257 related articles for article (PubMed ID: 28463240)
41. Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice.
Irwin SA; Idupulapati M; Gilbert ME; Harris JB; Chakravarti AB; Rogers EJ; Crisostomo RA; Larsen BP; Mehta A; Alcantara CJ; Patel B; Swain RA; Weiler IJ; Oostra BA; Greenough WT
Am J Med Genet; 2002 Aug; 111(2):140-6. PubMed ID: 12210340
[TBL] [Abstract][Full Text] [Related]
42. A potential gain-of-function variant of SLC9A6 leads to endosomal alkalinization and neuronal atrophy associated with Christianson Syndrome.
Ilie A; Gao AYL; Boucher A; Park J; Berghuis AM; Hoffer MJV; Hilhorst-Hofstee Y; McKinney RA; Orlowski J
Neurobiol Dis; 2019 Jan; 121():187-204. PubMed ID: 30296617
[TBL] [Abstract][Full Text] [Related]
43. Phosphorylation of CRMP2 by Cdk5 Regulates Dendritic Spine Development of Cortical Neuron in the Mouse Hippocampus.
Jin X; Sasamoto K; Nagai J; Yamazaki Y; Saito K; Goshima Y; Inoue T; Ohshima T
Neural Plast; 2016; 2016():6790743. PubMed ID: 26819770
[TBL] [Abstract][Full Text] [Related]
44. Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature.
Ansar M; Chung HL; Al-Otaibi A; Elagabani MN; Ravenscroft TA; Paracha SA; Scholz R; Abdel Magid T; Sarwar MT; Shah SF; Qaisar AA; Makrythanasis P; Marcogliese PC; Kamsteeg EJ; Falconnet E; Ranza E; Santoni FA; Aldhalaan H; Al-Asmari A; Faqeih EA; Ahmed J; Kornau HC; Bellen HJ; Antonarakis SE
Am J Hum Genet; 2019 Nov; 105(5):907-920. PubMed ID: 31607425
[TBL] [Abstract][Full Text] [Related]
45. Characterization of spontaneous seizures and EEG abnormalities in a mouse model of the human A350V IQSEC2 mutation and identification of a possible target for precision medicine based therapy.
Kane O; McCoy A; Jada R; Borisov V; Zag L; Zag A; Schragenheim-Rozales K; Shalgi R; Levy NS; Levy AP; Marsh ED
Epilepsy Res; 2022 May; 182():106907. PubMed ID: 35344748
[TBL] [Abstract][Full Text] [Related]
46. Molecular modeling of ARF6 dysregulation caused by mutations in IQSEC2.
Shokhen M; Walikonis R; Uversky VN; Allbeck A; Zezelic C; Feldman D; Levy NS; Levy AP
J Biomol Struct Dyn; 2024; 42(3):1268-1279. PubMed ID: 37078745
[TBL] [Abstract][Full Text] [Related]
47. The ROR2 tyrosine kinase receptor regulates dendritic spine morphogenesis in hippocampal neurons.
Alfaro IE; Varela-Nallar L; Varas-Godoy M; Inestrosa NC
Mol Cell Neurosci; 2015 Jul; 67():22-30. PubMed ID: 26003414
[TBL] [Abstract][Full Text] [Related]
48. Daily Brief Heat Therapy Reduces Seizures in A350V IQSEC2 Mice and Is Associated with Correction of AMPA Receptor-Mediated Synaptic Dysfunction.
Jada R; Borisov V; Laury E; Halpert S; Levy NS; Wagner S; Netser S; Walikonis R; Carmi I; Berlin S; Levy AP
Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36835332
[TBL] [Abstract][Full Text] [Related]
49. Synapse formation is regulated by the signaling adaptor GIT1.
Zhang H; Webb DJ; Asmussen H; Horwitz AF
J Cell Biol; 2003 Apr; 161(1):131-42. PubMed ID: 12695502
[TBL] [Abstract][Full Text] [Related]
50. Fragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice.
Han K; Chen H; Gennarino VA; Richman R; Lu HC; Zoghbi HY
Hum Mol Genet; 2015 Apr; 24(7):1813-23. PubMed ID: 25432536
[TBL] [Abstract][Full Text] [Related]
51. The epilepsy and intellectual disability-associated protein TBC1D24 regulates the maintenance of excitatory synapses and animal behaviors.
