Human iPS cell-derived mural cells as an in vitro model of hereditary cerebral small vessel disease
Human iPS cell-derived mural cells as an in vitro model of hereditary cerebral small vessel disease
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Author / Creator
Yamamoto, Yumi , Kojima, Katsutoshi , Taura, Daisuke , Sone, Masakatsu , Washida, Kazuo , Egawa, Naohiro , Kondo, Takayuki , Minakawa, Eiko N. , Tsukita, Kayoko , Enami, Takako , Tomimoto, Hidekazu , Mizuno, Toshiki , Kalaria, Raj N. , Inagaki, Nobuya , Takahashi, Ryosuke , Harada-Shiba, Mariko , Ihara, Masafumi and Inoue, Haruhisa
Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is one of the most common forms of hereditary cerebral small vessel diseases and is caused by mutations in
NOTCH3
. Our group has previously reported incorporation of NOTCH3 extracellular domain (N3ECD) in the CADASIL-specific granular osmioph...
Alternative Titles
Full title
Human iPS cell-derived mural cells as an in vitro model of hereditary cerebral small vessel disease
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Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_b9af76ea335a4855af63285e62998857
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b9af76ea335a4855af63285e62998857
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ISSN
1756-6606
E-ISSN
1756-6606
DOI
10.1186/s13041-020-00573-w
