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DPY-17 and MUA-3 Interact for Connective Tissue-Like Tissue Integrity in Caenorhabditis elegans: A Model for Marfan Syndrome

mua-3 is a Caenorhabditis elegans homolog of the mammalian fibrillin1, a monogenic cause of Marfan syndrome. We identified a new mutation of mua-3 that carries an in-frame deletion of 131 amino acids in the extracellular domain, which allows the mutants to survive in a temperature-dependent manner;...

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Detalhes bibliográficos
Publicado no:G3 (Bethesda)
Main Authors: Fotopoulos, Pauline, Kim, Jeongho, Hyun, Moonjung, Qamari, Waiss, Lee, Inhwan, You, Young-Jai
Formato: Artigo
Idioma:Inglês
Publicado em: Genetics Society of America 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4502371/
https://ncbi.nlm.nih.gov/pubmed/25917920
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/g3.115.018465
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