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Results: 1 to 20 of 59

Cited In for PubMed (Select 18231125)

1.

ZNF804A Transcriptional Networks in Differentiating Neurons Derived from Induced Pluripotent Stem Cells of Human Origin.

Chen J, Lin M, Hrabovsky A, Pedrosa E, Dean J, Jain S, Zheng D, Lachman HM.

PLoS One. 2015 Apr 23;10(4):e0124597. doi: 10.1371/journal.pone.0124597. eCollection 2015.

2.

The interplay between synaptic activity and neuroligin function in the CNS.

Hu X, Luo JH, Xu J.

Biomed Res Int. 2015;2015:498957. doi: 10.1155/2015/498957. Epub 2015 Mar 9. Review.

3.

Autism-associated mutation inhibits protein kinase C-mediated neuroligin-4X enhancement of excitatory synapses.

Bemben MA, Nguyen QA, Wang T, Li Y, Nicoll RA, Roche KW.

Proc Natl Acad Sci U S A. 2015 Feb 24;112(8):2551-6. doi: 10.1073/pnas.1500501112. Epub 2015 Feb 9.

PMID:
25675530
4.

The Inheritance of Tourette Disorder: A review.

Pauls DL, Fernandez TV, Mathews CA, State MW, Scharf JM.

J Obsessive Compuls Relat Disord. 2014 Oct 1;3(4):380-385.

PMID:
25506544
5.

Animal models of tic disorders: a translational perspective.

Godar SC, Mosher LJ, Di Giovanni G, Bortolato M.

J Neurosci Methods. 2014 Dec 30;238:54-69. doi: 10.1016/j.jneumeth.2014.09.008. Epub 2014 Sep 20.

PMID:
25244952
6.

An inside job: how endosomal Na(+)/H(+) exchangers link to autism and neurological disease.

Kondapalli KC, Prasad H, Rao R.

Front Cell Neurosci. 2014 Jun 23;8:172. doi: 10.3389/fncel.2014.00172. eCollection 2014. Review.

7.

Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators.

Bellott DW, Hughes JF, Skaletsky H, Brown LG, Pyntikova T, Cho TJ, Koutseva N, Zaghlul S, Graves T, Rock S, Kremitzki C, Fulton RS, Dugan S, Ding Y, Morton D, Khan Z, Lewis L, Buhay C, Wang Q, Watt J, Holder M, Lee S, Nazareth L, Alföldi J, Rozen S, Muzny DM, Warren WC, Gibbs RA, Wilson RK, Page DC.

Nature. 2014 Apr 24;508(7497):494-9. doi: 10.1038/nature13206. Erratum in: Nature. 2014 Oct 2;514(7520):126. Alföldi, Jessica [added].

8.

Balance within the Neurexin Trans-Synaptic Connexus Stabilizes Behavioral Control.

Clarke RA, Eapen V.

Front Hum Neurosci. 2014 Feb 27;8:52. doi: 10.3389/fnhum.2014.00052. eCollection 2014. Review.

9.

The role of ionotropic glutamate receptors in childhood neurodevelopmental disorders: autism spectrum disorders and fragile x syndrome.

Uzunova G, Hollander E, Shepherd J.

Curr Neuropharmacol. 2014 Jan;12(1):71-98. doi: 10.2174/1570159X113116660046.

10.

Emerging links between homeostatic synaptic plasticity and neurological disease.

Wondolowski J, Dickman D.

Front Cell Neurosci. 2013 Nov 21;7:223. doi: 10.3389/fncel.2013.00223. Review.

11.

Genetic susceptibility and neurotransmitters in Tourette syndrome.

Paschou P, Fernandez TV, Sharp F, Heiman GA, Hoekstra PJ.

Int Rev Neurobiol. 2013;112:155-77. doi: 10.1016/B978-0-12-411546-0.00006-8. Review.

12.

Sex chromosome-wide association analysis suggested male-specific risk genes for alcohol dependence.

Zuo L, Wang K, Zhang X, Pan X, Wang G, Krystal JH, Zhang H, Luo X.

Psychiatr Genet. 2013 Dec;23(6):233-8. doi: 10.1097/YPG.0b013e328364b8c7.

13.

The implication of neuroactive steroids in Tourette's syndrome pathogenesis: A role for 5α-reductase?

Bortolato M, Frau R, Godar SC, Mosher LJ, Paba S, Marrosu F, Devoto P.

J Neuroendocrinol. 2013 Nov;25(11):1196-208. doi: 10.1111/jne.12066. Review.

14.

The functional genetic link of NLGN4X knockdown and neurodevelopment in neural stem cells.

Shi L, Chang X, Zhang P, Coba MP, Lu W, Wang K.

Hum Mol Genet. 2013 Sep 15;22(18):3749-60. doi: 10.1093/hmg/ddt226. Epub 2013 May 24.

15.

Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.

Liu Y, Du Y, Liu W, Yang C, Liu Y, Wang H, Gong X.

PLoS One. 2013;8(2):e56639. doi: 10.1371/journal.pone.0056639. Epub 2013 Feb 26.

16.

Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder.

Hooper SD, Johansson AC, Tellgren-Roth C, Stattin EL, Dahl N, Cavelier L, Feuk L.

BMC Med Genet. 2012 Dec 19;13:123. doi: 10.1186/1471-2350-13-123.

17.

Lighting a path: genetic studies pinpoint neurodevelopmental mechanisms in autism and related disorders.

Pescosolido MF, Yang U, Sabbagh M, Morrow EM.

Dialogues Clin Neurosci. 2012 Sep;14(3):239-52. Review.

18.

Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder.

Steinberg KM, Ramachandran D, Patel VC, Shetty AC, Cutler DJ, Zwick ME.

Mol Autism. 2012 Sep 28;3(1):8. doi: 10.1186/2040-2392-3-8.

19.

Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism.

Clarke RA, Lee S, Eapen V.

Transl Psychiatry. 2012 Sep 4;2:e158. doi: 10.1038/tp.2012.75. Review. Erratum in: Transl Psychiatry. 2012;2:e163.

20.

Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder.

Yanagi K, Kaname T, Wakui K, Hashimoto O, Fukushima Y, Naritomi K.

Autism Res Treat. 2012;2012:724072. doi: 10.1155/2012/724072. Epub 2012 Jul 16.

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