-
1
-
-
0029006974
-
Collagens: Molecular biology, diseases, and potentials for therapy
-
Kivirikko K.I., Prockop D.J. Collagens: molecular biology, diseases, and potentials for therapy. Annu. Rev. Biochem. 64:1995;403-443.
-
(1995)
Annu. Rev. Biochem.
, vol.64
, pp. 403-443
-
-
Kivirikko, K.I.1
Prockop, D.J.2
-
2
-
-
0029176870
-
Extracellular matrix 1: Fibril-forming collagens
-
Kadler K. Extracellular matrix 1: fibril-forming collagens. Protein Profile. 2:1995;491-619.
-
(1995)
Protein Profile
, vol.2
, pp. 491-619
-
-
Kadler, K.1
-
3
-
-
0035068434
-
Collagens and collagen-related diseases
-
Myllyharju J., Kivirikko K.I. Collagens and collagen-related diseases. Ann. Med. 33:2001;7-21.
-
(2001)
Ann. Med.
, vol.33
, pp. 7-21
-
-
Myllyharju, J.1
Kivirikko, K.I.2
-
4
-
-
0002846317
-
The collagen family: Structure, assembly, and organization in the extracellular matrix
-
P.M. Royce, & B. Steinmann. Wiley-Liss
-
Kielty C.M., Grant M.E. The collagen family: structure, assembly, and organization in the extracellular matrix. Royce P.M., Steinmann B. Connective Tissue and Its Heritable Disorders. Molecular, Genetic, and Medical Aspects. 2nd edn :2002;159-221 Wiley-Liss.
-
(2002)
Connective Tissue and Its Heritable Disorders. Molecular, Genetic, and Medical Aspects 2nd Edn
, pp. 159-221
-
-
Kielty, C.M.1
Grant, M.E.2
-
5
-
-
0036007873
-
Insights on the conformational stability of collagen
-
Jenkins C.L., Raines R.T. Insights on the conformational stability of collagen. Nat. Prod. Rep. 19:2002;49-59.
-
(2002)
Nat. Prod. Rep.
, vol.19
, pp. 49-59
-
-
Jenkins, C.L.1
Raines, R.T.2
-
6
-
-
0042664095
-
Collagenous transmembrane proteins: Collagen XVII as a prototype
-
Franzke C.F., et al. Collagenous transmembrane proteins: collagen XVII as a prototype. Matrix Biol. 22:2003;299-309.
-
(2003)
Matrix Biol.
, vol.22
, pp. 299-309
-
-
Franzke, C.F.1
-
7
-
-
0035933862
-
α1(XX) collagen, a new member of the collagen subfamily, fibril-associated collagens with interrupted triple helices
-
Koch M., et al. α1(XX) collagen, a new member of the collagen subfamily, fibril-associated collagens with interrupted triple helices. J. Biol. Chem. 276:2001;23120-23126.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 23120-23126
-
-
Koch, M.1
-
8
-
-
0035860389
-
A new FACIT of the collagen family: COL21A1
-
Fitzgerald J., Bateman J.F. A new FACIT of the collagen family: COL21A1. FEBS Lett. 505:2001;275-280.
-
(2001)
FEBS Lett.
, vol.505
, pp. 275-280
-
-
Fitzgerald, J.1
Bateman, J.F.2
-
9
-
-
0038756787
-
Type XXIII collagen, a new transmembrane collagen identified in metastatic tumor cells
-
Banyard J., et al. Type XXIII collagen, a new transmembrane collagen identified in metastatic tumor cells. J. Biol. Chem. 278:2003;20989-20994.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 20989-20994
-
-
Banyard, J.1
-
10
-
-
0242290312
-
Collagen XXIV, a vertebrate fibrillar collagen with structural features of invertebrate collagens: Selective expression in developing cornea and bone
-
Koch M., et al. Collagen XXIV, a vertebrate fibrillar collagen with structural features of invertebrate collagens: selective expression in developing cornea and bone. J. Biol. Chem. 278:2003;43236-43244.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 43236-43244
-
-
Koch, M.1
-
11
-
-
18444418272
-
CLAC: A novel Alzheimer amyloid plaque component derived from a transmembrane precursor, CLAC-P/collagen type XXV
-
Hashimoto T., et al. CLAC: a novel Alzheimer amyloid plaque component derived from a transmembrane precursor, CLAC-P/collagen type XXV. EMBO J. 21:2002;1524-1534.
