-
1
-
-
77957727477
-
Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta
-
Alanay Y. Avaygan H. Camacho N. Utine G. E. Boduroglu K. Aktas D. Alikasifoglu M. Tuncbilek E. Orhan D. Bakar F. T. et al. (2010). Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta. Am. J. Hum. Genet. 87 572-573.
-
(2010)
Am. J. Hum. Genet
, vol.87
, pp. 572-573
-
-
Alanay, Y.1
Avaygan, H.2
Camacho, N.3
Utine, G.E.4
Boduroglu, K.5
Aktas, D.6
Alikasifoglu, M.7
Tuncbilek, E.8
Orhan, D.9
Bakar, F.T.10
-
2
-
-
0032583171
-
Collagen II is essential for the removal of the notochord and the formation of intervertebral discs
-
Aszodi A. Chan D. Hunziker E. Bateman J. F. and Fassler R. (1998). Collagen II is essential for the removal of the notochord and the formation of intervertebral discs. J. Cell. Biol. 143 1399-1412.
-
(1998)
J. Cell. Biol
, vol.143
, pp. 1399-1412
-
-
Aszodi, A.1
Chan, D.2
Hunziker, E.3
Bateman, J.F.4
Fassler, R.5
-
3
-
-
0018959643
-
Folding mechanism of the triple helix in type-III collagen and type-III pN-collagen. Role of disulfide bridges and peptide bond isomerization
-
Bachinger H. P. Bruckner P. Timpl R. Prockop D. J. and Engel J. (1980). Folding mechanism of the triple helix in type-III collagen and type-III pN-collagen. Role of disulfide bridges and peptide bond isomerization. Eur. J. Biochem. 106 619-632.
-
(1980)
Eur. J. Biochem
, vol.106
, pp. 619-632
-
-
Bachinger, H.P.1
Bruckner, P.2
Timpl, R.3
Prockop, D.J.4
Engel, J.5
-
4
-
-
55849106161
-
Baldridge D. Schwarze U. Morello R. Lennington J. Bertin T. K. Pace J. M. Pepin M. G. Weis M. Eyre D. R. Walsh J. et al.
-
Baldridge D. Schwarze U. Morello R. Lennington J. Bertin T. K. Pace J. M. Pepin M. G. Weis M. Eyre D. R. Walsh J. et al. (2008). CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta. Hum. Mutat. 29 1435-1442.
-
(2008)
Hum. Mutat
, vol.29
, pp. 1435-1442
-
-
-
5
-
-
0033782015
-
Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response
-
Bertolotti A. Zhang Y. Hendershot L. M. Harding H. P. and Ron D. (2000). Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response. Nat. Cell Biol. 2 326-332.
-
(2000)
Nat. Cell Biol
, vol.2
, pp. 326-332
-
-
Bertolotti, A.1
Zhang, Y.2
Hendershot, L.M.3
Harding, H.P.4
Ron, D.5
-
6
-
-
0029070079
-
Briggs M. D. Hoffman S. M. King L. M. Olsen A. S. Mohrenweiser H. Leroy J. G. Mortier G. R. Rimoin D. L. Lachman R. S. Gaines E. S. et al.
-
Briggs M. D. Hoffman S. M. King L. M. Olsen A. S. Mohrenweiser H. Leroy J. G. Mortier G. R. Rimoin D. L. Lachman R. S. Gaines E. S. et al. (1995). Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene. Nat. Genet. 10 330-336.
-
(1995)
Nat. Genet
, vol.10
, pp. 330-336
-
-
-
7
-
-
0038578294
-
Dynamic imaging of collagen and its modulation in tumors in vivo using second-harmonic generation
-
Brown E. McKee T. diTomaso E. Pluen A. Seed B. Boucher Y. and Jain R. K. (2003). Dynamic imaging of collagen and its modulation in tumors in vivo using second-harmonic generation. Nat. Med. 9 796-800.
-
(2003)
Nat. Med
, vol.9
, pp. 796-800
-
-
Brown, E.1
McKee, T.2
diTomaso, E.3
Pluen, A.4
Seed, B.5
Boucher, Y.6
Jain, R.K.7
-
8
-
-
0030812651
-
The C-propeptide domain of procollagen can be replaced with a transmembrane domain without affecting trimer formation or collagen triple helix folding during biosynthesis
-
Bulleid N. J. Dalley J. A. and Lees J. F. (1997). The C-propeptide domain of procollagen can be replaced with a transmembrane domain without affecting trimer formation or collagen triple helix folding during biosynthesis. EMBO J. 16 6694-6701.
-
(1997)
EMBO J
, vol.16
, pp. 6694-6701
-
-
Bulleid, N.J.1
Dalley, J.A.2
Lees, J.F.3
-
9
-
-
0028938776
-
A COL2A1 mutation in achondrogenesis type II results in the replacement of type II collagen by type I and III collagens in cartilage
-
Chan D. Cole W. G. Chow C. W. Mundlos S. and Bateman J. F. (1995). A COL2A1 mutation in achondrogenesis type II results in the replacement of type II collagen by type I and III collagens in cartilage. J. Biol. Chem. 270 1747-1753.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 1747-1753
-
-
Chan, D.1
Cole, W.G.2
Chow, C.W.3
Mundlos, S.4
Bateman, J.F.5
-
10
-
-
0034933884
-
Mutations in the region encoding the von Willebrand factor Adomain of matrilin-3 are associated with multiple epiphyseal dysplasia
-
Chapman K. L. Mortier G. R. Chapman K. Loughlin J. Grant M. E. and Briggs M. D. (2001). Mutations in the region encoding the von Willebrand factor Adomain of matrilin-3 are associated with multiple epiphyseal dysplasia. Nat. Genet. 28 393-396.
