| Literature DB >> 30327838 |
Philipp Karschnia1, Sayoko Nishimura1, Angeliki Louvi2.
Abstract
Cerebrovascular disorders are underlain by perturbations in cerebral blood flow and abnormalities in blood vessel structure. Here, we provide an overview of the current knowledge of select cerebrovascular disorders that are associated with genetic lesions and connect genomic findings with analyses aiming to elucidate the cellular and molecular mechanisms of disease pathogenesis. We argue that a mechanistic understanding of genetic (familial) forms of cerebrovascular disease is a prerequisite for the development of rational therapeutic approaches, and has wider implications for treatment of sporadic (non-familial) forms, which are usually more common.Entities:
Keywords: Cerebrovascular disease; Genetics; Hemorrhagic cerebrovascular disease; Model organisms; Small vessel disease
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Year: 2018 PMID: 30327838 PMCID: PMC6450555 DOI: 10.1007/s00018-018-2934-5
Source DB: PubMed Journal: Cell Mol Life Sci ISSN: 1420-682X Impact factor: 9.261