-
1
-
-
0030801002
-
Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
-
Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25:3389-3402
-
(1997)
Nucleic Acids Res
, vol.25
, pp. 3389-3402
-
-
Altschul, S.F.1
Madden, T.L.2
Schäffer, A.A.3
Zhang, J.4
Zhang, Z.5
Miller, W.6
Lipman, D.J.7
-
2
-
-
0024339149
-
Fibulin, a novel protein that interacts with the fibronectin receptor-beta subunit cytoplasmic domain
-
Argraves WS, Dickerson K, Burgess WH, Ruoslahti E (1989) Fibulin, a novel protein that interacts with the fibronectin receptor-beta subunit cytoplasmic domain. Cell 58:623-629
-
(1989)
Cell
, vol.58
, pp. 623-629
-
-
Argraves, W.S.1
Dickerson, K.2
Burgess, W.H.3
Ruoslahti, E.4
-
3
-
-
0025642484
-
Fibulin is an extracellular matrix and plasma glycoprotein with repeated domain structure
-
Argraves WS, Tran H, Burgess WH, Dickerson K (1990) Fibulin is an extracellular matrix and plasma glycoprotein with repeated domain structure. J Cell Biol 111:3155-3164
-
(1990)
J Cell Biol
, vol.111
, pp. 3155-3164
-
-
Argraves, W.S.1
Tran, H.2
Burgess, W.H.3
Dickerson, K.4
-
5
-
-
0027261517
-
Four novel FBNI mutations: Significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndrome
-
Dietz HC, McIntosh I, Sakai LY, Corson GM, Chalberg SC, Pyeritz RE, Francomano CA (1993) Four novel FBNI mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndrome. Genomics 17:468-475
-
(1993)
Genomics
, vol.17
, pp. 468-475
-
-
Dietz, H.C.1
McIntosh, I.2
Sakai, L.Y.3
Corson, G.M.4
Chalberg, S.C.5
Pyeritz, R.E.6
Francomano, C.A.7
-
6
-
-
0030000090
-
Solution structure of a pair of calcium-binding epidermal growth factor-like domains: Implications for the Marfan syndrome and other genetic disorders
-
Downing AK, Knott V, Werner JM, Cardy CM, Campbell ID, Handford PA (1996) Solution structure of a pair of calcium-binding epidermal growth factor-like domains: implications for the Marfan syndrome and other genetic disorders. Cell 85:597-605
-
(1996)
Cell
, vol.85
, pp. 597-605
-
-
Downing, A.K.1
Knott, V.2
Werner, J.M.3
Cardy, C.M.4
Campbell, I.D.5
Handford, P.A.6
-
7
-
-
0025277746
-
Molecular interactions between the protein products of the neurogenic loci Notch and Delta. Two EGF-homologous genes in Drosophila
-
Fehon RG, Kooh PJ, Rebay I, Regan CL, Xu T, Muskavitch MA, Artavanis-Tsakonas S (1990) Molecular interactions between the protein products of the neurogenic loci Notch and Delta. two EGF-homologous genes in Drosophila. Cell 61:523-534
-
(1990)
Cell
, vol.61
, pp. 523-534
-
-
Fehon, R.G.1
Kooh, P.J.2
Rebay, I.3
Regan, C.L.4
Xu, T.5
Muskavitch, M.A.6
Artavanis-Tsakonas, S.7
-
8
-
-
0029937085
-
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13
-
Gong Y, Vikkula M, Boon L, Beighton P, Ramesar R, Peltonen L, Somer H, Hirose T, Dallapiccola B, De Paepe A, Swoboda W, Zabel B, Superti-Furga A, Steinmann B, Brunner HG, Jans A, Boles RG, Adkins W, van den Boogaard M-J, Olsen BR, Warman ML (1996) Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13. Am J Hum Genet 59:145-151
-
(1996)
Am J Hum Genet
, vol.59
, pp. 145-151
-
-
Gong, Y.1
Vikkula, M.2
Boon, L.3
Beighton, P.4
Ramesar, R.5
Peltonen, L.6
Somer, H.7
Hirose, T.8
Dallapiccola, B.9
De Paepe, A.10
Swoboda, W.11
Zabel, B.12
Superti-Furga, A.13
Steinmann, B.14
Brunner, H.G.15
Jans, A.16
Boles, R.G.17
Adkins, W.18
Van Den Boogaard, M.-J.19
Olsen, B.R.20
Warman, M.L.21
more..
