i>elmo3</i> <sup></sup> Zebrafish Mutants Identified a Functional Non-Redundancy of the Elmo ProteinsMike Boger, Katrin Bennewitz, David Philipp Wohlfart, et al.
Molecular Microbiology|January 8, 2013
ClpV recycles VipA/VipB tubules and prevents non-productive tubule formation to ensure efficient type VI protein secretionNicole Kapitein, Gabriele Bönemann, Aleksandra Pietrosiuk, et al.
The Journal of Pediatrics|July 9, 2004
Variable clinical expression of an identical mutation in the ATP7A gene for Menkes disease/occipital horn syndrome in three affected males in a single familyBettina Borm, Lisbeth Birk Møller, Ingrid Hausser, et al.
The Journal of Investigative Dermatology|October 10, 2008
Ichthyosis, follicular atrophoderma, and hypotrichosis caused by mutations in ST14 is associated with impaired profilaggrin processingThomas Alef, Serena Torres, Ingrid Hausser, et al.
The Journal of Investigative Dermatology|February 23, 2016
Collagen VII Half-Life at the Dermal-Epidermal Junction Zone: Implications for Mechanisms and Therapy of GenodermatosesTobias Kühl, Markus Mezger, Ingrid Hausser, et al.
Molecular Genetics & Genomic Medicine|February 15, 2018
Familial aortic disease and a large duplication in chromosome 16p13.1Philipp Erhart, Tobias Brandt, Beate K Straub, et al.
Annals of Neurology|September 3, 2002
Exclusion mapping of the genetic predisposition for cervical artery dissections by linkage analysisCaspar Grond-Ginsbach, Bernhard Klima, Ralf Weber, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 24, 2018
Constitutional absence of epithelial integrin α3 impacts the composition of the cellular microenvironment of ILNEB keratinocytesYinghong He, Kerstin Thriene, Melanie Boerries, et al.
Human Mutation|October 31, 2008
COL5A1 signal peptide mutations interfere with protein secretion and cause classic Ehlers-Danlos syndromeSofie Symoens, Fransiska Malfait, Marjolijn Renard, et al.
Pageof 12