Jiang YH - Search Results

1

Human disorders of ubiquitination and proteasomal degradation.

Jiang YH, Beaudet AL. Jiang YH, et al. Curr Opin Pediatr. 2004 Aug;16(4):419-26. doi: 10.1097/01.mop.0000133634.79661.cd. Curr Opin Pediatr. 2004. PMID: 15273504 Review.

2

Epigenetics and human disease.

Jiang YH, Bressler J, Beaudet AL. Jiang YH, et al. 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.

3

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. 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

4

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.

5

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: jiang yh. Genesis. 2003 Dec;37(4):151-61. doi: 10.1002/gene.10237. Genesis. 2003. PMID: 14666508

6

Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.

Jiang YH, Pan Y, Zhu L, Landa L, Yoo J, Spencer C, Lorenzo I, Brilliant M, Noebels J, Beaudet AL. Jiang YH, et al. PLoS One. 2010 Aug 20;5(8):e12278. doi: 10.1371/journal.pone.0012278. PLoS One. 2010. PMID: 20808828 Free PMC article.

7

Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome.

Su H, Fan W, Coskun PE, Vesa J, Gold JA, Jiang YH, Potluri P, Procaccio V, Acab A, Weiss JH, Wallace DC, Kimonis VE. Su H, et al. Among authors: jiang yh. Neurosci Lett. 2011 Jan 7;487(2):129-33. doi: 10.1016/j.neulet.2009.06.079. Epub 2009 Jun 27. Neurosci Lett. 2011. PMID: 19563863 Free PMC article.

8

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

9

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

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results