-
1
-
-
0037162885
-
Whole-genome shotgun assembly and analysis of the genome of Fugu rubripes
-
S. Aparicio Whole-genome shotgun assembly and analysis of the genome of Fugu rubripes Science 297 2002 1301 1310
-
(2002)
Science
, vol.297
, pp. 1301-1310
-
-
Aparicio, S.1
-
2
-
-
0034855377
-
The molecular genetics of inherited cartilage disease
-
J.F. Bateman The molecular genetics of inherited cartilage disease Osteoarthr. Cartil. 9 2001 S141 149
-
(2001)
Osteoarthr. Cartil.
, vol.9
-
-
Bateman, J.F.1
-
3
-
-
0030513640
-
Variability in the upstream promoter and intron sequences of the human, mouse and chick type X collagen genes
-
F. Beier, I. Eerola, E. Vuorio, P. Luvalle, E. Reichenberger, W. Bertling, K. von der Mark, and M.J. Lammi Variability in the upstream promoter and intron sequences of the human, mouse and chick type X collagen genes Matrix Biol. 15 1996 415 422
-
(1996)
Matrix Biol.
, vol.15
, pp. 415-422
-
-
Beier, F.1
Eerola, I.2
Vuorio, E.3
Luvalle, P.4
Reichenberger, E.5
Bertling, W.6
Von Der Mark, K.7
Lammi, M.J.8
-
4
-
-
0026528501
-
The fibrillar collagens, collagen VIII, collagen X and the C1q complement proteins share a similar domain in their C-terminal non-collagenous regions
-
A. Brass, K.E. Kadler, J.T. Thomas, M.E. Grant, and R.P. Boot-Handford The fibrillar collagens, collagen VIII, collagen X and the C1q complement proteins share a similar domain in their C-terminal non-collagenous regions FEBS Lett. 303 1992 126 128
-
(1992)
FEBS Lett.
, vol.303
, pp. 126-128
-
-
Brass, A.1
Kadler, K.E.2
Thomas, J.T.3
Grant, M.E.4
Boot-Handford, R.P.5
-
5
-
-
0028965555
-
Type X collagen multimer assembly in vitro is prevented by a Gly618 to Val mutation in the alpha 1(X) NC1 domain resulting in Schmid metaphyseal chondrodysplasia
-
D. Chan, W.G. Cole, J.G. Rogers, and J.F. Bateman Type X collagen multimer assembly in vitro is prevented by a Gly618 to Val mutation in the alpha 1(X) NC1 domain resulting in Schmid metaphyseal chondrodysplasia J. Biol. Chem. 270 1995 4558 4562
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 4558-4562
-
-
Chan, D.1
Cole, W.G.2
Rogers, J.G.3
Bateman, J.F.4
-
6
-
-
0000937043
-
A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in Schmid metaphyseal chondrodysplasia
-
D. Chan, Y.M. Weng, H.K. Graham, D.O. Sillence, and J.F. Bateman A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in Schmid metaphyseal chondrodysplasia J. Clin. Invest. 101 1998 1490 1499
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 1490-1499
-
-
Chan, D.1
Weng, Y.M.2
Graham, H.K.3
Sillence, D.O.4
Bateman, J.F.5
-
7
-
-
0027459150
-
The mouse collagen X gene: Complete nucleotide sequence, exon structure and expression pattern
-
K. Elima, I. Eerola, R. Rosati, M. Metsaranta, S. Garofalo, M. Perala, B. De Crombrugghe, and E. Vuorio The mouse collagen X gene: complete nucleotide sequence, exon structure and expression pattern Biochem. J. 289 1993 247 253
-
(1993)
Biochem. J.
, vol.289
, pp. 247-253
-
-
Elima, K.1
Eerola, I.2
Rosati, R.3
Metsaranta, M.4
Garofalo, S.5
Perala, M.6
De Crombrugghe, B.7
Vuorio, E.8
-
8
-
-
0021795012
-
Type X collagen, a product of hypertrophic chondrocytes
-
C.M. Kielty, A.P. Kwan, D.F. Holmes, S.L. Schor, and M.E. Grant Type X collagen, a product of hypertrophic chondrocytes Biochem. J. 227 1985 545 554
-
(1985)
Biochem. J.
, vol.227
, pp. 545-554
-
-
Kielty, C.M.1
Kwan, A.P.2
Holmes, D.F.3
Schor, S.L.4
Grant, M.E.5
-
9
-
-
0027531910
-
Intron-exon structure, alternative use of promoter and expression of the mouse collagen X gene, Col10a-1
-
R.Y. Kong, K.M. Kwan, E.T. Lau, J.T. Thomas, R.P. Boot-Handford, M.E. Grant, and K.S. Cheah Intron-exon structure, alternative use of promoter and expression of the mouse collagen X gene, Col10a-1 Eur. J. Biochem. 213 1993 99 111
-
(1993)
Eur. J. Biochem.