-
9
-
-
0031570711
-
A 2.8-Mb clone contig of the multiple endocrine neoplasia type I (MEN1) region at 11q13
-
Guru SC, Olufemi SE, Manickam P, Cummings C, Gieser LM, Pike BL, Bittner ML, Jiang Y, Chinault AC, Nowak NJ, Brzozowska A, Crabtree JS, Wang Y, Roe BA, Weisemann JM, Boguski MS, Agarwal SK, Burns AL, Spiegel AM, Marx SJ, Flejter WL, Jong PJ de, Collins FS, Chandrasekharappa SC (1997) A 2.8-Mb clone contig of the multiple endocrine neoplasia type I (MEN1) region at 11q13. Genomics 42:436-445
-
(1997)
Genomics
, vol.42
, pp. 436-445
-
-
Guru, S.C.1
Olufemi, S.E.2
Manickam, P.3
Cummings, C.4
Gieser, L.M.5
Pike, B.L.6
Bittner, M.L.7
Jiang, Y.8
Chinault, A.C.9
Nowak, N.J.10
Brzozowska, A.11
Crabtree, J.S.12
Wang, Y.13
Roe, B.A.14
Weisemann, J.M.15
Boguski, M.S.16
Agarwal, S.K.17
Burns, A.L.18
Spiegel, A.M.19
Marx, S.J.20
Flejter, W.L.21
De Jong, P.J.22
Collins, F.S.23
Chandrasekharappa, S.C.24
more..
-
11
-
-
0028931325
-
The calcium binding properties and molecular organization of the epidermal growth factor-like domians in human fibrillin-1
-
Handford PA, Downing AK, Rao Z, Hewett DR, Sykes BC, Kielty CM (1995) The calcium binding properties and molecular organization of the epidermal growth factor-like domians in human fibrillin-1. J Biol Chem 270:6751-6756
-
(1995)
J Biol Chem
, vol.270
, pp. 6751-6756
-
-
Handford, P.A.1
Downing, A.K.2
Rao, Z.3
Hewett, D.R.4
Sykes, B.C.5
Kielty, C.M.6
-
12
-
-
0027412003
-
A novel fibrillin mutation in Marfan syndrome which could disrupt calcium binding of the epidermal growth factor-like module
-
Hewett DR, Lynch JR, Smith R, Sykes BC (1993) A novel fibrillin mutation in Marfan syndrome which could disrupt calcium binding of the epidermal growth factor-like module. Hum Mol Genet 2:475-477
-
(1993)
Hum Mol Genet
, vol.2
, pp. 475-477
-
-
Hewett, D.R.1
Lynch, J.R.2
Smith, R.3
Sykes, B.C.4
-
13
-
-
0030219709
-
Structure and chromosomal assignment of the human s1-5 gene (FBNL) that is highly homologous to fibrillin
-
Ikewaga S, Toda T, Okui K, Nakamura Y (1996) Structure and chromosomal assignment of the human S1-5 gene (FBNL) that is highly homologous to fibrillin. Genomics 35:590-592
-
(1996)
Genomics
, vol.35
, pp. 590-592
-
-
Ikewaga, S.1
Toda, T.2
Okui, K.3
Nakamura, Y.4
-
14
-
-
0030908846
-
Linkage of a gene causing high bone mass to human chromosome 11 (11q12-13)
-
Johnson ML, Gong G, Kimberling W, Recker SM, Kimmel DB, Recker RR (1997) Linkage of a gene causing high bone mass to human chromosome 11 (11q12-13). Am J Hum Genet 60: 1326-1332
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1326-1332
-
-
Johnson, M.L.1
Gong, G.2
Kimberling, W.3
Recker, S.M.4
Kimmel, D.B.5
Recker, R.R.6
-
15
-
-
0029791627
-
The gene encoding the p60 subunit of chromatin assembly factor I (CAF1P60) maps to human chromosome 21q22.2, a region associated with some of the major features of Down syndrome
