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Journal Abstract Search

447 related items for PubMed ID: 12379852

  • 1.
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  • 2. 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
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  • 3. 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
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  • 4. Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neurons.
    Poirier K, Van Esch H, Friocourt G, Saillour Y, Bahi N, Backer S, Souil E, Castelnau-Ptakhine L, Beldjord C, Francis F, Bienvenu T, Chelly J.
    Brain Res Mol Brain Res; 2004 Mar 17; 122(1):35-46. PubMed ID: 14992814
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  • 5. 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 01; 18(19):3708-24. PubMed ID: 19605412
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  • 6. Partial loss of pancreas endocrine and exocrine cells of human ARX-null mutation: consideration of pancreas differentiation.
    Itoh M, Takizawa Y, Hanai S, Okazaki S, Miyata R, Inoue T, Akashi T, Hayashi M, Goto Y.
    Differentiation; 2010 Oct 01; 80(2-3):118-22. PubMed ID: 20538404
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  • 7. Agenesis of the corpus callosum, abnormal genitalia and intractable epilepsy due to a novel familial mutation in the Aristaless-related homeobox gene.
    Hartmann H, Uyanik G, Gross C, Hehr U, Lücke T, Arslan-Kirchner M, Antosch B, Das AM, Winkler J.
    Neuropediatrics; 2004 Jun 01; 35(3):157-60. PubMed ID: 15248097
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  • 9. The vertebrate ortholog of Aristaless is regulated by Dlx genes in the developing forebrain.
    Cobos I, Broccoli V, Rubenstein JL.
    J Comp Neurol; 2005 Mar 14; 483(3):292-303. PubMed ID: 15682394
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  • 10. A novel mutation of the ARX gene in a male with nonsyndromic mental retardation.
    Troester MM, Trachtenberg T, Narayanan V.
    J Child Neurol; 2007 Jun 14; 22(6):744-8. PubMed ID: 17641262
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  • 11. Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand.
    Rujirabanjerd S, Tongsippunyoo K, Sripo T, Limprasert P.
    Eur J Med Genet; 2007 Jun 14; 50(5):346-54. PubMed ID: 17613295
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  • 12. A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females.
    Ekşioğlu YZ, Pong AW, Takeoka M.
    Epilepsia; 2011 May 14; 52(5):984-92. PubMed ID: 21426321
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  • 13. The role of ARX in cortical development.
    Friocourt G, Poirier K, Rakić S, Parnavelas JG, Chelly J.
    Eur J Neurosci; 2006 Feb 14; 23(4):869-76. PubMed ID: 16519652
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  • 14. X-linked lissencephaly with abnormal genitalia associated with renal phosphate wasting.
    Hahn A, Gross C, Uyanik G, Hehr U, Hügens-Penzel M, Alzen G, Neubauer BA.
    Neuropediatrics; 2004 Jun 14; 35(3):202-5. PubMed ID: 15248105
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  • 15. ARX spectrum disorders: making inroads into the molecular pathology.
    Shoubridge C, Fullston T, Gécz J.
    Hum Mutat; 2010 Aug 14; 31(8):889-900. PubMed ID: 20506206
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  • 17. 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 14; 20(4):392-7. PubMed ID: 15921244
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  • 19. A new paradigm for West syndrome based on molecular and cell biology.
    Kato M.
    Epilepsy Res; 2006 Aug 14; 70 Suppl 1():S87-95. PubMed ID: 16806828
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  • 20. 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 25; 27(17):4786-98. PubMed ID: 17460091
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