Osteoblastic differentiation of bone marrow mesenchymal stromal cells in Bruck Syndrome

BACKGROUND: Osteogenesis Imperfecta (OI) (OMIM %259450) is a heterogeneous group of inherited disorders characterized by increased bone fragility, with clinical severity ranging from mild to lethal. The majority of OI cases are caused by mutations in COL1A1 or COL1A2. Bruck Syndrome (BS) is a furthe...

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Gepubliceerd in:BMC Med Genet
Hoofdauteurs: Kaneto, Carla M., Lima, Patrícia S. P., Zanette, Dalila Lucíola, Oliveira, Thiago Yukio Kikuchi, de Assis Pereira, Francisco, Lorenzi, Julio Cesar Cetrulo, dos Santos, Jane Lima, Prata, Karen L., Neto, João M. Pina, de Paula, Francisco J. A., Silva, Wilson A.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2016
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4857408/
https://ncbi.nlm.nih.gov/pubmed/27146342
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-016-0301-7
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