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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 gene
L 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'-hexachlorobiphenyl
H 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 rat
J A Goldstein, P Linko, M E Hahn, et al.
Biochemical and Biophysical Research Communications
|
September 10, 1998
Altered posttranslational modifications of collagen in keloid
K 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 gene
V 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 VI
H 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 system
B 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 gene
L C Walker, A S Teebi, J C Marini, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 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 gene
L 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'-hexachlorobiphenyl
H 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 rat
J A Goldstein, P Linko, M E Hahn, et al.
Biochemical and Biophysical Research Communications
|
September 10, 1998
Altered posttranslational modifications of collagen in keloid
K 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 gene
V 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 VI
H 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 system
B 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 gene
L C Walker, A S Teebi, J C Marini, et al.
Page
of 3