-
1
-
-
0023755112
-
Cervical incompetence and preterm labor
-
Parisi VM. Cervical incompetence and preterm labor. Clin Obstet Gynecol 1988;31:585-98.
-
(1988)
Clin Obstet Gynecol
, vol.31
, pp. 585-598
-
-
Parisi, V.M.1
-
2
-
-
0023912503
-
Connective tissue changes during normal pregnancy and pregnancy complicated by cervical incompetence
-
Rechberger T, Uldbjerg N, Oxlund H. Connective tissue changes during normal pregnancy and pregnancy complicated by cervical incompetence. Obstet Gynecol 1988;71:563-7.
-
(1988)
Obstet Gynecol
, vol.71
, pp. 563-567
-
-
Rechberger, T.1
Uldbjerg, N.2
Oxlund, H.3
-
3
-
-
0030007713
-
Cervical collagen in non-pregnant women with previous cervical incompetence
-
Petersen LK, Uldbjerg N. Cervical collagen in non-pregnant women with previous cervical incompetence. Eur J Obstet Gynecol Reprod Biol 1996;67:41-5.
-
(1996)
Eur J Obstet Gynecol Reprod Biol
, vol.67
, pp. 41-45
-
-
Petersen, L.K.1
Uldbjerg, N.2
-
4
-
-
0029836744
-
Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I alpha 1 gene
-
Grant SF, Reid DM, Blake G, Herd R, Fogelman I, Ralston SH. Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I alpha 1 gene. Nat Genet 1996;14:203-5.
-
(1996)
Nat Genet
, vol.14
, pp. 203-205
-
-
Grant, S.F.1
Reid, D.M.2
Blake, G.3
Herd, R.4
Fogelman, I.5
Ralston, S.H.6
-
5
-
-
0035060434
-
A COL1A1 Sp1 binding site polymorphism predisposes to osteoporotic fracture by affecting bone density and quality
-
Mann V, Hobson EE, Li B, Stewart TL, Grant SF, Robins SP, et al. A COL1A1 Sp1 binding site polymorphism predisposes to osteoporotic fracture by affecting bone density and quality. J Clin Invest 2001;107:899-907.
-
(2001)
J Clin Invest
, vol.107
, pp. 899-907
-
-
Mann, V.1
Hobson, E.E.2
Li, B.3
Stewart, T.L.4
Grant, S.F.5
Robins, S.P.6
-
6
-
-
0034604110
-
Role of transforming growth factor β in human disease
-
Blobe GC, Schiemann WP, Lodish HF. Role of transforming growth factor β in human disease. N Engl J Med 2000;342:1350-8.
-
(2000)
N Engl J Med
, vol.342
, pp. 1350-1358
-
-
Blobe, G.C.1
Schiemann, W.P.2
Lodish, H.F.3
-
7
-
-
33747030405
-
TGFBR1 and TGFBR2 mutations in patients with features of Marfan Syndrome and Loeys-Dietz Syndrome
-
Singh KK, Rommel K, Mishra A, Karck M, Haverich A, Schmidtke J, et al. TGFBR1 and TGFBR2 mutations in patients with features of Marfan Syndrome and Loeys-Dietz Syndrome. Hum Mutat 2006;27:770-7.
-
(2006)
Hum Mutat
, vol.27
, pp. 770-777
-
-
Singh, K.K.1
Rommel, K.2
Mishra, A.3
Karck, M.4
Haverich, A.5
Schmidtke, J.6
-
8
-
-
33747016789
-
Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan Syndrome-related disorders
-
Mátyás G, Arnold E, Carrel T, Baumgartner D, Boileau C, Berger W, et al. Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan Syndrome-related disorders. Hum Mutat 2006;27:760-9.
-
(2006)
Hum Mutat
, vol.27
, pp. 760-769
-
-
Mátyás, G.1
Arnold, E.2
Carrel, T.3
Baumgartner, D.4
Boileau, C.5
Berger, W.6
-
9
-
-
0035997478
-
Analysis of transforming growth factor β1 gene polymorophisms in patients with systemic sclerosis
-
Crilly A, Hamilton J, Clark CJ, Jardine A, Madhok R. Analysis of transforming growth factor β1 gene polymorophisms in patients with systemic sclerosis. Ann Rheum Dis 2002;61:678-81.
