SDQLCHi014-A

Registration Summary:

A P E C

The cell line is not submitted yet.

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General

iPSC Line
hPSCreg name	SDQLCHi014-A
Cite as:	SDQLCHi014-A (RRID:CVCL_YI67)
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	4th November 2019
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Provider
Generator	Children’s Hospital affiliated to Shandong University (SDQLCH)
External iPSC Databases
Cellosaurus	CVCL_YI67
Wikidata	Q98129475
General iPSC Information
Publications	Yang X et al. An induced pluripotent stem cells line (SDQLCHi014-A) derived from urine cells of a patient with ASD and hyperactivity carrying a 303 kb de novo deletion at chr3p26.1 implicating GRM7 gene. Stem cell research. 2019 Dec;41:101635. Casamassa A et al. A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15. International journal of molecular sciences. 2020 Mar 9;21(5). Wang X et al. Overexpression of mGluR7 in the Prefrontal Cortex Attenuates Autistic Behaviors in Mice. Frontiers in cellular neuroscience. 2021;15:689611. 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. Baliña-Sánchez C et al. Generation of mesenchymal stromal cells from urine-derived iPSCs of pediatric brain tumor patients. Frontiers in immunology. 2023;14:1022676. Zaki-Dizaji Majid et al. GRM7 deficiency, from excitotoxicity and neuroinflammation to neurodegeneration: Systematic review of GRM7 deficient patients. Brain, Behavior, & Immunity - Health. 2024-08-00.

iPSC Derivation

General