-
(2001)
Nat. Genet
, vol.28
, pp. 393-396
-
-
Chapman, K.L.1
Mortier, G.R.2
Chapman, K.3
Loughlin, J.4
Grant, M.E.5
Briggs, M.D.6
-
11
-
-
0027182875
-
BiP binds type I procollagen pro alpha chains with mutations in the carboxyl-terminal propeptide synthesized by cells from patients with osteogenesis imperfecta
-
Chessler S. D. and Byers P. H. (1993). BiP binds type I procollagen pro alpha chains with mutations in the carboxyl-terminal propeptide synthesized by cells from patients with osteogenesis imperfecta. J. Biol. Chem. 268 18226-18233.
-
(1993)
J. Biol. Chem
, vol.268
, pp. 18226-18233
-
-
Chessler, S.D.1
Byers, P.H.2
-
12
-
-
77949262259
-
Homozygosity for a missense mutation in SERPINH1 which encodes the collagen chaperone protein HSP47 results in severe recessive osteogenesis imperfecta
-
Christiansen H. E. Schwarze U. Pyott S. M. AlSwaid A. Al Balwi M. Alrasheed S. Pepin M. G. Weis M. A. Eyre D. R. and Byers P. H. (2010). Homozygosity for a missense mutation in SERPINH1 which encodes the collagen chaperone protein HSP47 results in severe recessive osteogenesis imperfecta. Am. J. Hum. Genet. 86 389-398.
-
(2010)
Am. J. Hum. Genet
, vol.86
, pp. 389-398
-
-
Christiansen, H.E.1
Schwarze, U.2
Pyott, S.M.3
AlSwaid, A.4
Al Balwi, M.5
Alrasheed, S.6
Pepin, M.G.7
Weis, M.A.8
Eyre, D.R.9
Byers, P.H.10
-
14
-
-
0027468569
-
Parallel regulation of procollagen I and colligin a collagen-binding protein and a member of the serine protease inhibitor family
-
Clarke E. P. Jain N. Brickenden A. Lorimer I. A. and Sanwal B. D. (1993). Parallel regulation of procollagen I and colligin a collagen-binding protein and a member of the serine protease inhibitor family. J. Cell Biol. 121 193-199.
-
(1993)
J. Cell Biol
, vol.121
, pp. 193-199
-
-
Clarke, E.P.1
Jain, N.2
Brickenden, A.3
Lorimer, I.A.4
Sanwal, B.D.5
-
15
-
-
0028254163
-
Collagen genes: mutations affecting collagen structure and expression. Prog. Nucl
-
Cole W. G. (1994). Collagen genes: mutations affecting collagen structure and expression. Prog. Nucl. Acid Res. Mol. Biol. 47 29-80.
-
(1994)
Acid Res. Mol. Biol
, vol.47
, pp. 29-80
-
-
Cole, W.G.1
-
16
-
-
68549083862
-
Sulfation of chondroitin sulfate proteoglycans is necessary for proper Indian hedgehog signaling in the developing growth plate
-
Development
-
Cortes M. Baria A. T. and Schwartz N. B. (2009). Sulfation of chondroitin sulfate proteoglycans is necessary for proper Indian hedgehog signaling in the developing growth plate. Development 136 1697-1706.
-
(2009)
, vol.136
, pp. 1697-1706
-
-
Cortes, M.1
Baria, A.T.2
Schwartz, N.B.3
-
17
-
-
68249130696
-
A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta
-
Drogemuller C. Becker D. Brunner A. Haase B. Kircher P. Seeliger F. Fehr M. Baumann U. Lindblad-Toh K. and Leeb T. (2009). A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta. PLoS Genet. 5 e1000579.
-
(2009)
PLoS Genet
, vol.5
-
-
Drogemuller, C.1
Becker, D.2
Brunner, A.3
Haase, B.4
Kircher, P.5
Seeliger, F.6
Fehr, M.7
Baumann, U.8
Lindblad-Toh, K.9
Leeb, T.10
-
18
-
-
0025904728
-
The zipper-like folding of collagen triple helices and the effects of mutations that disrupt the zipper. Annu
-
Engel J. and Prockop D. J. (1991). The zipper-like folding of collagen triple helices and the effects of mutations that disrupt the zipper. Annu. Rev. Biophys. Biophys. Chem. 20 137-152.
-
(1991)
Rev. Biophys. Biophys. Chem
, vol.20
, pp. 137-152
-
-
Engel, J.1
Prockop, D.J.2
-
19
-
-
0036151502
-
Collagen of articular cartilage
-
Eyre D. (2002) Collagen of articular cartilage. Arthritis Res. 4 30-35
-
(2002)
Arthritis Res
, vol.4
, pp. 30-35
-
-
Eyre, D.1
-
21
-
-
36549034372
-
Collagen XI chain misassembly in cartilage of the chondrodysplasia (cho) mouse
-
Fernandes R. J. Weis M. Scott M. A. Seegmiller R. E. and Eyre D. R. (2007). Collagen XI chain misassembly in cartilage of the chondrodysplasia (cho) mouse. Matrix Biol. 26 597-603.
