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Results: 1 to 20 of 41

References for PMC Articles for PubMed (Select 19717458)

1.

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism.

Loat CS, Curran S, Lewis CM, Duvall J, Geschwind D, Bolton P, Craig IW.

Genes Brain Behav. 2008 Oct;7(7):754-60. doi: 10.1111/j.1601-183X.2008.00414.x.

2.

Brain-derived neurotrophic factor polymorphisms and frontal cortex morphology in schizophrenia.

Varnäs K, Lawyer G, Jönsson EG, Kulle B, Nesvåg R, Hall H, Terenius L, Agartz I.

Psychiatr Genet. 2008 Aug;18(4):177-83. doi: 10.1097/YPG.0b013e3283050a94.

PMID:
18628679
3.

MeCP2, a key contributor to neurological disease, activates and represses transcription.

Chahrour M, Jung SY, Shaw C, Zhou X, Wong ST, Qin J, Zoghbi HY.

Science. 2008 May 30;320(5880):1224-9. doi: 10.1126/science.1153252.

4.

Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure.

Schüle B, Armstrong DD, Vogel H, Oviedo A, Francke U.

Clin Genet. 2008 Aug;74(2):116-26. doi: 10.1111/j.1399-0004.2008.01005.x. Epub 2008 May 8. Review.

PMID:
18477000
5.

Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome.

Belichenko NP, Belichenko PV, Li HH, Mobley WC, Francke U.

J Comp Neurol. 2008 May 1;508(1):184-95. doi: 10.1002/cne.21673.

PMID:
18306326
6.

Abnormal functional connectivity in autism spectrum disorders during face processing.

Kleinhans NM, Richards T, Sterling L, Stegbauer KC, Mahurin R, Johnson LC, Greenson J, Dawson G, Aylward E.

Brain. 2008 Apr;131(Pt 4):1000-12. doi: 10.1093/brain/awm334. Epub 2008 Jan 29.

7.

Role of intermediate progenitor cells in cerebral cortex development.

Pontious A, Kowalczyk T, Englund C, Hevner RF.

Dev Neurosci. 2008;30(1-3):24-32. Review.

PMID:
18075251
8.

Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study.

Carter JC, Lanham DC, Pham D, Bibat G, Naidu S, Kaufmann WE.

AJNR Am J Neuroradiol. 2008 Mar;29(3):436-41. Epub 2007 Dec 7.

9.

Sex difference in mecp2 expression during a critical period of rat brain development.

Kurian JR, Forbes-Lorman RM, Auger AP.

Epigenetics. 2007 Sep;2(3):173-8. Epub 2007 Aug 6.

10.

PLINK: a tool set for whole-genome association and population-based linkage analyses.

Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC.

Am J Hum Genet. 2007 Sep;81(3):559-75. Epub 2007 Jul 25.

11.

The odyssey of MeCP2 and parental imprinting.

LaSalle JM.

Epigenetics. 2007 Jan-Mar;2(1):5-10. Review.

12.

Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation.

Nagarajan RP, Hogart AR, Gwye Y, Martin MR, LaSalle JM.

Epigenetics. 2006 Oct-Dec;1(4):e1-11.

13.

MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.

Coutinho AM, Oliveira G, Katz C, Feng J, Yan J, Yang C, Marques C, Ataíde A, Miguel TS, Borges L, Almeida J, Correia C, Currais A, Bento C, Mota-Vieira L, Temudo T, Santos M, Maciel P, Sommer SS, Vicente AM.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):475-83.

PMID:
17427193
14.

Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.

Stearns NA, Schaevitz LR, Bowling H, Nag N, Berger UV, Berger-Sweeney J.

Neuroscience. 2007 May 25;146(3):907-21. Epub 2007 Mar 23.

PMID:
17383101
15.

Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis.

Baala L, Briault S, Etchevers HC, Laumonnier F, Natiq A, Amiel J, Boddaert N, Picard C, Sbiti A, Asermouh A, Attié-Bitach T, Encha-Razavi F, Munnich A, Sefiani A, Lyonnet S.

Nat Genet. 2007 Apr;39(4):454-6. Epub 2007 Mar 11.

PMID:
17353897
16.

Gait function in newly diagnosed children with autism: Cerebellar and basal ganglia related motor disorder.

Rinehart NJ, Tonge BJ, Iansek R, McGinley J, Brereton AV, Enticott PG, Bradshaw JL.

Dev Med Child Neurol. 2006 Oct;48(10):819-24.

PMID:
16978461
17.

Principal components analysis corrects for stratification in genome-wide association studies.

Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D.

Nat Genet. 2006 Aug;38(8):904-9. Epub 2006 Jul 23.

PMID:
16862161
18.

Early progressive encephalopathy in boys and MECP2 mutations.

Kankirawatana P, Leonard H, Ellaway C, Scurlock J, Mansour A, Makris CM, Dure LS 4th, Friez M, Lane J, Kiraly-Borri C, Fabian V, Davis M, Jackson J, Christodoulou J, Kaufmann WE, Ravine D, Percy AK.

Neurology. 2006 Jul 11;67(1):164-6.

PMID:
16832102
19.

Identification of cis-regulatory elements for MECP2 expression.

Liu J, Francke U.

Hum Mol Genet. 2006 Jun 1;15(11):1769-82. Epub 2006 Apr 13.

20.

A map of recent positive selection in the human genome.

Voight BF, Kudaravalli S, Wen X, Pritchard JK.

PLoS Biol. 2006 Mar;4(3):e72. Epub 2006 Mar 7. Erratum in: PLoS Biol. 2006 Apr;4(4):e154. PLoS Biol. 2007 Jun;5(6):e147.

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