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Volumn 35, Issue 3, 1996, Pages 590-592

Structure and chromosomal assignment of the human S1-5 gene (FBNL) that is highly homologous to fibrillin

Author keywords

[No Author keywords available]

Indexed keywords

FIBRILLIN;

EID: 0030219709     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0402     Document Type: Article
Times cited : (26)

References (11)
  • 1
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    • Organization and expression of eukaryotic split genes coding for proteins
    • 1. Breathnach, R., and Chambon, P. (1981). Organization and expression of eukaryotic split genes coding for proteins. Annu. Rev. Biochem. 50: 349-383.
    • (1981) Annu. Rev. Biochem. , vol.50 , pp. 349-383
    • Breathnach, R.1    Chambon, P.2
  • 2
    • 0023261492 scopus 로고
    • Diagnosis and classification of severity of mitral valve prolapse: Methodologic, biologic, and prognostic considerations
    • 2. Devereaux, R. B. (1987). Diagnosis and classification of severity of mitral valve prolapse: Methodologic, biologic, and prognostic considerations. Am. Heart J. 113: 1265-1280.
    • (1987) Am. Heart J. , vol.113 , pp. 1265-1280
    • Devereaux, R.B.1
  • 4
    • 0013907774 scopus 로고
    • Werner syndrome: A review of its symptomatology, natural history, pathological features, genetics and relationship to the natural aging process
    • 4. Epstein, C. J., Martin, G. M., Schultz, A. L., and Motulsky, A. G. (1966). Werner syndrome: A review of its symptomatology, natural history, pathological features, genetics and relationship to the natural aging process. Medicine 45: 177-221.
    • (1966) Medicine , vol.45 , pp. 177-221
    • Epstein, C.J.1    Martin, G.M.2    Schultz, A.L.3    Motulsky, A.G.4
  • 5
    • 0026502062 scopus 로고
    • Genetic linkage of Werner's syndrome to five markers on chromosome 8
    • 5. Goto, M., Rubenstein, M., Weber, J., Wood, K., and Drayna, D. (1992). Genetic linkage of Werner's syndrome to five markers on chromosome 8. Nature 355: 735-738.
    • (1992) Nature , vol.355 , pp. 735-738
    • Goto, M.1    Rubenstein, M.2    Weber, J.3    Wood, K.4    Drayna, D.5
  • 7
    • 0028943214 scopus 로고
    • An overexpressed gene transcript in senescent and quiescent human fibroblasts encoding a novel protein in the epidermal growth factor-like repeat family stimulates DNA synthesis
    • 7. Lecka-Czernik, B., Lumpkin, C. K., and Goldstein, S. (1995). An overexpressed gene transcript in senescent and quiescent human fibroblasts encoding a novel protein in the epidermal growth factor-like repeat family stimulates DNA synthesis. Mol. Cell. Biol. 15: 120-128.
    • (1995) Mol. Cell. Biol. , vol.15 , pp. 120-128
    • Lecka-Czernik, B.1    Lumpkin, C.K.2    Goldstein, S.3
  • 8
    • 0028828221 scopus 로고
    • Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, cogenital contractual arachnodactyly
    • 8. Putnam, E. A., Zang, H., Ramirez, F., and Milewicz, D. M. (1995). Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, cogenital contractual arachnodactyly. Nature Genet. 11: 456-458.
    • (1995) Nature Genet. , vol.11 , pp. 456-458
    • Putnam, E.A.1    Zang, H.2    Ramirez, F.3    Milewicz, D.M.4
  • 10
    • 0028670603 scopus 로고
    • 2058 expressed sequence tags (ESTs) from a human fetal lung cDNA library
    • 10. Sudo, K., Chinen, K., and Nakamura, Y. (1994). 2058 expressed sequence tags (ESTs) from a human fetal lung cDNA library. Genomics 24: 276-278.
    • (1994) Genomics , vol.24 , pp. 276-278
    • Sudo, K.1    Chinen, K.2    Nakamura, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.