-
1
-
-
0031768531
-
Roles of Aggrecan, a large chondroitin sulfate proteoglycan, in cartilage structure and function
-
Watanabe H, Yamada Y, Kimata K. Roles of Aggrecan, a large chondroitin sulfate proteoglycan, in cartilage structure and function. J Biochem 1998;124:687-93.
-
(1998)
J Biochem
, vol.124
, pp. 687-693
-
-
Watanabe, H.1
Yamada, Y.2
Kimata, K.3
-
3
-
-
0033459532
-
Association between and aggrecan gene polymorphism and lumbar disc degeneration
-
Kawaguchi Y, Osada R, Kanamori M, et al. Association between and aggrecan gene polymorphism and lumbar disc degeneration. Spine 1999;24:2456-60.
-
(1999)
Spine
, vol.24
, pp. 2456-2460
-
-
Kawaguchi, Y.1
Osada, R.2
Kanamori, M.3
-
4
-
-
0032126314
-
An association between an aggrecan polymorphic allele and bilateral hand osteoarthritis in elderly white men: Data from the Baltimore longitudinal Study of Aging (BLSA)
-
Horton WE Jr, Lethbridge-Cejku M, Hochberg M, et al. An association between an aggrecan polymorphic allele and bilateral hand osteoarthritis in elderly white men: data from the Baltimore longitudinal Study of Aging (BLSA). Osteoarthritis Cartilage 1998;6:245-51.
-
(1998)
Osteoarthritis Cartilage
, vol.6
, pp. 245-251
-
-
Horton Jr., W.E.1
Lethbridge-Cejku, M.2
Hochberg, M.3
-
5
-
-
0037319787
-
Osteoarthritis of the hands, hips and knees in an Australian twin sample: Evidence of association with the aggrecan VNTR polymorphism
-
Kirk KM, Doege KJ, Hecht J, et al. Osteoarthritis of the hands, hips and knees in an Australian twin sample: evidence of association with the aggrecan VNTR polymorphism. Twin Res 2003;6:62-6.
-
(2003)
Twin Res
, vol.6
, pp. 62-66
-
-
Kirk, K.M.1
Doege, K.J.2
Hecht, J.3
-
6
-
-
0034983846
-
Localization of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26
-
Bayoumi R, Saar K, Lee YA, et al. Localization of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26. J Med Genet 2001;38:369-73.
-
(2001)
J Med Genet
, vol.38
, pp. 369-373
-
-
Bayoumi, R.1
Saar, K.2
Lee, Y.A.3
-
7
-
-
0017904533
-
Cartilage matrix deficiency (cmd) a new autosomal recessive lethal mutation in the mouse
-
Rittenhouse E, Dunn LC, Cookingham J, et al. Cartilage matrix deficiency (cmd) a new autosomal recessive lethal mutation in the mouse. J Embryol Exp Morphol 1978;43:71-84.
-
(1978)
J Embryol Exp Morphol
, vol.43
, pp. 71-84
-
-
Rittenhouse, E.1
Dunn, L.C.2
Cookingham, J.3
-
8
-
-
0028225528
-
Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene
-
Watanabe H, Kimata K, Line S, et al. Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene. Nat Genet 1994;7:154-7.
-
(1994)
Nat Genet
, vol.7
, pp. 154-157
-
-
Watanabe, H.1
Kimata, K.2
Line, S.3
-
9
-
-
0030917155
-
Dwarfism and age-associated spinal degeneration of heterozygote cmd mice defective in aggrecan
-
Watanabe H, Nakata K, Kimata K, et al. Dwarfism and age-associated spinal degeneration of heterozygote cmd mice defective in aggrecan. Proc Natl Acad Sci USA 1997;94:6943-7.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 6943-6947
-
-
Watanabe, H.1
Nakata, K.2
Kimata, K.3
-
10
-
-
0027373233
-
CDNA cloning of chick cartilage chondroitin sulfate (aggrecan) core protein and identification of a stop codon in the aggrecan gene associated with the chondrodystrophy nanomelia
-
Li H, Schwartz NB, Vertel BM. CDNA cloning of chick cartilage chondroitin sulfate (aggrecan) core protein and identification of a stop codon in the aggrecan gene associated with the chondrodystrophy nanomelia. J Biol Chem 1993;268:23504-11.
