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

A Roscher

Showing results (81-90 of 186) with videos related to

Pageof 19
Sort By:
Human Genetics|May 1, 1996
A novel sequence polymorphism in the promoter region of the human B2-bradykinin receptor geneA Braun, E Maier, S Kammerer, et al.
Immunopharmacology|June 1, 1996
Polymorphisms in the gene for the human B2-bradykinin receptor. New tools in assessing a genetic risk for bradykinin-associated diseasesA Braun, S Kammerer, E Maier, et al.
Journal of Cardiovascular Pharmacology|January 1, 1990
Regulation of bradykinin action at the receptor levelA A Roscher, C Klier, R Dengler, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2000
Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern GermanyN Krone, A Braun, A A Roscher, et al.
Pediatric Research|September 1, 1985
The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detectionA Roscher, B Molzer, H Bernheimer, et al.
Clinical Genetics|May 1, 1986
Infantile type of sialic acid storage disease with sialuriaE Paschke, G Trinkl, W Erwa, et al.
European Journal of Pharmacology|September 5, 1995
Autoradiographic localization and characterization of bradykinin receptors in human skinE Schremmer-Danninger, P Heinz-Erian, E Töpfer-Petersen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 30, 1986
Very long chain fatty acids in genetic peroxisomal disease fibroblasts: differences between the cerebro-hepato-renal (Zellweger) syndrome and adrenoleukodystrophy variantsB Molzer, M Korschinsky, H Bernheimer, et al.
European Journal of Cell Biology|October 10, 2003
Targeting of the human adrenoleukodystrophy protein to the peroxisomal membrane by an internal region containing a highly conserved motifPablo Landgraf, Peter U Mayerhofer, Roman Polanetz, et al.
Clinical Endocrinology|October 27, 2001
Mothers with congenital adrenal hyperplasia and their children: outcome of pregnancy, birth and childhoodN Krone, I Wachter, M Stefanidou, et al.
Pageof 19

Showing results (81-90 of 186) with videos related to

Sort By:
Pageof 19
Human Genetics|May 1, 1996
A novel sequence polymorphism in the promoter region of the human B2-bradykinin receptor geneA Braun, E Maier, S Kammerer, et al.
Immunopharmacology|June 1, 1996
Polymorphisms in the gene for the human B2-bradykinin receptor. New tools in assessing a genetic risk for bradykinin-associated diseasesA Braun, S Kammerer, E Maier, et al.
Journal of Cardiovascular Pharmacology|January 1, 1990
Regulation of bradykinin action at the receptor levelA A Roscher, C Klier, R Dengler, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2000
Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern GermanyN Krone, A Braun, A A Roscher, et al.
Pediatric Research|September 1, 1985
The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detectionA Roscher, B Molzer, H Bernheimer, et al.
Clinical Genetics|May 1, 1986
Infantile type of sialic acid storage disease with sialuriaE Paschke, G Trinkl, W Erwa, et al.
European Journal of Pharmacology|September 5, 1995
Autoradiographic localization and characterization of bradykinin receptors in human skinE Schremmer-Danninger, P Heinz-Erian, E Töpfer-Petersen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 30, 1986
Very long chain fatty acids in genetic peroxisomal disease fibroblasts: differences between the cerebro-hepato-renal (Zellweger) syndrome and adrenoleukodystrophy variantsB Molzer, M Korschinsky, H Bernheimer, et al.
European Journal of Cell Biology|October 10, 2003
Targeting of the human adrenoleukodystrophy protein to the peroxisomal membrane by an internal region containing a highly conserved motifPablo Landgraf, Peter U Mayerhofer, Roman Polanetz, et al.
Clinical Endocrinology|October 27, 2001
Mothers with congenital adrenal hyperplasia and their children: outcome of pregnancy, birth and childhoodN Krone, I Wachter, M Stefanidou, et al.
Pageof 19