IMEDEAi004-B

Registration Summary:

A P E C

iPS GM00879CL9

The cell line is not submitted yet.

(only basic data is shown)

General

iPSC Line
hPSCreg name	IMEDEAi004-B
Cite as:	IMEDEAi004-B (RRID:CVCL_UD90)
Alternative name(s)	iPS GM00879CL9
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	18th July 2018
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Provider
Generator	Instituto Mediterraneo de Estudios Avanzados (IMEDEA)
External iPSC Databases
Cellosaurus	CVCL_UD90
Wikidata	Q94316119
General iPSC Information
Publications	Vallejo S et al. Generation of two induced pluripotent stem cells lines from Mucopolysaccharydosis IIIA patient: IMEDEAi004-A and IMEDEAi004-B. Stem cell research. 2018 Oct;32:110-114. Wang AYL et al. Episomal Induced Pluripotent Stem Cells: Functional and Potential Therapeutic Applications. Cell transplantation. 2019 Dec;28(1_suppl):112S-131S. Pearse Y et al. A Cure for Sanfilippo Syndrome? A Summary of Current Therapeutic Approaches and their Promise. Medical research archives. 2020 Feb 1;8(2). Benetó N et al. Sanfilippo Syndrome: Molecular Basis, Disease Models and Therapeutic Approaches. International journal of molecular sciences. 2020 Oct 22;21(21). Lehmann RJ et al. Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells. Molecular genetics and metabolism reports. 2021 Dec;29:100811. Veraldi N et al. Characterization of a spontaneous cell line from primary mouse fibroblasts as a model to study Sanfilippo syndrome. The international journal of biochemistry & cell biology. 2022 Jan;142:106119. Carvalho Sofia et al. Neurological Disease Modeling Using Pluripotent and Multipotent Stem Cells: A Key Step towards Understanding and Treating Mucopolysaccharidoses. Biomedicines. 2023-04-21.

iPSC Derivation

General