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Volumn 6, Issue 2, 2000, Pages 136-137

The envelope, please: Nuclear lamins and disease

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; LAMININ;

EID: 0033973777     PISSN: 10788956     EISSN: None     Source Type: Journal    
DOI: 10.1038/72221     Document Type: Short Survey
Times cited : (18)

References (10)
  • 2
    • 0343756803 scopus 로고    scopus 로고
    • Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
    • Bonne, G. et al. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nature Genet. 9, 102-112 (1999).
    • (1999) Nature Genet. , vol.9 , pp. 102-112
    • Bonne, G.1
  • 3
    • 0033518282 scopus 로고    scopus 로고
    • Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
    • Fatkin, D. et al. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N. Engl. J. Med. 341, 1715-1724 (1999).
    • (1999) N. Engl. J. Med. , vol.341 , pp. 1715-1724
    • Fatkin, D.1
  • 4
    • 0034059075 scopus 로고    scopus 로고
    • Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy
    • Cao, H. & Hegele, R.A. Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy. Hum. Molec. Genet. 9, 109-112 (2000).
    • (2000) Hum. Molec. Genet. , vol.9 , pp. 109-112
    • Cao, H.1    Hegele, R.A.2
  • 5
    • 0027985787 scopus 로고
    • Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy
    • Bione, S. et al. Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. Nature Genet. 8, 323-327 (1994).
    • (1994) Nature Genet. , vol.8 , pp. 323-327
    • Bione, S.1
  • 6
    • 0033951216 scopus 로고    scopus 로고
    • The LMNA gene encoding lamin A/C is mutated in partial lipodystrophy
    • in press
    • Shackleton, S. et al. The LMNA gene encoding lamin A/C is mutated in partial lipodystrophy. Nature Genet. in press (2000)
    • (2000) Nature Genet.
    • Shackleton, S.1
  • 7
    • 0023032014 scopus 로고
    • cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins
    • Fisher, D.Z., Chaudhary, N. & Blobel, G. cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins. Proc. Natl. Acad. Sci. USA 83, 6450-6454 (1986)
    • (1986) Proc. Natl. Acad. Sci. USA , vol.83 , pp. 6450-6454
    • Fisher, D.Z.1    Chaudhary, N.2    Blobel, G.3
  • 8
    • 0031686054 scopus 로고    scopus 로고
    • Nuclear lamins: Their structure, assembly and interactions
    • Stuurman, N., Heins, S. & Aebi, U. Nuclear lamins: their structure, assembly and interactions. J. Struct. Biol. 122, 42-66 (1998)
    • (1998) J. Struct. Biol. , vol.122 , pp. 42-66
    • Stuurman, N.1    Heins, S.2    Aebi, U.3
  • 9
    • 0032852110 scopus 로고    scopus 로고
    • Heart to heart: From nuclear proteins to Emery-Dreifuss muscular dystrophy
    • Morris, G.E. & Manlial, S. Heart to heart: from nuclear proteins to Emery-Dreifuss muscular dystrophy. Hum. Molec. Genet. 8, 1847-1851 (1999)
    • (1999) Hum. Molec. Genet. , vol.8 , pp. 1847-1851
    • Morris, G.E.1    Manlial, S.2
  • 10
    • 0033517284 scopus 로고    scopus 로고
    • Leptin reverses insulin resistance and diabetes mellitus in mice with congenital lipodystrophy
    • Shimomura I., Hammer, R.E., Ikemoto, S., Brown, M.S. & Goldstein, J.L. Leptin reverses insulin resistance and diabetes mellitus in mice with congenital lipodystrophy. Nature 401, 73-76 (1999).
    • (1999) Nature , vol.401 , pp. 73-76
    • Shimomura, I.1    Hammer, R.E.2    Ikemoto, S.3    Brown, M.S.4    Goldstein, J.L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.