Ohta T - Search Results

1

Imprinting-mutation mechanisms in Prader-Willi syndrome.

Ohta T, Gray TA, Rogan PK, Buiting K, Gabriel JM, Saitoh S, Muralidhar B, Bilienska B, Krajewska-Walasek M, Driscoll DJ, Horsthemke B, Butler MG, Nicholls RD. Ohta T, et al. Am J Hum Genet. 1999 Feb;64(2):397-413. doi: 10.1086/302233. Am J Hum Genet. 1999. PMID: 9973278 Free PMC article.

2

Structure and function correlations at the imprinted mouse Snrpn locus.

Gabriel JM, Gray TA, Stubbs L, Saitoh S, Ohta T, Nicholls RD. Gabriel JM, et al. Among authors: ohta t. Mamm Genome. 1998 Oct;9(10):788-93. doi: 10.1007/s003359900868. Mamm Genome. 1998. PMID: 9745031

3

Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation.

Ohta T, Buiting K, Kokkonen H, McCandless S, Heeger S, Leisti H, Driscoll DJ, Cassidy SB, Horsthemke B, Nicholls RD. Ohta T, et al. Am J Hum Genet. 1999 Feb;64(2):385-96. doi: 10.1086/302232. Am J Hum Genet. 1999. PMID: 9973277 Free PMC article.

4

A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes.

Gabriel JM, Merchant M, Ohta T, Ji Y, Caldwell RG, Ramsey MJ, Tucker JD, Longnecker R, Nicholls RD. Gabriel JM, et al. Among authors: ohta t. Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9258-63. doi: 10.1073/pnas.96.16.9258. Proc Natl Acad Sci U S A. 1999. PMID: 10430930 Free PMC article.

5

Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models.

Nicholls RD, Ohta T, Gray TA. Nicholls RD, et al. Among authors: ohta t. Acta Paediatr Suppl. 1999 Dec;88(433):99-104. doi: 10.1111/j.1651-2227.1999.tb14414.x. Acta Paediatr Suppl. 1999. PMID: 10626556 Review.

6

Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site.

Chai JH, Locke DP, Ohta T, Greally JM, Nicholls RD. Chai JH, et al. Among authors: ohta t. Mamm Genome. 2001 Nov;12(11):813-21. doi: 10.1007/s00335-001-2083-1. Mamm Genome. 2001. PMID: 11845283

7

Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons.

Chai JH, Locke DP, Greally JM, Knoll JH, Ohta T, Dunai J, Yavor A, Eichler EE, Nicholls RD. Chai JH, et al. Among authors: ohta t. Am J Hum Genet. 2003 Oct;73(4):898-925. doi: 10.1086/378816. Epub 2003 Sep 23. Am J Hum Genet. 2003. PMID: 14508708 Free PMC article.

8

Report of the fourth international workshop on human chromosome 15 mapping 1997.

Morton CC, Christian SL, Donlon TA, Driscoll DJ, Fink JK, Gabriel JM, Gotway G, Greally JM, Hitchins MP, Howard HC, Ji Y, Leonard S, Lerner T, Magenis E, Malcolm S, Ohta T, Rainier S, Rees M, Riley B, Robinson WP, Saitoh S, Schultz R, Sell S, Sharp JD, Nicholls RD, et al. Morton CC, et al. Among authors: ohta t. Cytogenet Cell Genet. 1999;84(1-2):12-21. doi: 10.1159/000015203. Cytogenet Cell Genet. 1999. PMID: 10343092 No abstract available.

9

Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a.

Yamasaki K, Joh K, Ohta T, Masuzaki H, Ishimaru T, Mukai T, Niikawa N, Ogawa M, Wagstaff J, Kishino T. Yamasaki K, et al. Among authors: ohta t. Hum Mol Genet. 2003 Apr 15;12(8):837-47. doi: 10.1093/hmg/ddg106. Hum Mol Genet. 2003. PMID: 12668607

10

Physical map of a YAC contig containing the region of the human gene (HYRC) complementing hyper-radiosensitivity of the scid mouse mutation.

Watanabe Y, Matsumoto N, Ohta T, Tsujita T, Niikawa N. Watanabe Y, et al. Among authors: ohta t. Jpn J Hum Genet. 1996 Mar;41(1):149-58. doi: 10.1007/BF01892622. Jpn J Hum Genet. 1996. PMID: 8914630

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