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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:BMC Med Genet
Päätekijät: 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.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2016
Aiheet:
Research Article
Linkit: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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