TRNDi007-B

Registration Summary:

A P E C

iPSC HT521B

The cell line is not submitted yet.

(only basic data is shown)

General

iPSC Line
hPSCreg name	TRNDi007-B
Cite as:	TRNDi007-B (RRID:CVCL_UL27)
Alternative name(s)	iPSC HT521B
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	27th March 2019
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Provider
Generator	NIH/NCATS-TRND Branch (TRND)
External iPSC Databases
Cellosaurus	CVCL_UL27
Wikidata	Q98133596
General iPSC Information
Publications	Corbett JL et al. iPSC-Derived Hepatocytes as a Platform for Disease Modeling and Drug Discovery. Frontiers in medicine. 2019;6:265. Cheng YS et al. A human induced pluripotent stem cell line (TRNDi007-B) from an infantile onset Pompe patient carrying p.R854X mutation in the GAA gene. Stem cell research. 2019 May;37:101435. Chulpanova Daria S. et al. iPSCs for modeling lysosomal storage diseases. Recent Advances in iPSC Disease Modeling, Volume 1. 2020-00-00. Cheng YS et al. Modeling CNS Involvement in Pompe Disease Using Neural Stem Cells Generated from Patient-Derived Induced Pluripotent Stem Cells. Cells. 2020 Dec 22;10(1). Escribá R et al. Inborn errors of metabolism: Lessons from iPSC models. Reviews in endocrine & metabolic disorders. 2021 Dec;22(4):1189-1200. Zhang H et al. Case Report: Identification of Compound Heterozygous Mutations in a Patient With Late-Onset Glycogen Storage Disease Type II (Pompe Disease). Frontiers in neurology. 2022;13:839263. Aguilar-González A et al. Isogenic GAA-KO Murine Muscle Cell Lines Mimicking Severe Pompe Mutations as Preclinical Models for the Screening of Potential Gene Therapy Strategies. International journal of molecular sciences. 2022 Jun 4;23(11). Christensen C et al. Generation of two induced pluripotent stem cell lines (CHOCi002-A and CHOCi003-A) from Pompe disease patients with compound heterozygous mutations in the GAA gene. Stem cell research. 2023 Jun;69:103117. Cheng Yu‐Shan et al. A Protocol for Culture and Characterization of Human Induced Pluripotent Stem Cells After Induction. Current Protocols. 2023-08-00. Martinez‐Montoya Valentina et al. Mutational spectrum and genotype–phenotype correlation in Mexican patients with infantile‐onset and late‐onset Pompe disease. Molecular Genetics & Genomic Medicine. 2024-07-00. Andriianov Vladimir et al. Application of Induced Pluripotent Stem Cells (iPSCs) in Hereditary and Viral Diseases of the Liver: Modeling and Treatment. International Journal of Molecular Sciences. 2025-09-26.

iPSC Derivation

General