TRNDi009-C

Registration Summary:

A P E C

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General

Cell Line
hPSCreg name	TRNDi009-C
Cite as:	TRNDi009-C (RRID:CVCL_WU20)
Cell line type	Human induced pluripotent stem cell (hiPSC)
Similar lines	No similar lines found.
Last update	9th January 2019
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Provider
Generator	NIH/NCATS-TRND Branch (TRND)
External Databases
Cellosaurus	CVCL_WU20
Wikidata	Q98133601
General Information
Publications	Baskfield A et al. An induced pluripotent stem cell line (TRNDi009-C) from a Niemann-Pick disease type A patient carrying a heterozygous p.L302P (c.905 T>C) mutation in the SMPD1 gene. Stem cell research. 2019 Jul;38:101461. Ruiz JP et al. Robust generation of erythroid and multilineage hematopoietic progenitors from human iPSCs using a scalable monolayer culture system. Stem cell research. 2019 Dec;41:101600. Chulpanova Daria S. et al. iPSCs for modeling lysosomal storage diseases. Recent Advances in iPSC Disease Modeling, Volume 1. 2020-00-00. Zhou H et al. Rare Diseases Related with Lipoprotein Metabolism. Advances in experimental medicine and biology. 2020;1276:171-188. Zhou H et al. Rare Diseases in Glycosphingolipid Metabolism. Advances in experimental medicine and biology. 2022;1372:189-213. 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. Dursun FE et al. SMPD1 gene variants in patients with β-Thalassemia major. Molecular biology reports. 2023 Apr;50(4):3355-3363. Li Y et al. Modulation of WNT, Activin/Nodal, and MAPK Signaling Pathways Increases Arterial Hemogenic Endothelium and Hematopoietic Stem/Progenitor Cell Formation During Human iPSC Differentiation. Stem cells (Dayton, Ohio). 2023 Jul 14;41(7):685-697.

hIPSC Derivation

General