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Items: 1 to 20 of 104

1.

Angelman syndrome: advancing the research frontier of neurodevelopmental disorders.

Philpot BD, Thompson CE, Franco L, Williams CA.

J Neurodev Disord. 2011 Mar;3(1):50-6. doi: 10.1007/s11689-010-9066-z.

2.

Normal social seeking behavior, hypoactivity and reduced exploratory range in a mouse model of Angelman syndrome.

Allensworth M, Saha A, Reiter LT, Heck DH.

BMC Genet. 2011 Jan 14;12:7. doi: 10.1186/1471-2156-12-7.

3.

Highly parallel SNP genotyping reveals high-resolution landscape of mono-allelic Ube3a expression associated with locus-wide antisense transcription.

Numata K, Kohama C, Abe K, Kiyosawa H.

Nucleic Acids Res. 2011 Apr;39(7):2649-57. doi: 10.1093/nar/gkq1201.

4.

EphB-mediated degradation of the RhoA GEF Ephexin5 relieves a developmental brake on excitatory synapse formation.

Margolis SS, Salogiannis J, Lipton DM, Mandel-Brehm C, Wills ZP, Mardinly AR, Hu L, Greer PL, Bikoff JB, Ho HY, Soskis MJ, Sahin M, Greenberg ME.

Cell. 2010 Oct 29;143(3):442-55. doi: 10.1016/j.cell.2010.09.038.

5.

Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes.

Chamberlain SJ, Chen PF, Ng KY, Bourgois-Rocha F, Lemtiri-Chlieh F, Levine ES, Lalande M.

Proc Natl Acad Sci U S A. 2010 Oct 12;107(41):17668-73. doi: 10.1073/pnas.1004487107.

6.

Clarke's column neurons as the focus of a corticospinal corollary circuit.

Hantman AW, Jessell TM.

Nat Neurosci. 2010 Oct;13(10):1233-9. doi: 10.1038/nn.2637.

7.

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.

PLoS One. 2010 Aug 20;5(8):e12278. doi: 10.1371/journal.pone.0012278.

8.

Genome-wide analysis of expression modes and DNA methylation status at sense-antisense transcript loci in mouse.

Watanabe Y, Numata K, Murata S, Osada Y, Saito R, Nakaoka H, Yamamoto N, Watanabe K, Kato H, Abe K, Kiyosawa H.

Genomics. 2010 Dec;96(6):333-41. doi: 10.1016/j.ygeno.2010.08.007.

9.

Characterization of the Brain 26S Proteasome and its Interacting Proteins.

Tai HC, Besche H, Goldberg AL, Schuman EM.

Front Mol Neurosci. 2010 May 21;3. pii: 12. doi: 10.3389/fnmol.2010.00012.

10.

Loss of dopaminergic neurons and resulting behavioural deficits in mouse model of Angelman syndrome.

Mulherkar SA, Jana NR.

Neurobiol Dis. 2010 Dec;40(3):586-92. doi: 10.1016/j.nbd.2010.08.002.

PMID:
20696245
11.

Double-blind therapeutic trial in Angelman syndrome using betaine and folic acid.

Peters SU, Bird LM, Kimonis V, Glaze DG, Shinawi LM, Bichell TJ, Barbieri-Welge R, Nespeca M, Anselm I, Waisbren S, Sanborn E, Sun Q, O'Brien WE, Beaudet AL, Bacino CA.

Am J Med Genet A. 2010 Aug;152A(8):1994-2001. doi: 10.1002/ajmg.a.33509.

12.

Sex-specific parent-of-origin allelic expression in the mouse brain.

Gregg C, Zhang J, Butler JE, Haig D, Dulac C.

Science. 2010 Aug 6;329(5992):682-5. doi: 10.1126/science.1190831.

13.

High-resolution analysis of parent-of-origin allelic expression in the mouse brain.

Gregg C, Zhang J, Weissbourd B, Luo S, Schroth GP, Haig D, Dulac C.

Science. 2010 Aug 6;329(5992):643-8. doi: 10.1126/science.1190830.

14.

Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry.

Kravitz AV, Freeze BS, Parker PR, Kay K, Thwin MT, Deisseroth K, Kreitzer AC.

Nature. 2010 Jul 29;466(7306):622-6. doi: 10.1038/nature09159.

15.

Clinical and genetic aspects of Angelman syndrome.

Williams CA, Driscoll DJ, Dagli AI.

Genet Med. 2010 Jul;12(7):385-95. doi: 10.1097/GIM.0b013e3181def138. Review.

PMID:
20445456
16.

Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome.

Gustin RM, Bichell TJ, Bubser M, Daily J, Filonova I, Mrelashvili D, Deutch AY, Colbran RJ, Weeber EJ, Haas KF.

Neurobiol Dis. 2010 Sep;39(3):283-91. doi: 10.1016/j.nbd.2010.04.012.

17.

Genomic imprinting of experience-dependent cortical plasticity by the ubiquitin ligase gene Ube3a.

Sato M, Stryker MP.

Proc Natl Acad Sci U S A. 2010 Mar 23;107(12):5611-6. doi: 10.1073/pnas.1001281107.

18.

The Angelman Syndrome protein Ube3A regulates synapse development by ubiquitinating arc.

Greer PL, Hanayama R, Bloodgood BL, Mardinly AR, Lipton DM, Flavell SW, Kim TK, Griffith EC, Waldon Z, Maehr R, Ploegh HL, Chowdhury S, Worley PF, Steen J, Greenberg ME.

Cell. 2010 Mar 5;140(5):704-16. doi: 10.1016/j.cell.2010.01.026.

19.

Long nuclear-retained non-coding RNAs and allele-specific higher-order chromatin organization at imprinted snoRNA gene arrays.

Vitali P, Royo H, Marty V, Bortolin-Cavaillé ML, Cavaillé J.

J Cell Sci. 2010 Jan 1;123(Pt 1):70-83. doi: 10.1242/jcs.054957.

20.

Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.

Leung KN, Vallero RO, DuBose AJ, Resnick JL, LaSalle JM.

Hum Mol Genet. 2009 Nov 15;18(22):4227-38. doi: 10.1093/hmg/ddp373.

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