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Quantitative proteomic analysis of amniocytes reveals potentially dysregulated molecular networks in Down syndrome

BACKGROUND: Down syndrome (DS), caused by an extra copy of chromosome 21, affects 1 in 750 live births and is characterized by cognitive impairment and a constellation of congenital defects. Currently, little is known about the molecular pathogenesis and no direct genotype-phenotype relationship has...

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Détails bibliographiques
Auteurs principaux: Cho, Chan-Kyung J, Drabovich, Andrei P, Karagiannis, George S, Martínez-Morillo, Eduardo, Dason, Shawn, Dimitromanolakis, Apostolos, Diamandis, Eleftherios P
Format: Artigo
Langue:Inglês
Publié: Springer 2013
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3626793/
https://ncbi.nlm.nih.gov/pubmed/23394617
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1559-0275-10-2
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