-
1
-
-
84862266982
-
The Ehlers-Danlos syndrome, a disorder with many faces
-
De Paepe, A., and Malfait, F. (2012) The Ehlers-Danlos syndrome, a disorder with many faces. Clin. Genet. 82, 1-11
-
(2012)
Clin. Genet.
, vol.82
, pp. 1-11
-
-
De Paepe, A.1
Malfait, F.2
-
3
-
-
0015502702
-
A heritable disorder of connective tissue. Hydroxylysine-deficient collagen disease
-
Pinnell, S. R., Krane, S. M., Kenzora, J. E., and Glimcher, M. J. (1972) A heritable disorder of connective tissue. Hydroxylysine-deficient collagen disease. N. Engl. J. Med. 286, 1013-1020
-
(1972)
N. Engl. J. Med.
, vol.286
, pp. 1013-1020
-
-
Pinnell, S.R.1
Krane, S.M.2
Kenzora, J.E.3
Glimcher, M.J.4
-
4
-
-
4644297498
-
Novel types of mutation responsible for the dermatosparactic type of Ehlers-Danlos syndrome (type VIIC) and common polymorphisms in the ADAMTS2 gene
-
DOI 10.1111/j.0022-202X.2004.23406.x
-
Colige, A., Nuytinck, L., Hausser, I., van Essen, A. J., Thiry, M., Herens, C., Adès, L. C., Malfait, F., Paepe, A. D., Franck, P., Wolff, G., Oosterwijk, J. C., Smitt, J. H., Lapière, C. M., and Nusgens, B. V. (2004) Novel types of mutation responsible for the dermatosparactic type of Ehlers-Danlos syndrome (type VIIC) and common polymorphisms in the ADAMTS2 gene. J. Invest. Dermatol. 123, 656-663 (Pubitemid 39281605)
-
(2004)
Journal of Investigative Dermatology
, vol.123
, Issue.4
, pp. 656-663
-
-
Colige, A.1
Nuytinck, L.2
Hausser, I.3
Van Essen, A.J.4
Thiry, M.5
Herens, C.6
Ades, L.C.7
Malfait, F.8
De Paepe, A.9
Franck, P.10
Wolff, G.11
Oosterwijk, J.C.12
Smitt, J.H.S.13
Lapiere, C.M.14
Nusgens, B.V.15
-
5
-
-
84862780507
-
Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss
-
Baumann, M., Giunta, C., Krabichler, B., Rüschendorf, F., Zoppi, N., Colombi, M., Bittner, R. E., Quijano-Roy, S., Muntoni, F., Cirak, S., Schreiber, G., Zou, Y., Hu, Y., Romero, N. B., Carlier, R. Y., Amberger, A., Deutschmann, A., Straub, V., Rohrbach, M., Steinmann, B., Rostásy, K., Karall, D., Bönnemann, C. G., Zschocke, J., and Fauth, C. (2012) Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss. Am. J. Hum. Genet. 90, 201-216
-
(2012)
Am. J. Hum. Genet.
, vol.90
, pp. 201-216
-
-
Baumann, M.1
Giunta, C.2
Krabichler, B.3
Rüschendorf, F.4
Zoppi, N.5
Colombi, M.6
Bittner, R.E.7
Quijano-Roy, S.8
Muntoni, F.9
Cirak, S.10
Schreiber, G.11
Zou, Y.12
Hu, Y.13
Romero, N.B.14
Carlier, R.Y.15
Amberger, A.16
Deutschmann, A.17
Straub, V.18
Rohrbach, M.19
Steinmann, B.20
Rostásy, K.21
Karall, D.22
Bönnemann, C.G.23
Zschocke, J.24
Fauth, C.25
more..
-
6
-
-
0030843025
-
Tenascin-X deficiency is associated with Ehlers-Danlos syndrome
-
DOI 10.1038/ng0997-104
-
Burch, G. H., Gong, Y., Liu, W., Dettman, R. W., Curry, C. J., Smith, L., Miller, W. L., and Bristow, J. (1997) Tenascin-X deficiency is associated with Ehlers-Danlos syndrome. Nat. Genet. 17, 104-108 (Pubitemid 27377542)
-
(1997)
Nature Genetics
, vol.17
, Issue.1
, pp. 104-108
-
-
Burch, G.H.1
Gong, Y.2
Liu, W.3
Dettman, R.W.4
Curry, C.J.5
Smith, L.6
Miller, W.L.7
Bristow, J.8
-
7
-
-
53049110420
-
Aconnective tissue disorder caused by mutations of the lysyl hydroxylase 3 gene
-
Salo, A. M., Cox, H., Farndon, P., Moss, C., Grindulis, H., Risteli, M., Robins, S. P., and Myllylä, R. (2008)Aconnective tissue disorder caused by mutations of the lysyl hydroxylase 3 gene. Am. J. Hum. Genet. 83, 495-503
-
(2008)
Am. J. Hum. Genet.