-
(2002)
EMBO J.
, vol.21
, pp. 1524-1534
-
-
Hashimoto, T.1
-
12
-
-
0037020171
-
Type XXVI collagen, a new member of the collagen family, is specifically expressed in the testis and ovary
-
Sato K., et al. Type XXVI collagen, a new member of the collagen family, is specifically expressed in the testis and ovary. J. Biol. Chem. 277:2002;37678-37684.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 37678-37684
-
-
Sato, K.1
-
13
-
-
0344088437
-
Identification, characterization and expression analysis of a new fibrillar collagen gene, COL27A1
-
Pace J.M., et al. Identification, characterization and expression analysis of a new fibrillar collagen gene, COL27A1. Matrix Biol. 22:2003;3-14.
-
(2003)
Matrix Biol.
, vol.22
, pp. 3-14
-
-
Pace, J.M.1
-
14
-
-
0041731789
-
A novel and highly conserved collagen [proα1(XXVII)] with a unique expression pattern and unusual molecular characteristics establishes a new clade within the vertebrate fibrillar collagen family
-
Boot-Handford R.P., et al. A novel and highly conserved collagen [proα1(XXVII)] with a unique expression pattern and unusual molecular characteristics establishes a new clade within the vertebrate fibrillar collagen family. J. Biol. Chem. 278:2003;31067-31077.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 31067-31077
-
-
Boot-Handford, R.P.1
-
15
-
-
0041534400
-
Collectins and ficolins: Humoral lectins of the innate immune defense
-
Holmskov U., et al. Collectins and ficolins: humoral lectins of the innate immune defense. Annu. Rev. Immunol. 21:2003;547-578.
-
(2003)
Annu. Rev. Immunol.
, vol.21
, pp. 547-578
-
-
Holmskov, U.1
-
16
-
-
0035958849
-
The NC1 domain of collagen IV encodes a novel network composed of the α1, α2, α5, and α6 chains in smooth muscle basement membranes
-
Borza D.-B., et al. The NC1 domain of collagen IV encodes a novel network composed of the α1, α2, α5, and α6 chains in smooth muscle basement membranes. J. Biol. Chem. 276:2001;28532-28540.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 28532-28540
-
-
Borza, D.-B.1
-
17
-
-
0034848340
-
The role of collagen-derived proteolytic fragments in angiogenesis
-
Marneros A.G., Olsen B.R. The role of collagen-derived proteolytic fragments in angiogenesis. Matrix Biol. 20:2001;337-345.
-
(2001)
Matrix Biol.
, vol.20
, pp. 337-345
-
-
Marneros, A.G.1
Olsen, B.R.2
-
18
-
-
0031616949
-
Collagen hydroxylases and the protein disulfide isomerase subunit of prolyl 4-hydroxylases
-
Kivirikko K.I., Pihlajaniemi T. Collagen hydroxylases and the protein disulfide isomerase subunit of prolyl 4-hydroxylases. Adv. Enzymol. Relat. Areas Mol. Biol. 72:1998;325-398.
-
(1998)
Adv. Enzymol. Relat. Areas Mol. Biol.
, vol.72
, pp. 325-398
-
-
Kivirikko, K.I.1
Pihlajaniemi, T.2
-
19
-
-
0037358282
-
Prolyl 4-hydroxylases, the key enzymes of collagen biosynthesis
-
Myllyharju J. Prolyl 4-hydroxylases, the key enzymes of collagen biosynthesis. Matrix Biol. 22:2003;15-24.
-
(2003)
Matrix Biol.
, vol.22
, pp. 15-24
-
-
Myllyharju, J.1
-
20
-
-
0031940912
-
Two unusual metalloproteinases that are essential for procollagen processing probably have important roles in development and cell signaling
-
Prockop D.J., et al. Two unusual metalloproteinases that are essential for procollagen processing probably have important roles in development and cell signaling. Matrix Biol. 16:1998;399-408.
-
(1998)
Matrix Biol.
, vol.16
, pp. 399-408
-
-
Prockop, D.J.1
-
21
-
-
0037371153
-
Lysyl oxidase: Properties, specificity, and biological roles inside and outside of the cell
-
Kagan H.M., Li W. Lysyl oxidase: properties, specificity, and biological roles inside and outside of the cell. J. Cell. Biochem. 88:2003;660-672.
