TRNDi004-I

Registration Summary:

A P E C

HT222I

The cell line is not submitted yet.

(only basic data is shown)

General

iPSC Line
hPSCreg name	TRNDi004-I
Cite as:	TRNDi004-I (RRID:CVCL_UL22)
Alternative name(s)	HT222I
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	7th August 2018
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Provider
Generator	NIH/NCATS-TRND Branch (TRND)
External iPSC Databases
Cellosaurus	CVCL_UL22
Wikidata	Q98133589
General iPSC Information
Publications	Baskfield A et al. Generation of an induced pluripotent stem cell line (TRNDi004-I) from a Niemann-Pick disease type B patient carrying a heterozygous mutation of p.L43_A44delLA in the SMPD1 gene. Stem cell research. 2019 May;37:101436. Chulpanova Daria S. et al. iPSCs for modeling lysosomal storage diseases. Recent Advances in iPSC Disease Modeling, Volume 1. 2020-00-00. Sabitha KR et al. Delineating the Neuropathology of Lysosomal Storage Diseases Using Patient-Derived Induced Pluripotent Stem Cells. Stem cells and development. 2022 May;31(9-10):221-238. Gaudioso Á et al. Models to study basic and applied aspects of lysosomal storage disorders. Advanced drug delivery reviews. 2022 Nov;190:114532.

iPSC Derivation

General