Zobrazeno 1 - 10
of 606
pro vyhledávání: '"Bjorn R, Olsen"'
Autor:
Aikta Sharma, Alice Goring, Peter B. Johnson, Roger J. H. Emery, Eric Hesse, Alan Boyde, Bjorn R. Olsen, Andrew A. Pitsillides, Richard O. C. Oreffo, Sumeet Mahajan, Claire E. Clarkin
Publikováno v:
Disease Models & Mechanisms, Vol 14, Iss 3 (2021)
Collagen assembly during development is essential for successful matrix mineralisation, which determines bone quality and mechanocompetence. However, the biochemical and structural perturbations that drive pathological skeletal collagen configuration
Externí odkaz:
https://doaj.org/article/7641ca0ae1294d25a608e315cdaa11d3
Providing easy-to-access information, this unique sourcebook covers the wide range of topics that a researcher must be familiar with in order to become a successful experimental scientist. Perfect for aspiring as well as practicing professionals in t
Autor:
Masashi Nagao, John L. Hamilton, Ranjan Kc, Agnes D. Berendsen, Xuchen Duan, Chan Wook Cheong, Xin Li, Hee-Jeong Im, Bjorn R. Olsen
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-16 (2017)
Abstract Genome wide studies indicate that vascular endothelial growth factor A (VEGF) is associated with osteoarthritis (OA), and increased VEGF expression correlates with increased disease severity. VEGF is also a chondrocyte survival factor during
Externí odkaz:
https://doaj.org/article/4517a81285e945cda04564b0bb576f94
Autor:
Worrachet Intachai, Abigail S. Tucker, Sissades Tongsima, Chumpol Ngamphiw, Nutsuchar Wangtiraumnuay, Piranit Nik Kantaputra, Bjorn R. Olsen
Publikováno v:
Journal of Human Genetics. 67:115-118
FREM2 is a member of the FREM2–FRAS1–FREM1 protein complex which contributes to epithelial–mesenchymal coupling. We report a Thai woman with cryptophthalmos, dental anomalies, and oral vestibule defect. A compound heterozygous mutation (c.6499C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d19cc02daafd7c7ddb27b81d5623354
https://doi.org/10.1038/s10038-021-00972-4
https://doi.org/10.1038/s10038-021-00972-4
Autor:
Teruhito Yoshitaka, Tomoyuki Mukai, Mizuho Kittaka, Lisa M. Alford, Salome Masrani, Shu Ishida, Ken Yamaguchi, Motohiko Yamada, Noriyoshi Mizuno, Bjorn R. Olsen, Ernst J. Reichenberger, Yasuyoshi Ueki
Publikováno v:
Cell Reports, Vol 8, Iss 6, Pp 1752-1766 (2014)
Cherubism is caused by mutations in SH3BP2. Studies of cherubism mice showed that tumor necrosis factor α (TNF-α)-dependent autoinflammation is a major cause of the disorder but failed to explain why human cherubism lesions are restricted to jaws a
Externí odkaz:
https://doaj.org/article/5453dcbdd4d64aed8b946a1fbb2113bc
Autor:
Michael B. Duncan, Changqing Yang, Harikrishna Tanjore, Patrick M. Boyle, Doruk Keskin, Hikaru Sugimoto, Michael Zeisberg, Bjorn R. Olsen, Raghu Kalluri
Publikováno v:
Disease Models & Mechanisms, Vol 6, Iss 4, Pp 942-951 (2013)
SUMMARY The regenerative response to drug- and toxin-induced liver injury induces changes to the hepatic stroma, including the extracellular matrix. Although the extracellular matrix is known to undergo changes during the injury response, its impact
Externí odkaz:
https://doaj.org/article/7994aafa55724d89bf4a4b41388274ea
Autor:
Shuxian Lin, X. Baozhi Yuan, Yin Xiao, Zheng Wang, Xianglong Han, Yan Jing, Yinshi Ren, Bjorn R. Olsen, Minghao Zheng, Chi Ma, Jian Q. Feng, Ke Wang, Hu Zhao, Jun Wang, Lin Chen
Publikováno v:
International Journal of Biological Sciences
Bone-forming osteoblasts have been a cornerstone of bone biology for more than a century. Most research toward bone biology and bone diseases center on osteoblasts. Overlooked are the 90% of bone cells, called osteocytes. This study aims to test the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fafae0f08561dae0961326b0fd503fd
https://doi.org/10.7150/ijbs.61012
https://doi.org/10.7150/ijbs.61012
Autor:
Pongsak Mahanupab, Bjorn R. Olsen, Metawee Srikummool, Wattana Chartapisak, Piranit Nik Kantaputra, Rak Tananuvat, James R. Ketudat Cairns, Jatupol Kampuansai, Worrachet Intachai, Napaporn Tananuvat, Chananya Hokierti
Publikováno v:
Journal of Human Genetics. 66:193-203
Harboyan syndrome or corneal dystrophy and progressive deafness (MIM #217400) is characterized by congenital hereditary endothelial dystrophy (CHED) and progressive, sensorineural hearing loss. Mutations in SLC4A11 are responsible for this rare genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fccfc1f0f7064502987d97a71bffd5f3
https://doi.org/10.1038/s10038-020-00834-5
https://doi.org/10.1038/s10038-020-00834-5
Autor:
Kenneth Nilsson, Andreas Mårtensson, Augustinas Sakinis, Christine Wennerås, Martin Stenson, Linda Wass, Bjorn R. Olsen, Linnea Höper, Elisabet Skoog, Anna Grankvist, Jacob Söderlind
Publikováno v:
Clinical Infectious Diseases. 73:e2372-e2378
Background Candidatus (Ca.) Neoehrlichia (N.) mikurensis is an emerging tick-borne pathogen of humans that is closely related to Ehrlichia and Anaplasma species. This strict intracellular bacterium escapes detection by routine microbiologic diagnosti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e93e2009d1e8af28b52636d0c646095a
https://doi.org/10.1093/cid/ciaa1217
https://doi.org/10.1093/cid/ciaa1217
Autor:
Chumpol Ngamphiw, Suttichai Krisanaprakornkit, Bjorn R. Olsen, Sissades Tongsima, Jame R Ketudat Cairns, Worrachet Intachai, Katsushige Kawasaki, Atsushi Ohazama, Prapai Dejkhamron, Piranit Nik Kantaputra
Publikováno v:
European Journal of Orthodontics. 43:45-50
Summary Background Juberg-Hayward syndrome (JHS; MIM 216100) is a rare autosomal recessive malformation syndrome, characterized by cleft lip/palate, microcephaly, ptosis, short stature, hypoplasia or aplasia of thumbs, and dislocation of radial head
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be4c2a84e41b3bacd1f1939bb152d661
https://doi.org/10.1093/ejo/cjaa023
https://doi.org/10.1093/ejo/cjaa023