-
Katsanis N, Fisher EMC (1996) The gene encoding the p60 subunit of chromatin assembly factor I (CAF1P60) maps to human chromosome 21q22.2, a region associated with some of the major features of Down syndrome. Hum Genet 98:497-499
-
(1996)
Hum Genet
, vol.98
, pp. 497-499
-
-
Katsanis, N.1
Fisher, E.M.C.2
-
16
-
-
0033365397
-
Delineation of the critical interval of Burdet-Biedl syndrome 1 (BBS1) to a small region of 11q13 trough linkage and haplotype analysis of q1 pedigrees
-
Katsanis N, Lewis RA, Stockton DW, Mai PMT, Baird L, Beales PL, Leppert M, Lupski JR (1999) Delineation of the critical interval of Burdet-Biedl syndrome 1 (BBS1) to a small region of 11q13 trough linkage and haplotype analysis of q1 pedigrees. Am J Hum Genet 65:1672-1679
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1672-1679
-
-
Katsanis, N.1
Lewis, R.A.2
Stockton, D.W.3
Mai, P.M.T.4
Baird, L.5
Beales, P.L.6
Leppert, M.7
Lupski, J.R.8
-
17
-
-
0029977996
-
Calcium binding properties of an epidermal growth factor-like domain pair from human fibrillin-1
-
Knott V, Downing AK, Cardy CM, Handford P (1996) Calcium binding properties of an epidermal growth factor-like domain pair from human fibrillin-1. J Mol Biol 255:22-27
-
(1996)
J Mol Biol
, vol.255
, pp. 22-27
-
-
Knott, V.1
Downing, A.K.2
Cardy, C.M.3
Handford, P.4
-
18
-
-
0028943214
-
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
-
Lecka-Czernik B, Lumpkin CKJ, 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.J.2
Goldstein, S.3
-
19
-
-
0025900544
-
Linkage of marfan syndrome and a phenotypically related disorder to two different fibrillin genes
-
Lee B, Godfrey M, Vitale E, Hori H, Mattei M-G, Sarfarazi M, Tsipouras P, Ramirez F, Hollister DW (1991) Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes. Nature 352:330-334
-
(1991)
Nature
, vol.352
, pp. 330-334
-
-
Lee, B.1
Godfrey, M.2
Vitale, E.3
Hori, H.4
Mattei, M.-G.5
Sarfarazi, M.6
Tsipouras, P.7
Ramirez, F.8
Hollister, D.W.9
-
20
-
-
0026756530
-
The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533
-
Li Y, Muller B, Fuhrmann C, van Nouhuys CE, Laqua H, Humphries P, Schwinger E, Gal A (1992) The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533. Am J Hum Genet 51:749-754
-
(1992)
Am J Hum Genet
, vol.51
, pp. 749-754
-
-
Li, Y.1
Muller, B.2
Fuhrmann, C.3
Van Nouhuys, C.E.4
Laqua, H.5
Humphries, P.6
Schwinger, E.7
Gal, A.8
-
22
-
-
0028342664
-
Cloning of senescent cell-derived inhibitors of DNA synthesis using an expression system
-
Noda A, Ning Y, Venable SF, Pereira-Smith O, Smith JR (1994) Cloning of senescent cell-derived inhibitors of DNA synthesis using an expression system. Exp Cell Res 211:90-98
-
(1994)
Exp Cell Res
, vol.211
, pp. 90-98
-
-
Noda, A.1
Ning, Y.2
Venable, S.F.3
Pereira-Smith, O.4
Smith, J.R.5
-
23
-
-
0031577468
-
