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 *

233 related articles for article (PubMed ID: 24452264)

  • 1. Neonatal estradiol stimulation prevents epilepsy in Arx model of X-linked infantile spasms syndrome.
    Olivetti PR; Maheshwari A; Noebels JL
    Sci Transl Med; 2014 Jan; 6(220):220ra12. PubMed ID: 24452264
    [TBL] [Abstract][Full Text] [Related]  

  • 2.
    Siehr MS; Massey CA; Noebels JL
    Dis Model Mech; 2020 Mar; 13(3):. PubMed ID: 32033960
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females.
    Marsh E; Fulp C; Gomez E; Nasrallah I; Minarcik J; Sudi J; Christian SL; Mancini G; Labosky P; Dobyns W; Brooks-Kayal A; Golden JA
    Brain; 2009 Jun; 132(Pt 6):1563-76. PubMed ID: 19439424
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new paradigm for West syndrome based on molecular and cell biology.
    Kato M
    Epilepsy Res; 2006 Aug; 70 Suppl 1():S87-95. PubMed ID: 16806828
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cortical Parvalbumin-Positive Interneuron Development and Function Are Altered in the APC Conditional Knockout Mouse Model of Infantile and Epileptic Spasms Syndrome.
    Ryner RF; Derera ID; Armbruster M; Kansara A; Sommer ME; Pirone A; Noubary F; Jacob M; Dulla CG
    J Neurosci; 2023 Feb; 43(8):1422-1440. PubMed ID: 36717229
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Combination of infantile spasms, non-epileptic seizures and complex movement disorder: a new case of ARX-related epilepsy.
    Poirier K; Eisermann M; Caubel I; Kaminska A; Peudonnier S; Boddaert N; Saillour Y; Dulac O; Souville I; Beldjord C; Lascelles K; Plouin P; Chelly J; Bahi-Buisson N
    Epilepsy Res; 2008 Aug; 80(2-3):224-8. PubMed ID: 18468866
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes.
    Sherr EH
    Curr Opin Pediatr; 2003 Dec; 15(6):567-71. PubMed ID: 14631200
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bilaterally independent epileptic spasms in a case of Aicardi syndrome.
    Kobayashi K; Watanabe K; Yoshinaga H; Ohtsuka Y
    Epileptic Disord; 2011 Sep; 13(3):326-30. PubMed ID: 21873145
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome).
    Kato M; Saitoh S; Kamei A; Shiraishi H; Ueda Y; Akasaka M; Tohyama J; Akasaka N; Hayasaka K
    Am J Hum Genet; 2007 Aug; 81(2):361-6. PubMed ID: 17668384
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Reinitiation of mRNA translation in a patient with X-linked infantile spasms with a protein-truncating variant in ARX.
    Moey C; Topper S; Karn M; Johnson AK; Das S; Vidaurre J; Shoubridge C
    Eur J Hum Genet; 2016 May; 24(5):681-9. PubMed ID: 26306640
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Frameshift mutations of the ARX gene in familial Ohtahara syndrome.
    Kato M; Koyama N; Ohta M; Miura K; Hayasaka K
    Epilepsia; 2010 Sep; 51(9):1679-84. PubMed ID: 20384723
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early 17β-estradiol treatment reduces seizures but not abnormal behaviour in mice with expanded polyalanine tracts in the Aristaless related homeobox gene (ARX).
    Loring KE; Mattiske T; Lee K; Zysk A; Jackson MR; Noebels JL; Shoubridge C
    Neurobiol Dis; 2021 Jun; 153():105329. PubMed ID: 33711494
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expansion of the first polyalanine tract of the ARX gene in a boy presenting with generalized dystonia in the absence of infantile spasms.
    Shinozaki Y; Osawa M; Sakuma H; Komaki H; Nakagawa E; Sugai K; Sasaki M; Goto Y
    Brain Dev; 2009 Jun; 31(6):469-72. PubMed ID: 18823727
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Estradiol does not affect spasms in the betamethasone-NMDA rat model of infantile spasms.
    Chachua T; Di Grazia P; Chern CR; Johnkutty M; Hellman B; Lau HA; Shakil F; Daniel M; Goletiani C; Velíšková J; Velíšek L
    Epilepsia; 2016 Aug; 57(8):1326-36. PubMed ID: 27328917
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus.
    Guerrini R; Moro F; Kato M; Barkovich AJ; Shiihara T; McShane MA; Hurst J; Loi M; Tohyama J; Norci V; Hayasaka K; Kang UJ; Das S; Dobyns WB
    Neurology; 2007 Jul; 69(5):427-33. PubMed ID: 17664401
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.