-
(1993)
J Biol Chem
, vol.268
, pp. 23504-23511
-
-
Li, H.1
Schwartz, N.B.2
Vertel, B.M.3
-
11
-
-
0002918488
-
Structure and function of aggrecan
-
Kiani C, Chen L, Wu YJ, et al. Structure and function of aggrecan. Cell Res 2002;12:19-32.
-
(2002)
Cell Res
, vol.12
, pp. 19-32
-
-
Kiani, C.1
Chen, L.2
Wu, Y.J.3
-
12
-
-
0031010469
-
A human-specific polymorphism in the coding region of the aggrecan gene
-
Doege KJ, Coulter SN, Meek LM, et al. A human-specific polymorphism in the coding region of the aggrecan gene. J Biol Chem 1997;23:13974-9.
-
(1997)
J Biol Chem
, vol.23
, pp. 13974-13979
-
-
Doege, K.J.1
Coulter, S.N.2
Meek, L.M.3
-
13
-
-
0001166390
-
Adolescent idiopathic scoliosis: Prevalence and natural history
-
Weinstein SL, ed. New York: Raven Press
-
Weinstein SL. Adolescent idiopathic scoliosis: prevalence and natural history. In: Weinstein SL, ed. The Pediatric Spine: Principles and Practice. New York: Raven Press, 1994:463-78.
-
(1994)
The Pediatric Spine: Principles and Practice
, pp. 463-478
-
-
Weinstein, S.L.1
-
14
-
-
0017746233
-
Scoliosis prevalence: A call for a statement of terms
-
Kane WJ. Scoliosis prevalence: a call for a statement of terms. Clin Orthop 1977;126:43-6.
-
(1977)
Clin Orthop
, vol.126
, pp. 43-46
-
-
Kane, W.J.1
-
17
-
-
0025054396
-
Adolescent idiopathic scoliosis in identical twins
-
Carr AJ. Adolescent idiopathic scoliosis in identical twins. J Bone Joint Surg Br 1990;72:1077.
-
(1990)
J Bone Joint Surg Br
, vol.72
, pp. 1077
-
-
Carr, A.J.1
-
18
-
-
0018241706
-
Genetics of adolescent idiopathic scoliosis
-
Czeizel A, Bellyei A, Barta O, et al. Genetics of adolescent idiopathic scoliosis. J Med Genet 1978;15:424-7.
-
(1978)
J Med Genet
, vol.15
, pp. 424-427
-
-
Czeizel, A.1
Bellyei, A.2
Barta, O.3
-
20
-
-
84965341182
-
Hereditary scoliosis
-
Garland HG. Hereditary scoliosis. Br Med J 1934;1:328.
-
(1934)
Br Med J
, vol.1
, pp. 328
-
-
Garland, H.G.1
-
21
-
-
0031417826
-
Scoliosis in twins: A meta-analysis of the literature and report of six cases
-
Kesling KL, Reinker KA. Scoliosis in twins: a meta-analysis of the literature and report of six cases. Spine 1997;22:2009-15.
-
(1997)
Spine
, vol.22
, pp. 2009-2015
-
-
Kesling, K.L.1
Reinker, K.A.2
-
22
-
-
0014253676
-
Familial (idiopathic) scoliosis: A family survey
-
Wynne-Davies R. Familial (idiopathic) scoliosis: a family survey. J Bone Joint Surg Br 1968;50:24-30.
-
(1968)
J Bone Joint Surg Br
, vol.50
, pp. 24-30
-
-
Wynne-Davies, R.1
-
23
-
-
0015786694
-
A genetic survey of idiopathic scoliosis in Boston, MA
-
Riseborough EJ, Wynne-Davies R. A genetic survey of idiopathic scoliosis in Boston, MA. J Bone Joint Surg Am 1973;55:974-82.
