Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Marjo Hyry"'
Autor:
Olga Ovchinnikova, Per Eriksson, Peter Libby, Eduardo J. Folco, Göran K. Hansson, Dick Wågsäter, Marjo Hyry, Johanna Myllyharju, Anna-Karin L. Robertson
Publikováno v:
The American Journal of Pathology. 174:693-700
Rupture of the collagenous, fibrous cap of an atherosclerotic plaque commonly causes thrombosis. Activated immune cells can secrete mediators that jeopardize the integrity of the fibrous cap. This study aimed to determine the relationship between T-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff78889d8875851cee3f4d8da5bc4d2b
https://doi.org/10.2353/ajpath.2009.080561
https://doi.org/10.2353/ajpath.2009.080561
Autor:
Johanna Myllyharju, Raija Soininen, Ruud A. Bank, Marjo Hyry, Kati Takaluoma, Raija Sormunen, Juha Lantto, Kari I. Kivirikko
Publikováno v:
The Journal of Biological Chemistry, 282, 6588-6596. American Society for Biochemistry and Molecular Biology Inc.
Takaluoma, K, Hyry, M, Lantto, J, Sormunen, R, Bank, R A, Kivirikko, K I, Myllyharja, J & Soininen, R 2007, ' Tissue-specific changes in the hydroxylysine content and cross-links of collagens and alterations in fibril morphology in lysyl hydroxylase 1 knock-out mice ', The Journal of Biological Chemistry, vol. 282, pp. 6588-6596 . https://doi.org/10.1074/jbc.M608830200
Takaluoma, K, Hyry, M, Lantto, J, Sormunen, R, Bank, R A, Kivirikko, K I, Myllyharja, J & Soininen, R 2007, ' Tissue-specific changes in the hydroxylysine content and cross-links of collagens and alterations in fibril morphology in lysyl hydroxylase 1 knock-out mice ', The Journal of Biological Chemistry, vol. 282, pp. 6588-6596 . https://doi.org/10.1074/jbc.M608830200
We have generated mice with targeted inactivation of the Plod1 gene for lysyl hydroxylase 1 (LH1). Its human mutations cause Ehlers-Danlos syndrome VIA (EDS VIA) characterized by muscular hypotonia, joint laxity, and kyphoscoliosis. The Plod1(-/-) mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e149613c36654917e5fdaf937f53d832
https://hdl.handle.net/11245/1.277700
https://hdl.handle.net/11245/1.277700
Bruck syndrome is a rare autosomal recessive connective tissue disorder characterized by fragile bones, joint contractures, scoliosis, and osteoporosis. The telopeptides of bone collagen I are underhydroxylated in these patients, leading to abnormal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45198b7c9859bb4b60c864510ddffb9d
https://europepmc.org/articles/PMC2781491/
https://europepmc.org/articles/PMC2781491/
