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The relationship between CTP17 -34T/C polymorphism and acne in chinese subjects revealed by sequencingLI HE; ZHI YANG; HAIJING YU et al.Dermatology (Basel). 2006, Vol 212, Num 4, pp 338-342, issn 1018-8665, 5 p.Article

Exogenous granulocyte-macrophage colony-stimulating factor promotes follicular development in the newborn rat in vivoHONGBO WANG; YAN WEN; POLAN, Mary Lake et al.Human reproduction (Oxford. Print). 2005, Vol 20, Num 10, pp 2749-2756, issn 0268-1161, 8 p.Article

In vitro metabolism of dexamethasone (DEX) in human liver and kidney : The involvement of CYP3A4 and CYP17 (17,20 LYASE) and molecular modelling studiesTOMLINSON, E. S; LEWIS, D. F. V; MAGGS, J. L et al.Biochemical pharmacology. 1997, Vol 54, Num 5, pp 605-611, issn 0006-2952Article

CYP17 genotype predicts serum hormone levels among pre-menopausal womenSMALL, Chanley M; MARCUS, Michele; SHERMAN, Stephanie L et al.Human reproduction (Oxford. Print). 2005, Vol 20, Num 8, pp 2162-2167, issn 0268-1161, 6 p.Article

A polymorphism in the CYP17 gene relates to the risk of recurrent pregnancy lossSATA, F; YAMADA, H; YAMADA, A et al.Molecular human reproduction. 2003, Vol 9, Num 11-12, pp 725-728, issn 1360-9947, 4 p.Article

Two intronic mutations cause 17-hydroxylase deficiency by disrupting splice acceptor sites: Direct demonstration of aberrant splicing and absent enzyme activity by expression of the entire CYP17 gene in HEK-293 cellsCOSTA-SANTOS, Marivania; KATER, Claudio E; DIAS, Eduardo P et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 1, pp 43-48, issn 0021-972X, 6 p.Article

Gene for 17α-hydroxylase/C(17-20) lyase P-450 : complete nucleotide sequence of the porcine gene and 5' upstream sequence of the rat genePEILIN ZHANG; NASON, T. F; XU-GUANG HAN et al.Biochimica et biophysica acta, N. Gene structure and expression. 1992, Vol 1131, Num 3, pp 345-348, issn 0167-4781Article

Association study of CYP17 and HSDIIBI in polycystic ovary syndrome utilizing comprehensive gene coverageCHUA, Angela K; AZZIZ, Ricardo; GOODARZI, Mark O et al.Molecular human reproduction. 2012, Vol 18, Num 5-6, pp 320-324, issn 1360-9947, 5 p.Article

17α-Hydroxylase (CYP I7) Expression and Subsequent Androstenedione Production in the Human OvaryPATEL, Satin S; BESHAY, Victor E; ESCOBAR, Julian C et al.Reproductive sciences (Thousand Oaks, Calif.). 2010, Vol 17, Num 11, pp 978-986, issn 1933-7191, 9 p.Article

CYP17 and CYP19 gene polymorphisms in women affected with endometriosisVIETRI, Maria Teresa; CIOFFI, Michele; SESSA, Marcella et al.Fertility and sterility. 2009, Vol 92, Num 5, pp 1532-1535, issn 0015-0282, 4 p.Article

Association of the CYP17 gene and CYP19 gene polymorphisms with risk of endometriosis in Japanese womenKADO, Noriko; KITAWAKI, Jo; HONJO, Hideo et al.Human reproduction (Oxford. Print). 2002, Vol 17, Num 4, pp 897-902, issn 0268-1161Article

Demethylation of specific sites in the 5'-flanking region of the CYP17 genes when bovine adrenocortical cells are placed in cultureHORNSBY, P. J; YANG, L; RAJU, S. G et al.DNA and cell biology. 1992, Vol 11, Num 5, pp 385-395, issn 1044-5498Article