-
(2007)
Matrix Biol
, vol.26
, pp. 597-603
-
-
Fernandes, R.J.1
Weis, M.2
Scott, M.A.3
Seegmiller, R.E.4
Eyre, D.R.5
-
22
-
-
0028656507
-
Association of Hsp47 Grp78 and Grp94 with procollagen supports the successive or coupled action of molecular chaperones
-
Ferreira L. R. Norris K. Smith T. Hebert C. and Sauk J. J. (1994). Association of Hsp47 Grp78 and Grp94 with procollagen supports the successive or coupled action of molecular chaperones. J. Cell. Biochem. 56 518-526.
-
(1994)
J. Cell. Biochem
, vol.56
, pp. 518-526
-
-
Ferreira, L.R.1
Norris, K.2
Smith, T.3
Hebert, C.4
Sauk, J.J.5
-
23
-
-
0028263628
-
Mutation in the COL2A1 gene in a patient with hypochondrogenesis. Expression of mutated COL2A1 gene is accompanied by expression of genes for type I procollagen in chondrocytes
-
Freisinger P. Ala-Kokko L. LeGuellec D. Franc S. Bouvier R. Ritvaniemi P. Prockop D. J. and Bonaventure J. (1994). Mutation in the COL2A1 gene in a patient with hypochondrogenesis. Expression of mutated COL2A1 gene is accompanied by expression of genes for type I procollagen in chondrocytes. J. Biol. Chem. 269 13663-13669.
-
(1994)
J. Biol. Chem
, vol.269
, pp. 13663-13669
-
-
Freisinger, P.1
Ala-Kokko, L.2
LeGuellec, D.3
Franc, S.4
Bouvier, R.5
Ritvaniemi, P.6
Prockop, D.J.7
Bonaventure, J.8
-
24
-
-
0028361309
-
Folding of nascent polypeptide chains in a high molecular mass assembly with molecular chaperones
-
Frydman J. Nimmesgern E. Ohtsuka K. and Hartl F. U. (1994). Folding of nascent polypeptide chains in a high molecular mass assembly with molecular chaperones. Nature 370 111-117.
-
(1994)
Nature
, vol.370
, pp. 111-117
-
-
Frydman, J.1
Nimmesgern, E.2
Ohtsuka, K.3
Hartl, F.U.4
-
25
-
-
0028059099
-
Deletion of a DNA polymerase beta gene segment in T cells using cell type-specific gene targeting
-
Gu H. Marth J. D. Orban P. C. Mossmann H. and Rajewsky K. (1994). Deletion of a DNA polymerase beta gene segment in T cells using cell type-specific gene targeting. Science 265 103-106.
-
(1994)
Science
, vol.265
, pp. 103-106
-
-
Gu, H.1
Marth, J.D.2
Orban, P.C.3
Mossmann, H.4
Rajewsky, K.5
-
26
-
-
0037040541
-
Molecular chaperones in the cytosol: from nascent chain to folded protein
-
Hartl F. U. and Hayer-Hartl M. (2002). Molecular chaperones in the cytosol: from nascent chain to folded protein. Science 295 1852-1858.
-
(2002)
Science
, vol.295
, pp. 1852-1858
-
-
Hartl, F.U.1
Hayer-Hartl, M.2
-
27
-
-
0032693671
-
Mammalian transcription factor ATF6 is synthesized as a transmembrane protein and activated by proteolysis in response to endoplasmic reticulum stress
-
Haze K. Yoshida H. Yanagi H. Yura T. and Mori K. (1999). Mammalian transcription factor ATF6 is synthesized as a transmembrane protein and activated by proteolysis in response to endoplasmic reticulum stress. Mol. Biol. Cell 10 3787-3799.
-
(1999)
Mol. Biol. Cell
, vol.10
, pp. 3787-3799
-
-
Haze, K.1
Yoshida, H.2
Yanagi, H.3
Yura, T.4
Mori, K.5
-
28
-
-
0027184721
-
Molecular chaperone functions of heat-shock proteins
-
Hendrick J. P. and Hartl F. U. (1993). Molecular chaperone functions of heat-shock proteins. Annu. Rev. Biochem. 62 349-384.
-
(1993)
Annu. Rev. Biochem
, vol.62
, pp. 349-384
-
-
Hendrick, J.P.1
Hartl, F.U.2
-
30
-
-
33748250907
-
Regeneration of osteonecrosis of canine scapho-lunate using bone marrow stromal cells: possible therapeutic approach for Kienbock disease
-
Ikeguchi R. Kakinoki R. Aoyama T. Shibata K. R. Otsuka S. Fukiage K. Nishijo K. Ishibe T. Shima Y. Otsuki B. et al. (2006). Regeneration of osteonecrosis of canine scapho-lunate using bone marrow stromal cells: possible therapeutic approach for Kienbock disease. Cell Transplant. 15 411-422.
-
(2006)
Cell Transplant
, vol.15
, pp. 411-422
-
-
Ikeguchi, R.1
Kakinoki, R.2
Aoyama, T.3
Shibata, K.R.4
Otsuka, S.5
Fukiage, K.6
Nishijo, K.7
Ishibe, T.8
Shima, Y.9
Otsuki, B.10
-
31
-
-
33745747824
-
Type I collagen in Hsp47-null cells is aggregated in endoplasmic reticulum and deficient in N-propeptide processing and fibrillogenesis
-
Ishida Y. Kubota H. Yamamoto A. Kitamura A. Bachinger H. P. and Nagata K. (2006). Type I collagen in Hsp47-null cells is aggregated in endoplasmic reticulum and deficient in N-propeptide processing and fibrillogenesis. Mol. Biol. Cell 17 2346-2355.
