158 related articles for article (PubMed ID: 12932438)
1. 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. PubMed ID: 12932438
[TBL] [Abstract][Full Text] [Related]
2. The human orthologue of CdGAP is a phosphoprotein and a GTPase-activating protein for Cdc42 and Rac1 but not RhoA.
Tcherkezian J; Triki I; Stenne R; Danek EI; Lamarche-Vane N
Biol Cell; 2006 Aug; 98(8):445-56. PubMed ID: 16519628
[TBL] [Abstract][Full Text] [Related]
3. 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; 94(3):526-36. PubMed ID: 22298643
[TBL] [Abstract][Full Text] [Related]
4. Cloning of rat ARHGAP4/C1, a RhoGAP family member expressed in the nervous system that colocalizes with the Golgi complex and microtubules.
Foletta VC; Brown FD; Young WS
Brain Res Mol Brain Res; 2002 Oct; 107(1):65-79. PubMed ID: 12414125
[TBL] [Abstract][Full Text] [Related]
5. 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; 18(14):2575-83. PubMed ID: 19401298
[TBL] [Abstract][Full Text] [Related]
6. DEF6, a novel PH-DH-like domain protein, is an upstream activator of the Rho GTPases Rac1, Cdc42, and RhoA.
Mavrakis KJ; McKinlay KJ; Jones P; Sablitzky F
Exp Cell Res; 2004 Apr; 294(2):335-44. PubMed ID: 15023524
[TBL] [Abstract][Full Text] [Related]
7. Oligophrenin1 protects mice against myocardial ischemia and reperfusion injury by modulating inflammation and myocardial apoptosis.
Niermann C; Gorressen S; Klier M; Gowert NS; Billuart P; Kelm M; Merx MW; Elvers M
Cell Signal; 2016 Aug; 28(8):967-78. PubMed ID: 27117132
[TBL] [Abstract][Full Text] [Related]
8. Oligophrenin-1, a Rho GTPase-activating protein (RhoGAP) involved in X-linked mental retardation, is expressed in the enteric nervous system.
Xiao J; Neylon CB; Hunne B; Furness JB
Anat Rec A Discov Mol Cell Evol Biol; 2003 Aug; 273(2):671-6. PubMed ID: 12845702
[TBL] [Abstract][Full Text] [Related]
9. Loss of oligophrenin1 leads to uncontrolled Rho activation and increased thrombus formation in mice.
Fotinos A; Klier M; Gowert NS; Münzer P; Klatt C; Beck S; Borst O; Billuart P; Schaller M; Lang F; Gawaz M; Elvers M
J Thromb Haemost; 2015 Apr; 13(4):619-30. PubMed ID: 25556321
[TBL] [Abstract][Full Text] [Related]
10. Isoform-specific roles of the GTPase activating protein Nadrin in cytoskeletal reorganization of platelets.
Beck S; Fotinos A; Lang F; Gawaz M; Elvers M
Cell Signal; 2013 Jan; 25(1):236-46. PubMed ID: 22975681
[TBL] [Abstract][Full Text] [Related]
11. A stretch of polybasic residues mediates Cdc42 GTPase-activating protein (CdGAP) binding to phosphatidylinositol 3,4,5-trisphosphate and regulates its GAP activity.
Karimzadeh F; Primeau M; Mountassif D; Rouiller I; Lamarche-Vane N
J Biol Chem; 2012 Jun; 287(23):19610-21. PubMed ID: 22518840
[TBL] [Abstract][Full Text] [Related]
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; 12(1-2):63-7. PubMed ID: 22119667
[TBL] [Abstract][Full Text] [Related]
13. Hippocampal Excitatory Synaptic Transmission and Plasticity Are Differentially Altered during Postnatal Development by Loss of the X-Linked Intellectual Disability Protein Oligophrenin-1.
Cresto N; Lebrun N; Dumont F; Letourneur F; Billuart P; Rouach N
Cells; 2022 May; 11(9):. PubMed ID: 35563851
[TBL] [Abstract][Full Text] [Related]
14. 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; 23(11):1289-302. PubMed ID: 19487570
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 24105372
[TBL] [Abstract][Full Text] [Related]
16. The cellular function of srGAP3 and its role in neuronal morphogenesis.
Bacon C; Endris V; Rappold GA
Mech Dev; 2013; 130(6-8):391-5. PubMed ID: 23127797
[TBL] [Abstract][Full Text] [Related]
17. Novel unconventional variants expand the allelic spectrum of OPHN1 gene.
Nuovo S; Brankovic V; Caputi C; Casella A; Nigro V; Leuzzi V; Valente EM
Am J Med Genet A; 2021 May; 185(5):1575-1581. PubMed ID: 33638601
[TBL] [Abstract][Full Text] [Related]
18. 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; 35(31):11045-55. PubMed ID: 26245966
[TBL] [Abstract][Full Text] [Related]
19. FilGAP and its close relatives: a mediator of Rho-Rac antagonism that regulates cell morphology and migration.
Nakamura F
Biochem J; 2013 Jul; 453(1):17-25. PubMed ID: 23763313
[TBL] [Abstract][Full Text] [Related]
20. Expanding the phenotypic spectrum associated with OPHN1 mutations: Report of 17 individuals with intellectual disability but no cerebellar hypoplasia.
Moortgat S; Lederer D; Deprez M; Buzatu M; Clapuyt P; Boulanger S; Benoit V; Mary S; Guichet A; Ziegler A; Colin E; Bonneau D; Maystadt I
Eur J Med Genet; 2018 Aug; 61(8):442-450. PubMed ID: 29510240
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
