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

Heiko Traupe

Showing results (41-50 of 80) with videos related to

Pageof 8
Sort By:
Molecular and Cellular Endocrinology|August 18, 2016
Role of steroid sulfatase in steroid homeostasis and characterization of the sulfated steroid pathway: Evidence from steroid sulfatase deficiencyAlberto Sánchez-Guijo, Jens Neunzig, Adrian Gerber, et al.
The Journal of Investigative Dermatology|September 19, 2008
Genetic variants of the IL-23R pathway: association with psoriatic arthritis and psoriasis vulgaris, but no specific risk factor for arthritisUlrike Hüffmeier, Jesús Lascorz, Beate Böhm, et al.
Dermatopathology (Basel, Switzerland)|March 27, 2026
Defining Histological Patterns in Inherited Ichthyoses: Toward a Diagnostic Algorithm Based on 66 Confirmed CasesKira Süßmuth, Vinzenz Oji, Jacqueline Bodes, et al.
The Journal of Investigative Dermatology|June 19, 2009
In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growthSandra M Pasternack, Ivar von Kügelgen, Melanie Müller, et al.
The Journal of Investigative Dermatology|November 22, 2005
Systematic linkage disequilibrium analysis of SLC12A8 at PSORS5 confirms a role in susceptibility to psoriasis vulgarisUlrike Hüffmeier, Jesús Lascorz, Heiko Traupe, et al.
The Journal of Investigative Dermatology|February 4, 2006
Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritisUlrike Hüffmeier, André Reis, Michael Steffens, et al.
American Journal of Human Genetics|June 10, 2020
Mutations in ASPRV1 Cause Dominantly Inherited IchthyosisLynn M Boyden, Jing Zhou, Ronghua Hu, et al.
The Journal of Investigative Dermatology|December 30, 2006
The alpha and beta subunits of the metalloprotease meprin are expressed in separate layers of human epidermis, revealing different functions in keratinocyte proliferation and differentiationChristoph Becker-Pauly, Markus Höwel, Tatjana Walker, et al.
The Journal of Investigative Dermatology|July 16, 2010
Processing of procollagen III by meprins: new players in extracellular matrix assembly?Daniel Kronenberg, Bernd C Bruns, Catherine Moali, et al.
Human Molecular Genetics|September 14, 2006
Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotypeVinzenz Oji, Juliette Mazereeuw Hautier, Bijan Ahvazi, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Molecular and Cellular Endocrinology|August 18, 2016
Role of steroid sulfatase in steroid homeostasis and characterization of the sulfated steroid pathway: Evidence from steroid sulfatase deficiencyAlberto Sánchez-Guijo, Jens Neunzig, Adrian Gerber, et al.
The Journal of Investigative Dermatology|September 19, 2008
Genetic variants of the IL-23R pathway: association with psoriatic arthritis and psoriasis vulgaris, but no specific risk factor for arthritisUlrike Hüffmeier, Jesús Lascorz, Beate Böhm, et al.
Dermatopathology (Basel, Switzerland)|March 27, 2026
Defining Histological Patterns in Inherited Ichthyoses: Toward a Diagnostic Algorithm Based on 66 Confirmed CasesKira Süßmuth, Vinzenz Oji, Jacqueline Bodes, et al.
The Journal of Investigative Dermatology|June 19, 2009
In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growthSandra M Pasternack, Ivar von Kügelgen, Melanie Müller, et al.
The Journal of Investigative Dermatology|November 22, 2005
Systematic linkage disequilibrium analysis of SLC12A8 at PSORS5 confirms a role in susceptibility to psoriasis vulgarisUlrike Hüffmeier, Jesús Lascorz, Heiko Traupe, et al.
The Journal of Investigative Dermatology|February 4, 2006
Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritisUlrike Hüffmeier, André Reis, Michael Steffens, et al.
American Journal of Human Genetics|June 10, 2020
Mutations in ASPRV1 Cause Dominantly Inherited IchthyosisLynn M Boyden, Jing Zhou, Ronghua Hu, et al.
The Journal of Investigative Dermatology|December 30, 2006
The alpha and beta subunits of the metalloprotease meprin are expressed in separate layers of human epidermis, revealing different functions in keratinocyte proliferation and differentiationChristoph Becker-Pauly, Markus Höwel, Tatjana Walker, et al.
The Journal of Investigative Dermatology|July 16, 2010
Processing of procollagen III by meprins: new players in extracellular matrix assembly?Daniel Kronenberg, Bernd C Bruns, Catherine Moali, et al.
Human Molecular Genetics|September 14, 2006
Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotypeVinzenz Oji, Juliette Mazereeuw Hautier, Bijan Ahvazi, et al.
Pageof 8