-
(2006)
Mol. Biol. Cell
, vol.17
, pp. 2346-2355
-
-
Ishida, Y.1
Kubota, H.2
Yamamoto, A.3
Kitamura, A.4
Bachinger, H.P.5
Nagata, K.6
-
32
-
-
66349112572
-
Autophagic elimination of misfolded procollagen aggregates in the endoplasmic reticulum as a means of cell protection
-
Ishida Y. Yamamoto A. Kitamura A. Lamande S. R. Yoshimori T. Bateman J. F. Kubota H. and Nagata K. (2009). Autophagic elimination of misfolded procollagen aggregates in the endoplasmic reticulum as a means of cell protection. Mol. Biol. Cell 20 2744-2754.
-
(2009)
Mol. Biol. Cell
, vol.20
, pp. 2744-2754
-
-
Ishida, Y.1
Yamamoto, A.2
Kitamura, A.3
Lamande, S.R.4
Yoshimori, T.5
Bateman, J.F.6
Kubota, H.7
Nagata, K.8
-
33
-
-
77950446292
-
Type IX collagen gene mutations can result in multiple epiphyseal dysplasia that is associated with osteochondritis dissecans and a mild myopathy
-
Jackson G. C. Marcus-Soekarman D. Stolte-Dijkstra I. Verrips A. Taylor J. A. and Briggs M. D. (2010) Type IX collagen gene mutations can result in multiple epiphyseal dysplasia that is associated with osteochondritis dissecans and a mild myopathy. Am. J. Hum. Genet. 152 863-869.
-
(2010)
Am. J. Hum. Genet
, vol.152
, pp. 863-869
-
-
Jackson, G.C.1
Marcus-Soekarman, D.2
Stolte-Dijkstra, I.3
Verrips, A.4
Taylor, J.A.5
Briggs, M.D.6
-
34
-
-
0032032089
-
Collagen cross-links in mineralizing tissues: a review of their chemistry function and clinical relevance
-
Knott L. and Bailey A. J. (1998). Collagen cross-links in mineralizing tissues: a review of their chemistry function and clinical relevance. Bone 22 181-187.
-
(1998)
Bone
, vol.22
, pp. 181-187
-
-
Knott, L.1
Bailey, A.J.2
-
35
-
-
0037155282
-
Xaa-Arg-Gly triplets in the collagen triple helix are dominant binding sites for the molecular chaperone HSP47
-
Koide T. Takahara Y. Asada S. and Nagata K. (2002). Xaa-Arg-Gly triplets in the collagen triple helix are dominant binding sites for the molecular chaperone HSP47. J. Biol. Chem. 277 6178-6182.
-
(2002)
J. Biol. Chem
, vol.277
, pp. 6178-6182
-
-
Koide, T.1
Takahara, Y.2
Asada, S.3
Nagata, K.4
-
36
-
-
0032923886
-
Easy assessment of ES cell clone potency for chimeric development and germ-line competency by an optimized aggregation method
-
Kondoh G. Yamamoto Y. Yoshida K. Suzuki Y. Osuka S. Nakano Y. Morita T. and Takeda J. (1999). Easy assessment of ES cell clone potency for chimeric development and germ-line competency by an optimized aggregation method. J. Biochem. Biophys. Methods 39 137-142.
-
(1999)
J. Biochem. Biophys. Methods
, vol.39
, pp. 137-142
-
-
Kondoh, G.1
Yamamoto, Y.2
Yoshida, K.3
Suzuki, Y.4
Osuka, S.5
Nakano, Y.6
Morita, T.7
Takeda, J.8
-
37
-
-
0030955414
-
Mutations in fibrillar collagens (types I II III and XI) fibril-associated collagen (type IX) and network-forming collagen (type X) cause a spectrum of diseases of bone cartilage and blood vessels
-
Kuivaniemi H. Tromp G. and Prockop D. J. (1997). Mutations in fibrillar collagens (types I II III and XI) fibril-associated collagen (type IX) and network-forming collagen (type X) cause a spectrum of diseases of bone cartilage and blood vessels. Hum. Mutat. 9 300-315.
-
(1997)
Hum. Mutat
, vol.9
, pp. 300-315
-
-
Kuivaniemi, H.1
Tromp, G.2
Prockop, D.J.3
-
38
-
-
0028902639
-
Endoplasmic reticulum-mediated quality control of type I collagen production by cells from osteogenesis imperfecta patients with mutations in the pro alpha 1 (I) chain carboxyl-terminal propeptide which impair subunit assembly
-
Lamande S. R. Chessler S. D. Golub S. B. Byers P. H. Chan D. Cole W. G. Sillence D. O. and Bateman J. F. (1995). Endoplasmic reticulum-mediated quality control of type I collagen production by cells from osteogenesis imperfecta patients with mutations in the pro alpha 1 (I) chain carboxyl-terminal propeptide which impair subunit assembly. J. Biol. Chem. 270 8642-8649.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 8642-8649
-
-
Lamande, S.R.1
Chessler, S.D.2
Golub, S.B.3
Byers, P.H.4
Chan, D.5
Cole, W.G.6
Sillence, D.O.7
Bateman, J.F.8
-
39
-
-
0028856176
-
Transgenic mice with targeted inactivation of the Col2 alpha 1 gene for collagen II develop a skeleton with membranous and periosteal bone but no endochondral bone
-
Li S. W. Prockop D. J. Helminen H. Fassler R. Lapvetelainen T. Kiraly K. Peltarri A. Arokoski J. Lui H. Arita M. et al. (1995). Transgenic mice with targeted inactivation of the Col2 alpha 1 gene for collagen II develop a skeleton with membranous and periosteal bone but no endochondral bone. Genes Dev. 9 2821-2830.