, vol.83
, pp. 495-503
-
-
Salo, A.M.1
Cox, H.2
Farndon, P.3
Moss, C.4
Grindulis, H.5
Risteli, M.6
Robins, S.P.7
Myllylä, R.8
-
8
-
-
0026071008
-
Human bone contains type III collagen, type VI collagen, and fibrillin. Type III collagen is present on specific fibers that may mediate attachment of tendons, ligaments, and periosteum to calcified bone cortex
-
Keene, D. R., Sakai, L. Y., and Burgeson, R. E. (1991) Human bone contains type III collagen, type VI collagen, and fibrillin. Type III collagen is present on specific fibers that may mediate attachment of tendons, ligaments, and periosteum to calcified bone cortex. J. Histochem. Cytochem. 39, 59-69
-
(1991)
J. Histochem. Cytochem.
, vol.39
, pp. 59-69
-
-
Keene, D.R.1
Sakai, L.Y.2
Burgeson, R.E.3
-
9
-
-
77953298117
-
Type III collagen, a fibril network modifier in articular cartilage
-
Wu, J. J., Weis, M. A., Kim, L. S., and Eyre, D. R. (2010) Type III collagen, a fibril network modifier in articular cartilage. J. Biol. Chem. 285, 18537-18544
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 18537-18544
-
-
Wu, J.J.1
Weis, M.A.2
Kim, L.S.3
Eyre, D.R.4
-
10
-
-
27144449766
-
Domains and maturation processes that regulate the activity of ADAMTS-2, a metalloproteinase cleaving the aminopropeptide of fibrillar procollagens types I-III and V
-
DOI 10.1074/jbc.M506458200
-
Colige, A., Ruggiero, F., Vandenberghe, I., Dubail, J., Kesteloot, F., Van Beeumen, J., Beschin, A., Brys, L., Lapière, C. M., and Nusgens, B. (2005) Domains and maturation processes that regulate the activity of ADAMTS-2, a metalloproteinase cleaving the aminopropeptide of fibrillar procollagens types I-III and V. J. Biol. Chem. 280, 34397-34408 (Pubitemid 41504567)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.41
, pp. 34397-34408
-
-
Colige, A.1
Ruggiero, F.2
Vandenberghe, I.3
Dubail, J.4
Kesteloot, F.5
Van Beeumen, J.6
Beschin, A.7
Brys, L.8
Lapiere, C.M.9
Nusgens, B.10
-
11
-
-
0037805608
-
Transforming growth factor-β induces secretion of activated ADAMTS-2: A procollagen III N-proteinase
-
DOI 10.1074/jbc.M300767200
-
Wang, W. M., Lee, S., Steiglitz, B. M., Scott, I. C., Lebares, C. C., Allen, M. L., Brenner, M. C., Takahara, K., and Greenspan, D. S. (2003) Transforming growth factor-β induces secretion of activated ADAMTS-2. A procollagen III N-proteinase. J. Biol. Chem. 278, 19549-19557 (Pubitemid 36799353)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.21
, pp. 19549-19557
-
-
Wang, W.-M.1
Lee, S.2
Steiglitz, B.M.3
Scott, I.C.4
Lebares, C.C.5
Allen, M.L.6
Brenner, M.C.7
Takahara, K.8
Greenspan, D.S.9
-
12
-
-
0023576831
-
Type III collagen can be present on banded collagen fibrils regardless of fibril diameter
-
Keene, D. R., Sakai, L. Y., Bächinger, H. P., and Burgeson, R. E. (1987) Type III collagen can be present on banded collagen fibrils regardless of fibril diameter. J. Cell Biol. 105, 2393-2402 (Pubitemid 18019087)
-
(1987)
Journal of Cell Biology
, vol.105
, Issue.5
, pp. 2393-2402
-
-
Keene, D.R.1
Sakai, L.Y.2