, vol.213
, pp. 99-111
-
-
Kong, R.Y.1
Kwan, K.M.2
Lau, E.T.3
Thomas, J.T.4
Boot-Handford, R.P.5
Grant, M.E.6
Cheah, K.S.7
-
10
-
-
0024267226
-
The type X collagen gene. Intron sequences split the 5′- untranslated region and separate the coding regions for the non-collagenous amino-terminal and triple-helical domains
-
P. LuValle, Y. Ninomiya, N.D. Rosenblum, and B.R. Olsen The type X collagen gene. Intron sequences split the 5′-untranslated region and separate the coding regions for the non-collagenous amino-terminal and triple-helical domains J. Biol. Chem. 263 1988 18378 18385
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 18378-18385
-
-
Luvalle, P.1
Ninomiya, Y.2
Rosenblum, N.D.3
Olsen, B.R.4
-
11
-
-
0033525204
-
Metaphyseal chondrodysplasia type Schmid mutations are predicted to occur in two distinct three-dimensional clusters within type X collagen NC1 domains that retain the ability to trimerize
-
D.S. Marks, C.A. Gregory, G.A. Wallis, A. Brass, K.E. Kadler, and R.P. Boot-Handford Metaphyseal chondrodysplasia type Schmid mutations are predicted to occur in two distinct three-dimensional clusters within type X collagen NC1 domains that retain the ability to trimerize J. Biol. Chem. 274 1999 3632 3641
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 3632-3641
-
-
Marks, D.S.1
Gregory, C.A.2
Wallis, G.A.3
Brass, A.4
Kadler, K.E.5
Boot-Handford, R.P.6
-
12
-
-
0027976169
-
Additional mutations of type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locus
-
I. McIntosh, M.H. Abbott, M.L. Warman, B.R. Olsen, and C.A. Francomano Additional mutations of type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locus Hum. Mol. Genet. 3 1994 303 307
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 303-307
-
-
McIntosh, I.1
Abbott, M.H.2
Warman, M.L.3
Olsen, B.R.4
Francomano, C.A.5
-
13
-
-
0025887138
-
The alpha 2(VIII) collagen gene. A novel member of the short chain collagen family located on the human chromosome 1
-
Y. Muragaki, O. Jacenko, S. Apte, M.G. Mattei, Y. Ninomiya, and B.R. Olsen The alpha 2(VIII) collagen gene. A novel member of the short chain collagen family located on the human chromosome 1 J. Biol. Chem. 266 1991 7721 7727
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 7721-7727
-
-
Muragaki, Y.1
Jacenko, O.2
Apte, S.3
Mattei, M.G.4
Ninomiya, Y.5
Olsen, B.R.6
-
14
-
-
0025808789
-
The complete primary structure of the human alpha 1 (VIII) chain and assignment of its gene (COL8A1) to chromosome 3
-
Y. Muragaki, M.G. Mattei, N. Yamaguchi, B.R. Olsen, and Y. Ninomiya The complete primary structure of the human alpha 1 (VIII) chain and assignment of its gene (COL8A1) to chromosome 3 Eur. J. Biochem. 197 1991 615 622
-
(1991)
Eur. J. Biochem.
, vol.197
, pp. 615-622
-
-
Muragaki, Y.1
Mattei, M.G.2
Yamaguchi, N.3
Olsen, B.R.4
Ninomiya, Y.5
-
15
-
-
0026714635
-
Genomic organization and full-length cDNA sequence of human collagen X
-
E. Reichenberger, F. Beier, P. LuValle, B.R. Olsen, K. von der Mark, and W.M. Bertling Genomic organization and full-length cDNA sequence of human collagen X FEBS Lett. 311 1992 305 310
-
(1992)
FEBS Lett.
, vol.311
, pp. 305-310
-
-
Reichenberger, E.1
Beier, F.2
Luvalle, P.3
Olsen, B.R.4
Von Der Mark, K.5
Bertling, W.M.6
-
16
-
-
0020512378
-
A short chain (pro)collagen from aged endochondral chondrocytes, biochemical characterization
-
T. Schmid, and T. Linsenmayer A short chain (pro)collagen from aged endochondral chondrocytes, biochemical characterization J. Biol. Chem. 258 1983 9504 9509
-
(1983)
J. Biol. Chem.
, vol.258
, pp. 9504-9509
-
-
Schmid, T.1
Linsenmayer, T.2
-
17
-
-
1542314840
-
P38 MAP kinase signaling is required for hypertrophic chondrocyte differentiation
-
L.A. Stanton, S. Sabari, A.V. Sampaio, T.M. Underhill, and F. Beier p38 MAP kinase signaling is required for hypertrophic chondrocyte differentiation Biochem. J. 378 2004 53 62
-
(2004)
Biochem. J.
