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Items: 1 to 20 of 133

1.

The Rho-linked mental retardation protein OPHN1 controls synaptic vesicle endocytosis via endophilin A1.

Nakano-Kobayashi A, Kasri NN, Newey SE, Van Aelst L.

Curr Biol. 2009 Jul 14;19(13):1133-9. doi: 10.1016/j.cub.2009.05.022. Epub 2009 May 28.

2.

The X-linked mental retardation protein OPHN1 interacts with Homer1b/c to control spine endocytic zone positioning and expression of synaptic potentiation.

Nakano-Kobayashi A, Tai Y, Nadif Kasri N, Van Aelst L.

J Neurosci. 2014 Jun 25;34(26):8665-71. doi: 10.1523/JNEUROSCI.0894-14.2014.

3.

The Rho-linked mental retardation protein oligophrenin-1 controls synapse maturation and plasticity by stabilizing AMPA receptors.

Nadif Kasri N, Nakano-Kobayashi A, Malinow R, Li B, Van Aelst L.

Genes Dev. 2009 Jun 1;23(11):1289-302. doi: 10.1101/gad.1783809.

4.

Oligophrenin-1 Connects Exocytotic Fusion to Compensatory Endocytosis in Neuroendocrine Cells.

Houy S, Estay-Ahumada C, Croisé P, Calco V, Haeberlé AM, Bailly Y, Billuart P, Vitale N, Bader MF, Ory S, Gasman S.

J Neurosci. 2015 Aug 5;35(31):11045-55. doi: 10.1523/JNEUROSCI.4048-14.2015.

5.

Rapid synthesis of the X-linked mental retardation protein OPHN1 mediates mGluR-dependent LTD through interaction with the endocytic machinery.

Nadif Kasri N, Nakano-Kobayashi A, Van Aelst L.

Neuron. 2011 Oct 20;72(2):300-15. doi: 10.1016/j.neuron.2011.09.001.

6.

The X-linked mental retardation protein oligophrenin-1 is required for dendritic spine morphogenesis.

Govek EE, Newey SE, Akerman CJ, Cross JR, Van der Veken L, Van Aelst L.

Nat Neurosci. 2004 Apr;7(4):364-72. Epub 2004 Mar 14.

7.

Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation.

Khelfaoui M, Pavlowsky A, Powell AD, Valnegri P, Cheong KW, Blandin Y, Passafaro M, Jefferys JG, Chelly J, Billuart P.

Hum Mol Genet. 2009 Jul 15;18(14):2575-83. doi: 10.1093/hmg/ddp189. Epub 2009 Apr 28.

8.

Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturity.

Khelfaoui M, Denis C, van Galen E, de Bock F, Schmitt A, Houbron C, Morice E, Giros B, Ramakers G, Fagni L, Chelly J, Nosten-Bertrand M, Billuart P.

J Neurosci. 2007 Aug 29;27(35):9439-50.

9.

Formation of an endophilin-Ca2+ channel complex is critical for clathrin-mediated synaptic vesicle endocytosis.

Chen Y, Deng L, Maeno-Hikichi Y, Lai M, Chang S, Chen G, Zhang JF.

Cell. 2003 Oct 3;115(1):37-48.

PMID:
14532001
10.

The GRAF family member oligophrenin1 is a RhoGAP with BAR domain and regulates Rho GTPases in platelets.

Elvers M, Beck S, Fotinos A, Ziegler M, Gawaz M.

Cardiovasc Res. 2012 Jun 1;94(3):526-36. doi: 10.1093/cvr/cvs079. Epub 2012 Feb 1.

11.

Oligophrenin-1 (OPHN1), a gene involved in X-linked intellectual disability, undergoes RNA editing and alternative splicing during human brain development.

Barresi S, Tomaselli S, Athanasiadis A, Galeano F, Locatelli F, Bertini E, Zanni G, Gallo A.

PLoS One. 2014 Mar 17;9(3):e91351. doi: 10.1371/journal.pone.0091351. eCollection 2014.

12.

Oligophrenin-1 (Ophn1) is expressed in mouse retinal vessels.

Sel S, Kaiser M, Nass N, Trau S, Roepke A, Storsberg J, Hampel U, Paulsen F, Kalinski T.

Gene Expr Patterns. 2012 Jan-Feb;12(1-2):63-7. doi: 10.1016/j.gep.2011.11.003. Epub 2011 Nov 20.

PMID:
22119667
13.

The RhoGAP activity of OPHN1, a new F-actin-binding protein, is negatively controlled by its amino-terminal domain.

Fauchereau F, Herbrand U, Chafey P, Eberth A, Koulakoff A, Vinet MC, Ahmadian MR, Chelly J, Billuart P.

Mol Cell Neurosci. 2003 Aug;23(4):574-86.

PMID:
12932438
14.

Insertion of 16 amino acids in the BAR domain of the oligophrenin 1 protein causes mental retardation and cerebellar hypoplasia in an Italian family.

Pirozzi F, Di Raimo FR, Zanni G, Bertini E, Billuart P, Tartaglione T, Tabolacci E, Brancaccio A, Neri G, Chiurazzi P.

Hum Mutat. 2011 Nov;32(11):E2294-307. doi: 10.1002/humu.21567. Epub 2011 Sep 14.

PMID:
21796728
15.

Inhibition of dynamin completely blocks compensatory synaptic vesicle endocytosis.

Newton AJ, Kirchhausen T, Murthy VN.

Proc Natl Acad Sci U S A. 2006 Nov 21;103(47):17955-60. Epub 2006 Nov 8.

16.

Endophilin A1 regulates dendritic spine morphogenesis and stability through interaction with p140Cap.

Yang Y, Wei M, Xiong Y, Du X, Zhu S, Yang L, Zhang C, Liu JJ.

Cell Res. 2015 Apr;25(4):496-516. doi: 10.1038/cr.2015.31. Epub 2015 Mar 13.

17.

Two pathways of synaptic vesicle retrieval revealed by single-vesicle imaging.

Zhu Y, Xu J, Heinemann SF.

Neuron. 2009 Feb 12;61(3):397-411. doi: 10.1016/j.neuron.2008.12.024.

18.

A novel in-frame deletion affecting the BAR domain of OPHN1 in a family with intellectual disability and hippocampal alterations.

Santos-Rebouças CB, Belet S, Guedes de Almeida L, Ribeiro MG, Medina-Acosta E, Bahia PR, Alves da Silva AF, Lima dos Santos F, Borges de Lacerda GC, Pimentel MM, Froyen G.

Eur J Hum Genet. 2014 May;22(5):644-51. doi: 10.1038/ejhg.2013.216. Epub 2013 Oct 9.

19.

Oligophrenin-1 is associated with cell adhesion and migration in prostate cancer.

Goto K, Oue N, Hayashi T, Shinmei S, Sakamoto N, Sentani K, Teishima J, Matsubara A, Yasui W.

Pathobiology. 2014;81(4):190-8. doi: 10.1159/000363345. Epub 2014 Aug 27.

PMID:
25170626
20.
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