Jiang YH - Search Results

1

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

Matsuura T, Sutcliffe JS, Fang P, Galjaard RJ, Jiang YH, Benton CS, Rommens JM, Beaudet AL. Matsuura T, et al. Among authors: jiang yh. Nat Genet. 1997 Jan;15(1):74-7. doi: 10.1038/ng0197-74. Nat Genet. 1997. PMID: 8988172

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: jiang yh. 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. 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

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

Jiang YH, Armstrong D, Albrecht U, Atkins CM, Noebels JL, Eichele G, Sweatt JD, Beaudet AL. Jiang YH, et al. Neuron. 1998 Oct;21(4):799-811. doi: 10.1016/s0896-6273(00)80596-6. Neuron. 1998. PMID: 9808466 Free article.

5

Genetics of Angelman syndrome.

Jiang Y, Lev-Lehman E, Bressler J, Tsai TF, Beaudet AL. Jiang Y, et al. 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.

6

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: jiang yh. Hum Mol Genet. 1999 Aug;8(8):1357-64. doi: 10.1093/hmg/8.8.1357. Hum Mol Genet. 1999. PMID: 10400982

7

Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice.

Cummings CJ, Reinstein E, Sun Y, Antalffy B, Jiang Y, Ciechanover A, Orr HT, Beaudet AL, Zoghbi HY. Cummings CJ, et al. Neuron. 1999 Dec;24(4):879-92. doi: 10.1016/s0896-6273(00)81035-1. Neuron. 1999. PMID: 10624951 Free article.

8

Genetic ablation of the steroid receptor coactivator-ubiquitin ligase, E6-AP, results in tissue-selective steroid hormone resistance and defects in reproduction.

Smith CL, DeVera DG, Lamb DJ, Nawaz Z, Jiang YH, Beaudet AL, O'Malley BW. Smith CL, et al. Among authors: jiang yh. Mol Cell Biol. 2002 Jan;22(2):525-35. doi: 10.1128/MCB.22.2.525-535.2002. Mol Cell Biol. 2002. PMID: 11756548 Free PMC article.

9

A rheostat model for a rapid and reversible form of imprinting-dependent evolution.

Beaudet AL, Jiang YH. Beaudet AL, et al. Among authors: jiang yh. Am J Hum Genet. 2002 Jun;70(6):1389-97. doi: 10.1086/340969. Epub 2002 Apr 24. Am J Hum Genet. 2002. PMID: 11992247 Free PMC article.

10

Derangements of hippocampal calcium/calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndrome.

Weeber EJ, Jiang YH, Elgersma Y, Varga AW, Carrasquillo Y, Brown SE, Christian JM, Mirnikjoo B, Silva A, Beaudet AL, Sweatt JD. Weeber EJ, et al. Among authors: jiang yh. J Neurosci. 2003 Apr 1;23(7):2634-44. doi: 10.1523/JNEUROSCI.23-07-02634.2003. J Neurosci. 2003. PMID: 12684449 Free PMC article.

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