-
(1973)
J Bone Joint Surg Am
, vol.55
, pp. 974-982
-
-
Riseborough, E.J.1
Wynne-Davies, R.2
-
24
-
-
0015375048
-
Genetic aspects of idiopathic scoliosis: A Nicholas Andry Award essay
-
Cowell HR, Hall JN, MacEwen GD. Genetic aspects of idiopathic scoliosis: a Nicholas Andry Award essay. Clin Orthop 1972;86:121-31.
-
(1972)
Clin Orthop
, vol.86
, pp. 121-131
-
-
Cowell, H.R.1
Hall, J.N.2
MacEwen, G.D.3
-
25
-
-
0032872935
-
Segregation analysis of idiopathic scoliosis: Evidence for a major-gene effect
-
Axenovich TI, Zaidman AM, Zorkolseve IV, et al. Segregation analysis of idiopathic scoliosis: evidence for a major-gene effect. Am J Med Genet 1999;86:389-94.
-
(1999)
Am J Med Genet
, vol.86
, pp. 389-394
-
-
Axenovich, T.I.1
Zaidman, A.M.2
Zorkolseve, I.V.3
-
26
-
-
0034665178
-
Localization of susceptibility to familial idiopathic scoliosis
-
Wise CA, Barnes R, Gillum J, et al. Localization of susceptibility to familial idiopathic scoliosis. Spine 2000;25:2372-80.
-
(2000)
Spine
, vol.25
, pp. 2372-2380
-
-
Wise, C.A.1
Barnes, R.2
Gillum, J.3
-
27
-
-
0036821157
-
Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11
-
Salehi LB, Mangino M, De Serio S, et al. Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11. Hum Genet 2002;111:401-4.
-
(2002)
Hum Genet
, vol.111
, pp. 401-404
-
-
Salehi, L.B.1
Mangino, M.2
De Serio, S.3
-
28
-
-
0036074126
-
A genetic locus for adolescent idiopathic scoliosis linked to chromosome 19p13.3
-
Chan V, Fong GCY, Luk KDK, et al. A genetic locus for adolescent idiopathic scoliosis linked to chromosome 19p13.3. Am J Hum Genet 2002;71:401-6.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 401-406
-
-
Chan, V.1
Fong, G.C.Y.2
Luk, K.D.K.3
-
29
-
-
0037444167
-
Familial idiopathic scoliosis: Evidence of an X-linked susceptibility locus
-
Justice CM, Miller NH, Marosy B, et al. Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus. Spine 2003;6:589-94.
-
(2003)
Spine
, vol.6
, pp. 589-594
-
-
Justice, C.M.1
Miller, N.H.2
Marosy, B.3
-
30
-
-
18844369625
-
Identification of candidate regions for familial idiopathic scoliosis
-
Miller NH, Justice CM, Marosy B, et al. Identification of candidate regions for familial idiopathic scoliosis. Spine 2005;30:1181-7.
-
(2005)
Spine
, vol.30
, pp. 1181-1187
-
-
Miller, N.H.1
Justice, C.M.2
Marosy, B.3
-
31
-
-
0036480144
-
Analysis of polymorphism of the number of tandem repeats in the aggrecan gene exon G3 in the families with idiopathic scoliosis
-
Zorkoltseva IV, Liubinskii OA, Sharipov RN, et al. Analysis of polymorphism of the number of tandem repeats in the aggrecan gene exon G3 in the families with idiopathic scoliosis. Genetika 2002;38:259-63.
-
(2002)
Genetika
, vol.38
, pp. 259-263
-
-
Zorkoltseva, I.V.1
Liubinskii, O.A.2
Sharipov, R.N.3
-
32
-
-
33745072264
-
Polymorphism of the aggrecan gene as a marker for adolescent idiopathic scoliosis
-
Quebec, Canada, September
-
Merola AA, Mathur S, Igobou S, et al. Polymorphism of the aggrecan gene as a marker for adolescent idiopathic scoliosis. SRS 38th Annual Meeting, Quebec, Canada, September 2003.
