YAHKMUi001-A

A P E C

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Cell Line
hPSCreg name	YAHKMUi001-A
Cite as:	YAHKMUi001-A (RRID:CVCL_WU87)
Cell line type	Human induced pluripotent stem cell (hiPSC)
Similar lines	No similar lines found.
Last update	26th March 2019
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Provider
Generator	Yan'an Affiliated Hospital of Kunming Medical University (YAHKMU)
External Databases
Cellosaurus	CVCL_WU87
Wikidata	Q98136371
General Information
Publications	Han S et al. Generation of human iPSC line from a patient with Tetralogy of Fallot, YAHKMUi001-A, carrying a mutation in TBX1 gene. Stem cell research. 2020 Jan;42:101687. Rufaihah AJ et al. Mending a broken heart: In vitro, in vivo and in silico models of congenital heart disease. Disease models & mechanisms. 2021 Mar 28;14(3). Kalayinia S et al. Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot. Laboratory medicine. 2021 Nov 2;52(6):614-618. Yin XY et al. Genetic Variants of ISL1 Gene Promoter Identified from Congenital Tetralogy of Fallot Patients Alter Cellular Function Forming Disease Basis. Biomolecules. 2023 Feb 13;13(2). Maddhesiya Jyoti et al. Understanding the Genetic and Non-genetic Interconnections in the Aetiology of Isolated Congenital Heart Disease: An Updated Review: Part 1. Current Cardiology Reports. 2024-03-00.