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NCCDFWi001-A
Registration Summary
:
A
P
E
C
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
NCCDFWi001-A
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
NCCDFWi001-A (RRID:CVCL_YM45)
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar lines
No similar lines found.
Last update
19th December 2019
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Provider
Generator
National Center for Cardiovascular Diseases & Fuwai Hospital (NCCDFW)
External Databases
Cellosaurus
CVCL_YM45
Wikidata
Q95992665
General Information
Publications
Ma B et al. Generation of a human induced pluripotent stem cell line (NCCDFWi001-A) from a Marfan syndrome patient carrying two FBN1 variants (c.2613A > C and c.684_736 + 4del). Stem cell research. 2020 Jan;42:101690.
Iosef C et al. Quantitative proteomics reveal lineage-specific protein profiles in iPSC-derived Marfan syndrome smooth muscle cells. Scientific reports. 2020 Nov 23;10(1):20392.
Li T et al. Generation of a CRISPR/Cas9-corrected-hiPSC (NCCDFWi001-A-1) from a Marfan syndrome patient hiPSC with a heterozygous c.2613A>C variant in the fibrillin 1 (FBN1) gene. Stem cell research. 2021 Oct;56:102543.
Mansfield C et al. Translational potential of hiPSCs in predictive modeling of heart development and disease. Birth defects research. 2022 Oct 1;114(16):926-947.
Subclones
NCCDFWi001-A-1
hIPSC Derivation
General
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