-
(2003)
SRS 38th Annual Meeting
-
-
Merola, A.A.1
Mathur, S.2
Igobou, S.3
-
33
-
-
0020046727
-
Nonstandard vertebral rotation in scoliosis screening patients: Its prevalence and relation to the clinical deformity
-
Armstrong GW, Livermore NB, Suzuki N, et al. Nonstandard vertebral rotation in scoliosis screening patients: its prevalence and relation to the clinical deformity. Spine 1982;7:50-4.
-
(1982)
Spine
, vol.7
, pp. 50-54
-
-
Armstrong, G.W.1
Livermore, N.B.2
Suzuki, N.3
-
34
-
-
0000732804
-
The incidence of scoliosis in the State of Delaware: A study of 50,000 films of the chest made during a survey for tuberculosis
-
Shands AR Jr, Eisberg HB. The incidence of scoliosis in the State of Delaware: a study of 50,000 films of the chest made during a survey for tuberculosis. J Bone Joint Surg Am 1955;37:1243-7.
-
(1955)
J Bone Joint Surg Am
, vol.37
, pp. 1243-1247
-
-
Shands Jr., A.R.1
Eisberg, H.B.2
-
35
-
-
0027434893
-
Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes
-
Boileau C, Jondeau G, Babron MC, et al. Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes. Am J Hum Genet 1993;53:46-54.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 46-54
-
-
Boileau, C.1
Jondeau, G.2
Babron, M.C.3
-
36
-
-
0024820515
-
Osteoporosis and familial idiopathic scoliosis: Association with an abnormal alpha 2(I) collagen
-
Shapiro JR, Burn VE, Chipman SD, et al. Osteoporosis and familial idiopathic scoliosis: association with an abnormal alpha 2(I) collagen. Connect Tissue Res 1989;21:117-23.
-
(1989)
Connect Tissue Res
, vol.21
, pp. 117-123
-
-
Shapiro, J.R.1
Burn, V.E.2
Chipman, S.D.3
-
37
-
-
0035163544
-
Characterization of idiopathic scoliosis in a clinically well-defined population
-
Miller NH, Schwab DL, Sponseller PD, et al. Characterization of idiopathic scoliosis in a clinically well-defined population. Clin Orthop 2001;392:349-57.
-
(2001)
Clin Orthop
, vol.392
, pp. 349-357
-
-
Miller, N.H.1
Schwab, D.L.2
Sponseller, P.D.3
-
38
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recording and fuzzy inheritance
-
O'Connell JR, Weeks DE. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recording and fuzzy inheritance. Nat Genet 1995;11:402-8.
-
(1995)
Nat Genet
, vol.11
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
39
-
-
0000729548
-
Genomic search for X-linkage in familial adolescent idiopathic scoliosis
-
Stokes IAF, ed. Amsterdam: IOS Press
-
Miller NH, Schwab D, Sponseller P, et al. Genomic search for X-linkage in familial adolescent idiopathic scoliosis. In: Stokes IAF, ed. Research Into Spinal Deformities, vol. 2. Amsterdam: IOS Press, 1998:209-13.
-
(1998)
Research into Spinal Deformities
, vol.2
, pp. 209-213
-
-
Miller, N.H.1
Schwab, D.2
Sponseller, P.3
-
42
-
-
0001096896
-
Sib-pair: A program for non-parametric linkage/association analysis
-
Duffy D. Sib-pair: a program for non-parametric linkage/association analysis. Am J Hum Genet 1997;61(suppl):A197.
-
(1997)
Am J Hum Genet
, vol.61
, Issue.SUPPL.
-
-
Duffy, D.1
-
43
-
-
0030881661
-
Accurate inference of relationships in sib-pair linkage studies
-
Boehnke M, Cox NJ. Accurate inference of relationships in sib-pair linkage studies. Am J Hum Genet 1997;61:423-9.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 423-429
-
-
Boehnke, M.1
Cox, N.J.2
-
44
-
-
0032231347
-
Estimation of pairwise relationships in the presence of genotyping errors
-
Broman KW, Weber JL. Estimation of pairwise relationships in the presence of genotyping errors. Am J Hum Genet 1998;63:1563-4.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1563-1564
-
-
Broman, K.W.1
Weber, J.L.2
|