265 related articles for article (PubMed ID: 17460091)
1. Inactivation of Arx, the murine ortholog of the X-linked lissencephaly with ambiguous genitalia gene, leads to severe disorganization of the ventral telencephalon with impaired neuronal migration and differentiation.
Colombo E; Collombat P; Colasante G; Bianchi M; Long J; Mansouri A; Rubenstein JL; Broccoli V
J Neurosci; 2007 Apr; 27(17):4786-98. PubMed ID: 17460091
[TBL] [Abstract][Full Text] [Related]
2. Basal ganglia involvement in
Curie A; Friocourt G; des Portes V; Roy A; Nazir T; Brun A; Cheylus A; Marcorelles P; Retzepi K; Maleki N; Bussy G; Paulignan Y; Reboul A; Ibarrola D; Kong J; Hadjikhani N; Laquerrière A; Gollub RL
Neuroimage Clin; 2018; 19():454-465. PubMed ID: 29984154
[TBL] [Abstract][Full Text] [Related]
3. Aristaless-related homeobox gene disruption leads to abnormal distribution of GABAergic interneurons in human neocortex: evidence based on a case of X-linked lissencephaly with abnormal genitalia (XLAG).
Okazaki S; Ohsawa M; Kuki I; Kawawaki H; Koriyama T; Ri S; Ichiba H; Hai E; Inoue T; Nakamura H; Goto Y; Tomiwa K; Yamano T; Kitamura K; Itoh M
Acta Neuropathol; 2008 Oct; 116(4):453-62. PubMed ID: 18458920
[TBL] [Abstract][Full Text] [Related]
4. ARX mutations in X-linked lissencephaly with abnormal genitalia.
Uyanik G; Aigner L; Martin P; Gross C; Neumann D; Marschner-Schäfer H; Hehr U; Winkler J
Neurology; 2003 Jul; 61(2):232-5. PubMed ID: 12874405
[TBL] [Abstract][Full Text] [Related]
5. Arx acts as a regional key selector gene in the ventral telencephalon mainly through its transcriptional repression activity.
Colasante G; Sessa A; Crispi S; Calogero R; Mansouri A; Collombat P; Broccoli V
Dev Biol; 2009 Oct; 334(1):59-71. PubMed ID: 19627984
[TBL] [Abstract][Full Text] [Related]
6. X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy".
Kato M; Dobyns WB
J Child Neurol; 2005 Apr; 20(4):392-7. PubMed ID: 15921244
[TBL] [Abstract][Full Text] [Related]
7. ARX polyalanine expansion mutations lead to migration impediment in the rostral cortex coupled with a developmental deficit of calbindin-positive cortical GABAergic interneurons.
Lee K; Ireland K; Bleeze M; Shoubridge C
Neuroscience; 2017 Aug; 357():220-231. PubMed ID: 28627419
[TBL] [Abstract][Full Text] [Related]
8. Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.
Kitamura K; Yanazawa M; Sugiyama N; Miura H; Iizuka-Kogo A; Kusaka M; Omichi K; Suzuki R; Kato-Fukui Y; Kamiirisa K; Matsuo M; Kamijo S; Kasahara M; Yoshioka H; Ogata T; Fukuda T; Kondo I; Kato M; Dobyns WB; Yokoyama M; Morohashi K
Nat Genet; 2002 Nov; 32(3):359-69. PubMed ID: 12379852
[TBL] [Abstract][Full Text] [Related]
9. Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2.
De Mori R; Severino M; Mancardi MM; Anello D; Tardivo S; Biagini T; Capra V; Casella A; Cereda C; Copeland BR; Gagliardi S; Gamucci A; Ginevrino M; Illi B; Lorefice E; Musaev D; Stanley V; Micalizzi A; Gleeson JG; Mazza T; Rossi A; Valente EM
Brain; 2019 Oct; 142(10):2965-2978. PubMed ID: 31412107
[TBL] [Abstract][Full Text] [Related]
10. Cell-autonomous roles of ARX in cell proliferation and neuronal migration during corticogenesis.
Friocourt G; Kanatani S; Tabata H; Yozu M; Takahashi T; Antypa M; Raguénès O; Chelly J; Férec C; Nakajima K; Parnavelas JG
J Neurosci; 2008 May; 28(22):5794-805. PubMed ID: 18509041
[TBL] [Abstract][Full Text] [Related]
11. Origin and molecular specification of striatal interneurons.
Marin O; Anderson SA; Rubenstein JL
J Neurosci; 2000 Aug; 20(16):6063-76. PubMed ID: 10934256
[TBL] [Abstract][Full Text] [Related]
12. Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice.
