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The feelgood mutation in zebrafish dysregulates COPII-dependent secretion of select extracellular matrix proteins in skeletal morphogenesis

Craniofacial and skeletal dysmorphologies account for the majority of birth defects. A number of the disease phenotypes have been attributed to abnormal synthesis, maintenance and composition of extracellular matrix (ECM), yet the molecular and cellular mechanisms causing these ECM defects remain po...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Melville, David B., Montero-Balaguer, Mercedes, Levic, Daniel S., Bradley, Kevin, Smith, Jeffrey R., Hatzopoulos, Antonis K., Knapik, Ela W.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The Company of Biologists Limited 2011
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3209646/
https://ncbi.nlm.nih.gov/pubmed/21729877
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.007625
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