Joint hypermobility syndromes: the pathophysiologic role of tenascin-X gene defects.
作者： Manon C. Zweers , Alan J. Hakim , Rodney Grahame , Joost Schalkwijk
DOI: 10.1002/ART.20488
关键词: Gene 、 Tenascin X 、 Pathology 、 Pathophysiology 、 Medicine 、 Tenascin 、 Joint hypermobility
摘要:
ru.nl
core.ac.uk
sci-hub.se 参考文章(80)
Philipp Weber, Udo Bartsch, Matthew N. Rasband, Reiner Czaniera, Yolande Lang, Horst Bluethmann, Richard U. Margolis, S. Rock Levinson, Peter Shrager, Dirk Montag, Melitta Schachner, Mice Deficient for Tenascin-R Display Alterations of the Extracellular Matrix and Decreased Axonal Conduction Velocities in the CNS The Journal of Neuroscience. ,vol. 19, pp. 4245- 4262 ,(1999) , 10.1523/JNEUROSCI.19-11-04245.1999
A Gedalia, J Press, M Klein, D Buskila, Joint hypermobility and fibromyalgia in schoolchildren. Annals of the Rheumatic Diseases. ,vol. 52, pp. 494- 496 ,(1993) , 10.1136/ARD.52.7.494
David S Goldstein, David Robertson, Murray Esler, Stephen E Straus, Graeme Eisenhofer, Dysautonomias: Clinical Disorders of the Autonomic Nervous System Annals of Internal Medicine. ,vol. 137, pp. 753- 763 ,(2002) , 10.7326/0003-4819-137-9-200211050-00011
Peter N Robinson, Maurice Godfrey, The molecular genetics of Marfan syndrome and related microfibrillopathies Journal of Medical Genetics. ,vol. 37, pp. 9- 25 ,(2000) , 10.1136/JMG.37.1.9
Barbara Crippes Trask, Timothy M. Trask, Thomas Broekelmann, Robert P. Mecham, The Microfibrillar Proteins MAGP-1 and Fibrillin-1 Form a Ternary Complex with the Chondroitin Sulfate Proteoglycan Decorin Molecular Biology of the Cell. ,vol. 11, pp. 1499- 1507 ,(2000) , 10.1091/MBC.11.5.1499
Peter Beighton, Anne De Paepe, Beat Steinmann, Petros Tsipouras, Richard J. Wenstrup, Ehlers‐Danlos syndromes: Revised nosology, Villefranche, 1997 American Journal of Medical Genetics. ,vol. 77, pp. 31- 37 ,(1998) , 10.1002/(SICI)1096-8628(19980428)77:1<31::AID-AJMG8>3.0.CO;2-O
R. Grahame, Joint hypermobility and genetic collagen disorders: are they related? Archives of Disease in Childhood. ,vol. 80, pp. 188- 191 ,(1999) , 10.1136/ADC.80.2.188
P Beighton, L Solomon, C L Soskolne, Articular mobility in an African population. Annals of the Rheumatic Diseases. ,vol. 32, pp. 413- 418 ,(1973) , 10.1136/ARD.32.5.413
Carol A. Blanchong, Bi Zhou, Kristi L. Rupert, Erwin K. Chung, Karla N. Jones, Juan F. Sotos, William B. Zipf, Robert M. Rennebohm, C. Yung Yu, Deficiencies of Human Complement Component C4a and C4b and Heterozygosity in Length Variants of RP-C4-CYP21-TNX (Rccx) Modules in Caucasians The Load of Rccx Genetic Diversity on Major Histocompatibility Complex–Associated Disease Journal of Experimental Medicine. ,vol. 191, pp. 2183- 2196 ,(2000) , 10.1084/JEM.191.12.2183
Paolo Narcisi, Allan J.Richards, Stanley D. Ferguson, F.Michael Pope, A family with Ehlers — Danlos syndrome type III/articular hypermobility syndrome has a glycine 637 to serine substitution in type III collagen Human Molecular Genetics. ,vol. 3, pp. 1617- 1620 ,(1994) , 10.1093/HMG/3.9.1617