Kitamura K; Itou Y; Yanazawa M; Ohsawa M; Suzuki-Migishima R; Umeki Y; Hohjoh H; Yanagawa Y; Shinba T; Itoh M; Nakamura K; Goto Y
Hum Mol Genet; 2009 Oct; 18(19):3708-24. PubMed ID: 19605412
[TBL] [Abstract][Full Text] [Related]
13. Arx is a direct target of Dlx2 and thereby contributes to the tangential migration of GABAergic interneurons.
Colasante G; Collombat P; Raimondi V; Bonanomi D; Ferrai C; Maira M; Yoshikawa K; Mansouri A; Valtorta F; Rubenstein JL; Broccoli V
J Neurosci; 2008 Oct; 28(42):10674-86. PubMed ID: 18923043
[TBL] [Abstract][Full Text] [Related]
14. Evidence for tangential migration disturbances in human lissencephaly resulting from a defect in LIS1, DCX and ARX genes.
Marcorelles P; Laquerrière A; Adde-Michel C; Marret S; Saugier-Veber P; Beldjord C; Friocourt G
Acta Neuropathol; 2010 Oct; 120(4):503-15. PubMed ID: 20461390
[TBL] [Abstract][Full Text] [Related]
15. Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons.
Colombo E; Galli R; Cossu G; Gécz J; Broccoli V
Dev Dyn; 2004 Nov; 231(3):631-9. PubMed ID: 15376319
[TBL] [Abstract][Full Text] [Related]
16. Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation.
Kato M; Das S; Petras K; Kitamura K; Morohashi KI; Abuelo DN; Barr M; Bonneau D; Brady AF; Carpenter NJ; Cipero KL; Frisone F; Fukuda T; Guerrini R; Iida E; Itoh M; Lewanda AF; Nanba Y; Oka A; Proud VK; Saugier-Veber P; Schelley SL; Selicorni A; Shaner R; Silengo M; Stewart F; Sugiyama N; Toyama J; Toutain A; Vargas AL; Yanazawa M; Zackai EH; Dobyns WB
Hum Mutat; 2004 Feb; 23(2):147-159. PubMed ID: 14722918
[TBL] [Abstract][Full Text] [Related]
17. An Emerging Female Phenotype with Loss-of-Function Mutations in the Aristaless-Related Homeodomain Transcription Factor ARX.
Mattiske T; Moey C; Vissers LE; Thorne N; Georgeson P; Bakshi M; Shoubridge C
Hum Mutat; 2017 May; 38(5):548-555. PubMed ID: 28150386
[TBL] [Abstract][Full Text] [Related]
18. Analysis of the hypothalamus in a case of X-linked lissencephaly with abnormal genitalia (XLAG).
Miyata R; Hayashi M; Miyai K; Akashi T; Kato M; Kohyama J
Brain Dev; 2009 Jun; 31(6):456-60. PubMed ID: 18842366
[TBL] [Abstract][Full Text] [Related]
19. Arx polyalanine expansion in mice leads to reduced pancreatic α-cell specification and increased α-cell death.
Wilcox CL; Terry NA; May CL
PLoS One; 2013; 8(11):e78741. PubMed ID: 24236044
[TBL] [Abstract][Full Text] [Related]
20. Lhx6 activity is required for the normal migration and specification of cortical interneuron subtypes.
Liodis P; Denaxa M; Grigoriou M; Akufo-Addo C; Yanagawa Y; Pachnis V
J Neurosci; 2007 Mar; 27(12):3078-89. PubMed ID: 17376969
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
