Bressler J - Search Results

1

A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A.

Jiang YH, Sahoo T, Michaelis RC, Bercovich D, Bressler J, Kashork CD, Liu Q, Shaffer LG, Schroer RJ, Stockton DW, Spielman RS, Stevenson RE, Beaudet AL. Jiang YH, et al. Among authors: bressler j. Am J Med Genet A. 2004 Nov 15;131(1):1-10. doi: 10.1002/ajmg.a.30297. Am J Med Genet A. 2004. PMID: 15389703

2

The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region.

Sutcliffe JS, Jiang YH, Galijaard RJ, Matsuura T, Fang P, Kubota T, Christian SL, Bressler J, Cattanach B, Ledbetter DH, Beaudet AL. Sutcliffe JS, et al. Among authors: bressler j. Genome Res. 1997 Apr;7(4):368-77. doi: 10.1101/gr.7.4.368. Genome Res. 1997. PMID: 9110176 Free PMC article.

3

Imprinting in Angelman and Prader-Willi syndromes.

Jiang Y, Tsai TF, Bressler J, Beaudet AL. Jiang Y, et al. Among authors: bressler j. 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.

4

Genetics of Angelman syndrome.

Jiang Y, Lev-Lehman E, Bressler J, Tsai TF, Beaudet AL. Jiang Y, et al. Among authors: bressler j. 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.

5

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. Among authors: bressler j. Hum Mol Genet. 1999 Aug;8(8):1357-64. doi: 10.1093/hmg/8.8.1357. Hum Mol Genet. 1999. PMID: 10400982

6

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. Nat Genet. 2001 Jul;28(3):232-40. doi: 10.1038/90067. Nat Genet. 2001. PMID: 11431693

7

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. Among authors: bressler j. Genesis. 2003 Dec;37(4):151-61. doi: 10.1002/gene.10237. Genesis. 2003. PMID: 14666508

8

Epigenetics and human disease.

Jiang YH, Bressler J, Beaudet AL. Jiang YH, et al. Among authors: bressler j. Annu Rev Genomics Hum Genet. 2004;5:479-510. doi: 10.1146/annurev.genom.5.061903.180014. Annu Rev Genomics Hum Genet. 2004. PMID: 15485357 Review.

9

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: bressler j. Genesis. 2006 Jan;44(1):12-22. doi: 10.1002/gene.20179. Genesis. 2006. PMID: 16397868

10

Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.

Jiang YH, Wauki K, Liu Q, Bressler J, Pan Y, Kashork CD, Shaffer LG, Beaudet AL. Jiang YH, et al. Among authors: bressler j. BMC Genomics. 2008 Jan 28;9:50. doi: 10.1186/1471-2164-9-50. BMC Genomics. 2008. PMID: 18226259 Free PMC article.

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