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

C Rossier

Showing results (261-270 of 295) with videos related to

Pageof 30
Sort By:
Genomics|February 18, 1998
Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysisH S Scott, D S Kyriakou, P Peterson, et al.
Human Molecular Genetics|August 1, 1995
Localization of 102 exons to a 2.5 Mb region involved in Down syndromeD Lucente, H M Chen, D Shea, et al.
Arthritis and Rheumatism|January 1, 2008
Atacicept in patients with rheumatoid arthritis: results of a multicenter, phase Ib, double-blind, placebo-controlled, dose-escalating, single- and repeated-dose studyP P Tak, R M Thurlings, C Rossier, et al.
Genomics|December 19, 2006
Identification of corticosteroid-regulated genes in cardiomyocytes by serial analysis of gene expressionOlivier Muller, Sylvain Pradervand, Stefan Berger, et al.
Journal of the American Society of Nephrology : JASN|October 16, 2010
Sodium and potassium balance depends on αENaC expression in connecting tubuleBirgitte Mønster Christensen, Romain Perrier, Qing Wang, et al.
Human Genetics|July 16, 2005
A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the proteinMarie Wattenhofer, Nilüfer Sahin-Calapoglu, Ditte Andreasen, et al.
Biochemical and Biophysical Research Communications|March 2, 1999
Isolation and characterization of the mouse Aire geneL Mittaz, C Rossier, M Heino, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 1997
A mouse model for the renal salt-wasting syndrome pseudohypoaldosteronismE Hummler, P Barker, C Talbot, et al.
Blood|March 26, 1999
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiencyM Neerman-Arbez, K M Johnson, M A Morris, et al.
Journal of the American Society of Nephrology : JASN|December 25, 2015
Severe Salt-Losing Syndrome and Hyperkalemia Induced by Adult Nephron-Specific Knockout of the Epithelial Sodium Channel α-SubunitRomain Perrier, Emilie Boscardin, Sumedha Malsure, et al.
Pageof 30

Showing results (261-270 of 295) with videos related to

Sort By:
Pageof 30
Genomics|February 18, 1998
Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysisH S Scott, D S Kyriakou, P Peterson, et al.
Human Molecular Genetics|August 1, 1995
Localization of 102 exons to a 2.5 Mb region involved in Down syndromeD Lucente, H M Chen, D Shea, et al.
Arthritis and Rheumatism|January 1, 2008
Atacicept in patients with rheumatoid arthritis: results of a multicenter, phase Ib, double-blind, placebo-controlled, dose-escalating, single- and repeated-dose studyP P Tak, R M Thurlings, C Rossier, et al.
Genomics|December 19, 2006
Identification of corticosteroid-regulated genes in cardiomyocytes by serial analysis of gene expressionOlivier Muller, Sylvain Pradervand, Stefan Berger, et al.
Journal of the American Society of Nephrology : JASN|October 16, 2010
Sodium and potassium balance depends on αENaC expression in connecting tubuleBirgitte Mønster Christensen, Romain Perrier, Qing Wang, et al.
Human Genetics|July 16, 2005
A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the proteinMarie Wattenhofer, Nilüfer Sahin-Calapoglu, Ditte Andreasen, et al.
Biochemical and Biophysical Research Communications|March 2, 1999
Isolation and characterization of the mouse Aire geneL Mittaz, C Rossier, M Heino, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 1997
A mouse model for the renal salt-wasting syndrome pseudohypoaldosteronismE Hummler, P Barker, C Talbot, et al.
Blood|March 26, 1999
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiencyM Neerman-Arbez, K M Johnson, M A Morris, et al.
Journal of the American Society of Nephrology : JASN|December 25, 2015
Severe Salt-Losing Syndrome and Hyperkalemia Induced by Adult Nephron-Specific Knockout of the Epithelial Sodium Channel α-SubunitRomain Perrier, Emilie Boscardin, Sumedha Malsure, et al.
Pageof 30