-
(2002)
Ann Rheum Dis
, vol.61
, pp. 678-681
-
-
Crilly, A.1
Hamilton, J.2
Clark, C.J.3
Jardine, A.4
Madhok, R.5
-
10
-
-
0036597746
-
Genetic association studies: Design, analysis, and interpretation
-
Lewis CM. Genetic association studies: design, analysis, and interpretation. Brief Bioinform 2002;3:146-53.
-
(2002)
Brief Bioinform
, vol.3
, pp. 146-153
-
-
Lewis, C.M.1
-
11
-
-
0023720337
-
Complete nucleotide sequence of the region encompassing the first twenty-five exons of the human pro alpha 1(I) collagen gene (COL1A1)
-
D'Alessio M, Bernard M, Pretorius PJ, de Wet W, Ramirez F. Complete nucleotide sequence of the region encompassing the first twenty-five exons of the human pro alpha 1(I) collagen gene (COL1A1). Gene 1988;67:105-15.
-
(1988)
Gene
, vol.67
, pp. 105-115
-
-
D'Alessio, M.1
Bernard, M.2
Pretorius, P.J.3
de Wet, W.4
Ramirez, F.5
-
12
-
-
0035344688
-
Thirty-three novel COL1A1 and COL1A2 mutations in patients with osteogenesis imperfecta types I-IV
-
Ward LM, Lalic L, Roughley PJ, Glorieux FH. Thirty-three novel COL1A1 and COL1A2 mutations in patients with osteogenesis imperfecta types I-IV. Hum Mutat 2001;17:434.
-
(2001)
Hum Mutat
, vol.17
, pp. 434
-
-
Ward, L.M.1
Lalic, L.2
Roughley, P.J.3
Glorieux, F.H.4
-
13
-
-
33746702148
-
Mutation analysis of COL1A1 and COL1A2 in patients diagnosed with osteogenesis imperfecta types I-IV
-
Pollitt R, McMahon R, Nunn J, Bamford R, Afifi A, Bishop N, et al. Mutation analysis of COL1A1 and COL1A2 in patients diagnosed with osteogenesis imperfecta types I-IV. Hum Mutat 2006;27:716.
-
(2006)
Hum Mutat
, vol.27
, pp. 716
-
-
Pollitt, R.1
McMahon, R.2
Nunn, J.3
Bamford, R.4
Afifi, A.5
Bishop, N.6
-
14
-
-
26444456995
-
Analysis of polymorphic TGFB1 codons 10, 25, and 263 in a German patient group with non-syndromic cleft lip, alveolus, and palate compared with healthy adults
-
Stoll C, Mengsteab S, Stoll D, Riediger D, Gressner AM, Weiskirchen R. Analysis of polymorphic TGFB1 codons 10, 25, and 263 in a German patient group with non-syndromic cleft lip, alveolus, and palate compared with healthy adults. BMC Med Genet 2004;5:15.
-
(2004)
BMC Med Genet
, vol.5
, pp. 15
-
-
Stoll, C.1
Mengsteab, S.2
Stoll, D.3
Riediger, D.4
Gressner, A.M.5
Weiskirchen, R.6
-
15
-
-
0942276272
-
The length of the cervix and the risk of spontaneous preterm delivery
-
Iams JD, Goldenberg RL, Meis PJ, Mercer BM, Moawad A, Das A, et al. The length of the cervix and the risk of spontaneous preterm delivery. N Engl J Med 1996;334:567-72.
-
(1996)
N Engl J Med
, vol.334
, pp. 567-572
-
-
Iams, J.D.1
Goldenberg, R.L.2
Meis, P.J.3
Mercer, B.M.4
Moawad, A.5
Das, A.6
-
16
-
-
0035201481
-
Revisiting the short cervix found by transvaginal ultrasound in the second trimester: Why cerclage therapy may not help
-
Rust OA, Atlas RO, Reed J, van Gaalen J, Balducci J. Revisiting the short cervix found by transvaginal ultrasound in the second trimester: why cerclage therapy may not help. Am J Obstet Gynecol 2001;185:1098-105.
-
(2001)
Am J Obstet Gynecol
, vol.185
, pp. 1098-1105
-
-
Rust, O.A.1
Atlas, R.O.2
Reed, J.3
van Gaalen, J.4
Balducci, J.5
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