-
(2003)
J. Cell. Biochem.
, vol.88
, pp. 660-672
-
-
Kagan, H.M.1
Li, W.2
-
22
-
-
0034649591
-
Protein-specific chaperones: The role of hsp47 begins to gel
-
Hendershot L.M., Bulleid N.J. Protein-specific chaperones: the role of hsp47 begins to gel. Curr. Biol. 10:2000;R912-R915.
-
(2000)
Curr. Biol.
, vol.10
-
-
Hendershot, L.M.1
Bulleid, N.J.2
-
23
-
-
0034683570
-
Embryonic lethality of molecular chaperone hsp47 knockout mice is associated with defects in collagen biosynthesis
-
Nagai N., et al. Embryonic lethality of molecular chaperone hsp47 knockout mice is associated with defects in collagen biosynthesis. J. Cell Biol. 150:2000;1499-1506.
-
(2000)
J. Cell Biol.
, vol.150
, pp. 1499-1506
-
-
Nagai, N.1
-
24
-
-
0043075892
-
Cloning of a novel prolyl 4-hydroxylase subunit expressed in the fibrous cap of human atherosclerotic plaque
-
Van Den Diepstraten C., et al. Cloning of a novel prolyl 4-hydroxylase subunit expressed in the fibrous cap of human atherosclerotic plaque. Circulation. 108:2003;508-511.
-
(2003)
Circulation
, vol.108
, pp. 508-511
-
-
Van Den Diepstraten, C.1
-
25
-
-
85030932482
-
Identification and characterization of a third human, rat and mouse collagen prolyl 4-hydroxylase isoenzyme
-
in press
-
Kukkola, L. et al. Identification and characterization of a third human, rat and mouse collagen prolyl 4-hydroxylase isoenzyme. J. Biol. Chem. (in press).
-
J. Biol. Chem.
-
-
Kukkola, L.1
-
26
-
-
17944375360
-
C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation
-
Epstein A.C.R., et al. C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation. Cell. 107:2001;43-54.
-
(2001)
Cell
, vol.107
, pp. 43-54
-
-
Epstein, A.C.R.1
-
27
-
-
0035834409
-
A conserved family of prolyl 4-hydroxylases that modify HIF
-
Bruick R.K., McKnight S.L. A conserved family of prolyl 4-hydroxylases that modify HIF. Science. 294:2001;1337-1340.
-
(2001)
Science
, vol.294
, pp. 1337-1340
-
-
Bruick, R.K.1
McKnight, S.L.2
-
28
-
-
0037108807
-
Biochemical purification and pharmacological inhibition of a mammalian prolyl hydroxylase acting on hypoxia-inducible factor
-
Ivan M., et al. Biochemical purification and pharmacological inhibition of a mammalian prolyl hydroxylase acting on hypoxia-inducible factor. Proc. Natl. Acad. Sci. U. S. A. 99:2002;13459-13464.
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, pp. 13459-13464
-
-
Ivan, M.1
-
29
-
-
0043234538
-
Characterization of the human prolyl 4-hydroxylases that modify the hypoxia-inducible factor HIF
-
Hirsilä M., et al. Characterization of the human prolyl 4-hydroxylases that modify the hypoxia-inducible factor HIF. J. Biol. Chem. 278:2003;30772-30780.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 30772-30780
-
-
Hirsilä, M.1
-
30
-
-
0032168062
-
Cloning and characterization of a third human lysyl hydroxylase isoform
-
Passoja K., et al. Cloning and characterization of a third human lysyl hydroxylase isoform. Proc. Natl. Acad. Sci. U. S. A. 95:1998;10482-10486.
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, pp. 10482-10486
-
-
Passoja, K.1
-
31
-
-
0032557436
-
Primary structure, tissue distribution, and chromosomal localization of a novel isoform of lysyl hydroxylase (lysyl hydroxylase 3)
-
Valtavaara M., et al. Primary structure, tissue distribution, and chromosomal localization of a novel isoform of lysyl hydroxylase (lysyl hydroxylase 3). J. Biol. Chem. 273:1998;12881-12886.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 12881-12886
-
-
Valtavaara, M.1
-
32
-
-
0034751557
-
Cloning and characterization of a fifth human lysyl oxidase isoenzyme: The third member of the lysyl oxidase-related subfamily with four scavenger receptor cysteine-rich domains
-
Mäki J.M., et al. Cloning and characterization of a fifth human lysyl oxidase isoenzyme: the third member of the lysyl oxidase-related subfamily with four scavenger receptor cysteine-rich domains. Matrix Biol. 20:2001;493-496.
