Differential response to intracellular stress in the skin from osteogenesis imperfecta Brtl mice with lethal and non lethal phenotype: A proteomic approach()

Phenotypic variability in the presence of an identical molecular defect is a recurrent feature in heritable disorders and it was also reported in osteogenesis imperfecta (OI). OI is a prototype for skeletal dysplasias mainly caused by mutations in the two genes coding for type I collagen. No definit...

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Dettagli Bibliografici
Pubblicato in:J Proteomics
Autori principali: Bianchi, Laura, Gagliardi, Assunta, Gioia, Roberta, Besio, Roberta, Tani, Chiara, Landi, Claudia, Cipriano, Maria, Gimigliano, Anna, Rossi, Antonio, Marini, Joan C., Forlino, Antonella, Bini, Luca
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2012
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7595140/
https://ncbi.nlm.nih.gov/pubmed/22846432
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jprot.2012.01.038
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