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Molecular Endocrinology (Baltimore, Md.)
|
March 1, 1994
Modeling and mutagenesis of the active site of human P450c17
D Lin, L H Zhang, E Chiao, et al.
The Journal of Biological Chemistry
|
December 23, 1999
Transcriptional regulatory elements of the human gene for cytochrome P450c21 (steroid 21-hydroxylase) lie within intron 35 of the linked C4B gene
S D Wijesuriya, G Zhang, A Dardis, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
January 6, 2012
Analysis of the duplicated human C4/P450c21/X gene cluster
W L Miller, S E Gitelman, J Bristow, et al.
The Journal of Clinical Investigation
|
December 1, 1991
Normal genes for the cholesterol side chain cleavage enzyme, P450scc, in congenital lipoid adrenal hyperplasia
D Lin, S E Gitelman, P Saenger, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1997
Transcription of the human genes for cytochrome P450scc and P450c17 is regulated differently in human adrenal NCI-H295 cells than in mouse adrenal Y1 cells
H Rodriguez, D W Hum, B Staels, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
April 1, 1993
Congenital lipoid adrenal hyperplasia--genes for P450scc, side chain cleavage enzyme, are normal
P Saenger, D Lin, S E Gitelman, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1989
Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus
Y Morel, J Bristow, S E Gitelman, et al.
The American Journal of Physiology
|
July 1, 1970
Contribution of glomerular and tubular RNA synthesis to compensatory renal growth
P Vancura, W L Miller, J W Little, et al.
Endocrine Research
|
February 24, 2001
Probing structural and functional domains of human P450c17
R J Auchus, K Worthy, D H Geller, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1994
Point mutation of Arg440 to His in cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency
C E Fardella, D W Hum, J Homoki, et al.
Page
of 33
Search research articles
Search
Showing results (171-180 of 323) with videos related to
Sort By:
Page
of 33
Molecular Endocrinology (Baltimore, Md.)
|
March 1, 1994
Modeling and mutagenesis of the active site of human P450c17
D Lin, L H Zhang, E Chiao, et al.
The Journal of Biological Chemistry
|
December 23, 1999
Transcriptional regulatory elements of the human gene for cytochrome P450c21 (steroid 21-hydroxylase) lie within intron 35 of the linked C4B gene
S D Wijesuriya, G Zhang, A Dardis, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
January 6, 2012
Analysis of the duplicated human C4/P450c21/X gene cluster
W L Miller, S E Gitelman, J Bristow, et al.
The Journal of Clinical Investigation
|
December 1, 1991
Normal genes for the cholesterol side chain cleavage enzyme, P450scc, in congenital lipoid adrenal hyperplasia
D Lin, S E Gitelman, P Saenger, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1997
Transcription of the human genes for cytochrome P450scc and P450c17 is regulated differently in human adrenal NCI-H295 cells than in mouse adrenal Y1 cells
H Rodriguez, D W Hum, B Staels, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
April 1, 1993
Congenital lipoid adrenal hyperplasia--genes for P450scc, side chain cleavage enzyme, are normal
P Saenger, D Lin, S E Gitelman, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1989
Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus
Y Morel, J Bristow, S E Gitelman, et al.
The American Journal of Physiology
|
July 1, 1970
Contribution of glomerular and tubular RNA synthesis to compensatory renal growth
P Vancura, W L Miller, J W Little, et al.
Endocrine Research
|
February 24, 2001
Probing structural and functional domains of human P450c17
R J Auchus, K Worthy, D H Geller, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1994
Point mutation of Arg440 to His in cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency
C E Fardella, D W Hum, J Homoki, et al.
Page
of 33