364 related articles for article (PubMed ID: 18271004)
21. Disturbed expression of Sox9 in pre-sertoli cells underlies sex-reversal in mice b6.Ytir.
Moreno-Mendoza N; Torres-Maldonado L; Chimal-Monroy J; Harley V; Merchant-Larios H
Biol Reprod; 2004 Jan; 70(1):114-22. PubMed ID: 13679320
[TBL] [Abstract][Full Text] [Related]
22. Sertoli cell differentiation is induced both cell-autonomously and through prostaglandin signaling during mammalian sex determination.
Wilhelm D; Martinson F; Bradford S; Wilson MJ; Combes AN; Beverdam A; Bowles J; Mizusaki H; Koopman P
Dev Biol; 2005 Nov; 287(1):111-24. PubMed ID: 16185683
[TBL] [Abstract][Full Text] [Related]
23. The porcine SRY promoter is transactivated within a male genital ridge environment.
Daneau I; Pilon N; Boyer A; Behdjani R; Overbeek PA; Viger R; Lussier J; Silversides DW
Genesis; 2002 Aug; 33(4):170-80. PubMed ID: 12203914
[TBL] [Abstract][Full Text] [Related]
24. From SRY to SOX9: mammalian testis differentiation.
Kanai Y; Hiramatsu R; Matoba S; Kidokoro T
J Biochem; 2005 Jul; 138(1):13-9. PubMed ID: 16046443
[TBL] [Abstract][Full Text] [Related]
25. Delayed Sry and Sox9 expression in developing mouse gonads underlies B6-Y(DOM) sex reversal.
Bullejos M; Koopman P
Dev Biol; 2005 Feb; 278(2):473-81. PubMed ID: 15680364
[TBL] [Abstract][Full Text] [Related]
26. Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.
Klamt B; Koziell A; Poulat F; Wieacker P; Scambler P; Berta P; Gessler M
Hum Mol Genet; 1998 Apr; 7(4):709-14. PubMed ID: 9499425
[TBL] [Abstract][Full Text] [Related]
27. [WT1 mutation as a cause of progressive nephropathy in Frasier syndrome--case report].
Wasilewska A; Zoch-Zwierz W; Tenderenda E; Rybi-Szumińska A; Kołodziejczyk Z
Pol Merkur Lekarski; 2009 Jun; 26(156):642-4. PubMed ID: 19711733
[TBL] [Abstract][Full Text] [Related]
28. Mutation analysis of five candidate genes in Chinese patients with hypospadias.
Wang Y; Li Q; Xu J; Liu Q; Wang W; Lin Y; Ma F; Chen T; Li S; Shen Y
Eur J Hum Genet; 2004 Sep; 12(9):706-12. PubMed ID: 15266301
[TBL] [Abstract][Full Text] [Related]
29. Transcription factor AP-2gamma is a developmentally regulated marker of testicular carcinoma in situ and germ cell tumors.
Hoei-Hansen CE; Nielsen JE; Almstrup K; Sonne SB; Graem N; Skakkebaek NE; Leffers H; Rajpert-De Meyts E
Clin Cancer Res; 2004 Dec; 10(24):8521-30. PubMed ID: 15623634
[TBL] [Abstract][Full Text] [Related]
30. Expression profiling of purified mouse gonadal somatic cells during the critical time window of sex determination reveals novel candidate genes for human sexual dysgenesis syndromes.
Beverdam A; Koopman P
Hum Mol Genet; 2006 Feb; 15(3):417-31. PubMed ID: 16399799
[TBL] [Abstract][Full Text] [Related]
31. Sertoli cell tumor and gonadoblastoma in an untreated 29-year-old 46,XY phenotypic male with Frasier syndrome carrying a WT1 IVS9+4C>T mutation.
Kitsiou-Tzeli S; Deligiorgi M; Malaktari-Skarantavou S; Vlachopoulos C; Megremis S; Fylaktou I; Traeger-Synodinos J; Kanaka-Gantenbein C; Stefanadis C; Kanavakis E
Hormones (Athens); 2012; 11(3):361-7. PubMed ID: 22908070
[TBL] [Abstract][Full Text] [Related]
32. Early gonadal development: exploring Wt1 and Sox9 function.
Guo JK; Hammes A; Chaboissier MC; Vidal V; Xing Y; Wong F; Schedl A
Novartis Found Symp; 2002; 244():23-31; discussion 31-42, 253-7. PubMed ID: 11990794
[TBL] [Abstract][Full Text] [Related]
33. Tumor risk in disorders of sex development (DSD).
Looijenga LH; Hersmus R; Oosterhuis JW; Cools M; Drop SL; Wolffenbuttel KP
Best Pract Res Clin Endocrinol Metab; 2007 Sep; 21(3):480-95. PubMed ID: 17875493
[TBL] [Abstract][Full Text] [Related]
34. Role of Wilms tumor 1 (WT1) in the transcriptional regulation of the Mullerian-inhibiting substance promoter.
Hossain A; Saunders GF
Biol Reprod; 2003 Dec; 69(6):1808-14. PubMed ID: 12855602
[TBL] [Abstract][Full Text] [Related]
35. Expanding the clinical spectrum of Frasier syndrome.
Gwin K; Cajaiba MM; Caminoa-Lizarralde A; Picazo ML; Nistal M; Reyes-Múgica M
Pediatr Dev Pathol; 2008; 11(2):122-7. PubMed ID: 17378674
[TBL] [Abstract][Full Text] [Related]
36. Sex-determining genes in mice: building pathways.
Lovell-Badge R; Canning C; Sekido R
Novartis Found Symp; 2002; 244():4-18; discussion 18-22, 35-42, 253-7. PubMed ID: 11990796
[TBL] [Abstract][Full Text] [Related]
37. Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms, are also responsible for Frasier syndrome.
Kohsaka T; Tagawa M; Takekoshi Y; Yanagisawa H; Tadokoro K; Yamada M
Hum Mutat; 1999; 14(6):466-70. PubMed ID: 10571943
[TBL] [Abstract][Full Text] [Related]
38. New insights into the function of the Wilms tumor suppressor gene WT1 in podocytes.
Morrison AA; Viney RL; Saleem MA; Ladomery MR
Am J Physiol Renal Physiol; 2008 Jul; 295(1):F12-7. PubMed ID: 18385267
[TBL] [Abstract][Full Text] [Related]
39. Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development.
Benko S; Gordon CT; Mallet D; Sreenivasan R; Thauvin-Robinet C; Brendehaug A; Thomas S; Bruland O; David M; Nicolino M; Labalme A; Sanlaville D; Callier P; Malan V; Huet F; Molven A; Dijoud F; Munnich A; Faivre L; Amiel J; Harley V; Houge G; Morel Y; Lyonnet S
J Med Genet; 2011 Dec; 48(12):825-30. PubMed ID: 22051515
[TBL] [Abstract][Full Text] [Related]
40. The Wilms tumor gene, Wt1, is required for Sox9 expression and maintenance of tubular architecture in the developing testis.
Gao F; Maiti S; Alam N; Zhang Z; Deng JM; Behringer RR; Lécureuil C; Guillou F; Huff V
Proc Natl Acad Sci U S A; 2006 Aug; 103(32):11987-92. PubMed ID: 16877546
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