-
(2001)
Matrix Biol.
, vol.20
, pp. 493-496
-
-
Mäki, J.M.1
-
33
-
-
0035968314
-
Molecular cloning and biological activity of a novel lysyl oxidase-related gene expressed in cartilage
-
Ito H., et al. Molecular cloning and biological activity of a novel lysyl oxidase-related gene expressed in cartilage. J. Biol. Chem. 276:2001;24023-24029.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 24023-24029
-
-
Ito, H.1
-
34
-
-
0038043187
-
Paired basic/furin-like proprotein convertase cleavage of pro-BMP-1 in the trans-Golgi network
-
Leighton M., Kadler K.E. Paired basic/furin-like proprotein convertase cleavage of pro-BMP-1 in the trans-Golgi network. J. Biol. Chem. 278:2003;18478-18484.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 18478-18484
-
-
Leighton, M.1
Kadler, K.E.2
-
35
-
-
0037155146
-
Cloning and characterization of ADAMTS-14, a novel ADAMTS displaying high homology with ADAMTS-2 and ADAMTS-3
-
Colige A., et al. Cloning and characterization of ADAMTS-14, a novel ADAMTS displaying high homology with ADAMTS-2 and ADAMTS-3. J. Biol. Chem. 277:2002;5756-5766.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 5756-5766
-
-
Colige, A.1
-
36
-
-
0037166347
-
Identification of amino acids important for the catalytic activity of the collagen glucosyltransferase associated with the multifunctional lysyl hydroxylase 3 (LH3)
-
Wang C., et al. Identification of amino acids important for the catalytic activity of the collagen glucosyltransferase associated with the multifunctional lysyl hydroxylase 3 (LH3). J. Biol. Chem. 277:2002;18568-18573.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 18568-18573
-
-
Wang, C.1
-
37
-
-
0037151077
-
Characterization of three fragments that constitute the monomers of the human lysyl hydroxylase isoenzymes 1-3. The 30-kDa N-terminal fragment is not required for lysyl hydroxylase activity
-
Rautavuoma K., et al. Characterization of three fragments that constitute the monomers of the human lysyl hydroxylase isoenzymes 1-3. The 30-kDa N-terminal fragment is not required for lysyl hydroxylase activity. J. Biol. Chem. 277:2002;23084-23091.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 23084-23091
-
-
Rautavuoma, K.1
-
38
-
-
0030789557
-
The human type I collagen mutation database
-
Dalgleish R. The human type I collagen mutation database. Nucleic Acids Res. 25:1997;181-187.
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 181-187
-
-
Dalgleish, R.1
-
39
-
-
0031092272
-
The human gene mutation database
-
Krawczak M., Cooper D.N. The human gene mutation database. Trends Genet. 13:1997;121-122.
-
(1997)
Trends Genet.
, vol.13
, pp. 121-122
-
-
Krawczak, M.1
Cooper, D.N.2
-
40
-
-
0043258821
-
Osteogenesis imperfecta
-
P.M. Royce, & B. Steinmann. Wiley-Liss
-
Byers P.H., Cole W.G. Osteogenesis imperfecta. Royce P.M., Steinmann B. Connective Tissue and Its Heritable Disorders. Molecular, Genetic, and Medical Aspects. 2nd edn :2002;385-430 Wiley-Liss.
-
(2002)
Connective Tissue and Its Heritable Disorders. Molecular, Genetic, and Medical Aspects 2nd Edn
, pp. 385-430
-
-
Byers, P.H.1
Cole, W.G.2
-
42
-
-
9644298890
-
Chondrodysplasias: Disorders of cartilage matrix proteins
-
P.M. Royce, & B. Steinmann. Wiley-Liss
-
Horton W.A., Hecht J.T. Chondrodysplasias: disorders of cartilage matrix proteins. Royce P.M., Steinmann B. Connective Tissue and Its Heritable Disorders. Molecular, Genetic, and Medical Aspects. 2nd edn :2002;909-937 Wiley-Liss.
-
(2002)
Connective Tissue and Its Heritable Disorders. Molecular, Genetic, and Medical Aspects 2nd Edn
, pp. 909-937
-
-
Horton, W.A.1
Hecht, J.T.2
-
43
-
-
0347395990
-
Alport syndrome
-
P.M. Royce, & B. Steinmann. Wiley-Liss
-
Tryggvason K., Martin P. Alport syndrome. Royce P.M., Steinmann B. Connective Tissue and Its Heritable Disorders. Molecular, Genetic, and Medical Aspects. 2nd edn :2002;1069-1102 Wiley-Liss.
