Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Rheumatology/Cartilage Biology and Osteoarthritis"'
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13520 (2010)
PLoS ONE
PLoS ONE
Background Most research on failure leading to revision total hip arthroplasty (THA) is reported from single centers. We searched PubMed between January 2000 and August 2010 to identify population- or community-based studies evaluating ten-year revis
Autor:
Claudia Kruger, Claudia Kappen
Publikováno v:
PLoS ONE, Vol 5, Iss 2, p e8978 (2010)
PLoS ONE
PLoS ONE
Hox genes encode transcription factors, which regulate skeletal patterning and chondrocyte differentiation during the development of cartilage, the precursor to mature bone. Overexpression of the homeobox transcription factors Hoxc8 and Hoxd4 causes
Autor:
Peiman Liu, Jacqueline T. Hecht, Karen L. Posey, Huiqiu R. Wang, Alka C. Veerisetty, Joseph L. Alcorn
Publikováno v:
PLoS ONE
PLoS ONE, Vol 5, Iss 4, p e10302 (2010)
PLoS ONE, Vol 5, Iss 4, p e10302 (2010)
Mutations in cartilage oligomeric matrix protein (COMP), a large extracellular glycoprotein expressed in musculoskeletal tissues, cause two skeletal dysplasias, pseudoachondroplasia and multiple epiphyseal dysplasia. These mutations lead to massive i
Autor:
Jean-Edouard Ombetta, Natacha Thelier, Chang Zhi Dong, Stéphanie Plocki, Lydia Tsagris, François Rannou, France Massicot, Atimé Djimdé, Elissar El-Hayek, Yiming Shi, Françoise Heymans, Nohad Gresh, Caroline Chauvet
Publikováno v:
PLoS ONE, Vol 5, Iss 6, p e10914 (2010)
PLoS ONE
PLoS ONE
Group IIA secreted/synovial phospholipase A(2) (GIIAPLA(2)) is an enzyme involved in the synthesis of eicosanoids such as prostaglandin E(2) (PGE(2)), the main eicosanoid contributing to pain and inflammation in rheumatic diseases. We designed, by mo
Autor:
Akihiro Sudo, Juan J. Gomez-Reino, Yusuke Nakamura, Aspasia Tsezou, Masahiro Nakajima, Konstantinos N. Malizos, Jin Dai, Shiro Ikegawa, Tatsuhiko Tsunoda, Naoyuki Kamatani, Tatsuya Furuichi, Ikuyo Kou, Antonio Gonzalez, Michiaki Kubo, Atsushi Takahashi, Atsumasa Uchida, Cristina Rodriguez-Fontenla, Naoshi Fukui
Publikováno v:
PLoS ONE, Vol 5, Iss 3, p e9723 (2010)
PLoS ONE
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
PLoS ONE
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Osteoarthritis (OA) is a common disease that has a definite genetic component. Only a few OA susceptibility genes that have definite functional evidence and replication of association have been reported, however. Through a genome-wide association stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b93222cb50626fdbee7c7a3411abca7
https://hdl.handle.net/10347/22836
https://hdl.handle.net/10347/22836
Autor:
Rachel Eardley, Louise H. W. Kung, Richard Poulsom, Mel Heeran, Lynnette Knowles, John F. Bateman, Michael D. Briggs, Raymond P. Boot-Handford, M. Helen Rajpar, Ben T. McDermott, Peter Arvan, Richard Wilson, Karl E. Kadler, David J. Thornton
Publikováno v:
Rajpar, M H, McDermott, B, Kung, L, Eardley, R, Knowles, L, Heeran, M, Thornton, D J, Wilson, R, Bateman, J F, Poulsom, R, Arvan, P, Kadler, K E, Briggs, M D & Boot-Handford, R P 2009, ' Targeted induction of endoplasmic reticulum stress induces cartilage pathology ', PL o S Genetics, vol. 5, no. 10, e1000691 . https://doi.org/10.1371/journal.pgen.1000691
PLoS Genetics
PLoS Genetics, Vol 5, Iss 10, p e1000691 (2009)
PLoS Genetics
PLoS Genetics, Vol 5, Iss 10, p e1000691 (2009)
Pathologies caused by mutations in extracellular matrix proteins are generally considered to result from the synthesis of extracellular matrices that are defective. Mutations in type X collagen cause metaphyseal chondrodysplasia type Schmid (MCDS), a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6820740417420de975724f13aaac4d58