Isolation, characterization, and chromosomal mapping of mouse P450 17α-hydroxylase/C_17-20 lyaseYOUNGBLOOD, G. L; SARTORIUS, C; TAYLOR, B. A et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 1, pp 270-275, issn 0888-7543, 6 p.Article

A polymorphism of the CYP17 gene related to sex steroid metabolism is associated with female-to-male but not male-to-female transsexualismBENTZ, Eva-Katrin; HEFLER, Lukas A; KAUFMANN, Ulrike et al.Fertility and sterility. 2008, Vol 90, Num 1, pp 56-59, issn 0015-0282, 4 p.Article

Prenatal alcohol exposure, CYP17 gene polymorphisms and fetal growth restrictionDELPISHEH, Ali; TOPPING, Joanne; REYAD, Manal et al.European journal of obstetrics, gynecology, and reproductive biology. 2008, Vol 138, Num 1, pp 49-53, issn 0301-2115, 5 p.Article

A novel point mutation in P450c17 (CYP17) causing combined 17α-hydroxylase/17,20-lyase deficiencyBROOKE, A. M; TAYLOR, N. F; MONSON, J. P et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 6, pp 2428-2431, issn 0021-972X, 4 p.Article

17a-hydroxylase/17,20-lyase deficiency caused by a novel homozygous mutation (Y27stop) in the cytochrome CYP17 geneMÜSSIG, Karsten; KALTENBACH, Simone; MACHICAO, Fausto et al.The Journal of clinical endocrinology and metabolism. 2005, Vol 90, Num 7, pp 4362-4365, issn 0021-972X, 4 p.Article

Estrogen receptor α dinucleotide repeat and cytochrome P450c17α gene polymorphisms are associated with susceptibility to endometriosisHSIEH, Yao-Yuan; CHANG, Chi-Chen; TSAI, Fuu-Jen et al.Fertility and sterility. 2005, Vol 83, Num 3, pp 567-572, issn 0015-0282, 6 p.Article

CYP17, CYP1A1 and COMT polymorphisms and the risk of adenomyosis and endometriosis in Taiwanese womenJUO, S. H; WANG, T. N; LEE, J. N et al.Human reproduction (Oxford. Print). 2006, Vol 21, Num 6, pp 1498-1502, issn 0268-1161, 5 p.Article

Cyclic AMP regulates expression of the rat gene for steroid 17α-hydroxylase/C_17-20 lyase P-450 (CYP17) in rat Leydig cellsNASON, T. F; XU-GUANG HAN; HALL, P. F et al.Biochimica et biophysica acta, N. Gene structure and expression. 1992, Vol 1171, Num 1, pp 73-80, issn 0167-4781Article

Isolation and characterization of the mouse P450 17α-hydroxylase/C_17-20-lyase gene (Cyp17) : transcriptional regulation of the gene by cyclic adenosine 3',5'-monophosphate in MA-10 Leydig cellsYOUNGBLOOD, G. L; PAYNE, A. H.Molecular endocrinology (Baltimore, Md.). 1992, Vol 6, Num 6, pp 927-934, issn 0888-8809Article

Deletion within the CYP17 gene together with insertion of foreign DNA is the cause of combined complete 17α-hydroxylase/17,20-lyase deficiency in an Italian patientBIASON, A; MANTERO, F; SCARONI, C et al.Molecular endocrinology (Baltimore, Md.). 1991, Vol 5, Num 12, pp 2037-2045, issn 0888-8809Article

Transcriptional regulation of the bovine CYP17 gene by cAMPLUND, J; BAKKE, M; MELLGREN, G et al.Steroids. 1997, Vol 62, Num 1, pp 43-45, issn 0039-128XConference Paper

A novel compound heterozygous mutation in the CYP17 (P450 17α-hydroxylase) gene leading to 17α-hydroxylase/17,20-lyase deficiencyJONG RYEAL HAHM; DEOK RYONG KIM; DONG KEE JEONG et al.Metabolism, clinical and experimental. 2003, Vol 52, Num 4, pp 488-492, issn 0026-0495, 5 p.Article