Bachinger, H.P.3
Burgerson, R.E.4
-
13
-
-
0025561019
-
Dermal collagen fibrils are hybrids of type I and type III collagen molecules
-
Fleischmajer, R., MacDonald, E. D., Perlish, J. S., Burgeson, R. E., and Fisher, L. W. (1990) Dermal collagen fibrils are hybrids of type I and type III collagen molecules. J. Struct. Biol 105, 162-169
-
(1990)
J. Struct. Biol
, vol.105
, pp. 162-169
-
-
Fleischmajer, R.1
MacDonald, E.D.2
Perlish, J.S.3
Burgeson, R.E.4
Fisher, L.W.5
-
14
-
-
69949138651
-
Re: Microfibrillar structure of type I collagen in situ
-
Okuyama, K., Bächinger, H. P., Mizuno, K., Boudko, S., Engel, J., Berisio, R., and Vitagliano, L. (2009) Re: microfibrillar structure of type I collagen in situ. Acta Crystallogr. D Biol. Crystallogr 65, 1007-1008
-
(2009)
Acta Crystallogr. D Biol. Crystallogr
, vol.65
, pp. 1007-1008
-
-
Okuyama, K.1
Bächinger, H.P.2
Mizuno, K.3
Boudko, S.4
Engel, J.5
Berisio, R.6
Vitagliano, L.7
-
15
-
-
0031055523
-
Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development
-
DOI 10.1073/pnas.94.5.1852
-
Liu, X., Wu, H., Byrne, M., Krane, S., and Jaenisch, R. (1997) Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development. Proc. Natl. Acad. Sci. U.S.A. 94, 1852-1856 (Pubitemid 27113925)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.5
, pp. 1852-1856
-
-
Liu, X.1
Wu, H.2
Byrne, M.3
Krane, S.4
Jaenisch, R.5
-
16
-
-
0030789557
-
The human type I collagen mutation database
-
Dalgleish, R. (1997) The human type I collagen mutation database. Nucleic Acids Res. 25, 181-187
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 181-187
-
-
Dalgleish, R.1
-
17
-
-
0031831307
-
The Human Collagen Mutation Database 1998
-
Dalgleish, R. (1998) The Human Collagen Mutation Database 1998. Nucleic Acids Res. 26, 253-255
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 253-255
-
-
Dalgleish, R.1
-
18
-
-
0034759627
-
Haploinsufficiency for one COL3A1 allele of type III procollagen results in a phenotype similar to the vascular form of Ehlers-Danlos syndrome, Ehlers-Danlos syndrome type IV
-
DOI 10.1086/324123
-
Schwarze, U., Schievink, W. I., Petty, E., Jaff, M. R., Babovic-Vuksanovic, D., Cherry, K. J., Pepin, M., and Byers, P. H. (2001) Haploinsufficiency for one COL3A1 allele of type III procollagen results in a phenotype similar to the vascular form of Ehlers-Danlos syndrome, Ehlers-Danlos syndrome type IV. Am. J. Hum. Genet. 69, 989-1001 (Pubitemid 33015814)
-
(2001)
American Journal of Human Genetics
, vol.69
, Issue.5
, pp. 989-1001
-
-
Schwarze, U.1
Schievink, W.I.2
Petty, E.3
Jaff, M.R.4
Babovic-Vuksanovic, D.5
Cherry, K.J.6
Pepin, M.7
Byers, P.H.8
-
19
-
-
78649916092
-
The haploinsufficient Col3a1 mouse as a model for vascular Ehlers-Danlos syndrome
-
Cooper, T. K., Zhong, Q., Krawczyk, M., Tae, H. J., Müller, G. A., Schubert, R., Myers, L. A., Dietz, H. C., Talan, M. I., and Briest, W. (2010) The haploinsufficient Col3a1 mouse as a model for vascular Ehlers-Danlos syndrome. Vet Pathol. 47, 1028-1039
-
(2010)
Vet Pathol.
