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Items: 1 to 20 of 93

1.

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model.

Stark KL, Xu B, Bagchi A, Lai WS, Liu H, Hsu R, Wan X, Pavlidis P, Mills AA, Karayiorgou M, Gogos JA.

Nat Genet. 2008 Jun;40(6):751-60. doi: 10.1038/ng.138. Epub 2008 May 11.

PMID:
18469815
2.

MicroRNA Profiling of Neurons Generated Using Induced Pluripotent Stem Cells Derived from Patients with Schizophrenia and Schizoaffective Disorder, and 22q11.2 Del.

Zhao D, Lin M, Chen J, Pedrosa E, Hrabovsky A, Fourcade HM, Zheng D, Lachman HM.

PLoS One. 2015 Jul 14;10(7):e0132387. doi: 10.1371/journal.pone.0132387. eCollection 2015.

3.

Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11 deletion syndrome mouse model.

Toritsuka M, Kimoto S, Muraki K, Landek-Salgado MA, Yoshida A, Yamamoto N, Horiuchi Y, Hiyama H, Tajinda K, Keni N, Illingworth E, Iwamoto T, Kishimoto T, Sawa A, Tanigaki K.

Proc Natl Acad Sci U S A. 2013 Oct 22;110(43):17552-7. doi: 10.1073/pnas.1312661110. Epub 2013 Oct 7.

4.

Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia.

Sivagnanasundaram S, Fletcher D, Hubank M, Illingworth E, Skuse D, Scambler P.

Brain Res. 2007 Mar 30;1139:48-59. Epub 2007 Jan 10.

PMID:
17292336
5.

Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex.

Fénelon K, Mukai J, Xu B, Hsu PK, Drew LJ, Karayiorgou M, Fischbach GD, Macdermott AB, Gogos JA.

Proc Natl Acad Sci U S A. 2011 Mar 15;108(11):4447-52. doi: 10.1073/pnas.1101219108. Epub 2011 Feb 28.

6.

Derepression of a neuronal inhibitor due to miRNA dysregulation in a schizophrenia-related microdeletion.

Xu B, Hsu PK, Stark KL, Karayiorgou M, Gogos JA.

Cell. 2013 Jan 17;152(1-2):262-75. doi: 10.1016/j.cell.2012.11.052.

7.

Monoallelic deletion of the microRNA biogenesis gene Dgcr8 produces deficits in the development of excitatory synaptic transmission in the prefrontal cortex.

Schofield CM, Hsu R, Barker AJ, Gertz CC, Blelloch R, Ullian EM.

Neural Dev. 2011 Apr 5;6:11. doi: 10.1186/1749-8104-6-11.

8.

Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome.

Sellier C, Hwang VJ, Dandekar R, Durbin-Johnson B, Charlet-Berguerand N, Ander BP, Sharp FR, Angkustsiri K, Simon TJ, Tassone F.

PLoS One. 2014 Aug 1;9(8):e103884. doi: 10.1371/journal.pone.0103884. eCollection 2014.

9.

A comprehensive analysis of 22q11 gene expression in the developing and adult brain.

Maynard TM, Haskell GT, Peters AZ, Sikich L, Lieberman JA, LaMantia AS.

Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14433-8. Epub 2003 Nov 12.

10.

Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion.

Mukai J, Dhilla A, Drew LJ, Stark KL, Cao L, MacDermott AB, Karayiorgou M, Gogos JA.

Nat Neurosci. 2008 Nov;11(11):1302-10. doi: 10.1038/nn.2204. Epub 2008 Oct 5.

11.

A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice.

Hiroi N, Zhu H, Lee M, Funke B, Arai M, Itokawa M, Kucherlapati R, Morrow B, Sawamura T, Agatsuma S.

Proc Natl Acad Sci U S A. 2005 Dec 27;102(52):19132-7. Epub 2005 Dec 19.

12.

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

Paylor R, McIlwain KL, McAninch R, Nellis A, Yuva-Paylor LA, Baldini A, Lindsay EA.

Hum Mol Genet. 2001 Nov 1;10(23):2645-50.

PMID:
11726551
13.

MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review.

Forstner AJ, Degenhardt F, Schratt G, Nöthen MM.

Front Mol Neurosci. 2013 Dec 5;6:47. doi: 10.3389/fnmol.2013.00047. Review.

14.

An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.

Frank DU, Fotheringham LK, Brewer JA, Muglia LJ, Tristani-Firouzi M, Capecchi MR, Moon AM.

Development. 2002 Oct;129(19):4591-603.

15.

Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome.

Philip N, Bassett A.

Behav Genet. 2011 May;41(3):403-12. doi: 10.1007/s10519-011-9468-z. Epub 2011 May 15. Review.

16.

Signature MicroRNA expression patterns identified in humans with 22q11.2 deletion/DiGeorge syndrome.

de la Morena MT, Eitson JL, Dozmorov IM, Belkaya S, Hoover AR, Anguiano E, Pascual MV, van Oers NS.

Clin Immunol. 2013 Apr;147(1):11-22. doi: 10.1016/j.clim.2013.01.011. Epub 2013 Jan 30.

17.

Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model.

Hiramoto T, Kang G, Suzuki G, Satoh Y, Kucherlapati R, Watanabe Y, Hiroi N.

Hum Mol Genet. 2011 Dec 15;20(24):4775-85. doi: 10.1093/hmg/ddr404. Epub 2011 Sep 9.

18.

Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain.

Harper KM, Hiramoto T, Tanigaki K, Kang G, Suzuki G, Trimble W, Hiroi N.

Hum Mol Genet. 2012 Aug 1;21(15):3489-99. doi: 10.1093/hmg/dds180. Epub 2012 May 15.

19.

MicroRNA in schizophrenia: genetic and expression analysis of miR-130b (22q11).

Burmistrova OA, Goltsov AY, Abramova LI, Kaleda VG, Orlova VA, Rogaev EI.

Biochemistry (Mosc). 2007 May;72(5):578-82.

20.

MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome.

Merico D, Costain G, Butcher NJ, Warnica W, Ogura L, Alfred SE, Brzustowicz LM, Bassett AS.

Front Neurol. 2014 Nov 21;5:238. doi: 10.3389/fneur.2014.00238. eCollection 2014.

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