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TRNDi004-I
Registration Summary
:
A
P
E
C
HT222I
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
TRNDi004-I
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
TRNDi004-I (RRID:CVCL_UL22)
Alternative name(s)
HT222I
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar lines
No similar lines found.
Last update
7th August 2018
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Provider
Generator
NIH/NCATS-TRND Branch (TRND)
External Databases
Cellosaurus
CVCL_UL22
Wikidata
Q98133589
General 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.
hIPSC Derivation
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