Tsai TF - Search Results

1

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome.

Tsai TF, Jiang YH, Bressler J, Armstrong D, Beaudet AL. Tsai TF, et al. Hum Mol Genet. 1999 Aug;8(8):1357-64. doi: 10.1093/hmg/8.8.1357. Hum Mol Genet. 1999. PMID: 10400982

2

Evidence for translational regulation of the imprinted Snurf-Snrpn locus in mice.

Tsai TF, Chen KS, Weber JS, Justice MJ, Beaudet AL. Tsai TF, et al. Hum Mol Genet. 2002 Jul 1;11(14):1659-68. doi: 10.1093/hmg/11.14.1659. Hum Mol Genet. 2002. PMID: 12075010

3

Disruption of the genomic imprint in trans with homologous recombination at Snrpn in ES cells.

Tsai TF, Bressler J, Jiang YH, Beaudet AL. Tsai TF, et al. Genesis. 2003 Dec;37(4):151-61. doi: 10.1002/gene.10237. Genesis. 2003. PMID: 14666508

4

Mouse imprinting defect mutations that model Angelman syndrome.

Wu MY, Chen KS, Bressler J, Hou A, Tsai TF, Beaudet AL. Wu MY, et al. Among authors: tsai tf. Genesis. 2006 Jan;44(1):12-22. doi: 10.1002/gene.20179. Genesis. 2006. PMID: 16397868

5

Imprinting in Angelman and Prader-Willi syndromes.

Jiang Y, Tsai TF, Bressler J, Beaudet AL. Jiang Y, et al. Among authors: tsai tf. Curr Opin Genet Dev. 1998 Jun;8(3):334-42. doi: 10.1016/s0959-437x(98)80091-9. Curr Opin Genet Dev. 1998. PMID: 9691003 Review.

6

The spectrum of mutations in UBE3A causing Angelman syndrome.

Fang P, Lev-Lehman E, Tsai TF, Matsuura T, Benton CS, Sutcliffe JS, Christian SL, Kubota T, Halley DJ, Meijers-Heijboer H, Langlois S, Graham JM Jr, Beuten J, Willems PJ, Ledbetter DH, Beaudet AL. Fang P, et al. Among authors: tsai tf. Hum Mol Genet. 1999 Jan;8(1):129-35. doi: 10.1093/hmg/8.1.129. Hum Mol Genet. 1999. PMID: 9887341

7

Genetics of Angelman syndrome.

Jiang Y, Lev-Lehman E, Bressler J, Tsai TF, Beaudet AL. Jiang Y, et al. Among authors: tsai tf. Am J Hum Genet. 1999 Jul;65(1):1-6. doi: 10.1086/302473. Am J Hum Genet. 1999. PMID: 10364509 Free PMC article. Review. No abstract available.

8

The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.

Bressler J, Tsai TF, Wu MY, Tsai SF, Ramirez MA, Armstrong D, Beaudet AL. Bressler J, et al. Among authors: tsai sf, tsai tf. Nat Genet. 2001 Jul;28(3):232-40. doi: 10.1038/90067. Nat Genet. 2001. PMID: 11431693

9

Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain.

Wu MY, Tsai TF, Beaudet AL. Wu MY, et al. Among authors: tsai tf. Genes Dev. 2006 Oct 15;20(20):2859-70. doi: 10.1101/gad.1452206. Genes Dev. 2006. PMID: 17043311 Free PMC article.

10

Prenatal diagnosis and carrier detection for a point mutation in UBE3A causing Angelman syndrome.

Tsai TF, Raas-Rothschild A, Ben-Neriah Z, Beaudet AL. Tsai TF, et al. Am J Hum Genet. 1998 Nov;63(5):1561-3. doi: 10.1086/302120. Am J Hum Genet. 1998. PMID: 9792887 Free PMC article. No abstract available.

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