, vol.378
, pp. 53-62
-
-
Stanton, L.A.1
Sabari, S.2
Sampaio, A.V.3
Underhill, T.M.4
Beier, F.5
-
18
-
-
0027958472
-
Amino acid substitutions of conserved residues in the carboxyl-terminal domain of the alpha 1(X) chain of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type Schmid
-
G.A. Wallis, B. Rash, W.A. Sweetman, J.T. Thomas, M. Super, G. Evans, M.E. Grant, and R.P. Boot-Handford Amino acid substitutions of conserved residues in the carboxyl-terminal domain of the alpha 1(X) chain of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type Schmid Am. J. Hum. Genet. 54 1994 169 178
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 169-178
-
-
Wallis, G.A.1
Rash, B.2
Sweetman, W.A.3
Thomas, J.T.4
Super, M.5
Evans, G.6
Grant, M.E.7
Boot-Handford, R.P.8
-
19
-
-
0029952201
-
Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasia
-
G.A. Wallis, B. Rash, B. Sykes, J. Bonaventure, P. Maroteaux, B. Zabel, R. Wynne-Davies, M.E. Grant, and R.P. Boot-Handford Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasia J. Med. Genet. 33 1996 450 457
-
(1996)
J. Med. Genet.
, vol.33
, pp. 450-457
-
-
Wallis, G.A.1
Rash, B.2
Sykes, B.3
Bonaventure, J.4
Maroteaux, P.5
Zabel, B.6
Wynne-Davies, R.7
Grant, M.E.8
Boot-Handford, R.P.9
-
20
-
-
1842581698
-
RhoA/ROCK signaling suppresses hypertrophic chondrocyte differentiation
-
G. Wang, A. Woods, S. Sabari, L. Pagnotta, L.-A. Stanton, and F. Beier RhoA/ROCK signaling suppresses hypertrophic chondrocyte differentiation J. Biol. Chem. 279 2004 13205 13214
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 13205-13214
-
-
Wang, G.1
Woods, A.2
Sabari, S.3
Pagnotta, L.4
Stanton, L.-A.5
Beier, F.6
-
21
-
-
0027282559
-
A type X collagen mutation causes Schmid metaphyseal chondrodysplasia
-
M.L. Warman, M. Abbott, S.S. Apte, T. Hefferon, I. McIntosh, D.H. Cohn, J.T. Hecht, B.R. Olsen, and C.A. Francomano A type X collagen mutation causes Schmid metaphyseal chondrodysplasia Nat. Genet. 5 1993 79 82
-
(1993)
Nat. Genet.
, vol.5
, pp. 79-82
-
-
Warman, M.L.1
Abbott, M.2
Apte, S.S.3
Hefferon, T.4
McIntosh, I.5
Cohn, D.H.6
Hecht, J.T.7
Olsen, B.R.8
Francomano, C.A.9
-
22
-
-
0024450805
-
The cloning and sequencing of alpha 1(VIII) collagen cDNAs demonstrate that type VIII collagen is a short chain collagen and contains triple-helical and carboxyl-terminal non-triple-helical domains similar to those of type X collagen
-
N. Yamaguchi, P.D. Benya, M. van der Rest, and Y. Ninomiya The cloning and sequencing of alpha 1(VIII) collagen cDNAs demonstrate that type VIII collagen is a short chain collagen and contains triple-helical and carboxyl-terminal non-triple-helical domains similar to those of type X collagen J. Biol. Chem. 264 1989 16022 16029
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 16022-16029
-
-
Yamaguchi, N.1
Benya, P.D.2
Van Der Rest, M.3
Ninomiya, Y.4
-
23
-
-
0025911342
-
The alpha 1 (VIII) collagen gene is homologous to the alpha 1 (X) collagen gene and contains a large exon encoding the entire triple helical and carboxyl-terminal non-triple helical domains of the alpha 1 (VIII) polypeptide
-
N. Yamaguchi, R. Mayne, and Y. Ninomiya The alpha 1 (VIII) collagen gene is homologous to the alpha 1 (X) collagen gene and contains a large exon encoding the entire triple helical and carboxyl-terminal non-triple helical domains of the alpha 1 (VIII) polypeptide J. Biol. Chem. 266 1991 4508 4513
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 4508-4513
-
-
Yamaguchi, N.1
Mayne, R.2
Ninomiya, Y.3
-
24
-
-
0042887424
-
Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo
-
Q. Zheng, G. Zhou, R. Morello, Y. Chen, X. Garcia-Rojas, and B. Lee Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo J. Cell Biol. 162 2003 833 842
-
(2003)
J. Cell Biol.
, vol.162
, pp. 833-842
-
-
Zheng, Q.1
Zhou, G.2
Morello, R.3
Chen, Y.4
Garcia-Rojas, X.5
Lee, B.6
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