TRNDi002-B

Registration Summary:

A P E C

iPSC HT519B

The cell line is not submitted yet.

(only basic data is shown)

General

Cell Line
hPSCreg name	TRNDi002-B
Cite as:	TRNDi002-B (RRID:CVCL_UL09)
Alternative name(s)	iPSC HT519B
Cell line type	Human induced pluripotent stem cell (hiPSC)
Similar lines	No similar lines found.
Last update	27th March 2019
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Provider
Generator	NIH/NCATS-TRND Branch (TRND)
External Databases
Cellosaurus	CVCL_UL09
Wikidata	Q98133573
General Information
Publications	Li R et al. Generation of an induced pluripotent stem cell line (TRNDi002-B) from a patient carrying compound heterozygous p.Q208X and p.G310G mutations in the NGLY1 gene. Stem cell research. 2019 Jan;34:101362. Farkhondeh A et al. Induced pluripotent stem cells for neural drug discovery. Drug discovery today. 2019 Apr;24(4):992-999. Hong J et al. Generation of an induced pluripotent stem cell line (TRNDi008-A) from a Hunter syndrome patient carrying a hemizygous 208insC mutation in the IDS gene. Stem cell research. 2019 May;37:101451. Huang W et al. An induced pluripotent stem cell line (TRNDi006-A) from a MPS IIIB patient carrying homozygous mutation of p.Glu153Lys in the NAGLU gene. Stem cell research. 2019 May;37:101427. Miller DB et al. CompoundHetVIP: Compound Heterozygous Variant Identification Pipeline. F1000Research. 2020;9:1211. Pradhan M et al. An induced pluripotent stem cell line (NCATS-CL9075) from a patient carrying compound heterozygote mutations, p.R390P and p.L318P, in the NGLY1 gene. Stem cell research. 2021 Jul;54:102400. Sasserath T et al. An induced pluripotent stem cell-derived NMJ platform for study of the NGLY1-Congenital Disorder of Deglycosylation. Advanced therapeutics. 2022 Nov;5(11). Abbott J et al. Generation and characterization of NGLY1 patient-derived midbrain organoids. Frontiers in cell and developmental biology. 2023;11:1039182.

hIPSC Derivation

General