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Volumn 46, Issue 3, 1996, Pages 789-790

Analysis of the KSP repeat of the neurofilament heavy subunit in familial amyotrophic lateral sclerosis

Author keywords

[No Author keywords available]

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; DNA; NEUROFILAMENT PROTEIN; PROTEIN SUBUNIT;

EID: 0030000608     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.46.3.789     Document Type: Article
Times cited : (61)

References (11)
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  • 3
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    • Progressive neuropathy in transgenic mice expressing the human neurofilament heavy gene: A mouse model of amyotrophic lateral sclerosis
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    • Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease
    • Xu Z, Cork LC, Griffin JW, Cleveland DW. Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease. Cell 1993;73:23-33.
    • (1993) Cell , vol.73 , pp. 23-33
    • Xu, Z.1    Cork, L.C.2    Griffin, J.W.3    Cleveland, D.W.4
  • 5
    • 0028116467 scopus 로고
    • A mutant neurofilament subunit causes massive, selective motor neuron death: Implications for the pathogenesis of human motor neuron disease
    • Lee MK, Marszalek JR, Cleveland DW. A mutant neurofilament subunit causes massive, selective motor neuron death: implications for the pathogenesis of human motor neuron disease. Neuron 1994;13:975-988.
    • (1994) Neuron , vol.13 , pp. 975-988
    • Lee, M.K.1    Marszalek, J.R.2    Cleveland, D.W.3
  • 6
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    • (1994) Hum Molec Genet , vol.3 , pp. 1757-1761
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  • 7
    • 0027424206 scopus 로고
    • Polymorphism in the multi-phosphorylation domain of the human neurofilament-heavy-subunit encoding gene
    • Figlewicz DA, Rouleau GA, Krizus A, Julien J-P. Polymorphism in the multi-phosphorylation domain of the human neurofilament-heavy-subunit encoding gene. Gene 1993;132:297-300.
    • (1993) Gene , vol.132 , pp. 297-300
    • Figlewicz, D.A.1    Rouleau, G.A.2    Krizus, A.3    Julien, J.-P.4
  • 8
    • 0024042469 scopus 로고
    • The structure and organization of the human heavy neurofilament subunit (NF-H) and the gene encoding it
    • Lees JF, Shneidman PS, Skuntz SF, Carden MJ, Lazzarini RA. The structure and organization of the human heavy neurofilament subunit (NF-H) and the gene encoding it. EMBO J 1988;7:1947-1955.
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    • Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis
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  • 10
    • 0028067985 scopus 로고
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    • Pramatarova A, Goto J, Nanba E, et al. A two basepair deletion in the SOD1 gene causes familial amyotrophic lateral sclerosis. Hum Molec Genet 1994;3:2061-2062.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.