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Volumn 48, Issue 11, 2003, Pages 3295-3296

Examination of the possible role of biologically relevant genes around FBN1 in systemic sclerosis in the Choctaw population [1]

Author keywords

[No Author keywords available]

Indexed keywords

FIBRILLIN;

EID: 0242495083     PISSN: 00043591     EISSN: None     Source Type: Journal    
DOI: 10.1002/art.11280     Document Type: Letter
Times cited : (10)

References (13)
  • 1
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  • 2
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    • Association of microsatellite markers near the fibrillin 1 gene on human chromosome 15q with scleroderma in a Native American population
    • Tan FK, Stivers DN, Foster MW, Chakraborty R, Howard RF, Milewicz DM, et al. Association of microsatellite markers near the fibrillin 1 gene on human chromosome 15q with scleroderma in a Native American population. Arthritis Rheum 1998;41:1729-37.
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  • 3
    • 0035052163 scopus 로고    scopus 로고
    • Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations
    • Tan FK, Wang N, Kuwana M, Chakraborty R, Bona CA, Milewicz DM, et al. Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations. Arthritis Rheum 2001;44:893-901.
    • (2001) Arthritis Rheum , vol.44 , pp. 893-901
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  • 4
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    • Association of 5′-untranslated region of the fibrillin-1 gene with Japanese scleroderma
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  • 5
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    • Wallis DD, Tan FK, Kielty CM, Kimball MD, Arnett FC, Milewicz DM. Abnormalities in fibrillin 1-containing microfibrils in dermal fibroblast cultures from patients with systemic sclerosis (scleroderma). Arthritis Rheum 2001;44:1855-64.
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  • 7
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    • Thrombospondin binds and activates the small and large forms of latent transforming growth factor-beta in a chemically defined system
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  • 8
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    • The function of KGF in morphogenesis of epithelium and reepithelialization of wounds
    • Werner S, Smola H, Liao X, Longaker MT, Krieg T, Hofschneider PH, et al. The function of KGF in morphogenesis of epithelium and reepithelialization of wounds. Science 1994;266:819-22.
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  • 9
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    • Liu W, Faraco J, Qian C, Francke U. The gene for microfibril-associated protein-1 (MFAP1) is located several megabases centromeric to FBN1 and is not mutated in Marfan syndrome. Hum Genet 1997;99:578-84.
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  • 10
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  • 12
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.