Lin L; Lyu Q; Kwan PY; Zhao J; Fan R; Chai A; Lai CSW; Chan YS; Shen X; Lai KO
PLoS Genet; 2020 Jan; 16(1):e1008587. PubMed ID: 32004315
[TBL] [Abstract][Full Text] [Related]
52. Reducing premature KCC2 expression rescues seizure susceptibility and spine morphology in atypical febrile seizures.
Awad PN; Sanon NT; Chattopadhyaya B; Carriço JN; Ouardouz M; Gagné J; Duss S; Wolf D; Desgent S; Cancedda L; Carmant L; Di Cristo G
Neurobiol Dis; 2016 Jul; 91():10-20. PubMed ID: 26875662
[TBL] [Abstract][Full Text] [Related]
53. The RhoGEF DOCK10 is essential for dendritic spine morphogenesis.
Jaudon F; Raynaud F; Wehrlé R; Bellanger JM; Doulazmi M; Vodjdani G; Gasman S; Fagni L; Dusart I; Debant A; Schmidt S
Mol Biol Cell; 2015 Jun; 26(11):2112-27. PubMed ID: 25851601
[TBL] [Abstract][Full Text] [Related]
54. Rho GTPases, dendritic structure, and mental retardation.
Newey SE; Velamoor V; Govek EE; Van Aelst L
J Neurobiol; 2005 Jul; 64(1):58-74. PubMed ID: 15884002
[TBL] [Abstract][Full Text] [Related]
55. Direct Visualisation of Abnormal Dendritic Spine Morphology in the Hippocampus of the R6/2 Transgenic Mouse Model of Huntington's Disease.
Bulley SJ; Drew CJ; Morton AJ
J Huntingtons Dis; 2012; 1(2):267-73. PubMed ID: 25063335
[TBL] [Abstract][Full Text] [Related]
56. IQSEC2 disorder: A new disease entity or a Rett spectrum continuum?
Lopergolo D; Privitera F; Castello G; Lo Rizzo C; Mencarelli MA; Pinto AM; Ariani F; Currò A; Lamacchia V; Canitano R; Vaghi E; Ferrarini A; Baltodano GM; Lederer D; Van Maldergem L; Serrano M; Pineda M; Fons-Estupina MDC; Van Esch H; Breckpot J; Kumps C; Callewaert B; Mueller S; Ramelli GP; Armstrong J; Renieri A; Mari F
Clin Genet; 2021 Mar; 99(3):462-474. PubMed ID: 33368194
[TBL] [Abstract][Full Text] [Related]
57. Region-specific dendritic simplification induced by Aβ, mediated by tau via dysregulation of microtubule dynamics: a mechanistic distinct event from other neurodegenerative processes.
Golovyashkina N; Penazzi L; Ballatore C; Smith AB; Bakota L; Brandt R
Mol Neurodegener; 2015 Nov; 10():60. PubMed ID: 26541821
[TBL] [Abstract][Full Text] [Related]
58. Psychiatric features and variable neurodevelopment outcome in four females with IQSEC2 spectrum disorder.
Accogli A; Eric Jarvis G; Schiavetto A; Lai L; Amirali EL; Jimenez Cruz DA; Rivière JB; Trakadis Y
J Genet; 2020; 99():. PubMed ID: 32529990
[No Abstract] [Full Text] [Related]
59. 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]
60. SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance.
Cordovado A; Schaettin M; Jeanne M; Panasenkava V; Denommé-Pichon AS; Keren B; Mignot C; Doco-Fenzy M; Rodan L; Ramsey K; Narayanan V; Jones JR; Prijoles EJ; Mitchell WG; Ozmore JR; Juliette K; Torti E; Normand EA; Granger L; Petersen AK; Au MG; Matheny JP; Phornphutkul C; Chambers MK; Fernández-Ramos JA; López-Laso E; Kruer MC; Bakhtiari S; Zollino M; Morleo M; Marangi G; Mei D; Pisano T; Guerrini R; Louie RJ; Childers A; Everman DB; Isidor B; Audebert-Bellanger S; Odent S; Bonneau D; Gilbert-Dussardier B; Redon R; Bézieau S; Laumonnier F; Stoeckli ET; Toutain A; Vuillaume ML
Hum Mol Genet; 2022 Sep; 31(19):3325-3340. PubMed ID: 35604360
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]