, vol.47
, pp. 1028-1039
-
-
Cooper, T.K.1
Zhong, Q.2
Krawczyk, M.3
Tae, H.J.4
Müller, G.A.5
Schubert, R.6
Myers, L.A.7
Dietz, H.C.8
Talan, M.I.9
Briest, W.10
-
20
-
-
79952836042
-
Haploinsufficiency of the murine Col3a1 locus causes aortic dissection. A novel model of the vascular type of Ehlers-Danlos syndrome
-
Smith, L. B., Hadoke, P. W., Dyer, E., Denvir, M. A., Brownstein, D., Miller, E., Nelson, N., Wells, S., Cheeseman, M., and Greenfield, A. (2011) Haploinsufficiency of the murine Col3a1 locus causes aortic dissection. A novel model of the vascular type of Ehlers-Danlos syndrome. Cardiovasc Res. 90, 182-190
-
(2011)
Cardiovasc Res.
, vol.90
, pp. 182-190
-
-
Smith, L.B.1
Hadoke, P.W.2
Dyer, E.3
Denvir, M.A.4
Brownstein, D.5
Miller, E.6
Nelson, N.7
Wells, S.8
Cheeseman, M.9
Greenfield, A.10
-
21
-
-
0027996196
-
Crystal and molecular structure of a collagen-like peptide at 1.9 Å resolution
-
Bella, J., Eaton, M., Brodsky, B., and Berman, H. M. (1994) Crystal and molecular structure of a collagen-like peptide at 1.9 Å resolution. Science 266, 75-81
-
(1994)
Science
, vol.266
, pp. 75-81
-
-
Bella, J.1
Eaton, M.2
Brodsky, B.3
Berman, H.M.4
-
22
-
-
47749145413
-
Triple-helical peptides. An approach to collagen conformation, stability, and self-association
-
Brodsky, B., Thiagarajan, G., Madhan, B., and Kar, K. (2008) Triple-helical peptides. An approach to collagen conformation, stability, and self-association. Biopolymers 89, 345-353
-
(2008)
Biopolymers
, vol.89
, pp. 345-353
-
-
Brodsky, B.1
Thiagarajan, G.2
Madhan, B.3
Kar, K.4
-
23
-
-
0021967252
-
Subtle structural alterations in the chains of type I procollagen produce osteogenesis imperfecta type II
-
DOI 10.1038/316363a0
-
Bonadio, J., and Byers, P. H. (1985) Subtle structural alterations in the chains of type I procollagen produce osteogenesis imperfecta type II. Nature 316, 363-366 (Pubitemid 15237813)
-
(1985)
Nature
, vol.316
, Issue.6026
, pp. 363-366
-
-
Bonadio, J.1
Byers, P.H.2
-
24
-
-
77952756514
-
Prolyl 3-hydroxylase 1 null mice display abnormalities in fibrillar collagen-rich tissues such as tendons, skin, and bones
-
Vranka, J. A., Pokidysheva, E., Hayashi, L., Zientek, K., Mizuno, K., Ishikawa, Y., Maddox, K., Tufa, S., Keene, D. R., Klein, R., and Bächinger, H. P. (2010) Prolyl 3-hydroxylase 1 null mice display abnormalities in fibrillar collagen-rich tissues such as tendons, skin, and bones. J. Biol. Chem. 285, 17253-17262
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 17253-17262
-
-
Vranka, J.A.1
Pokidysheva, E.2
Hayashi, L.3
Zientek, K.4
Mizuno, K.5
Ishikawa, Y.6
Maddox, K.7
Tufa, S.8
Keene, D.R.9
Klein, R.10
Bächinger, H.P.11
-
25
-
-
0002367129
-
-
(Royce, P. M., and Steinmann, B., eds.) 2nd Ed., Wiley-Liss, Inc.
-
Steinmann, B., Royce, P. M., and Superti-Furga, A. (2002) in Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects (Royce, P. M., and Steinmann, B., eds.) 2nd Ed., pp. 431-523, Wiley-Liss, Inc.
-
(2002)
Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects
, pp. 431-523
-
-
Steinmann, B.1
Royce, P.M.2
Superti-Furga, A.3
-
26
-
-
69549130585
-
Crystal structure of human collagen XVIII trimerization domain. A novel collagen trimerization fold
-
Boudko, S. P., Sasaki, T., Engel, J., Lerch, T. F., Nix, J., Chapman, M. S., and Bächinger, H. P. (2009) Crystal structure of human collagen XVIII trimerization domain. A novel collagen trimerization fold. J. Mol. Biol. 392, 787-802
-
(2009)
J. Mol. Biol.
, vol.392
, pp. 787-802
-
-
Boudko, S.P.1
Sasaki, T.2
Engel, J.3
Lerch, T.F.4
Nix, J.5
Chapman, M.S.6
Bächinger, H.P.7
-
27
-
-
78951488005
-
Crystal structure of the human collagen XV trimerization domain. A potent trimerizing unit common to multiplexin collagens
-
Wirz, J. A., Boudko, S. P., Lerch, T. F., Chapman, M. S., and Bächinger, H. P. (2011) Crystal structure of the human collagen XV trimerization domain. A potent trimerizing unit common to multiplexin collagens. Matrix Biol. 30, 9-15
-
(2011)
Matrix Biol.
