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Results: 1 to 20 of 70

References for PMC Articles for PubMed (Select 20471353)

1.

LRRTM2 interacts with Neurexin1 and regulates excitatory synapse formation.

de Wit J, Sylwestrak E, O'Sullivan ML, Otto S, Tiglio K, Savas JN, Yates JR 3rd, Comoletti D, Taylor P, Ghosh A.

Neuron. 2009 Dec 24;64(6):799-806. doi: 10.1016/j.neuron.2009.12.019.

2.

LRRTM2 functions as a neurexin ligand in promoting excitatory synapse formation.

Ko J, Fuccillo MV, Malenka RC, Südhof TC.

Neuron. 2009 Dec 24;64(6):791-8. doi: 10.1016/j.neuron.2009.12.012.

3.

Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.

Etherton MR, Blaiss CA, Powell CM, Südhof TC.

Proc Natl Acad Sci U S A. 2009 Oct 20;106(42):17998-8003. doi: 10.1073/pnas.0910297106. Epub 2009 Oct 12.

4.

Neuroligin-1 performs neurexin-dependent and neurexin-independent functions in synapse validation.

Ko J, Zhang C, Arac D, Boucard AA, Brunger AT, Südhof TC.

EMBO J. 2009 Oct 21;28(20):3244-55. doi: 10.1038/emboj.2009.249. Epub 2009 Sep 3.

5.

A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export.

Zhang C, Milunsky JM, Newton S, Ko J, Zhao G, Maher TA, Tager-Flusberg H, Bolliger MF, Carter AS, Boucard AA, Powell CM, Südhof TC.

J Neurosci. 2009 Sep 2;29(35):10843-54. doi: 10.1523/JNEUROSCI.1248-09.2009.

6.

Bridging the synaptic gap: neuroligins and neurexin I in Apis mellifera.

Biswas S, Russell RJ, Jackson CJ, Vidovic M, Ganeshina O, Oakeshott JG, Claudianos C.

PLoS One. 2008;3(10):e3542. doi: 10.1371/journal.pone.0003542. Epub 2008 Oct 31.

7.

Disruption of the neurexin 1 gene is associated with schizophrenia.

Rujescu D, Ingason A, Cichon S, Pietiläinen OP, Barnes MR, Toulopoulou T, Picchioni M, Vassos E, Ettinger U, Bramon E, Murray R, Ruggeri M, Tosato S, Bonetto C, Steinberg S, Sigurdsson E, Sigmundsson T, Petursson H, Gylfason A, Olason PI, Hardarsson G, Jonsdottir GA, Gustafsson O, Fossdal R, Giegling I, Möller HJ, Hartmann AM, Hoffmann P, Crombie C, Fraser G, Walker N, Lonnqvist J, Suvisaari J, Tuulio-Henriksson A, Djurovic S, Melle I, Andreassen OA, Hansen T, Werge T, Kiemeney LA, Franke B, Veltman J, Buizer-Voskamp JE; GROUP Investigators, Sabatti C, Ophoff RA, Rietschel M, Nöthen MM, Stefansson K, Peltonen L, St Clair D, Stefansson H, Collier DA.

Hum Mol Genet. 2009 Mar 1;18(5):988-96. doi: 10.1093/hmg/ddn351. Epub 2008 Oct 22.

8.

Neuroligins and neurexins link synaptic function to cognitive disease.

Südhof TC.

Nature. 2008 Oct 16;455(7215):903-11. doi: 10.1038/nature07456. Review.

9.

GABA(A) receptor downregulation in brains of subjects with autism.

Fatemi SH, Reutiman TJ, Folsom TD, Thuras PD.

J Autism Dev Disord. 2009 Feb;39(2):223-30. doi: 10.1007/s10803-008-0646-7. Epub 2008 Sep 23.

10.

Mutational analysis of the neurexin/neuroligin complex reveals essential and regulatory components.

Reissner C, Klose M, Fairless R, Missler M.

Proc Natl Acad Sci U S A. 2008 Sep 30;105(39):15124-9. doi: 10.1073/pnas.0801639105. Epub 2008 Sep 23.

11.

Neurexin 1alpha structural variants associated with autism.

Yan J, Noltner K, Feng J, Li W, Schroer R, Skinner C, Zeng W, Schwartz CE, Sommer SS.

Neurosci Lett. 2008 Jun 27;438(3):368-70. doi: 10.1016/j.neulet.2008.04.074. Epub 2008 Apr 25.

PMID:
18490107
12.

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.

Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM, Nord AS, Kusenda M, Malhotra D, Bhandari A, Stray SM, Rippey CF, Roccanova P, Makarov V, Lakshmi B, Findling RL, Sikich L, Stromberg T, Merriman B, Gogtay N, Butler P, Eckstrand K, Noory L, Gochman P, Long R, Chen Z, Davis S, Baker C, Eichler EE, Meltzer PS, Nelson SF, Singleton AB, Lee MK, Rapoport JL, King MC, Sebat J.

Science. 2008 Apr 25;320(5875):539-43. doi: 10.1126/science.1155174. Epub 2008 Mar 27.

13.

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.

14.

Disruption of neurexin 1 associated with autism spectrum disorder.

Kim HG, Kishikawa S, Higgins AW, Seong IS, Donovan DJ, Shen Y, Lally E, Weiss LA, Najm J, Kutsche K, Descartes M, Holt L, Braddock S, Troxell R, Kaplan L, Volkmar F, Klin A, Tsatsanis K, Harris DJ, Noens I, Pauls DL, Daly MJ, MacDonald ME, Morton CC, Quade BJ, Gusella JF.

Am J Hum Genet. 2008 Jan;82(1):199-207. doi: 10.1016/j.ajhg.2007.09.011.

15.

Structures of neuroligin-1 and the neuroligin-1/neurexin-1 beta complex reveal specific protein-protein and protein-Ca2+ interactions.

Araç D, Boucard AA, Ozkan E, Strop P, Newell E, Südhof TC, Brunger AT.

Neuron. 2007 Dec 20;56(6):992-1003.

16.

A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alpha.

Zahir FR, Baross A, Delaney AD, Eydoux P, Fernandes ND, Pugh T, Marra MA, Friedman JM.

J Med Genet. 2008 Apr;45(4):239-43. Epub 2007 Dec 5.

PMID:
18057082
17.

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.

Kirov G, Gumus D, Chen W, Norton N, Georgieva L, Sari M, O'Donovan MC, Erdogan F, Owen MJ, Ropers HH, Ullmann R.

Hum Mol Genet. 2008 Feb 1;17(3):458-65. Epub 2007 Nov 6.

18.

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice.

Tabuchi K, Blundell J, Etherton MR, Hammer RE, Liu X, Powell CM, Südhof TC.

Science. 2007 Oct 5;318(5847):71-6. Epub 2007 Sep 6.

19.

Neurexin 3 polymorphisms are associated with alcohol dependence and altered expression of specific isoforms.

Hishimoto A, Liu QR, Drgon T, Pletnikova O, Walther D, Zhu XG, Troncoso JC, Uhl GR.

Hum Mol Genet. 2007 Dec 1;16(23):2880-91. Epub 2007 Sep 4.

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