These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

83 related articles for article (PubMed ID: 10720067)

  • 41. Molecular study of five Chinese patients with 46XX partial 17a-hydroxylase/17,20-lyase deficiency.
    Tian Q; Yao F; Zhang Y; Tseng H; Lang J
    Gynecol Endocrinol; 2012 Mar; 28(3):234-8. PubMed ID: 21846181
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Haploinsufficiency of cytochrome P450 17alpha-hydroxylase/17,20 lyase (CYP17) causes infertility in male mice.
    Liu Y; Yao ZX; Bendavid C; Borgmeyer C; Han Z; Cavalli LR; Chan WY; Folmer J; Zirkin BR; Haddad BR; Gallicano GI; Papadopoulos V
    Mol Endocrinol; 2005 Sep; 19(9):2380-9. PubMed ID: 15890676
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Developmentally regulated expression and activity of 17alpha-hydroxylase/C-17,20-lyase cytochrome P450 in rat liver.
    Vianello S; Waterman MR; Dalla Valle L; Colombo L
    Endocrinology; 1997 Aug; 138(8):3166-74. PubMed ID: 9231764
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mutagenesis of putative serine-threonine phosphorylation sites proximal to Arg255 of human cytochrome P450c17 does not selectively promote its 17,20-lyase activity.
    Souter I; Munir I; Mallick P; Weitsman SR; Geller DH; Magoffin DA
    Fertil Steril; 2006 Apr; 85 Suppl 1():1290-9. PubMed ID: 16616104
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Functional Identification of Compound Heterozygous Mutations in the
    Mo EY; Lee JY; Kim SY; Kim MJ; Kim ES; Lee S; Han JH; Moon SD
    Endocrinol Metab (Seoul); 2018 Sep; 33(3):413-422. PubMed ID: 30229581
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Abnormal morphology of spermatozoa in cytochrome P450 17alpha-hydroxylase/17, 20-lyase (CYP17) deficient mice.
    Liu Y; Dettin LE; Folmer J; Zirkin BR; Papadopoulos V
    J Androl; 2007; 28(3):453-60. PubMed ID: 17251596
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 17alpha-hydroxylase/C17-20 lyase cytochrome P450 mRNA expressions and enzyme activities during the development of arthritis in collagen-induced arthritis mice.
    Tagawa N; Muraoka K; Okamoto Y; Nishida M; Katagiri M; Kobayashi Y
    Biol Pharm Bull; 2004 Oct; 27(10):1663-5. PubMed ID: 15467215
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Two CYP17 genes in the South African Angora goat (Capra hircus) - the identification of three genotypes that differ in copy number and steroidogenic output.
    Storbeck KH; Swart AC; Snyman MA; Swart P
    FEBS J; 2008 Aug; 275(15):3934-43. PubMed ID: 18616460
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [New mutation in the CYP17 gene: description of a case].
    Dzeranova LK; Tyulpakov AN; Pigarova YA; Rubtsov PM; Artemova AM; Vorontsov AV; Yarovaya IS; Rozhinskaya LY; Dedov II
    Probl Endokrinol (Mosk); 2006 Dec; 52(6):41-45. PubMed ID: 31627669
    [TBL] [Abstract][Full Text] [Related]  

  • 50. CYP17 causes hypocortisolism in the South African Angora goat.
    Storbeck KH; Swart AC; Swart P
    Mol Cell Endocrinol; 2009 Mar; 300(1-2):121-5. PubMed ID: 18840497
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 17 alpha-hydroxylase/17,20-lyase dysregulation is not caused by mutations in the coding regions of CYP17.
    Witchel SF; Lee PA; Suda-Hartman M; Smith R; Hoffman EP
    J Pediatr Adolesc Gynecol; 1998 Aug; 11(3):133-7. PubMed ID: 9704303
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Gene symbol: M19489, CYP17. Disease: 17-alpha-hydroxylase/17,20-lyase deficiency.
    Hong T; Zhao-Lin L
    Hum Genet; 2003 Oct; 113(5):465. PubMed ID: 14552332
    [No Abstract]   [Full Text] [Related]  

  • 53. Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency.
    Lin D; Harikrishna JA; Moore CC; Jones KL; Miller WL
    J Biol Chem; 1991 Aug; 266(24):15992-8. PubMed ID: 1714904
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Molecular basis of apparent isolated 17,20-lyase deficiency: compound heterozygous mutations in the C-terminal region (Arg(496)----Cys, Gln(461)----Stop) actually cause combined 17 alpha-hydroxylase/17,20-lyase deficiency.
    Yanase T; Waterman MR; Zachmann M; Winter JS; Simpson ER; Kagimoto M
    Biochim Biophys Acta; 1992 Aug; 1139(4):275-9. PubMed ID: 1515452
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Mutation R96W in cytochrome P450c17 gene causes combined 17 alpha-hydroxylase/17-20-lyase deficiency in two French Canadian patients.
    Laflamme N; Leblanc JF; Mailloux J; Faure N; Labrie F; Simard J
    J Clin Endocrinol Metab; 1996 Jan; 81(1):264-8. PubMed ID: 8550762
    [TBL] [Abstract][Full Text] [Related]  

  • 56. P450c17 deficiency in Brazilian patients: biochemical diagnosis through progesterone levels confirmed by CYP17 genotyping.
    Martin RM; Lin CJ; Costa EM; de Oliveira ML; Carrilho A; Villar H; Longui CA; Mendonca BB
    J Clin Endocrinol Metab; 2003 Dec; 88(12):5739-46. PubMed ID: 14671162
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Gonadal tumor risk in pediatric and adolescent phenotypic females with disorders of sex development and Y chromosomal constitution with different genetic etiologies.
    Lu L; Luo F; Wang X
    Front Pediatr; 2022; 10():856128. PubMed ID: 35935368
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Genetic screening for monogenic hypertension in hypertensive individuals in a clinical setting.
    Bao M; Li P; Li Q; Chen H; Zhong Y; Li S; Jin L; Wang W; Chen Z; Zhong J; Geng B; Fan Y; Yang X; Cai J
    J Med Genet; 2020 Aug; 57(8):571-580. PubMed ID: 32561571
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A Novel Compound Heterozygous
    Chen H; Yuan K; Zhang B; Jia Z; Chen C; Zhu Y; Sun Y; Zhou H; Huang W; Liang L; Yan Q; Wang C
    Front Genet; 2019; 10():996. PubMed ID: 31695722
    [No Abstract]   [Full Text] [Related]  

  • 60. Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population.
    Wang M; Wang H; Zhao H; Li L; Liu M; Liu F; Meng F; Fan C
    Clin Hypertens; 2019; 25():23. PubMed ID: 31636948
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.