, vol.30
, pp. 9-15
-
-
Wirz, J.A.1
Boudko, S.P.2
Lerch, T.F.3
Chapman, M.S.4
Bächinger, H.P.5
-
28
-
-
57749083515
-
Trimerization and triple helix stabilization of the collagen XIX NC2 domain
-
Boudko, S. P., Engel, J., and Bächinger, H. P. (2008) Trimerization and triple helix stabilization of the collagen XIX NC2 domain. J. Biol. Chem. 283, 34345-34351
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 34345-34351
-
-
Boudko, S.P.1
Engel, J.2
Bächinger, H.P.3
-
29
-
-
83555174430
-
The crucial role of trimerization domains in collagen folding
-
Boudko, S. P., Engel, J., and Bächinger, H. P. (2012) The crucial role of trimerization domains in collagen folding. Int. J. Biochem. Cell Biol. 44, 21-32
-
(2012)
Int. J. Biochem. Cell Biol.
, vol.44
, pp. 21-32
-
-
Boudko, S.P.1
Engel, J.2
Bächinger, H.P.3
-
30
-
-
77953583346
-
Kinetic hysteresis in collagen folding
-
Mizuno, K., Boudko, S. P., Engel, J., and Bächinger, H. P. (2010) Kinetic hysteresis in collagen folding. Biophys. J. 98, 3004-3014
-
(2010)
Biophys. J.
, vol.98
, pp. 3004-3014
-
-
Mizuno, K.1
Boudko, S.P.2
Engel, J.3
Bächinger, H.P.4
-
31
-
-
84871801157
-
The NC2 domain of type IX collagen determines the chain register of the triple helix
-
Boudko, S. P., and Bächinger, H. P. (2012) The NC2 domain of type IX collagen determines the chain register of the triple helix. J. Biol. Chem. 287, 44536-44545
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 44536-44545
-
-
Boudko, S.P.1
Bächinger, H.P.2
-
32
-
-
0025917316
-
Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IV
-
Richards, A. J., Lloyd, J. C., Ward, P. N., De Paepe, A., Narcisi, P., and Pope, F. M. (1991) Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IV. J. Med. Genet. 28, 458-463 (Pubitemid 21922639)
-
(1991)
Journal of Medical Genetics
, vol.28
, Issue.7
, pp. 458-463
-
-
Richards, A.J.1
Lloyd, J.C.2
Ward, P.N.3
De Paepe, A.4
Narcisi, P.5
Pope, F.M.6
-
33
-
-
0031050915
-
Mutations in the COL3A1 gene result in the Ehlers-Danlos syndrome type IV and alterations in the size and distribution of the major collagen fibrils of the dermis
-
Smith, L. T., Schwarze, U., Goldstein, J., and Byers, P. H. (1997) Mutations in the COL3A1 gene result in the Ehlers-Danlos syndrome type IV and alterations in the size and distribution of the major collagen fibrils of the dermis. J. Invest. Dermatol. 108, 241-247 (Pubitemid 27116217)
-
(1997)
Journal of Investigative Dermatology
, vol.108
, Issue.3
, pp. 241-247
-
-
Smith, L.T.1
Schwarze, U.2
Goldstein, J.3
Byers, P.H.4
-
34
-
-
0022998720
-
The tissue form of Type VII collagen is an antiparallel dimer
-
Morris, N. P., Keene, D. R., Glanville, R. W., Bentz, H., and Burgeson, R. E. (1986) The tissue form of type VII collagen is an antiparallel dimer. J. Biol. Chem. 261, 5638-5644 (Pubitemid 17204384)
-
(1986)
Journal of Biological Chemistry
, vol.261
, Issue.12
, pp. 5638-5644
-
-
Morris, N.P.1
Keene, D.R.2
Glanville, R.W.3
-
35
-
-
0018959643
-
Folding mechanism of the triple helix in type-III collagen and type-III pN-collagen. Role of disulfide bridges and peptide bond isomerization
-
Bächinger, 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
