LAMA2 Neuropathies: Human Findings and Pathomechanisms From Mouse Models
Sign Up to like & getrecommendations! Published in 2020 at "Frontiers in Molecular Neuroscience"
DOI: 10.3389/fnmol.2020.00060
Abstract: Merosin deficient Congenital Muscular Dystrophy (MDC1A), or LAMA2-related muscular dystrophy (LAMA2-RD), is a recessive disorder resulting from mutations in the LAMA2 gene, encoding for the alpha-2 chain of laminin-211. The disease is predominantly characterized by… read more here.
Keywords: mouse models; neuropathies human; findings pathomechanisms; muscular dystrophy ... See more keywords
Benzene Exposure and MicroRNAs Expression: In Vitro, In Vivo and Human Findings
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DOI: 10.3390/ijerph20031920
Abstract: MicroRNAs (miRNAs) are important regulators of gene expression and define part of the epigenetic signature. Their influence on human health is established and interest in them is progressively increasing. Environmental and occupational risk factors affecting… read more here.
Keywords: health; benzene exposure; expression; human findings ... See more keywords