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

H N Yeowell

Showing results (21-30 of 28) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 28 results.
Molecular Genetics and Metabolism|May 18, 1999
A patient with Ehlers-Danlos syndrome type VI is homozygous for a premature termination codon in exon 14 of the lysyl hydroxylase 1 geneL C Walker, J C Marini, D K Grange, et al.
Molecular Pharmacology|March 1, 1988
Induction of rat cytochrome P-450 3 and its mRNA by 3,4,5,3',4',5'-hexachlorobiphenylH N Yeowell, D J Waxman, G A LeBlanc, et al.
IARC Scientific Publications|January 1, 1986
Structure-activity relationships of chlorinated benzenes as inducers of hepatic cytochrome P-450 isozymes in the ratJ A Goldstein, P Linko, M E Hahn, et al.
Biochemical and Biophysical Research Communications|September 10, 1998
Altered posttranslational modifications of collagen in keloidK Uzawa, M K Marshall, E P Katz, et al.
The Journal of Clinical Investigation|April 1, 1994
A patient with Ehlers-Danlos syndrome type VI is a compound heterozygote for mutations in the lysyl hydroxylase geneV T Ha, M K Marshall, L J Elsas, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|February 25, 2000
Deletion of cysteine 369 in lysyl hydroxylase 1 eliminates enzyme activity and causes Ehlers-Danlos syndrome type VIH N Yeowell, J D Allen, L C Walker, et al.
The Journal of Investigative Dermatology|January 1, 1996
The expression of a functional, secreted human lysyl hydroxylase in a baculovirus systemB J Krol, S Murad, L C Walker, et al.
Molecular Genetics and Metabolism|December 14, 2004
Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 geneL C Walker, A S Teebi, J C Marini, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Molecular Genetics and Metabolism|May 18, 1999
A patient with Ehlers-Danlos syndrome type VI is homozygous for a premature termination codon in exon 14 of the lysyl hydroxylase 1 geneL C Walker, J C Marini, D K Grange, et al.
Molecular Pharmacology|March 1, 1988
Induction of rat cytochrome P-450 3 and its mRNA by 3,4,5,3',4',5'-hexachlorobiphenylH N Yeowell, D J Waxman, G A LeBlanc, et al.
IARC Scientific Publications|January 1, 1986
Structure-activity relationships of chlorinated benzenes as inducers of hepatic cytochrome P-450 isozymes in the ratJ A Goldstein, P Linko, M E Hahn, et al.
Biochemical and Biophysical Research Communications|September 10, 1998
Altered posttranslational modifications of collagen in keloidK Uzawa, M K Marshall, E P Katz, et al.
The Journal of Clinical Investigation|April 1, 1994
A patient with Ehlers-Danlos syndrome type VI is a compound heterozygote for mutations in the lysyl hydroxylase geneV T Ha, M K Marshall, L J Elsas, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|February 25, 2000
Deletion of cysteine 369 in lysyl hydroxylase 1 eliminates enzyme activity and causes Ehlers-Danlos syndrome type VIH N Yeowell, J D Allen, L C Walker, et al.
The Journal of Investigative Dermatology|January 1, 1996
The expression of a functional, secreted human lysyl hydroxylase in a baculovirus systemB J Krol, S Murad, L C Walker, et al.
Molecular Genetics and Metabolism|December 14, 2004
Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 geneL C Walker, A S Teebi, J C Marini, et al.
Pageof 3