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

R J Wenstrup

Showing results (1-10 of 37) with videos related to

Pageof 4
Sort By:
The Journal of Pediatrics|September 1, 1989
Ehlers-Danlos syndrome type VI: clinical manifestations of collagen lysyl hydroxylase deficiencyR J Wenstrup, S Murad, S R Pinnell
The Journal of Clinical Investigation|December 1, 1986
Osteogenesis imperfecta type IV. Biochemical confirmation of genetic linkage to the pro alpha 2(I) gene of type I collagenR J Wenstrup, P Tsipouras, P H Byers
The Journal of Investigative Dermatology|August 1, 1991
DNA sequence analysis and restriction fragment length polymorphism (RFLP) typing of the HLA-DQw2 alleles associated with dermatitis herpetiformisC C Otley, R J Wenstrup, R P Hall
Human Genetics|September 1, 1986
Osteogenesis imperfecta type IV: evidence of abnormal triple helical structure of type I collagenR J Wenstrup, A G Hunter, P H Byers
The Journal of Investigative Dermatology|August 1, 1990
An HLA class II region restriction fragment length polymorphism (RFLP) in patients with dermatitis herpetiformis: association with HLA-DP phenotypeR P Hall, F E Ward, R J Wenstrup
Connective Tissue Research|January 1, 1996
Abnormal differentiation in MC3T3-E1 preosteoblasts expressing a dominant-negative type I collagen mutationR J Wenstrup, D P Witte, J B Florer
The Journal of Biological Chemistry|June 5, 1988
Arginine for glycine substitution in the triple-helical domain of the products of one alpha 2(I) collagen allele (COL1A2) produces the osteogenesis imperfecta type IV phenotypeR J Wenstrup, D H Cohn, T Cohen, et al.
Clinical Genetics|August 26, 1998
Aortic root dilatation in Ehlers-Danlos syndrome types I, II and III. A report of five casesG E Tiller, S B Cassidy, C Wensel, et al.
The British Journal of Radiology|May 31, 2002
Skeletal aspects of Gaucher disease: a reviewR J Wenstrup, M Roca-Espiau, N J Weinreb, et al.
Antisense & Nucleic Acid Drug Development|January 5, 2002
Delivery of a hammerhead ribozyme specifically downregulates mutant type I collagen mRNA in a murine model of osteogenesis imperfectaI Toudjarska, M W Kilpatrick, J Niu, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
The Journal of Pediatrics|September 1, 1989
Ehlers-Danlos syndrome type VI: clinical manifestations of collagen lysyl hydroxylase deficiencyR J Wenstrup, S Murad, S R Pinnell
The Journal of Clinical Investigation|December 1, 1986
Osteogenesis imperfecta type IV. Biochemical confirmation of genetic linkage to the pro alpha 2(I) gene of type I collagenR J Wenstrup, P Tsipouras, P H Byers
The Journal of Investigative Dermatology|August 1, 1991
DNA sequence analysis and restriction fragment length polymorphism (RFLP) typing of the HLA-DQw2 alleles associated with dermatitis herpetiformisC C Otley, R J Wenstrup, R P Hall
Human Genetics|September 1, 1986
Osteogenesis imperfecta type IV: evidence of abnormal triple helical structure of type I collagenR J Wenstrup, A G Hunter, P H Byers
The Journal of Investigative Dermatology|August 1, 1990
An HLA class II region restriction fragment length polymorphism (RFLP) in patients with dermatitis herpetiformis: association with HLA-DP phenotypeR P Hall, F E Ward, R J Wenstrup
Connective Tissue Research|January 1, 1996
Abnormal differentiation in MC3T3-E1 preosteoblasts expressing a dominant-negative type I collagen mutationR J Wenstrup, D P Witte, J B Florer
The Journal of Biological Chemistry|June 5, 1988
Arginine for glycine substitution in the triple-helical domain of the products of one alpha 2(I) collagen allele (COL1A2) produces the osteogenesis imperfecta type IV phenotypeR J Wenstrup, D H Cohn, T Cohen, et al.
Clinical Genetics|August 26, 1998
Aortic root dilatation in Ehlers-Danlos syndrome types I, II and III. A report of five casesG E Tiller, S B Cassidy, C Wensel, et al.
The British Journal of Radiology|May 31, 2002
Skeletal aspects of Gaucher disease: a reviewR J Wenstrup, M Roca-Espiau, N J Weinreb, et al.
Antisense & Nucleic Acid Drug Development|January 5, 2002
Delivery of a hammerhead ribozyme specifically downregulates mutant type I collagen mRNA in a murine model of osteogenesis imperfectaI Toudjarska, M W Kilpatrick, J Niu, et al.
Pageof 4