-
(1995)
Genes Dev
, vol.9
, pp. 2821-2830
-
-
Li, S.W.1
Prockop, D.J.2
Helminen, H.3
Fassler, R.4
Lapvetelainen, T.5
Kiraly, K.6
Peltarri, A.7
Arokoski, J.8
Lui, H.9
Arita, M.10
-
40
-
-
0028815297
-
A fibrillar collagen gene Col11a1 is essential for skeletal morphogenesis
-
Li Y. Lacerda D. A. Warman M. L. Beier D. R. Yoshioka H. Ninomiya Y. Oxford J. T. Morris N. P. Andrikopoulos K. Ramirez F. et al. (1995). A fibrillar collagen gene Col11a1 is essential for skeletal morphogenesis. Cell 80 423-430.
-
(1995)
Cell
, vol.80
, pp. 423-430
-
-
Li, Y.1
Lacerda, D.A.2
Warman, M.L.3
Beier, D.R.4
Yoshioka, H.5
Ninomiya, Y.6
Oxford, J.T.7
Morris, N.P.8
Andrikopoulos, K.9
Ramirez, F.10
-
42
-
-
33847227672
-
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans
-
Marini J. C. Forlino A. Cabral W. A. Barnes A. M. San Antonio J. D. Milgrom S. Hyland J. C. Korkko J. Prockop D. J. De Paepe A. et al. (2007). Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans. Hum. Mutat. 28 209-221.
-
(2007)
Hum. Mutat
, vol.28
, pp. 209-221
-
-
Marini, J.C.1
Forlino, A.2
Cabral, W.A.3
Barnes, A.M.4
San Antonio, J.D.5
Milgrom, S.6
Hyland, J.C.7
Korkko, J.8
Prockop, D.J.9
De Paepe, A.10
-
43
-
-
84861408086
-
-
Coexpression of the collagen-binding stress protein HSP47 gene and the alpha 1(I) and alpha 1(III)
-
Masuda H. Fukumoto M. Hirayoshi K. and Nagata K. (1994). Coexpression of the collagen-binding stress protein HSP47 gene and the alpha 1(I) and alpha 1(III)
-
(1994)
-
-
Masuda, H.1
Fukumoto, M.2
Hirayoshi, K.3
Nagata, K.4
-
44
-
-
84872268657
-
-
Collagen genes in carbon tetrachloride-induced rat liver fibrosis
-
Collagen genes in carbon tetrachloride-induced rat liver fibrosis. J. Clin. Invest. 94 2481-2488.
-
J. Clin. Invest
, vol.94
, pp. 2481-2488
-
-
-
45
-
-
69049108804
-
Conditional inactivation of Has2 reveals a crucial role for hyaluronan in skeletal growth patterning chondrocyte maturation and joint formation in the developing limb
-
Development
-
Matsumoto K. Li Y. Jakuba C. Sugiyama Y. Sayo T. Okuno M. Dealy C. N. Toole B. P. Takeda J. Yamaguchi Y. and Kosher R. A. (2009). Conditional inactivation of Has2 reveals a crucial role for hyaluronan in skeletal growth patterning chondrocyte maturation and joint formation in the developing limb. Development 136 2825-2835.
-
(2009)
, vol.136
, pp. 2825-2835
-
-
Matsumoto, K.1
Li, Y.2
Jakuba, C.3
Sugiyama, Y.4
Sayo, T.5
Okuno, M.6
Dealy, C.N.7
Toole, B.P.8
Takeda, J.9
Yamaguchi, Y.10
Kosher, R.A.11
-
46
-
-
4644234938
-
Insufficient folding of type IV collagen and formation of abnormal basement membrane-like structure in embryoid bodies derived from Hsp47- null embryonic stem cells
-
Matsuoka Y. Kubota H. Adachi E. Nagai N. Marutani T. Hosokawa N. and Nagata K. (2004). Insufficient folding of type IV collagen and formation of abnormal basement membrane-like structure in embryoid bodies derived from Hsp47- null embryonic stem cells. Mol. Biol. Cell 15 4467-4475.
-
(2004)
Mol. Biol. Cell
, vol.15
, pp. 4467-4475
-
-
Matsuoka, Y.1
Kubota, H.2
Adachi, E.3
Nagai, N.4
Marutani, T.5
Hosokawa, N.6
Nagata, K.7
-
47
-
-
0019126423
-
Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S. Teratology
-
McLeod M. J. (1980). Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S. Teratology 22 299-301.
-
(1980)
, vol.22
, pp. 299-301
-
-
McLeod, M.J.1
-
48
-
-
0026710239
-
Chondrodysplasia in transgenic mice harboring a 15-amino acid deletion in the triple helical domain of pro alpha 1(II) collagen chain
-
Metsaranta M. Garofalo S. Decker G. Rintala M. de Crombrugghe B. and Vuorio E. (1992). Chondrodysplasia in transgenic mice harboring a 15-amino acid deletion in the triple helical domain of pro alpha 1(II) collagen chain. J. Cell Biol. 118 203-212.
