-
1
-
-
0023002893
-
Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils
-
Sakai LY, Keene DR, Engvall E: Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils. J Cell Biol 1986; 103: 2499-2509.
-
(1986)
J Cell Biol
, vol.103
, pp. 2499-2509
-
-
Sakai, L.Y.1
Keene, D.R.2
Engvall, E.3
-
2
-
-
0031252407
-
Targeting of the gene-encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome
-
Pereira L, Andrikopoulos K, Tian J et al: Targeting of the gene-encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome. Nat Genet 1997; 17: 218-222.
-
(1997)
Nat Genet
, vol.17
, pp. 218-222
-
-
Pereira, L.1
Andrikopoulos, K.2
Tian, J.3
-
4
-
-
0026002215
-
Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1
-
Magenis RE, Maslen CL, Smith L, Allen L, Sakai LY: Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1. Genomics 1991; 2: 346-351.
-
(1991)
Genomics
, vol.2
, pp. 346-351
-
-
Magenis, R.E.1
Maslen, C.L.2
Smith, L.3
Allen, L.4
Sakai, L.Y.5
-
5
-
-
0033558206
-
Revised genomic organization of FBN1 and significance for regulated gene expression
-
Biery NJ, Eldadah ZA, Moore CS, Stetten G, Spencer F, Dietz HC: Revised genomic organization of FBN1 and significance for regulated gene expression. Genomics 1999; 56: 70-77.
-
(1999)
Genomics
, vol.56
, pp. 70-77
-
-
Biery, N.J.1
Eldadah, Z.A.2
Moore, C.S.3
Stetten, G.4
Spencer, F.5
Dietz, H.C.6
-
6
-
-
0028902039
-
A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features af the Marfan syndrome
-
Milewicz DM, Grossfield J, Cao SN, Kielty C, Covitz W, Jewett T: A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features af the Marfan syndrome. J Clin Invest 1995; 95: 2373-2378.
-
(1995)
J Clin Invest
, vol.95
, pp. 2373-2378
-
-
Milewicz, D.M.1
Grossfield, J.2
Cao, S.N.3
Kielty, C.4
Covitz, W.5
Jewett, T.6
-
7
-
-
0027257818
-
Fibrillin binds calcium and is coded by cDNAs that reveal a multidomain structure and alternatively spliced exons at the 5′ end
-
Corson GM, Chalberg SC, Dietz HC, Charbonneau NL, Sakai LY: Fibrillin binds calcium and is coded by cDNAs that reveal a multidomain structure and alternatively spliced exons at the 5′ end. Genomics 1993; 17: 476-484.
-
(1993)
Genomics
, vol.17
, pp. 476-484
-
-
Corson, G.M.1
Chalberg, S.C.2
Dietz, H.C.3
Charbonneau, N.L.4
Sakai, L.Y.5
-
8
-
-
0026342613
-
An analysis of vertebrate mINA sequences: Intimations of translational control
-
Review
-
Kozak M: An analysis of vertebrate mINA sequences: intimations of translational control. J Cell Biol 1991; 115: 887-903. Review.
-
(1991)
J Cell Biol
, vol.115
, pp. 887-903
-
-
Kozak, M.1
-
9
-
-
0035052163
-
Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations
-
Tan FK, Wang N, Kuwana M 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
-
-
Tan, F.K.1
Wang, N.2
Kuwana, M.3
-
10
-
-
0037019552
-
Association of 5′-untranslated region of the fibrillin-1 gene with Japanese scleroderma
-
Kodera T, Tan FK, Sasaki T, Arnett FC, Bona CA: Association of 5′-untranslated region of the fibrillin-1 gene with Japanese scleroderma. Gene 2002; 297: 61-67.
-
(2002)
Gene
, vol.297
, pp. 61-67
-
-
Kodera, T.1
Tan, F.K.2
Sasaki, T.3
Arnett, F.C.4
Bona, C.A.5
-
11
-
-
33745281284
-
Sequence variations in the 5′ upstream regions of the FBN1 gene associated with Marfan syndrome
-
Singh KK, Shukla PC, Rommel K, Schmidtke J, Arslan-Kirchner M: Sequence variations in the 5′ upstream regions of the FBN1 gene associated with Marfan syndrome. Eur J Hum Genet 2006; 14: 876-879.
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 876-879
-
-
Singh, K.K.1
Shukla, P.C.2
Rommel, K.3
Schmidtke, J.4
Arslan-Kirchner, M.5
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