Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ingrid Hausser

Showing results (31-40 of 112) with videos related to

Pageof 12
Sort By:
Plos One|May 30, 2013
Rat model for dominant dystrophic epidermolysis bullosa: glycine substitution reduces collagen VII stability and shows gene-dosage effectAlexander Nyström, Jens Buttgereit, Michael Bader, et al.
The Journal of Investigative Dermatology|January 6, 2009
Development of an ichthyosiform phenotype in Alox12b-deficient mouse skin transplantsSilvia de Juanes, Nikolas Epp, Susanne Latzko, et al.
The Journal of Biological Chemistry|May 26, 2015
Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis ImperfectaUschi Lindert, Mary Ann Weis, Jyoti Rai, et al.
Metabolism: Clinical and Experimental|February 1, 2025
Combined loss of glyoxalase 1 and aldehyde dehydrogenase 3a1 amplifies dicarbonyl stress, impairs proteasome activity resulting in hyperglycemia and activated retinal angiogenesisShu Li, Hao Li, Katrin Bennewitz, et al.
American Journal of Human Genetics|September 24, 2013
Topical enzyme-replacement therapy restores transglutaminase 1 activity and corrects architecture of transglutaminase-1-deficient skin graftsKarin Aufenvenne, Fernando Larcher, Ingrid Hausser, et al.
Journal of the American Academy of Dermatology|February 10, 2023
Dermatologic manifestations and diagnostic assessments of the Ehlers-Danlos syndromes: A clinical reviewBrent J Doolan, Mark Lavallee, Ingrid Hausser, et al.
The American Journal of Dermatopathology|July 28, 2009
The evolution of osseous metaplasia in localized cutaneous nephrogenic systemic fibrosis: a case reportKatharina Wiedemeyer, Heinz Kutzner, Jerrold L Abraham, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2021
Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagenTibbe Dhooge, Delfien Syx, Trinh Hermanns-Lê, et al.
Journal of Inherited Metabolic Disease|April 14, 2011
Defect in proline synthesis: pyrroline-5-carboxylate reductase 1 deficiency leads to a complex clinical phenotype with collagen and elastin abnormalitiesRita Kretz, Bita Bozorgmehr, Mohamad Hasan Kariminejad, et al.
Journal of the American Academy of Dermatology|August 23, 2011
Ichthyosis prematurity syndrome: clinical evaluation of 17 families with a rare disorder of lipid metabolismDenis Khnykin, Jørgen Rønnevig, Margareta Johnsson, et al.
Pageof 12

Showing results (31-40 of 112) with videos related to

Sort By:
Pageof 12
Plos One|May 30, 2013
Rat model for dominant dystrophic epidermolysis bullosa: glycine substitution reduces collagen VII stability and shows gene-dosage effectAlexander Nyström, Jens Buttgereit, Michael Bader, et al.
The Journal of Investigative Dermatology|January 6, 2009
Development of an ichthyosiform phenotype in Alox12b-deficient mouse skin transplantsSilvia de Juanes, Nikolas Epp, Susanne Latzko, et al.
The Journal of Biological Chemistry|May 26, 2015
Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis ImperfectaUschi Lindert, Mary Ann Weis, Jyoti Rai, et al.
Metabolism: Clinical and Experimental|February 1, 2025
Combined loss of glyoxalase 1 and aldehyde dehydrogenase 3a1 amplifies dicarbonyl stress, impairs proteasome activity resulting in hyperglycemia and activated retinal angiogenesisShu Li, Hao Li, Katrin Bennewitz, et al.
American Journal of Human Genetics|September 24, 2013
Topical enzyme-replacement therapy restores transglutaminase 1 activity and corrects architecture of transglutaminase-1-deficient skin graftsKarin Aufenvenne, Fernando Larcher, Ingrid Hausser, et al.
Journal of the American Academy of Dermatology|February 10, 2023
Dermatologic manifestations and diagnostic assessments of the Ehlers-Danlos syndromes: A clinical reviewBrent J Doolan, Mark Lavallee, Ingrid Hausser, et al.
The American Journal of Dermatopathology|July 28, 2009
The evolution of osseous metaplasia in localized cutaneous nephrogenic systemic fibrosis: a case reportKatharina Wiedemeyer, Heinz Kutzner, Jerrold L Abraham, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2021
Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagenTibbe Dhooge, Delfien Syx, Trinh Hermanns-Lê, et al.
Journal of Inherited Metabolic Disease|April 14, 2011
Defect in proline synthesis: pyrroline-5-carboxylate reductase 1 deficiency leads to a complex clinical phenotype with collagen and elastin abnormalitiesRita Kretz, Bita Bozorgmehr, Mohamad Hasan Kariminejad, et al.
Journal of the American Academy of Dermatology|August 23, 2011
Ichthyosis prematurity syndrome: clinical evaluation of 17 families with a rare disorder of lipid metabolismDenis Khnykin, Jørgen Rønnevig, Margareta Johnsson, et al.
Pageof 12