-
(2002)
Connective Tissue and Its Heritable Disorders. Molecular, Genetic, and Medical Aspects 2nd Edn
, pp. 1069-1102
-
-
Tryggvason, K.1
Martin, P.2
-
45
-
-
0041664084
-
New molecular mechanism for Ullrich congenital muscular dystrophy: A heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
-
Pan T.C., et al. New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype. Am. J. Hum. Genet. 73:2003;355-369.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 355-369
-
-
Pan, T.C.1
-
46
-
-
0035504694
-
Missense mutations in COL8A2, the gene encoding the α2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy
-
Biswas S., et al. Missense mutations in COL8A2, the gene encoding the α2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy. Hum. Mol. Genet. 10:2001;2415-2423.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2415-2423
-
-
Biswas, S.1
-
47
-
-
0036913635
-
Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome
-
Suzuki O.T., et al. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. Am. J. Hum. Genet. 71:2002;1320-1329.
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 1320-1329
-
-
Suzuki, O.T.1
-
48
-
-
0032913989
-
Sequence dependent conformational variations of collagen triple-helical structure
-
Kramer R.Z., et al. Sequence dependent conformational variations of collagen triple-helical structure. Nat. Struct. Biol. 6:1999;454-457.
-
(1999)
Nat. Struct. Biol.
, vol.6
, pp. 454-457
-
-
Kramer, R.Z.1
-
49
-
-
0033575339
-
An allele of COL9A2 associated with intervertebral disc disease
-
Annunen S., et al. An allele of COL9A2 associated with intervertebral disc disease. Science. 285:1999;409-412.
-
(1999)
Science
, vol.285
, pp. 409-412
-
-
Annunen, S.1
-
50
-
-
0035843638
-
Identification of a novel common genetic risk factor for lumbar disk disease
-
Paassilta P., et al. Identification of a novel common genetic risk factor for lumbar disk disease. J.A.M.A. 285:2001;1843-1849.
-
(2001)
J.A.M.A.
, vol.285
, pp. 1843-1849
-
-
Paassilta, P.1
-
51
-
-
0034715896
-
Insights into extracellular matrix functions from mutant mouse models
-
Gustafsson E., Fässler R. Insights into extracellular matrix functions from mutant mouse models. Exp. Cell Res. 261:2000;52-68.
-
(2000)
Exp. Cell Res.
, vol.261
, pp. 52-68
-
-
Gustafsson, E.1
Fässler, R.2
-
52
-
-
0034443786
-
Collagen XII mutation disrupts matrix structure of periodontal ligament and skin
-
Reichenberger E., et al. Collagen XII mutation disrupts matrix structure of periodontal ligament and skin. J. Dent. Res. 79:2000;1962-1968.
-
(2000)
J. Dent. Res.
, vol.79
, pp. 1962-1968
-
-
Reichenberger, E.1
-
53
-
-
0035903442
-
Abnormal adherence junctions in the heart and reduced angiogenesis in transgenic mice overexpressing mutant type XIII collagen
-
Sund M., et al. Abnormal adherence junctions in the heart and reduced angiogenesis in transgenic mice overexpressing mutant type XIII collagen. EMBO J. 20:2001;5153-5164.
-
(2001)
EMBO J.
, vol.20
, pp. 5153-5164
-
-
Sund, M.1
-
54
-
-
0034785475
-
Lack of cytosolic and transmembrane domains of type XIII collagen results in progressive myopathy
-
Kvist A.-P., et al. Lack of cytosolic and transmembrane domains of type XIII collagen results in progressive myopathy. Am. J. Pathol. 159:2001;1581-1592.
-
(2001)
Am. J. Pathol.
, vol.159
, pp. 1581-1592
-
-
Kvist, A.-P.1
-
55
-
-
0035970075
-
Lack of type XV collagen causes a skeletal myopathy and cardiovascular defects in mice
-
Eklund L., et al. Lack of type XV collagen causes a skeletal myopathy and cardiovascular defects in mice. Proc. Natl. Acad. Sci. U. S. A. 98:2001;1194-1199.
-
(2001)
Proc. Natl. Acad. Sci. U. S. A.
