Hata J - Search Results

1

Constitutional WT1 correlate with clinical features in children with progressive nephropathy.

Takata A, Kikuchi H, Fukuzawa R, Ito S, Honda M, Hata J. Takata A, et al. Among authors: hata j. J Med Genet. 2000 Sep;37(9):698-701. doi: 10.1136/jmg.37.9.698. J Med Genet. 2000. PMID: 11182928 Free PMC article. No abstract available.

2

Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?

Kikuchi H, Takata A, Akasaka Y, Fukuzawa R, Yoneyama H, Kurosawa Y, Honda M, Kamiyama Y, Hata J. Kikuchi H, et al. Among authors: hata j. J Med Genet. 1998 Jan;35(1):45-8. doi: 10.1136/jmg.35.1.45. J Med Genet. 1998. PMID: 9475094 Free PMC article.

3

Nephrotic syndrome and end-stage renal disease with WT1 mutation detected at 3 years.

Ito S, Ikeda M, Takata A, Kikuchi H, Hata J, Honda M. Ito S, et al. Among authors: hata j. Pediatr Nephrol. 1999 Nov;13(9):790-1. doi: 10.1007/s004670050702. Pediatr Nephrol. 1999. PMID: 10603123

4

A novel WT1 gene mutation associated with wilms' tumor and congenital male genitourinary malformation.

Sakamoto J, Takata A, Fukuzawa R, Kikuchi H, Sugiyama M, Kanamori Y, Hashizume K, Hata JI. Sakamoto J, et al. Among authors: hata ji. Pediatr Res. 2001 Sep;50(3):337-44. doi: 10.1203/00006450-200109000-00008. Pediatr Res. 2001. PMID: 11518820

5

Embryonal hyperplasia of Bowman's capsular epithelium in patients with WT1 mutations.

Fukuzawa R, Eccles MR, Ikeda M, Hata J. Fukuzawa R, et al. Among authors: hata j. Pediatr Nephrol. 2003 Jan;18(1):9-13. doi: 10.1007/s00467-002-1019-7. Epub 2002 Nov 22. Pediatr Nephrol. 2003. PMID: 12488983

6

[Wilms' tumors and malformation complexes].

Hata J, Fukuzawa R, Takata A, Kikuchi H. Hata J, et al. Nihon Rinsho. 2000 Jul;58(7):1419-25. Nihon Rinsho. 2000. PMID: 10921316 Review. Japanese.

7

Isolated diffuse mesangial sclerosis and Wilms tumor suppressor gene.

Ito S, Takata A, Hataya H, Ikeda M, Kikuchi H, Hata J, Honda M. Ito S, et al. Among authors: hata j. J Pediatr. 2001 Mar;138(3):425-7. doi: 10.1067/mpd.2001.111317. J Pediatr. 2001. PMID: 11241056

8

Alport syndrome-like basement membrane changes in Frasier syndrome: an electron microscopy study.

Ito S, Hataya H, Ikeda M, Takata A, Kikuchi H, Hata J, Morikawa Y, Kawamura S, Honda M. Ito S, et al. Among authors: hata j. Am J Kidney Dis. 2003 May;41(5):1110-5. doi: 10.1016/s0272-6386(03)00209-9. Am J Kidney Dis. 2003. PMID: 12722046

9

Beckwith-Wiedemann syndrome-associated hepatoblastoma: wnt signal activation occurs later in tumorigenesis in patients with 11p15.5 uniparental disomy.

Fukuzawa R, Hata J, Hayashi Y, Ikeda H, Reeve AE. Fukuzawa R, et al. Among authors: hata j. Pediatr Dev Pathol. 2003 Jul-Aug;6(4):299-306. doi: 10.1007/s10024-003-1009-1. Pediatr Dev Pathol. 2003. PMID: 14692643

10

Responsiveness of chemotherapy based on the histological type and Wilms' tumor suppressor gene mutation in bilateral Wilms' tumor.

Shibata R, Takata A, Hashiguchi A, Umezawa A, Yamada T, Hata J. Shibata R, et al. Among authors: hata j. Pathol Int. 2003 Apr;53(4):214-20. doi: 10.1046/j.1320-5463.2003.01457.x. Pathol Int. 2003. PMID: 12675764

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