Cargando…
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...
Autores principales: | Gagliardi, Assunta, Besio, Roberta, Carnemolla, Chiara, Landi, Claudia, Armini, Alessandro, Aglan, Mona, Otaify, Ghada, Temtamy, Samia A., Forlino, Antonella, Bini, Luca, Bianchi, Laura |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584732/ https://www.ncbi.nlm.nih.gov/pubmed/28802583 http://dx.doi.org/10.1016/j.jprot.2017.08.007 |
Ejemplares similares
-
Intracellular and Extracellular Markers of Lethality in Osteogenesis Imperfecta: A Quantitative Proteomic Approach
por: Bini, Luca, et al.
Publicado: (2021) -
Molecular spectrum and differential diagnosis in patients referred with sporadic or autosomal recessive osteogenesis imperfecta
por: Caparros‐Martin, Jose A., et al.
Publicado: (2016) -
Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate
por: Besio, Roberta, et al.
Publicado: (2019) -
Dissecting the phenotypic variability of osteogenesis imperfecta
por: Garibaldi, Nadia, et al.
Publicado: (2022) -
TAPT1—at the crossroads of extracellular matrix and signaling in Osteogenesis imperfecta
por: Etich, Julia, et al.
Publicado: (2023)