, vol.98
, pp. 1194-1199
-
-
Eklund, L.1
-
56
-
-
18444389460
-
Lack of collagen XVIII/endostatin results in eye abnormalities
-
Fukai N., et al. Lack of collagen XVIII/endostatin results in eye abnormalities. EMBO J. 21:2002;1535-1544.
-
(2002)
EMBO J.
, vol.21
, pp. 1535-1544
-
-
Fukai, N.1
-
57
-
-
17044454221
-
Identification of PLOD2 as telopeptide lysyl hydroxylase, an important enzyme in fibrosis
-
Van der Slot A.J., et al. Identification of PLOD2 as telopeptide lysyl hydroxylase, an important enzyme in fibrosis. J. Biol. Chem. 278:2003;40967-40972.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 40967-40972
-
-
Van Der Slot, A.J.1
-
58
-
-
0035870995
-
Transgenic mice with inactive alleles for procollagen N-proteinase (ADAMTS-2) develop fragile skin and male sterility
-
Li S.-W., et al. Transgenic mice with inactive alleles for procollagen N-proteinase (ADAMTS-2) develop fragile skin and male sterility. Biochem. J. 355:2001;271-278.
-
(2001)
Biochem. J.
, vol.355
, pp. 271-278
-
-
Li, S.-W.1
-
59
-
-
0032805098
-
The mammalian Tolloid-like 1 gene, Tll1, is necessary for normal septation and positioning of the heart
-
Clark T.G., et al. The mammalian Tolloid-like 1 gene, Tll1, is necessary for normal septation and positioning of the heart. Development. 126:1999;2631-2642.
-
(1999)
Development
, vol.126
, pp. 2631-2642
-
-
Clark, T.G.1
-
60
-
-
0037027504
-
Inactivation of the lysyl oxidase gene Lox leads to aortic aneurysms, cardiovascular dysfunction, and perinatal death in mice
-
Mäki J.M., et al. Inactivation of the lysyl oxidase gene Lox leads to aortic aneurysms, cardiovascular dysfunction, and perinatal death in mice. Circulation. 106:2002;2503-2509.
-
(2002)
Circulation
, vol.106
, pp. 2503-2509
-
-
Mäki, J.M.1
-
61
-
-
0038529805
-
Lysyl oxidase is required for vascular and diaphragmatic development in mice
-
Hornstra I.K., et al. Lysyl oxidase is required for vascular and diaphragmatic development in mice. J. Biol. Chem. 278:2003;14387-14393.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 14387-14393
-
-
Hornstra, I.K.1
-
62
-
-
0034710157
-
The evolution of cell adhesion
-
Hynes R.O., Zhao Q. The evolution of cell adhesion. J. Cell Biol. 150:2000;F89-F95.
-
(2000)
J. Cell Biol.
, vol.150
-
-
Hynes, R.O.1
Zhao, Q.2
-
63
-
-
0036337733
-
Pericardin, a Drosophila type IV collagen-like protein is involved in the morphogenesis and maintenance of the heart epithelium during dorsal ectoderm closure
-
Chartier A., et al. Pericardin, a Drosophila type IV collagen-like protein is involved in the morphogenesis and maintenance of the heart epithelium during dorsal ectoderm closure. Development. 129:2002;3241-3253.
-
(2002)
Development
, vol.129
, pp. 3241-3253
-
-
Chartier, A.1
-
64
-
-
0036180819
-
Prolyl 4-hydroxylase α-related proteins in Drosophila melanogaster: Tissue-specific embryonic expression of the 99F8-9 cluster
-
Abrams E.W., Andrew D.J. Prolyl 4-hydroxylase α-related proteins in Drosophila melanogaster: tissue-specific embryonic expression of the 99F8-9 cluster. Mech. Dev. 112:2002;165-171.
-
(2002)
Mech. Dev.
, vol.112
, pp. 165-171
-
-
Abrams, E.W.1
Andrew, D.J.2
-
65
-
-
0033525689
-
Cloning of the α subunit of prolyl 4-hydroxylase from Drosophila and expression and characterization of the corresponding enzyme tetramer with some unique properties
-
Annunen P., et al. Cloning of the α subunit of prolyl 4-hydroxylase from Drosophila and expression and characterization of the corresponding enzyme tetramer with some unique properties. J. Biol. Chem. 274:1999;6790-6796.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 6790-6796
-
-
Annunen, P.1
-
66
-
-
0001531616
-
Extracellular matrix
-
D.L. et al. Riddle. Cold Spring Harbor Laboratory Press
-
Kramer J.M. Extracellular matrix. Riddle D.L., et al. C. elegans II. 1997;471-500 Cold Spring Harbor Laboratory Press.
