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European Heart Journal
|
October 26, 2002
Strong predictive value of TIMI risk score analysis for in-hospital and long-term survival of patients with right ventricular infarction
R J Gumina, R S Wright, S L Kopecky, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 30, 2000
Enzymatic activities of P450c17 stably expressed in fibroblasts from patients with the polycystic ovary syndrome
J W Martens, D H Geller, W Arlt, et al.
Endocrinology
|
May 1, 1987
Cholesterol side-chain cleavage P450 messenger ribonucleic acid: evidence for hormonal regulation in rat ovarian follicles and constitutive expression in corpora lutea
N B Goldring, J M Durica, J Lifka, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1987
P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia
K J Matteson, J A Phillips, W L Miller, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 26, 1996
Steroidogenic acute regulatory protein (StAR) retains activity in the absence of its mitochondrial import sequence: implications for the mechanism of StAR action
F Arakane, T Sugawara, H Nishino, et al.
AIDS (London, England)
|
December 1, 1992
Infection of cultured human adrenal cells by different strains of HIV
A Barboza, B A Castro, M Whalen, et al.
Journal of the American College of Cardiology
|
October 1, 1996
C-type natriuretic peptide-mediated coronary vasodilation: role of the coronary nitric oxide and particulate guanylate cyclase systems
R S Wright, C M Wei, C H Kim, et al.
Molecular Genetics and Metabolism
|
March 13, 2001
Mutation of proline 409 to arginine in the meander region of cytochrome p450c17 causes severe 17 alpha-hydroxylase deficiency
C W Lam, W Arlt, C K Chan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 1, 1995
Prenatal diagnosis of congenital lipoid adrenal hyperplasia
P Saenger, Z Klonari, S M Black, et al.
The Journal of Clinical Investigation
|
February 1, 1989
Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia
Y Morel, J André, B Uring-Lambert, et al.
Page
of 26
Search research articles
Search
Showing results (241-250 of 256) with videos related to
Sort By:
Page
of 26
European Heart Journal
|
October 26, 2002
Strong predictive value of TIMI risk score analysis for in-hospital and long-term survival of patients with right ventricular infarction
R J Gumina, R S Wright, S L Kopecky, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 30, 2000
Enzymatic activities of P450c17 stably expressed in fibroblasts from patients with the polycystic ovary syndrome
J W Martens, D H Geller, W Arlt, et al.
Endocrinology
|
May 1, 1987
Cholesterol side-chain cleavage P450 messenger ribonucleic acid: evidence for hormonal regulation in rat ovarian follicles and constitutive expression in corpora lutea
N B Goldring, J M Durica, J Lifka, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1987
P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia
K J Matteson, J A Phillips, W L Miller, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 26, 1996
Steroidogenic acute regulatory protein (StAR) retains activity in the absence of its mitochondrial import sequence: implications for the mechanism of StAR action
F Arakane, T Sugawara, H Nishino, et al.
AIDS (London, England)
|
December 1, 1992
Infection of cultured human adrenal cells by different strains of HIV
A Barboza, B A Castro, M Whalen, et al.
Journal of the American College of Cardiology
|
October 1, 1996
C-type natriuretic peptide-mediated coronary vasodilation: role of the coronary nitric oxide and particulate guanylate cyclase systems
R S Wright, C M Wei, C H Kim, et al.
Molecular Genetics and Metabolism
|
March 13, 2001
Mutation of proline 409 to arginine in the meander region of cytochrome p450c17 causes severe 17 alpha-hydroxylase deficiency
C W Lam, W Arlt, C K Chan, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 1, 1995
Prenatal diagnosis of congenital lipoid adrenal hyperplasia
P Saenger, Z Klonari, S M Black, et al.
The Journal of Clinical Investigation
|
February 1, 1989
Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia
Y Morel, J André, B Uring-Lambert, et al.
Page
of 26