https://doi.org/10.1371/journal.pgen.1000691
https://doi.org/10.1371/journal.pgen.1000691
Autor:
Bradley A. Carlson, Chelsea R. Horton, Dolph L. Hatfield, Frank R. Jirik, Trish E. Parsons, Benedikt Hallgrímsson, Charlene M. Downey
Publikováno v:
PLoS Genetics, Vol 5, Iss 8, p e1000616 (2009)
PLoS Genetics
PLoS Genetics
Kashin-Beck disease, a syndrome characterized by short stature, skeletal deformities, and arthropathy of multiple joints, is highly prevalent in specific regions of Asia. The disease has been postulated to result from a combination of different envir
Autor:
Claudine G. James, Lee-Anne Stanton, Frank Beier, Veronica Ulici, Hanga Agoston, T. Michael Underhill
Publikováno v:
PLoS ONE
Paediatrics Publications
PLoS ONE, Vol 5, Iss 1, p e8693 (2010)
Paediatrics Publications
PLoS ONE, Vol 5, Iss 1, p e8693 (2010)
Background: Endochondral ossification is a complex process involving a series of events that are initiated by the establishment of a chondrogenic template and culminate in its replacement through the coordinated activity of osteoblasts, osteoclasts a
Autor:
Jonathan Stephens, Huibert A. P. Pols, Deborah J. Hart, Mohammed J. R. Ghori, Ida Malkina, Wendy L. McArdle, Simon C. Potter, Rhian Gwilliam, David P. Strachan, Alexandra C. Nica, Kourosh R. Ahmadi, Radhi Ravindrarajah, Michael Inouye, Albert Hofman, Tim D. Spector, Karol Estrada, Lisette Stolk, Frances M K Williams, Gregory Livshits, Eleanor Wheeler, Naomi Hammond, P. Mila Jhamai, Sergey Ermakov, Usha Chinappen-Horsley, Pascal P. Arp, André G. Uitterlinden, Emmanouil T. Dermitzakis, Panos Deloukas, Nicholas J. Wareham, Ruth J. F. Loos, Amy Chaney, Inês Barroso, J. Brent Richards, Willem H. Ouwehand, Joyce B. J. van Meurs, Nicole Soranzo, Fernando Rivadeneira, Manjinder S. Sandhu
Publikováno v:
PLoS Genetics, Vol 5, Iss 4, p e1000445 (2009)
PLoS Genetics
PLOS Genetics, Vol. 5, No 4 (2009) P. e1000445
PLoS Genetics (print), 5(4). Public Library of Science
PLoS Genetics
PLOS Genetics, Vol. 5, No 4 (2009) P. e1000445
PLoS Genetics (print), 5(4). Public Library of Science
Recent genome-wide (GW) scans have identified several independent loci affecting human stature, but their contribution through the different skeletal components of height is still poorly understood. We carried out a genome-wide scan in 12,611 partici
Autor:
Anne-Lise Delezoide, Laurence Legeai-Mallet, Jean-Philippe Jais, Philippe Loget, Charles Decraene, Marie Gonzales, Arnold Munnich, Catherine Benoist-Lasselin, Linda Gibbs, Jelena Martinovic, Laurent Schibler
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2009, 4, online (10), Non paginé. ⟨10.1371/journal.pone.0007633⟩
PLoS ONE, Public Library of Science, 2009, 4, online (10), Non paginé. 〈10.1371/journal.pone.0007633〉
PLoS ONE, Vol 4, Iss 10, p e7633 (2009)
Plos One 10 (4, online), Non paginé. (2009)
PLoS ONE, Public Library of Science, 2009, 4, online (10), Non paginé. ⟨10.1371/journal.pone.0007633⟩
PLoS ONE, Public Library of Science, 2009, 4, online (10), Non paginé. 〈10.1371/journal.pone.0007633〉
PLoS ONE, Vol 4, Iss 10, p e7633 (2009)
Plos One 10 (4, online), Non paginé. (2009)
Endochondral ossification is the process by which the appendicular skeleton, facial bones, vertebrae and medial clavicles are formed and relies on the tight control of chondrocyte maturation. Fibroblast growth factor receptor (FGFR)3 plays a role in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5531d7a4d595607bae9da382ec85c984
https://hal.archives-ouvertes.fr/hal-01193364/document
https://hal.archives-ouvertes.fr/hal-01193364/document