-
(1997)
C. Elegans II
, pp. 471-500
-
-
Kramer, J.M.1
-
67
-
-
0033621541
-
Cuticle collagen genes. Expression in Caenorhabditis elegans
-
Johnstone I.L. Cuticle collagen genes. Expression in Caenorhabditis elegans. Trends Genet. 16:2000;21-27.
-
(2000)
Trends Genet.
, vol.16
, pp. 21-27
-
-
Johnstone, I.L.1
-
68
-
-
0002237158
-
The nematode cuticle: Synthesis, modification and mutants
-
M.W. Kennedy, & W. Harnett. CABI Press
-
Page A.P. The nematode cuticle: synthesis, modification and mutants. Kennedy M.W., Harnett W. Parasitic Nematodes. 2001;167-193 CABI Press.
-
(2001)
Parasitic Nematodes
, pp. 167-193
-
-
Page, A.P.1
-
69
-
-
0037373288
-
Caenorhabditis elegans exoskeleton collagen COL-19: An adult-specific marker for collagen modification and assembly, and the analysis of organismal morphology
-
Thein M.C., et al. Caenorhabditis elegans exoskeleton collagen COL-19: an adult-specific marker for collagen modification and assembly, and the analysis of organismal morphology. Dev. Dyn. 226:2003;523-539.
-
(2003)
Dev. Dyn.
, vol.226
, pp. 523-539
-
-
Thein, M.C.1
-
70
-
-
0013459508
-
Two sets of interacting collagens form functionally distinct substructures within a Caenorhabditis elegans extracellular matrix
-
McMahon L., et al. Two sets of interacting collagens form functionally distinct substructures within a Caenorhabditis elegans extracellular matrix. Mol. Biol. Cell. 14:2003;1366-1378.
-
(2003)
Mol. Biol. Cell
, vol.14
, pp. 1366-1378
-
-
McMahon, L.1
-
71
-
-
0035911968
-
The NC1/endostatin domain of Caenorhabditis elegans type XVIII collagen affects cell migration and axon guidance
-
Ackley B.D., et al. The NC1/endostatin domain of Caenorhabditis elegans type XVIII collagen affects cell migration and axon guidance. J. Cell Biol. 152:2001;1219-1232.
-
(2001)
J. Cell Biol.
, vol.152
, pp. 1219-1232
-
-
Ackley, B.D.1
-
72
-
-
0034712971
-
Prolyl 4-hydroxylase is required for viability and morphogenesis in Caenorhabditis elegans
-
Friedman L., et al. Prolyl 4-hydroxylase is required for viability and morphogenesis in Caenorhabditis elegans. Proc. Natl. Acad. Sci. U. S. A. 97:2000;4736-4741.
-
(2000)
Proc. Natl. Acad. Sci. U. S. A.
, vol.97
, pp. 4736-4741
-
-
Friedman, L.1
-
73
-
-
0033624045
-
Dpy-18 encodes an α-subunit of prolyl 4-hydroxylase in Caenorhabditis elegans
-
Hill K.L., et al. dpy-18 encodes an α-subunit of prolyl 4-hydroxylase in Caenorhabditis elegans. Genetics. 155:2000;1139-1148.
-
(2000)
Genetics
, vol.155
, pp. 1139-1148
-
-
Hill, K.L.1
-
74
-
-
0034111331
-
Prolyl 4-hydroxylase is an essential procollagen-modifying enzyme required for exoskeleton formation and the maintenance of body shape in the nematode Caenorhabditis elegans
-
Winter A.D., Page A.P. Prolyl 4-hydroxylase is an essential procollagen-modifying enzyme required for exoskeleton formation and the maintenance of body shape in the nematode Caenorhabditis elegans. Mol. Cell. Biol. 20:2000;4084-4093.
