Cytoskeleton and nuclear lamina affection in recessive osteogenesis imperfecta: A functional proteomics perspective

Osteogenesis imperfecta (OI) is a collagen-related disorder associated to dominant, recessive or X-linked transmission, mainly caused by mutations in type I collagen genes or in genes involved in type I collagen metabolism. Among the recessive forms, OI types VII, VIII, and IX are due to mutations i...

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Bibliografiset tiedot
Julkaisussa:J Proteomics
Päätekijät: Gagliardi, Assunta, Besio, Roberta, Carnemolla, Chiara, Landi, Claudia, Armini, Alessandro, Aglan, Mona, Otaify, Ghada, Temtamy, Samia A., Forlino, Antonella, Bini, Luca, Bianchi, Laura
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2017
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5584732/
https://ncbi.nlm.nih.gov/pubmed/28802583
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jprot.2017.08.007
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