-
(1992)
J. Cell Biol
, vol.118
, pp. 203-212
-
-
Metsaranta, M.1
Garofalo, S.2
Decker, G.3
Rintala, M.4
de Crombrugghe, B.5
Vuorio, E.6
-
49
-
-
0034108294
-
Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorder
-
Mortier G. R. Weis M. Nuytinck L. King L. M. Wilkin D. J. De Paepe A. Lachman R. S. Rimoin D. L. Eyre D. R. and Cohn D. H. (2000). Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorder. J. Med. Genet. 37 263-271.
-
(2000)
J. Med. Genet
, vol.37
, pp. 263-271
-
-
Mortier, G.R.1
Weis, M.2
Nuytinck, L.3
King, L.M.4
Wilkin, D.J.5
De Paepe, A.6
Lachman, R.S.7
Rimoin, D.L.8
Eyre, D.9
Cohn, D.H.10
-
50
-
-
36148952129
-
Functional gene screening system identified TRPV4 as a regulator of chondrogenic differentiation
-
Muramatsu S. Wakabayashi M. Ohno T. Amano K. Ooishi R. Sugahara T. Shiojiri S. Tashiro K. Suzuki Y. Nishimura R. et al. (2007). Functional gene screening system identified TRPV4 as a regulator of chondrogenic differentiation. J. Biol. Chem. 282 32158-32167.
-
(2007)
J. Biol. Chem
, vol.282
, pp. 32158-32167
-
-
Muramatsu, S.1
Wakabayashi, M.2
Ohno, T.3
Amano, K.4
Ooishi, R.5
Sugahara, T.6
Shiojiri, S.7
Tashiro, K.8
Suzuki, Y.9
Nishimura, R.10
-
51
-
-
0034683570
-
Embryonic lethality of molecular chaperone hsp47 knockout mice is associated with defects in collagen biosynthesis
-
Nagai N. Hosokawa M. Itohara S. Adachi E. Matsushita T. Hosokawa N. and Nagata K. (2000). Embryonic lethality of molecular chaperone hsp47 knockout mice is associated with defects in collagen biosynthesis. J. Cell Biol. 150 1499-1506.
-
(2000)
J. Cell Biol
, vol.150
, pp. 1499-1506
-
-
Nagai, N.1
Hosokawa, M.2
Itohara, S.3
Adachi, E.4
Matsushita, T.5
Hosokawa, N.6
Nagata, K.7
-
52
-
-
0742304951
-
HSP47 as a collagen-specific molecular chaperone: function and expression in normal mouse development
-
Nagata K. (2003). HSP47 as a collagen-specific molecular chaperone: function and expression in normal mouse development. Semin. Cell Dev. Biol. 14 275-282
-
(2003)
Semin. Cell Dev. Biol
, vol.14
, pp. 275-282
-
-
Nagata, K.1
-
53
-
-
0022548519
-
A major collagen-binding protein of chick embryo fibroblasts is a novel heat shock protein
-
Nagata K. Saga S. and Yamada K. M. (1986). A major collagen-binding protein of chick embryo fibroblasts is a novel heat shock protein. J. Cell Biol. 103 223-229.
-
(1986)
J. Cell Biol
, vol.103
, pp. 223-229
-
-
Nagata, K.1
Saga, S.2
Yamada, K.M.3
-
54
-
-
0034810624
-
Upregulation of HSP47 and collagen type III in the dermal fibrotic disease keloid. Biochem
-
Naitoh M. Hosokawa N. Kubota H. Tanaka T. Shirane H. Sawada M. Nishimura Y. and Nagata K. (2001). Upregulation of HSP47 and collagen type III in the dermal fibrotic disease keloid. Biochem. Biophys. Res. Commun. 280 1316-1322.
-
(2001)
Biophys. Res. Commun
, vol.280
, pp. 1316-1322
-
-
Naitoh, M.1
Hosokawa, N.2
Kubota, H.3
Tanaka, T.4
Shirane, H.5
Sawada, M.6
Nishimura, Y.7
Nagata, K.8
-
55
-
-
0027988156
-
Interactions between collagen-binding stress protein HSP47 and collagen. Analysis of kinetic parameters by surface plasmon resonance biosensor
-
Natsume T. Koide T. Yokota S. Hirayoshi K. and Nagata K. (1994). Interactions between collagen-binding stress protein HSP47 and collagen. Analysis of kinetic parameters by surface plasmon resonance biosensor. J. Biol. Chem. 269 31224-31228.
-
(1994)
J. Biol. Chem
, vol.269
, pp. 31224-31228
-
-
Natsume, T.1
Koide, T.2
Yokota, S.3
Hirayoshi, K.4
Nagata, K.5
-
56
-
-
12944265540
-
Col2a1- directed expression of Cre recombinase in differentiating chondrocytes in transgenic mice
-
Ovchinnikov D. A. Deng J. M. Ogunrinu G. and Behringer R. R. (2000). Col2a1- directed expression of Cre recombinase in differentiating chondrocytes in transgenic mice. Genesis 26 145-146.