-
-
Bächinger, H.P.1
Bruckner, P.2
Timpl, R.3
Prockop, D.J.4
Engel, J.5
-
36
-
-
0027934571
-
Crystal structure of an isoleucine-zipper trimer
-
DOI 10.1038/371080a0
-
Harbury, P. B., Kim, P. S., and Alber, T. (1994) Crystal structure of an isoleucine-zipper trimer. Nature 371, 80-83 (Pubitemid 24277468)
-
(1994)
Nature
, vol.371
, Issue.6492
, pp. 80-83
-
-
Harbury, P.B.1
Kim, P.S.2
Alber, T.3
-
37
-
-
57749106685
-
Crystal structure of human type III collagen Gly-991-Gly-1032 cystine knot-containing peptide shows both 7/2 and 10/3 triple helical symmetries
-
Boudko, S. P., Engel, J., Okuyama, K., Mizuno, K., Bächinger, H. P., and Schumacher, M. A. (2008) Crystal structure of human type III collagen Gly-991-Gly-1032 cystine knot-containing peptide shows both 7/2 and 10/3 triple helical symmetries. J. Biol. Chem. 283, 32580-32589
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 32580-32589
-
-
Boudko, S.P.1
Engel, J.2
Okuyama, K.3
Mizuno, K.4
Bächinger, H.P.5
Schumacher, M.A.6
-
38
-
-
84884893019
-
-
(Celis, J. E., ed.) 3rd Ed., Academic Press, New York
-
Aebi, U., and Baschong, W. (2006) in Cell Biology (Celis, J. E., ed.) pp 241-246, 3rd Ed., Academic Press, New York
-
(2006)
Cell Biology
, pp. 241-246
-
-
Aebi, U.1
Baschong, W.2
-
39
-
-
0000523565
-
Structure of collagen
-
Ramachandran, G. N., and Kartha, G. (1955) Structure of collagen. Nature 176, 593-595
-
(1955)
Nature
, vol.176
, pp. 593-595
-
-
Ramachandran, G.N.1
Kartha, G.2
-
40
-
-
33645742624
-
Revision of collagen molecular structure
-
Okuyama, K., Xu, X., Iguchi, M., and Noguchi, K. (2006) Revision of collagen molecular structure. Biopolymers 84, 181-191
-
(2006)
Biopolymers
, vol.84
, pp. 181-191
-
-
Okuyama, K.1
Xu, X.2
Iguchi, M.3
Noguchi, K.4
-
41
-
-
0024289472
-
Folding of collagen IV
-
Dölz, R., Engel, J., and Kühn, K. (1988) Folding of collagen IV. Eur. J. Biochem. 178, 357-366
-
(1988)
Eur. J. Biochem.
, vol.178
, pp. 357-366
-
-
Dölz, R.1
Engel, J.2
Kühn, K.3
-
42
-
-
25444466358
-
-
(Buchner, J., and Kiefhaber, T. eds.) John Wiley & Sons, Inc., New York
-
Bächinger, H. P., and Engel, J. (2005) in Protein Folding Handbook (Buchner, J., and Kiefhaber, T. eds.) pp. 1059-1110, John Wiley & Sons, Inc., New York
-
(2005)
Protein Folding Handbook
, pp. 1059-1110
-
-
Bächinger, H.P.1
Engel, J.2
-
43
-
-
0036290657
-
Nucleation and propagation of the collagen triple helix in single-chain and trimerized peptides: Transition from third to first order kinetics
-
DOI 10.1006/jmbi.2002.5439
-
Boudko, S., Frank, S., Kammerer, R. A., Stetefeld, J., Schulthess, T., Landwehr, R., Lustig, A., Bächinger, H. P., and Engel, J. (2002) Nucleation and propagation of the collagen triple helix in single-chain and trimerized peptides. Transition from third to first order kinetics. J. Mol. Biol. 317, 459-470 (Pubitemid 34722183)
-
(2002)
Journal of Molecular Biology
, vol.317
, Issue.3
, pp. 459-470
-
-
Boudko, S.1
Frank, S.2
Kammerer, R.A.3
Stetefeld, J.4
Schulthess, T.5
Landwehr, R.6
Lustig, A.7
Bachinger, H.P.8
Engel, J.9
-
44
-
-
0035715945
-
Prolyl isomerases
-
Schmid, F. X. (2001) Prolyl isomerases. Adv. Protein. Chem. 59, 243-282
-
(2001)
Adv. Protein. Chem.
