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

Yves de Prost

Showing results (41-50 of 46) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 46 results.
The Journal of Investigative Dermatology|February 14, 2002
Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 familiesEmmanuelle Bitoun, Stéphane Chavanas, Alan D Irvine, et al.
The Journal of Allergy and Clinical Immunology|March 19, 2002
Efficacy and safety of tacrolimus ointment compared with that of hydrocortisone acetate ointment in children with atopic dermatitisSakari Reitamo, Edwin J M Van Leent, Vincent Ho, et al.
The Journal of Allergy and Clinical Immunology|March 7, 2006
Proceedings of the 4th Georg Rajka International Symposium on Atopic Dermatitis, Arcachon, France, September 15-17, 2005Alain Taïeb, Jon Hanifin, Kevin Cooper, et al.
Human Mutation|October 28, 2010
Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia casesCéline Cluzeau, Smail Hadj-Rabia, Marguerite Jambou, et al.
The Journal of Investigative Dermatology|October 30, 2009
Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutationsChristine Bodemer, Olivier Hermine, Fabienne Palmérini, et al.
Nature Genetics|January 6, 2009
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosisYaran Wen, Yang Liu, Yiming Xu, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
The Journal of Investigative Dermatology|February 14, 2002
Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 familiesEmmanuelle Bitoun, Stéphane Chavanas, Alan D Irvine, et al.
The Journal of Allergy and Clinical Immunology|March 19, 2002
Efficacy and safety of tacrolimus ointment compared with that of hydrocortisone acetate ointment in children with atopic dermatitisSakari Reitamo, Edwin J M Van Leent, Vincent Ho, et al.
The Journal of Allergy and Clinical Immunology|March 7, 2006
Proceedings of the 4th Georg Rajka International Symposium on Atopic Dermatitis, Arcachon, France, September 15-17, 2005Alain Taïeb, Jon Hanifin, Kevin Cooper, et al.
Human Mutation|October 28, 2010
Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia casesCéline Cluzeau, Smail Hadj-Rabia, Marguerite Jambou, et al.
The Journal of Investigative Dermatology|October 30, 2009
Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutationsChristine Bodemer, Olivier Hermine, Fabienne Palmérini, et al.
Nature Genetics|January 6, 2009
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosisYaran Wen, Yang Liu, Yiming Xu, et al.
Pageof 5