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Volumn 17, Issue 12, 1997, Pages 4562-4569

Sensitivity to jerky gene dosage underlies epileptic seizures in mice

Author keywords

c Fos; Epilepsy; Gene dosage; Haploinsufficiency; In situ hybridization; Jerky gene; PTZ; Seizure

Indexed keywords

PENTETRAZOLE;

EID: 0030925348     PISSN: 02706474     EISSN: None     Source Type: Journal    
DOI: 10.1523/jneurosci.17-12-04562.1997     Document Type: Article
Times cited : (27)

References (9)
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    • Ceccatelli, S.1    Villar, M.J.2    Goldstein, M.3    Hokfelt, T.4
  • 2
    • 0025311047 scopus 로고
    • CENP-B: A major human centromere protein located beneath the kinetochore
    • Cooke CA, Bernat RL, Earnshaw WC (1990) CENP-B: a major human centromere protein located beneath the kinetochore. J Cell Biol 110:1475-1488.
    • (1990) J Cell Biol , vol.110 , pp. 1475-1488
    • Cooke, C.A.1    Bernat, R.L.2    Earnshaw, W.C.3
  • 3
    • 0026096204 scopus 로고
    • Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myodonic epilepsy patients
    • Durner M, Sander T, Greenberg DA, Johnson K, Beck-Mannagetta G, Janz D (1991) Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myodonic epilepsy patients. Neurology 41:1651-1655.
    • (1991) Neurology , vol.41 , pp. 1651-1655
    • Durner, M.1    Sander, T.2    Greenberg, D.A.3    Johnson, K.4    Beck-Mannagetta, G.5    Janz, D.6
  • 4
    • 0027299118 scopus 로고
    • The chromosome 6p epilepsy locus: Exploring mode of inheritance and heterogeneity through linkage analysis
    • Greenberg DA, Delgado-Escueta AV (1993) The chromosome 6p epilepsy locus: exploring mode of inheritance and heterogeneity through linkage analysis. Epilepsia [Suppl]34:pS12-pS18.
    • (1993) Epilepsia [Suppl] , vol.34
    • Greenberg, D.A.1    Delgado-Escueta, A.V.2
  • 5
    • 0027731681 scopus 로고
    • Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease
    • Halford S, Wadey R, Roberts C, Daw SC, Whiting JA, O'Donnell H, Dunham I, Bentley D, Lindsay E, Baldini A (1993) Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease. Hum Mol Genet 2:2099-2107.
    • (1993) Hum Mol Genet , vol.2 , pp. 2099-2107
    • Halford, S.1    Wadey, R.2    Roberts, C.3    Daw, S.C.4    Whiting, J.A.5    O'Donnell, H.6    Dunham, I.7    Bentley, D.8    Lindsay, E.9    Baldini, A.10
  • 6
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    • A mouse model of Greig cephalopolysyndactyly syndrome: The extra-toesJ mutation contains an intragenic deletion of the Gli3 gene
    • Hui CC, Joyner AL (1993) A mouse model of Greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene. Nat Genet 3:241-246.
    • (1993) Nat Genet , vol.3 , pp. 241-246
    • Hui, C.C.1    Joyner, A.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.