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Items: 1 to 20 of 96

1.

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.

Jamain S, Radyushkin K, Hammerschmidt K, Granon S, Boretius S, Varoqueaux F, Ramanantsoa N, Gallego J, Ronnenberg A, Winter D, Frahm J, Fischer J, Bourgeron T, Ehrenreich H, Brose N.

Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1710-5. doi: 10.1073/pnas.0711555105. Epub 2008 Jan 28.

2.

Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism.

El-Kordi A, Winkler D, Hammerschmidt K, Kästner A, Krueger D, Ronnenberg A, Ritter C, Jatho J, Radyushkin K, Bourgeron T, Fischer J, Brose N, Ehrenreich H.

Behav Brain Res. 2013 Aug 15;251:41-9. doi: 10.1016/j.bbr.2012.11.016. Epub 2012 Nov 23.

PMID:
23183221
3.

Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.

Radyushkin K, Hammerschmidt K, Boretius S, Varoqueaux F, El-Kordi A, Ronnenberg A, Winter D, Frahm J, Fischer J, Brose N, Ehrenreich H.

Genes Brain Behav. 2009 Jun;8(4):416-25. doi: 10.1111/j.1601-183X.2009.00487.x. Epub 2009 Feb 11.

4.

Juvenile manifestation of ultrasound communication deficits in the neuroligin-4 null mutant mouse model of autism.

Ju A, Hammerschmidt K, Tantra M, Krueger D, Brose N, Ehrenreich H.

Behav Brain Res. 2014 Aug 15;270:159-64. doi: 10.1016/j.bbr.2014.05.019. Epub 2014 May 20.

PMID:
24855039
5.

[Synapse maturation and autism: learning from neuroligin model mice].

Tabuchi K, Chang W, Asgar NF, Pramanik G.

Nihon Shinkei Seishin Yakurigaku Zasshi. 2014 Feb;34(1):1-4. Review. Japanese. Erratum in: Nihon Shinkei Seishin Yakurigaku Zasshi. 2015 Jun;35(3):79. Hang, WenHsin [corrected to Chang, WenHsin]; Asgar, Nur Farehan Mohamed [corrected to Asgar, Nur Farehan].

PMID:
25069265
6.

The possible interplay of synaptic and clock genes in autism spectrum disorders.

Bourgeron T.

Cold Spring Harb Symp Quant Biol. 2007;72:645-54. doi: 10.1101/sqb.2007.72.020. Review.

PMID:
18419324
7.

Analysis of four neuroligin genes as candidates for autism.

Ylisaukko-oja T, Rehnström K, Auranen M, Vanhala R, Alen R, Kempas E, Ellonen P, Turunen JA, Makkonen I, Riikonen R, Nieminen-von Wendt T, von Wendt L, Peltonen L, Järvelä I.

Eur J Hum Genet. 2005 Dec;13(12):1285-92.

8.

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.

9.

Familial deletion within NLGN4 associated with autism and Tourette syndrome.

Lawson-Yuen A, Saldivar JS, Sommer S, Picker J.

Eur J Hum Genet. 2008 May;16(5):614-8. doi: 10.1038/sj.ejhg.5202006. Epub 2008 Jan 30.

10.

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.

11.

Medicine. Testing hypotheses about autism.

Crawley JN.

Science. 2007 Oct 5;318(5847):56-7. No abstract available.

PMID:
17916718
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.

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family.

Laumonnier F, Bonnet-Brilhault F, Gomot M, Blanc R, David A, Moizard MP, Raynaud M, Ronce N, Lemonnier E, Calvas P, Laudier B, Chelly J, Fryns JP, Ropers HH, Hamel BC, Andres C, Barthélémy C, Moraine C, Briault S.

Am J Hum Genet. 2004 Mar;74(3):552-7. Epub 2004 Feb 12.

14.

[Autism: more evidence of a genetic cause].

Bourgeron T, Leboyer M, Delorme R.

Bull Acad Natl Med. 2009 Feb;193(2):299-304; discussion 304-5. French.

PMID:
19718887
15.

Monogenic heritable autism gene neuroligin impacts Drosophila social behaviour.

Hahn N, Geurten B, Gurvich A, Piepenbrock D, Kästner A, Zanini D, Xing G, Xie W, Göpfert MC, Ehrenreich H, Heinrich R.

Behav Brain Res. 2013 Sep 1;252:450-7. doi: 10.1016/j.bbr.2013.06.020. Epub 2013 Jun 19. Erratum in: Behav Brain Res. 2013 Nov 1;256:690.

PMID:
23792025
16.

Mice genetically depleted of brain serotonin display social impairments, communication deficits and repetitive behaviors: possible relevance to autism.

Kane MJ, Angoa-Peréz M, Briggs DI, Sykes CE, Francescutti DM, Rosenberg DR, Kuhn DM.

PLoS One. 2012;7(11):e48975. doi: 10.1371/journal.pone.0048975. Epub 2012 Nov 6.

17.

A review on the current neuroligin mouse models.

Xu JY, Xia QQ, Xia J.

Sheng Li Xue Bao. 2012 Oct 25;64(5):550-62. Review.

18.

Lack of parvalbumin in mice leads to behavioral deficits relevant to all human autism core symptoms and related neural morphofunctional abnormalities.

Wöhr M, Orduz D, Gregory P, Moreno H, Khan U, Vörckel KJ, Wolfer DP, Welzl H, Gall D, Schiffmann SN, Schwaller B.

Transl Psychiatry. 2015 Mar 10;5:e525. doi: 10.1038/tp.2015.19.

19.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
20.

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

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