-
(2000)
Genesis
, vol.26
, pp. 145-146
-
-
Ovchinnikov, D.A.1
Deng, J.M.2
Ogunrinu, G.3
Behringer, R.R.4
-
57
-
-
0029006974
-
Collagens: molecular biology diseases and potentials for therapy
-
Prockop D. J. and Kivirikko K. I. (1995). Collagens: molecular biology diseases and potentials for therapy. Annu. Rev. Biochem. 64 403-434
-
(1995)
Annu. Rev. Biochem
, vol.64
, pp. 403-434
-
-
Prockop, D.J.1
Kivirikko, K.I.2
-
58
-
-
1942501149
-
Osteogenesis imperfecta
-
Rauch F. and Glorieux F. H. (2004). Osteogenesis imperfecta. Lancet 363 1377-1385
-
(2004)
Lancet
, vol.363
, pp. 1377-1385
-
-
Rauch, F.1
Glorieux, F.H.2
-
59
-
-
41849117310
-
Resolution of liver cirrhosis using vitamin A-coupled liposomes to deliver siRNA against a collagenspecific chaperone
-
Sato Y. Murase K. Kato J. Kobune M. Sato T. Kawano Y. Takimoto R. Takada K. Miyanishi K. Matsunaga T. et al. (2008). Resolution of liver cirrhosis using vitamin A-coupled liposomes to deliver siRNA against a collagenspecific chaperone. Nat. Biotechnol. 26 431-442.
-
(2008)
Nat. Biotechnol
, vol.26
, pp. 431-442
-
-
Sato, Y.1
Murase, K.2
Kato, J.3
Kobune, M.4
Sato, T.5
Kawano, Y.6
Takimoto, R.7
Takada, K.8
Miyanishi, K.9
Matsunaga, T.10
-
60
-
-
0029968576
-
Intracellular interaction of collagen-specific stress protein HSP47 with newly synthesized procollagen
-
Satoh M. Hirayoshi K. Yokota S. Hosokawa N. and Nagata K. (1996). Intracellular interaction of collagen-specific stress protein HSP47 with newly synthesized procollagen. J. Cell Biol. 133 469-483.
-
(1996)
J. Cell Biol
, vol.133
, pp. 469-483
-
-
Satoh, M.1
Hirayoshi, K.2
Yokota, S.3
Hosokawa, N.4
Nagata, K.5
-
61
-
-
0028943780
-
A constitutively active mutant PTHPTHrP receptor in Jansen-type metaphyseal chondrodysplasia
-
Schipani E. Kruse K. and Juppner H. (1995). A constitutively active mutant PTHPTHrP receptor in Jansen-type metaphyseal chondrodysplasia. Science 268 98-100.
-
(1995)
Science
, vol.268
, pp. 98-100
-
-
Schipani, E.1
Kruse, K.2
Juppner, H.3
-
62
-
-
0027964261
-
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism achondroplasia
-
Shiang R. Thompson L. M. Zhu Y. Z. Church D. M. Fielder T. J. Bocian M. Winokur S. T. and Wasmuth J. J. (1994). Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism achondroplasia. Cell 78 335-342.
-
(1994)
Cell
, vol.78
, pp. 335-342
-
-
Shiang, R.1
Thompson, L.M.2
Zhu, Y.Z.3
Church, D.M.4
Fielder, T.J.5
Bocian, M.6
Winokur, S.T.7
Wasmuth, J.J.8
-
63
-
-
41049109533
-
Chondromodulin-I and tenomodulin are differentially expressed in the avascular mesenchyme during mouse and chick development
-
Shukunami C. Takimoto A. Miura S. Nishizaki Y. and Hiraki Y. (2008) Chondromodulin-I and tenomodulin are differentially expressed in the avascular mesenchyme during mouse and chick development. Cell Tissue Res. 332 111-122.
-
(2008)
Cell Tissue Res
, vol.332
, pp. 111-122
-
-
Shukunami, C.1
Takimoto, A.2
Miura, S.3
Nishizaki, Y.4
Hiraki, Y.5
-
64
-
-
0024221225
-
Bone dysplasia 'families'. Pathol
-
Spranger J. (1988) Bone dysplasia 'families'. Pathol. Immunopathol. Res. 7 76-80.
-
(1988)
Immunopathol. Res
, vol.7
, pp. 76-80
-
-
Spranger, J.1
-
65
-
-
0028157152
-
The type II collagenopathies: a spectrum of chondrodysplasias
-
Spranger J. Winterpacht A. and Zabel B. (1994). The type II collagenopathies: a spectrum of chondrodysplasias. Eur. J. Pediatr. 153 56-65.
-
(1994)
Eur. J. Pediatr
, vol.153
, pp. 56-65
-
-
Spranger, J.1
Winterpacht, A.2
Zabel, B.3
-
66
-
-
19944426775
-
Altered endochondral bone development in matrix metalloproteinase 13-deficient mice
-
Stickens D. Behonick D. J. Ortega N. Heyer B. Hartenstein B. Yu Y. Fosang A. J. Schorpp-Kistner M. Angel P. and Werb Z. (2004). Altered endochondral bone development in matrix metalloproteinase 13-deficient mice. Development 131 5883-5895.
-
(2004)
Development
, vol.131
, pp. 5883-5895
-
-
Stickens, D.1
Behonick, D.J.2
Ortega, N.3
Heyer, B.4
Hartenstein, B.5
Yu, Y.6
Fosang, A.J.7
Schorpp-Kistner, M.8
Angel, P.9
Werb, Z.10
-
67
-
-
33845442361
-
Second harmonic generation confocal microscopy of collagen type I from rat tendon cryosections
-
Theodossiou T. A. Thrasivoulou C. Ekwobi C. and Becker D. L. (2006). Second harmonic generation confocal microscopy of collagen type I from rat tendon cryosections. Biophys. J. 91 4665-4677.
