These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 22355284)

  • 21. ARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repression.
    Shoubridge C; Tan MH; Seiboth G; Gécz J
    Hum Mol Genet; 2012 Apr; 21(7):1639-47. PubMed ID: 22194193
    [TBL] [Abstract][Full Text] [Related]  

  • 22. An epilepsy-related ARX polyalanine expansion modifies glutamatergic neurons excitability and morphology without affecting GABAergic neurons development.
    Beguin S; Crépel V; Aniksztejn L; Becq H; Pelosi B; Pallesi-Pocachard E; Bouamrane L; Pasqualetti M; Kitamura K; Cardoso C; Represa A
    Cereb Cortex; 2013 Jun; 23(6):1484-94. PubMed ID: 22628459
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Embryonic forebrain transcriptome of mice with polyalanine expansion mutations in the ARX homeobox gene.
    Mattiske T; Lee K; Gecz J; Friocourt G; Shoubridge C
    Hum Mol Genet; 2016 Dec; 25(24):5433-5443. PubMed ID: 27798109
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Interneuron, interrupted: molecular pathogenesis of ARX mutations and X-linked infantile spasms.
    Olivetti PR; Noebels JL
    Curr Opin Neurobiol; 2012 Oct; 22(5):859-65. PubMed ID: 22565167
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Arx homeobox gene is essential for development of mouse olfactory system.
    Yoshihara S; Omichi K; Yanazawa M; Kitamura K; Yoshihara Y
    Development; 2005 Feb; 132(4):751-62. PubMed ID: 15677725
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dual effects of
    Nieto-Estevez V; Varma P; Mirsadeghi S; Caballero J; Gamero-Alameda S; Hosseini A; Silvosa MJ; Thodeson DM; Lybrand ZR; Giugliano M; Navara C; Hsieh J
    bioRxiv; 2024 Sep; ():. PubMed ID: 38328230
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Differential gene expression in migrating cortical interneurons during mouse forebrain development.
    Faux C; Rakic S; Andrews W; Yanagawa Y; Obata K; Parnavelas JG
    J Comp Neurol; 2010 Apr; 518(8):1232-48. PubMed ID: 20151419
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment.
    Price MG; Yoo JW; Burgess DL; Deng F; Hrachovy RA; Frost JD; Noebels JL
    J Neurosci; 2009 Jul; 29(27):8752-63. PubMed ID: 19587282
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mutations in the nuclear localization sequence of the Aristaless related homeobox; sequestration of mutant ARX with IPO13 disrupts normal subcellular distribution of the transcription factor and retards cell division.
    Shoubridge C; Tan MH; Fullston T; Cloosterman D; Coman D; McGillivray G; Mancini GM; Kleefstra T; Gécz J
    Pathogenetics; 2010 Jan; 3():1. PubMed ID: 20148114
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Aristaless Related Homeobox (ARX) Interacts with β-Catenin, BCL9, and P300 to Regulate Canonical Wnt Signaling.
    Cho IT; Lim Y; Golden JA; Cho G
    PLoS One; 2017; 12(1):e0170282. PubMed ID: 28103279
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulation.
    Lee K; Mattiske T; Kitamura K; Gecz J; Shoubridge C
    Hum Mol Genet; 2014 Feb; 23(4):1084-94. PubMed ID: 24122442
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Estrogen Treatment Reverses Prematurity-Induced Disruption in Cortical Interneuron Population.
    Panda S; Dohare P; Jain S; Parikh N; Singla P; Mehdizadeh R; Klebe DW; Kleinman GM; Cheng B; Ballabh P
    J Neurosci; 2018 Aug; 38(34):7378-7391. PubMed ID: 30037831
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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; 483(3):292-303. PubMed ID: 15682394
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Human ARX gene: genomic characterization and expression.
    Ohira R; Zhang YH; Guo W; Dipple K; Shih SL; Doerr J; Huang BL; Fu LJ; Abu-Khalil A; Geschwind D; McCabe ER
    Mol Genet Metab; 2002; 77(1-2):179-88. PubMed ID: 12359145
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genotype-phenotype correlation in neuronal migration disorders and cortical dysplasias.
    Kato M
    Front Neurosci; 2015; 9():181. PubMed ID: 26052266
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Gene expression in cortical interneuron precursors is prescient of their mature function.
    Batista-Brito R; Machold R; Klein C; Fishell G
    Cereb Cortex; 2008 Oct; 18(10):2306-17. PubMed ID: 18250082
    [TBL] [Abstract][Full Text] [Related]  

  • 40. ARX spectrum disorders: making inroads into the molecular pathology.
    Shoubridge C; Fullston T; Gécz J
    Hum Mutat; 2010 Aug; 31(8):889-900. PubMed ID: 20506206
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.