Quantitative proteomics reveal lineage-specific protein profiles in iPSC-derived Marfan syndrome smooth muscle cells

Marfan syndrome (MFS) is a connective tissue disorder caused by mutations in the FBN1 gene that produces wide disease phenotypic variability. The lack of ample genotype–phenotype correlation hinders translational study development aimed at improving disease prognosis. In response to this need, an in...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Iosef, Cristiana, Pedroza, Albert J., Cui, Jason Z., Dalal, Alex R., Arakawa, Mamoru, Tashima, Yasushi, Koyano, Tiffany K., Burdon, Grayson, Churovich, Samantha M. P., Orrick, Joshua O., Pariani, Mitchel, Fischbein, Michael P.
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7683538/
https://ncbi.nlm.nih.gov/pubmed/33230159
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-77274-w
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