-
(2006)
Biophys. J
, vol.91
, pp. 4665-4677
-
-
Theodossiou, T.A.1
Thrasivoulou, C.2
Ekwobi, C.3
Becker, D.L.4
-
68
-
-
0025792023
-
Collagen family of proteins
-
Van der Rest M. and Garrone R. (1991). Collagen family of proteins. FASEB J. 5 2814-2823.
-
(1991)
FASEB J
, vol.5
, pp. 2814-2823
-
-
Van der Rest, M.1
Garrone, R.2
-
69
-
-
0028815298
-
Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus
-
Vikkula M. Mariman E. C. Lui V. C. Zhidkova N. I. Tiller G. E. Goldring M. B. van Beersum S. E. de Waal Malefijt M. C. van den Hoogen F. H. Ropers H. H. et al. (1995). Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus. Cell 80 431-437.
-
(1995)
Cell
, vol.80
, pp. 431-437
-
-
Vikkula, M.1
Mariman, E.C.2
Lui, V.C.3
Zhidkova, N.I.4
Tiller, G.E.5
Goldring, M.B.6
van Beersum, S.E.7
de Waal Malefijt, M.C.8
van den Hoogen, F.H.9
Ropers, H.H.10
-
70
-
-
2542497037
-
Prolyl 3-hydroxylase 1 enzyme characterization and identification of a novel family of enzymes
-
Vranka J. A. Sakai L. Y. and Bächinger H. P. (2004). Prolyl 3-hydroxylase 1 enzyme characterization and identification of a novel family of enzymes. J. Biol. Chem. 279 23615-23621.
-
(2004)
J. Biol. Chem
, vol.279
, pp. 23615-23621
-
-
Vranka, J.A.1
Sakai, L.Y.2
Bächinger, H.P.3
-
71
-
-
0033591252
-
Intracellular retention of procollagen within the endoplasmic reticulum is mediated by prolyl 4- hydroxylase
-
Walmsley A. R. Batten M. R. Lad U. and Bulleid N. J. (1999). Intracellular retention of procollagen within the endoplasmic reticulum is mediated by prolyl 4- hydroxylase. J. Biol. Chem. 274 14884-14892.
-
(1999)
J. Biol. Chem
, vol.274
, pp. 14884-14892
-
-
Walmsley, A.R.1
Batten, M.R.2
Lad, U.3
Bulleid, N.J.4
-
72
-
-
21244479321
-
Interpreting secondharmonic generation images of collagen I fibrils
-
Williams R. M. Zipfel W. R. and Webb W. W. (2005). Interpreting secondharmonic generation images of collagen I fibrils. Biophys. J. 88 1377-1386.
-
(2005)
Biophys. J
, vol.88
, pp. 1377-1386
-
-
Williams, R.M.1
Zipfel, W.R.2
Webb, W.W.3
-
73
-
-
0032540353
-
Protein disulfide isomerase acts as a molecular chaperone during the assembly of procollagen
-
Wilson R. Lees J. F. and Bulleid N. J. (1998). Protein disulfide isomerase acts as a molecular chaperone during the assembly of procollagen. J. Biol. Chem. 273 9637-9643.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 9637-9643
-
-
Wilson, R.1
Lees, J.F.2
Bulleid, N.J.3
-
74
-
-
0023461254
-
Type VI collagen of the intervertebral disc. Biochemical and electron-microscopic characterization of the native protein
-
Wu J. J. Eyre D. R. and Slayter H. S. (1987). Type VI collagen of the intervertebral disc. Biochemical and electron-microscopic characterization of the native protein. Biochem. J. 248 373-381.
-
(1987)
Biochem. J
, vol.248
, pp. 373-381
-
-
Wu, J.J.1
Eyre, D.R.2
Slayter, H.S.3
-
75
-
-
0026451141
-
Identification of cross-linking sites in bovine cartilage type IX collagen reveals an antiparallel type II-type IX molecular relationship and type IX to type IX bonding
-
Wu J. J. Woods P. E. and Eyre D. R. (1992). Identification of cross-linking sites in bovine cartilage type IX collagen reveals an antiparallel type II-type IX molecular relationship and type IX to type IX bonding. J. Biol. Chem. 267 23007-23014.
-
(1992)
J. Biol. Chem
, vol.267
, pp. 23007-23014
-
-
Wu, J.J.1
Woods, P.E.2
Eyre, D.R.3
-
76
-
-
0031574479
-
Synergistic action of transforming growth factor-beta and insulin-like growth factor-I induces expression of type II collagen and aggrecan genes in adult human articular chondrocytes
-
Yaeger P. C. Masi T. L. de Ortiz J. L. Binette F. Tubo R. and McPherson J. M. (1997). Synergistic action of transforming growth factor-beta and insulin-like growth factor-I induces expression of type II collagen and aggrecan genes in adult human articular chondrocytes. Exp. Cell Res. 237 318-325.
-
(1997)
Exp. Cell Res
, vol.237
, pp. 318-325
-
-
Yaeger, P.C.1
Masi, T.L.2
de Ortiz, J.L.3
Binette, F.4
Tubo, R.5
McPherson, J.M.6
|