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 4084-4093
-
-
Winter, A.D.1
Page, A.P.2
-
75
-
-
0037047409
-
The exoskeleton collagens in Caenorhabditis elegans are modified by prolyl 4-hydroxylases with unique combinations of subunits
-
Myllyharju J., et al. The exoskeleton collagens in Caenorhabditis elegans are modified by prolyl 4-hydroxylases with unique combinations of subunits. J. Biol. Chem. 277:2002;29187-29196.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 29187-29196
-
-
Myllyharju, J.1
-
76
-
-
0037124029
-
Egg shell collagen formation in Caenorhabditis elegans involves a novel prolyl 4-hydroxylase expressed in spermatheca and embryos and possessing many unique properties
-
Riihimaa P., et al. Egg shell collagen formation in Caenorhabditis elegans involves a novel prolyl 4-hydroxylase expressed in spermatheca and embryos and possessing many unique properties. J. Biol. Chem. 277:2002;18238-18243.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 18238-18243
-
-
Riihimaa, P.1
-
77
-
-
0034669227
-
The let-268 locus of Caenorhabditis elegans encodes a procollagen lysyl hydroxylase that is essential for type IV collagen secretion
-
Norman K.R., Moerman D.G. The let-268 locus of Caenorhabditis elegans encodes a procollagen lysyl hydroxylase that is essential for type IV collagen secretion. Dev. Biol. 227:2000;690-705.
-
(2000)
Dev. Biol.
, vol.227
, pp. 690-705
-
-
Norman, K.R.1
Moerman, D.G.2
-
78
-
-
0036336598
-
A novel thioredoxin-like protein encoded by the C. elegans dpy-11 gene is required for body and sensory organ morphogenesis
-
Ko F.C., Chow K.L. A novel thioredoxin-like protein encoded by the C. elegans dpy-11 gene is required for body and sensory organ morphogenesis. Development. 129:2002;1185-1194.
-
(2002)
Development
, vol.129
, pp. 1185-1194
-
-
Ko, F.C.1
Chow, K.L.2
-
79
-
-
0037423294
-
The Caenorhabditis elegans ERp60 homolog protein disulfide isomerase-3 has disulfide isomerase and transglutaminase-like cross-linking activity and is involved in the maintenance of body morphology
-
Eschenlauer C.P., Page A.P. The Caenorhabditis elegans ERp60 homolog protein disulfide isomerase-3 has disulfide isomerase and transglutaminase-like cross-linking activity and is involved in the maintenance of body morphology. J. Biol. Chem. 278:2003;4227-4237.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 4227-4237
-
-
Eschenlauer, C.P.1
Page, A.P.2
-
80
-
-
0035921417
-
Tyrosine cross-linking of extracellular matrix is catalyzed by Duox, a multidomain oxidase/peroxidase with homology to the phagocyte oxidase subunit gp91phox
-
Edens W.A., et al. Tyrosine cross-linking of extracellular matrix is catalyzed by Duox, a multidomain oxidase/peroxidase with homology to the phagocyte oxidase subunit gp91phox. J. Cell Biol. 154:2001;879-891.
-
(2001)
J. Cell Biol.
, vol.154
, pp. 879-891
-
-
Edens, W.A.1
-
81
-
-
0032722059
-
Proteolytic processing of Caenorhabditis elegans SQT-1 cuticle collagen is inhibited in right roller mutants whereas cross-linking is inhibited in left-roller mutants
-
Yang J., Kramer J.M. Proteolytic processing of Caenorhabditis elegans SQT-1 cuticle collagen is inhibited in right roller mutants whereas cross-linking is inhibited in left-roller mutants. J. Biol. Chem. 274:1999;32744-32749.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 32744-32749
-
-
Yang, J.1
Kramer, J.M.2
-
82
-
-
0030612084
-
Characterization of α1(IV) collagen mutations in Caenorhabditis elegans and the effects of α1 and α2(IV) mutations on type IV collagen distribution
-
Gupta M.C., et al. Characterization of α1(IV) collagen mutations in Caenorhabditis elegans and the effects of α1 and α2(IV) mutations on type IV collagen distribution. J. Cell Biol. 137:1997;1185-1196.
-
(1997)
J. Cell Biol.
, vol.137
, pp. 1185-1196
-
-
Gupta, M.C.1
-
83
-
-
0038545348
-
The basement membrane components nidogen and type XVIII collagen regulate organization of neuromuscular junctions in Caenorhabditis elegans
-
Ackley B.D., et al. The basement membrane components nidogen and type XVIII collagen regulate organization of neuromuscular junctions in Caenorhabditis elegans. J. Neurosci. 23:2003;3577-3587.
-
(2003)
J. Neurosci.
, vol.23
, pp. 3577-3587
-
-
Ackley, B.D.1
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