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Items: 1 to 20 of 31

1.

Modeling the functional genomics of autism using human neurons.

Konopka G, Wexler E, Rosen E, Mukamel Z, Osborn GE, Chen L, Lu D, Gao F, Gao K, Lowe JK, Geschwind DH.

Mol Psychiatry. 2012 Feb;17(2):202-14. doi: 10.1038/mp.2011.60. Epub 2011 Jun 7.

2.

Conserved subcortical and divergent cortical expression of proteins encoded by orthologs of the autism risk gene MET.

Judson MC, Amaral DG, Levitt P.

Cereb Cortex. 2011 Jul;21(7):1613-26. doi: 10.1093/cercor/bhq223. Epub 2010 Dec 1.

3.

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.

Roll P, Vernes SC, Bruneau N, Cillario J, Ponsole-Lenfant M, Massacrier A, Rudolf G, Khalife M, Hirsch E, Fisher SE, Szepetowski P.

Hum Mol Genet. 2010 Dec 15;19(24):4848-60. doi: 10.1093/hmg/ddq415. Epub 2010 Sep 21.

4.

Evidence of cell-nonautonomous changes in dendrite and dendritic spine morphology in the met-signaling-deficient mouse forebrain.

Judson MC, Eagleson KL, Wang L, Levitt P.

J Comp Neurol. 2010 Nov 1;518(21):4463-78. doi: 10.1002/cne.22467.

5.

Investigation of SERPINE1 genetic polymorphism in Macedonian patients with occlusive artery disease and deep vein thrombosis.

Spiroski I, Kedev S, Antov S, Trajkov D, Petlichkovski A, Dzhekova-Stojkova S, Kostovska S, Spiroski M.

Kardiol Pol. 2009 Oct;67(10):1088-94.

6.

Human-specific transcriptional regulation of CNS development genes by FOXP2.

Konopka G, Bomar JM, Winden K, Coppola G, Jonsson ZO, Gao F, Peng S, Preuss TM, Wohlschlegel JA, Geschwind DH.

Nature. 2009 Nov 12;462(7270):213-7. doi: 10.1038/nature08549.

7.

Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder.

Jackson PB, Boccuto L, Skinner C, Collins JS, Neri G, Gurrieri F, Schwartz CE.

Autism Res. 2009 Aug;2(4):232-6. doi: 10.1002/aur.87.

PMID:
19681062
8.

Genetic advances in autism: heterogeneity and convergence on shared pathways.

Bill BR, Geschwind DH.

Curr Opin Genet Dev. 2009 Jun;19(3):271-8. doi: 10.1016/j.gde.2009.04.004. Epub 2009 May 26. Review.

9.

Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.

Campbell DB, Li C, Sutcliffe JS, Persico AM, Levitt P.

Autism Res. 2008 Jun;1(3):159-68. doi: 10.1002/aur.27.

10.

Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain.

Judson MC, Bergman MY, Campbell DB, Eagleson KL, Levitt P.

J Comp Neurol. 2009 Apr 10;513(5):511-31. doi: 10.1002/cne.21969.

11.

MET and autism susceptibility: family and case-control studies.

Sousa I, Clark TG, Toma C, Kobayashi K, Choma M, Holt R, Sykes NH, Lamb JA, Bailey AJ, Battaglia A, Maestrini E, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC).

Eur J Hum Genet. 2009 Jun;17(6):749-58. doi: 10.1038/ejhg.2008.215. Epub 2008 Nov 12.

12.

A functional genetic link between distinct developmental language disorders.

Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE.

N Engl J Med. 2008 Nov 27;359(22):2337-45. doi: 10.1056/NEJMoa0802828. Epub 2008 Nov 5.

13.

Advances in autism genetics: on the threshold of a new neurobiology.

Abrahams BS, Geschwind DH.

Nat Rev Genet. 2008 May;9(5):341-55. doi: 10.1038/nrg2346. Review. Erratum in: Nat Rev Genet. 2008 Jun;9(6):493.

14.

Hepatocyte growth factor and c-Met promote dendritic maturation during hippocampal neuron differentiation via the Akt pathway.

Lim CS, Walikonis RS.

Cell Signal. 2008 May;20(5):825-35. doi: 10.1016/j.cellsig.2007.12.013. Epub 2007 Dec 27.

15.

Neuroanatomy of autism.

Amaral DG, Schumann CM, Nordahl CW.

Trends Neurosci. 2008 Mar;31(3):137-45. doi: 10.1016/j.tins.2007.12.005. Epub 2008 Feb 6. Review.

PMID:
18258309
16.

Structural variation of chromosomes in autism spectrum disorder.

Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J, Shago M, Moessner R, Pinto D, Ren Y, Thiruvahindrapduram B, Fiebig A, Schreiber S, Friedman J, Ketelaars CE, Vos YJ, Ficicioglu C, Kirkpatrick S, Nicolson R, Sloman L, Summers A, Gibbons CA, Teebi A, Chitayat D, Weksberg R, Thompson A, Vardy C, Crosbie V, Luscombe S, Baatjes R, Zwaigenbaum L, Roberts W, Fernandez B, Szatmari P, Scherer SW.

Am J Hum Genet. 2008 Feb;82(2):477-88. doi: 10.1016/j.ajhg.2007.12.009. Epub 2008 Jan 17.

17.

Mapping early brain development in autism.

Courchesne E, Pierce K, Schumann CM, Redcay E, Buckwalter JA, Kennedy DP, Morgan J.

Neuron. 2007 Oct 25;56(2):399-413. Review.

18.

Disruption of cerebral cortex MET signaling in autism spectrum disorder.

Campbell DB, D'Oronzio R, Garbett K, Ebert PJ, Mirnics K, Levitt P, Persico AM.

Ann Neurol. 2007 Sep;62(3):243-50.

PMID:
17696172
19.
20.

A genetic variant that disrupts MET transcription is associated with autism.

Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P.

Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16834-9. Epub 2006 Oct 19.

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