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Items: 1 to 20 of 25

1.

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.

2.

Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?

Koziell A, Charmandari E, Hindmarsh PC, Rees L, Scambler P, Brook CG.

Clin Endocrinol (Oxf). 2000 Apr;52(4):519-24. Review. Erratum in: Clin Endocrinol (Oxf) 2000 Jun;52(6):801.

PMID:
10762296
3.

WT1 and glomerular diseases.

Niaudet P, Gubler MC.

Pediatr Nephrol. 2006 Nov;21(11):1653-60. Epub 2006 Aug 23. Review.

PMID:
16927106
4.

An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.

Melo KF, Martin RM, Costa EM, Carvalho FM, Jorge AA, Arnhold IJ, Mendonca BB.

J Clin Endocrinol Metab. 2002 Jun;87(6):2500-5. Review.

PMID:
12050205
5.

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. doi: 10.1152/ajprenal.00597.2007. Epub 2008 Apr 2. Review.

6.

A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.

Heathcott RW, Morison IM, Gubler MC, Corbett R, Reeve AE.

Hum Mutat. 2002 Apr;19(4):462. Review.

PMID:
11933209
7.

Wilms tumor and the WT1 gene.

Lee SB, Haber DA.

Exp Cell Res. 2001 Mar 10;264(1):74-99. Review.

PMID:
11237525
8.

WT1 proteins: functions in growth and differentiation.

Scharnhorst V, van der Eb AJ, Jochemsen AG.

Gene. 2001 Aug 8;273(2):141-61. Review.

PMID:
11595161
9.

Multiple roles for the Wilms' tumor suppressor, WT1.

Davies R, Moore A, Schedl A, Bratt E, Miyahawa K, Ladomery M, Miles C, Menke A, van Heyningen V, Hastie N.

Cancer Res. 1999 Apr 1;59(7 Suppl):1747s-1750s; discussion 1751s. Review.

PMID:
10197591
10.

The complex life of WT1.

Wagner KD, Wagner N, Schedl A.

J Cell Sci. 2003 May 1;116(Pt 9):1653-8. Review.

11.

The role of Wilms' tumor genes.

Hirose M.

J Med Invest. 1999 Aug;46(3-4):130-40. Review.

PMID:
10687307
12.

Does the Wilms' tumour suppressor gene, WT1, play roles in both splicing and transcription?

Charlieu JP, Larsson S, Miyagawa K, van Heyningen V, Hastie ND.

J Cell Sci Suppl. 1995;19:95-9. Review.

PMID:
8655654
13.

Wilms' tumor suppressor gene WT1: from structure to renal pathophysiologic features.

Mrowka C, Schedl A.

J Am Soc Nephrol. 2000 Nov;11 Suppl 16:S106-15. Review.

14.

Multiple roles for the Wilms' tumour suppressor gene, WT1 in genitourinary development.

Schedl A, Hastie N.

Mol Cell Endocrinol. 1998 May 25;140(1-2):65-9. Review.

PMID:
9722170
16.

WT1: what has the last decade told us?

Little M, Holmes G, Walsh P.

Bioessays. 1999 Mar;21(3):191-202. Review.

PMID:
10333728
17.

Regulation of gene expression by WT1 in development and tumorigenesis.

Ellisen LW.

Int J Hematol. 2002 Aug;76(2):110-6. Review.

PMID:
12215008
18.

Atypical presentation of Denys-Drash syndrome in a female with a novel Wt1 gene mutation.

Machin GA.

Birth Defects Orig Artic Ser. 1996;30(1):269-86. Review. No abstract available.

PMID:
9125334
19.

[A case of Denys-Drash syndrome with prophylactic bilateral nephrectomy].

Yamamoto K, Santo Y, Satomura K.

Nihon Jinzo Gakkai Shi. 2003;45(1):42-6. Review. Japanese.

PMID:
12680320
20.

Chronic renal failure and XY gonadal dysgenesis: "Frasier" syndrome--a commentary on reported cases.

Moorthy AV, Chesney RW, Lubinsky M.

Am J Med Genet Suppl. 1987;3:297-302. Review.

PMID:
3130865
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