171 related articles for article (PubMed ID: 34014906)
21. A novel splice mutation in PAK3 gene underlying mental retardation with neuropsychiatric features.
Rejeb I; Saillour Y; Castelnau L; Julien C; Bienvenu T; Taga P; Chaabouni H; Chelly J; Ben Jemaa L; Bahi-Buisson N
Eur J Hum Genet; 2008 Nov; 16(11):1358-63. PubMed ID: 18523455
[TBL] [Abstract][Full Text] [Related]
22. The four mammalian splice variants encoded by the p21-activated kinase 3 gene have different biological properties.
Kreis P; Rousseau V; Thévenot E; Combeau G; Barnier JV
J Neurochem; 2008 Aug; 106(3):1184-97. PubMed ID: 18507705
[TBL] [Abstract][Full Text] [Related]
23. p21-Activated kinase 3 (PAK3) protein regulates synaptic transmission through its interaction with the Nck2/Grb4 protein adaptor.
Thévenot E; Moreau AW; Rousseau V; Combeau G; Domenichini F; Jacquet C; Goupille O; Amar M; Kreis P; Fossier P; Barnier JV
J Biol Chem; 2011 Nov; 286(46):40044-59. PubMed ID: 21949127
[TBL] [Abstract][Full Text] [Related]
24. Sequential implication of the mental retardation proteins ARHGEF6 and PAK3 in spine morphogenesis.
Nodé-Langlois R; Muller D; Boda B
J Cell Sci; 2006 Dec; 119(Pt 23):4986-93. PubMed ID: 17105769
[TBL] [Abstract][Full Text] [Related]
25. Sequence analysis of P21-activated kinase 3 (PAK3) in chronic schizophrenia with cognitive impairment.
Morrow EM; Kane A; Goff DC; Walsh CA
Schizophr Res; 2008 Dec; 106(2-3):265-7. PubMed ID: 18805672
[TBL] [Abstract][Full Text] [Related]
26. A novel VPS13B mutation in Cohen syndrome: a case report and review of literature.
Momtazmanesh S; Rayzan E; Shahkarami S; Rohlfs M; Klein C; Rezaei N
BMC Med Genet; 2020 Jun; 21(1):140. PubMed ID: 32605629
[TBL] [Abstract][Full Text] [Related]
27. Distinct, but compensatory roles of PAK1 and PAK3 in spine morphogenesis.
Boda B; Jourdain L; Muller D
Hippocampus; 2008; 18(9):857-61. PubMed ID: 18481281
[TBL] [Abstract][Full Text] [Related]
28. The mental retardation protein PAK3 contributes to synapse formation and plasticity in hippocampus.
Boda B; Alberi S; Nikonenko I; Node-Langlois R; Jourdain P; Moosmayer M; Parisi-Jourdain L; Muller D
J Neurosci; 2004 Dec; 24(48):10816-25. PubMed ID: 15574732
[TBL] [Abstract][Full Text] [Related]
29. Pak3 promotes cell cycle exit and differentiation of β-cells in the embryonic pancreas and is necessary to maintain glucose homeostasis in adult mice.
Piccand J; Meunier A; Merle C; Jia Z; Barnier JV; Gradwohl G
Diabetes; 2014 Jan; 63(1):203-15. PubMed ID: 24163148
[TBL] [Abstract][Full Text] [Related]
30. p21-activated kinase 3 (PAK3) is an AP-1 regulated gene contributing to actin organisation and migration of transformed fibroblasts.
Holderness Parker N; Donninger H; Birrer MJ; Leaner VD
PLoS One; 2013; 8(6):e66892. PubMed ID: 23818969
[TBL] [Abstract][Full Text] [Related]
31. p21-Activated kinase 3 promotes cancer stem cell phenotypes through activating the Akt-GSK3β-β-catenin signaling pathway in pancreatic cancer cells.
Wu HY; Yang MC; Ding LY; Chen CS; Chu PC
Cancer Lett; 2019 Aug; 456():13-22. PubMed ID: 31051214
[TBL] [Abstract][Full Text] [Related]
32. Interaction of paxillin with p21-activated Kinase (PAK). Association of paxillin alpha with the kinase-inactive and the Cdc42-activated forms of PAK3.
Hashimoto S; Tsubouchi A; Mazaki Y; Sabe H
J Biol Chem; 2001 Feb; 276(8):6037-45. PubMed ID: 11096073
[TBL] [Abstract][Full Text] [Related]
33. Novel CLCN4 variant associated with syndromic X-linked intellectual disability in a Chinese girl: a case report.
Xu X; Lu F; Zhang L; Li H; Du S; Tang J
BMC Pediatr; 2021 Sep; 21(1):384. PubMed ID: 34479510
[TBL] [Abstract][Full Text] [Related]
34. Abnormal long-lasting synaptic plasticity and cognition in mice lacking the mental retardation gene Pak3.
Meng J; Meng Y; Hanna A; Janus C; Jia Z
J Neurosci; 2005 Jul; 25(28):6641-50. PubMed ID: 16014725
[TBL] [Abstract][Full Text] [Related]
35. Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.
Kim HG; Rosenfeld JA; Scott DA; Bénédicte G; Labonne JD; Brown J; McGuire M; Mahida S; Naidu S; Gutierrez J; Lesca G; des Portes V; Bruel AL; Sorlin A; Xia F; Capri Y; Muller E; McKnight D; Torti E; Rüschendorf F; Hummel O; Islam Z; Kolatkar PR; Layman LC; Ryu D; Kong IK; Madan-Khetarpal S; Kim CH
Mol Autism; 2019; 10():35. PubMed ID: 31649809
[TBL] [Abstract][Full Text] [Related]
36. Molecular study of the PAK3 and GDI1 genes in nonsyndromic X-linked mental retardation spanish patients.
Rifé M; Mallolas J; Castellví-Bel S; Badenas C; Jiménez D; Milà M
Am J Med Genet; 2000 Oct; 94(5):389-91. PubMed ID: 11050624
[No Abstract] [Full Text] [Related]
37. Loss of Drosophila melanogaster p21-activated kinase 3 suppresses defects in synapse structure and function caused by spastin mutations.
Ozdowski EF; Gayle S; Bao H; Zhang B; Sherwood NT
Genetics; 2011 Sep; 189(1):123-35. PubMed ID: 21705760
[TBL] [Abstract][Full Text] [Related]
38. Lethality of PAK3 and SGK2 shRNAs to human papillomavirus positive cervical cancer cells is independent of PAK3 and SGK2 knockdown.
Zhou N; Ding B; Agler M; Cockett M; McPhee F
PLoS One; 2015; 10(1):e0117357. PubMed ID: 25615606
[TBL] [Abstract][Full Text] [Related]
39. Kinase requirements in human cells: V. Synthetic lethal interactions between p53 and the protein kinases SGK2 and PAK3.
Baldwin A; Grueneberg DA; Hellner K; Sawyer J; Grace M; Li W; Harlow E; Munger K
Proc Natl Acad Sci U S A; 2010 Jul; 107(28):12463-8. PubMed ID: 20616055
[TBL] [Abstract][Full Text] [Related]
40. Functional analysis of rare variants found in schizophrenia implicates a critical role for GIT1-PAK3 signaling in neuroplasticity.
Kim MJ; Biag J; Fass DM; Lewis MC; Zhang Q; Fleishman M; Gangwar SP; Machius M; Fromer M; Purcell SM; McCarroll SA; Rudenko G; Premont RT; Scolnick EM; Haggarty SJ
Mol Psychiatry; 2017 Mar; 22(3):417-429. PubMed ID: 27457813
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]