Interaction of DA41, a DAN-binding protein, with the epidermal growth factor-like protein, S(1-5)
-
Ozaki T, Kondo K, Nakamura Y, Ichimiya S, Nakagawara A, Sakiyama S (1997) Interaction of DA41, a DAN-binding protein, with the epidermal growth factor-like protein, S(1-5). Biochem Biophys Res Commun 237:245-250
-
(1997)
Biochem Biophys Res Commun
, vol.237
, pp. 245-250
-
-
Ozaki, T.1
Kondo, K.2
Nakamura, Y.3
Ichimiya, S.4
Nakagawara, A.5
Sakiyama, S.6
-
24
-
-
0024504538
-
Domains of laminin with growth-factor activity
-
Panayotou G, End E, Aumailley M, Timpl R, Engel J (1989) Domains of laminin with growth-factor activity. Cell 56:93-101
-
(1989)
Cell
, vol.56
, pp. 93-101
-
-
Panayotou, G.1
End, E.2
Aumailley, M.3
Timpl, R.4
Engel, J.5
-
26
-
-
0024039803
-
The role of b-hydroxyaspartate and adjacent carboxylate residues in the first EGF domain of human factor IX
-
Rees DJG, Jones IM, Handford PA, Waller SJ, Esnouf MP, Smith KJ, Brownlee GG (1988) The role of b-hydroxyaspartate and adjacent carboxylate residues in the first EGF domain of human factor IX. EMBO J 7:2053-2061
-
(1988)
EMBO J
, vol.7
, pp. 2053-2061
-
-
Rees, D.J.G.1
Jones, I.M.2
Handford, P.A.3
Waller, S.J.4
Esnouf, M.P.5
Smith, K.J.6
Brownlee, G.G.7
-
27
-
-
0031570669
-
A transcript map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13
-
Sawicki M, Arnold E, Ebrahimi S, Duell T, Jin S, Wood T, Chakrabarti R, Peters J, Wan Y, Samara G, Weier HU, Udar N, Passaro EJ, Srivatsan ES (1997) A transcript map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13. Genomics 42:405-412
-
(1997)
Genomics
, vol.42
, pp. 405-412
-
-
Sawicki, M.1
Arnold, E.2
Ebrahimi, S.3
Duell, T.4
Jin, S.5
Wood, T.6
Chakrabarti, R.7
Peters, J.8
Wan, Y.9
Samara, G.10
Weier, H.U.11
Udar, N.12
Passaro, E.J.13
Srivatsan, E.S.14
-
29
-
-
0027018441
-
Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13
-
Stone EM, Kimura AE, Folk JC, Bennett SR, Nichols BE, Streb LM, Sheffield VC (1992) Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13. Hum Mol Genet 1:685-689
-
(1992)
Hum Mol Genet
, vol.1
, pp. 685-689
-
-
Stone, E.M.1
Kimura, A.E.2
Folk, J.C.3
Bennett, S.R.4
Nichols, B.E.5
Streb, L.M.6
Sheffield, V.C.7
-
30
-
-
0033027071
-
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy
-
Stone EM, Lotery AJ, Munier FL, Heon E, Piguet B, Guymer RH, Vandenburgh K, Cousin P, Nishimura D, Swiderski RE, Silvestri G, Mackey DA, Hageman GS, Bird AC, Sheffield VC, Schorderet DF (1999) A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy. Nat Genet 22:199-202
-
(1999)
Nat Genet
, vol.22
, pp. 199-202
-
-
Stone, E.M.1
Lotery, A.J.2
Munier, F.L.3
Heon, E.4
Piguet, B.5
Guymer, R.H.6
Vandenburgh, K.7
Cousin, P.8
Nishimura, D.9
Swiderski, R.E.10
Silvestri, G.11
Mackey, D.A.12
Hageman, G.S.13
Bird, A.C.14
Sheffield, V.C.15
Schorderet, D.F.16
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