SDQLCHi007-A

Registration Summary:

A P E C

The cell line is not submitted yet.

(only basic data is shown)

General

Cell Line
hPSCreg name	SDQLCHi007-A
Cite as:	SDQLCHi007-A (RRID:CVCL_XJ79)
Cell line type	Human induced pluripotent stem cell (hiPSC)
Similar lines	No similar lines found.
Last update	27th November 2019
User feedback	Written by on No feedback available yet. Login to share your feedback, experiences or results with the research community.
Provider
Generator	Children’s Hospital affiliated to Shandong University (SDQLCH)
External Databases
Cellosaurus	CVCL_XJ79
Wikidata	Q98129458
General Information
Publications	Guan J et al. Reprogramming of human Peripheral Blood Mononuclear Cell (PBMC) from a Chinese patient suffering Duchenne muscular dystrophy to iPSC line (SDQLCHi007-A) carrying deletion of 49-50 exons in the DMD gene. Stem cell research. 2020 Jan;42:101666. Rovina D et al. "Betwixt Mine Eye and Heart a League Is Took": The Progress of Induced Pluripotent Stem-Cell-Based Models of Dystrophin-Associated Cardiomyopathy. International journal of molecular sciences. 2020 Sep 23;21(19). Ray A et al. An Overview on Promising Somatic Cell Sources Utilized for the Efficient Generation of Induced Pluripotent Stem Cells. Stem cell reviews and reports. 2021 Dec;17(6):1954-1974. Kim Hyun-Jun et al. Keeping your strength up: induced pluripotent stem cell-based approaches for the treatment and investigation of skeletal muscle disorders. All Life. 2023-12-04. Liu Yue et al. Duchenne muscular dystrophy caused by a deletion (c.5021del) in exon 35 of the DMD gene: A case report and review of the literature. Heliyon. 2024-04-00.

hIPSC Derivation

General