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Results: 1 to 20 of 116

Similar articles for PubMed (Select 19726642)

1.

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.

2.

Disorder-associated mutations lead to functional inactivation of neuroligins.

Chih B, Afridi SK, Clark L, Scheiffele P.

Hum Mol Genet. 2004 Jul 15;13(14):1471-7. Epub 2004 May 18.

3.

An autism-associated point mutation in the neuroligin cytoplasmic tail selectively impairs AMPA receptor-mediated synaptic transmission in hippocampus.

Etherton MR, Tabuchi K, Sharma M, Ko J, Südhof TC.

EMBO J. 2011 Jun 3;30(14):2908-19. doi: 10.1038/emboj.2011.182.

4.

Dissection of synapse induction by neuroligins: effect of a neuroligin mutation associated with autism.

Chubykin AA, Liu X, Comoletti D, Tsigelny I, Taylor P, Südhof TC.

J Biol Chem. 2005 Jun 10;280(23):22365-74. Epub 2005 Mar 29.

5.

Unusually rapid evolution of Neuroligin-4 in mice.

Bolliger MF, Pei J, Maxeiner S, Boucard AA, Grishin NV, Südhof TC.

Proc Natl Acad Sci U S A. 2008 Apr 29;105(17):6421-6. doi: 10.1073/pnas.0801383105. Epub 2008 Apr 23.

6.

Neuroligin trafficking deficiencies arising from mutations in the alpha/beta-hydrolase fold protein family.

De Jaco A, Lin MZ, Dubi N, Comoletti D, Miller MT, Camp S, Ellisman M, Butko MT, Tsien RY, Taylor P.

J Biol Chem. 2010 Sep 10;285(37):28674-82. doi: 10.1074/jbc.M110.139519. Epub 2010 Jul 8.

7.

Autism spectrum disorder is related to endoplasmic reticulum stress induced by mutations in the synaptic cell adhesion molecule, CADM1.

Fujita E, Dai H, Tanabe Y, Zhiling Y, Yamagata T, Miyakawa T, Tanokura M, Momoi MY, Momoi T.

Cell Death Dis. 2010 Jun 3;1:e47. doi: 10.1038/cddis.2010.23.

8.

Trafficking of cholinesterases and neuroligins mutant proteins. An association with autism.

De Jaco A, Comoletti D, King CC, Taylor P.

Chem Biol Interact. 2008 Sep 25;175(1-3):349-51. doi: 10.1016/j.cbi.2008.04.023. Epub 2008 Apr 29.

9.

The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing.

Comoletti D, De Jaco A, Jennings LL, Flynn RE, Gaietta G, Tsigelny I, Ellisman MH, Taylor P.

J Neurosci. 2004 May 19;24(20):4889-93.

10.

Homodimerization and isoform-specific heterodimerization of neuroligins.

Poulopoulos A, Soykan T, Tuffy LP, Hammer M, Varoqueaux F, Brose N.

Biochem J. 2012 Sep 1;446(2):321-30. doi: 10.1042/BJ20120808.

11.

Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection.

Blasi F, Bacchelli E, Pesaresi G, Carone S, Bailey AJ, Maestrini E; International Molecular Genetic Study of Autism Consortium (IMGSAC).

Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):220-1.

PMID:
16508939
12.

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism.

Talebizadeh Z, Lam DY, Theodoro MF, Bittel DC, Lushington GH, Butler MG.

J Med Genet. 2006 May;43(5):e21.

13.

A mutation linked with autism reveals a common mechanism of endoplasmic reticulum retention for the alpha,beta-hydrolase fold protein family.

De Jaco A, Comoletti D, Kovarik Z, Gaietta G, Radic Z, Lockridge O, Ellisman MH, Taylor P.

J Biol Chem. 2006 Apr 7;281(14):9667-76. Epub 2006 Jan 24.

14.

A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population.

Pampanos A, Volaki K, Kanavakis E, Papandreou O, Youroukos S, Thomaidis L, Karkelis S, Tzetis M, Kitsiou-Tzeli S.

Genet Test Mol Biomarkers. 2009 Oct;13(5):611-5. doi: 10.1089/gtmb.2009.0005.

PMID:
19645625
15.

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.

16.

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.

Jamain S, Quach H, Betancur C, Råstam M, Colineaux C, Gillberg IC, Soderstrom H, Giros B, Leboyer M, Gillberg C, Bourgeron T; Paris Autism Research International Sibpair Study.

Nat Genet. 2003 May;34(1):27-9.

17.

Neuroligin-4 is localized to glycinergic postsynapses and regulates inhibition in the retina.

Hoon M, Soykan T, Falkenburger B, Hammer M, Patrizi A, Schmidt KF, Sassoè-Pognetto M, Löwel S, Moser T, Taschenberger H, Brose N, Varoqueaux F.

Proc Natl Acad Sci U S A. 2011 Feb 15;108(7):3053-8. doi: 10.1073/pnas.1006946108. Epub 2011 Jan 31.

18.

Analysis of the neuroligin 4Y gene in patients with autism.

Yan J, Feng J, Schroer R, Li W, Skinner C, Schwartz CE, Cook EH Jr, Sommer SS.

Psychiatr Genet. 2008 Aug;18(4):204-7. doi: 10.1097/YPG.0b013e3282fb7fe6.

PMID:
18628683
19.

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.

Vincent JB, Kolozsvari D, Roberts WS, Bolton PF, Gurling HM, Scherer SW.

Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):82-4.

PMID:
15274046
20.

Structural insights into the exquisite selectivity of neurexin/neuroligin synaptic interactions.

Leone P, Comoletti D, Ferracci G, Conrod S, Garcia SU, Taylor P, Bourne Y, Marchot P.

EMBO J. 2010 Jul 21;29(14):2461-71. doi: 10.1038/emboj.2010.123. Epub 2010 Jun 11.

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