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 *

130 related articles for article (PubMed ID: 8570694)

  • 21. Porcine Dax-1 gene: isolation and expression during gonadal development.
    Parma P; Pailhoux E; Puissant C; Cotinot C
    Mol Cell Endocrinol; 1997 Nov; 135(1):49-58. PubMed ID: 9453240
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Role of Ahch in gonadal development and gametogenesis.
    Yu RN; Ito M; Saunders TL; Camper SA; Jameson JL
    Nat Genet; 1998 Dec; 20(4):353-7. PubMed ID: 9843206
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Dax-1 (dosage-sensitive sex reversal-adrenal hypoplasia congenita critical region on the X chromosome, gene 1) gene transcription is regulated by wnt4 in the female developing gonad.
    Mizusaki H; Kawabe K; Mukai T; Ariyoshi E; Kasahara M; Yoshioka H; Swain A; Morohashi K
    Mol Endocrinol; 2003 Apr; 17(4):507-19. PubMed ID: 12554773
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Four Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by DAX-1 gene mutations: mutant DAX-1 failed to repress steroidogenic acute regulatory protein (StAR) and luteinizing hormone beta-subunit gene promoter activity.
    Okuhara K; Abe S; Kondo T; Fujita K; Koda N; Mochizuki H; Fujieda K; Tajima T
    Endocr J; 2008 Mar; 55(1):97-103. PubMed ID: 18202527
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Delayed-onset adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by a novel mutation in
    Liu S; Yan L; Zhou X; Chen C; Wang D; Yuan G
    J Int Med Res; 2020 Feb; 48(2):300060519882151. PubMed ID: 31642359
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dax1 antagonizes Sry action in mammalian sex determination.
    Swain A; Narvaez V; Burgoyne P; Camerino G; Lovell-Badge R
    Nature; 1998 Feb; 391(6669):761-7. PubMed ID: 9486644
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Progressive onset of adrenal insufficiency and hypogonadism of pituitary origin caused by a complex genetic rearrangement within DAX-1.
    Salvi R; Gomez F; Fiaux M; Schorderet D; Jameson JL; Achermann JC; Gaillard RC; Pralong FP
    J Clin Endocrinol Metab; 2002 Sep; 87(9):4094-100. PubMed ID: 12213854
    [TBL] [Abstract][Full Text] [Related]  

  • 28. DAX-1 inhibits SF-1-mediated transactivation via a carboxy-terminal domain that is deleted in adrenal hypoplasia congenita.
    Ito M; Yu R; Jameson JL
    Mol Cell Biol; 1997 Mar; 17(3):1476-83. PubMed ID: 9032275
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Screening for mutations in the steroidogenic acute regulatory protein and steroidogenic factor-1 genes, and in CYP11A and dosage-sensitive sex reversal-adrenal hypoplasia gene on the X chromosome, gene-1 (DAX-1), in hyperandrogenic hirsute women.
    Calvo RM; Asunción M; Tellería D; Sancho J; San Millán JL; Escobar-Morreale HF
    J Clin Endocrinol Metab; 2001 Apr; 86(4):1746-9. PubMed ID: 11297612
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.
    Koh JW; Kang SY; Kim GH; Yoo HW; Yu J
    Ann Pediatr Endocrinol Metab; 2013 Jun; 18(2):90-4. PubMed ID: 24904859
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Sex determination: a 'window' of DAX1 activity.
    Ludbrook LM; Harley VR
    Trends Endocrinol Metab; 2004 Apr; 15(3):116-21. PubMed ID: 15046740
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Isolation and characterization of a MAGE gene family in the Xp21.3 region.
    Muscatelli F; Walker AP; De Plaen E; Stafford AN; Monaco AP
    Proc Natl Acad Sci U S A; 1995 May; 92(11):4987-91. PubMed ID: 7761436
    [TBL] [Abstract][Full Text] [Related]  

  • 33. An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita.
    Zanaria E; Muscatelli F; Bardoni B; Strom TM; Guioli S; Guo W; Lalli E; Moser C; Walker AP; McCabe ER
    Nature; 1994 Dec; 372(6507):635-41. PubMed ID: 7990953
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Female-to-male sex reversal associated with unique Xp21.2 deletion disrupting genomic regulatory architecture of the dosage-sensitive sex reversal region.
    Dangle P; Touzon MS; Reyes-Múgica M; Witchel SF; Rajkovic A; Schneck FX; Yatsenko SA
    J Med Genet; 2017 Oct; 54(10):705-709. PubMed ID: 28483799
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel DAX1 mutations in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism.
    Bassett JH; O'Halloran DJ; Williams GR; Beardwell CG; Shalet SM; Thakker RV
    Clin Endocrinol (Oxf); 1999 Jan; 50(1):69-75. PubMed ID: 10341858
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Phenotypic spectrum of mutations in DAX-1 and SF-1.
    Achermann JC; Meeks JJ; Jameson JL
    Mol Cell Endocrinol; 2001 Dec; 185(1-2):17-25. PubMed ID: 11738790
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Expression of DAX-1, the gene responsible for X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism, in the hypothalamic-pituitary-adrenal/gonadal axis.
    Guo W; Burris TP; McCabe ER
    Biochem Mol Med; 1995 Oct; 56(1):8-13. PubMed ID: 8593542
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Sex reversal in a child with duplication of sex reversing locus on the short arm of the X chromosome (Xp).
    Ito T; Kaino Y; Hirai H; Kida K; Nakahori Y; Nakagome Y
    J Pediatr Endocrinol Metab; 1996; 9(3):429-33. PubMed ID: 8887155
    [TBL] [Abstract][Full Text] [Related]  

  • 39. New mutations of DAX-1 genes in two Japanese patients with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism.
    Yanase T; Takayanagi R; Oba K; Nishi Y; Ohe K; Nawata H
    J Clin Endocrinol Metab; 1996 Feb; 81(2):530-5. PubMed ID: 8636263
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion.
    Bartley JA; Patil S; Davenport S; Goldstein D; Pickens J
    J Pediatr; 1986 Feb; 108(2):189-92. PubMed ID: 3003318
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.