, vol.59
, pp. 243-282
-
-
Schmid, F.X.1
-
45
-
-
0032486107
-
Side-chain effects on peptidyl-prolyl cis/trans isomerisation
-
DOI 10.1006/jmbi.1998.1770
-
Reimer, U., Scherer, G., Drewello, M., Kruber, S., Schutkowski, M., and Fischer, G. (1998) Side-chain effects on peptidyl-prolyl cis/trans isomerisation. J. Mol. Biol. 279, 449-460 (Pubitemid 28263982)
-
(1998)
Journal of Molecular Biology
, vol.279
, Issue.2
, pp. 449-460
-
-
Reimer, U.1
Scherer, G.2
Drewello, M.3
Kruber, S.4
Schutkowski, M.5
Fischer, G.6
-
46
-
-
79955972195
-
Designed coiled coils promote folding of a recombinant bacterial collagen
-
Yoshizumi, A., Fletcher, J. M., Yu, Z., Persikov, A. V., Bartlett, G. J., Boyle, A. L., Vincent, T. L., Woolfson, D. N., and Brodsky, B. (2011) Designed coiled coils promote folding of a recombinant bacterial collagen. J. Biol. Chem. 286, 17512-17520
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 17512-17520
-
-
Yoshizumi, A.1
Fletcher, J.M.2
Yu, Z.3
Persikov, A.V.4
Bartlett, G.J.5
Boyle, A.L.6
Vincent, T.L.7
Woolfson, D.N.8
Brodsky, B.9
-
47
-
-
77950259337
-
Noncollagenous region of the streptococcal collagen-like protein is a trimerization domain that supports refolding of adjacent homologous and heterologous collagenous domains
-
Yu, Z., Mirochnitchenko, O., Xu, C., Yoshizumi, A., Brodsky, B., and Inouye, M. (2010) Noncollagenous region of the streptococcal collagen-like protein is a trimerization domain that supports refolding of adjacent homologous and heterologous collagenous domains. Protein Sci. 19, 775-785
-
(2010)
Protein Sci.
, vol.19
, pp. 775-785
-
-
Yu, Z.1
Mirochnitchenko, O.2
Xu, C.3
Yoshizumi, A.4
Brodsky, B.5
Inouye, M.6
-
48
-
-
0027389056
-
Thermal stability and folding of the collagen triple helix and the effects of mutations in osteogenesis imperfecta on the triple helix of type I collagen
-
Bächinger, H. P., Morris, N. P., and Davis, J. M. (1993) Thermal stability and folding of the collagen triple helix and the effects of mutations in osteogenesis imperfecta on the triple helix of type I collagen. Am. J. Med. Genet. 45, 152-162
-
(1993)
Am. J. Med. Genet.
, vol.45
, pp. 152-162
-
-
Bächinger, H.P.1
Morris, N.P.2
Davis, J.M.3
-
49
-
-
0028220202
-
Delayed triple helix formation of mutant collagen from patients with osteogenesis imperfecta
-
DOI 10.1006/jmbi.1994.1199
-
Raghunath, M., Bruckner, P., and Steinmann, B. (1994) Delayed triple helix formation of mutant collagen from patients with osteogenesis imperfecta. J. Mol. Biol. 236, 940-949 (Pubitemid 24146332)
-
(1994)
Journal of Molecular Biology
, vol.236
, Issue.3
, pp. 940-949
-
-
Raghunath, M.1
Bruckner, P.2
Steinmann, B.3
-
50
-
-
77954946969
-
The NC2 domain of collagen IX provides chain selection and heterotrimerization
-
Boudko, S. P., Zientek, K. D., Vance, J., Hacker, J. L., Engel, J., and Bächinger, H. P. (2010) The NC2 domain of collagen IX provides chain selection and heterotrimerization. J. Biol. Chem. 285, 23721-23731
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 23721-23731
-
-
Boudko, S.P.1
Zientek, K.D.2
Vance, J.3
Hacker, J.L.4
Engel, J.5
Bächinger, H.P.6
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