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Cellosaurus NUIGi022-B (CVCL_XI98)

[Text version]

Cell line name NUIGi022-B
Synonyms ND11C7
Accession CVCL_XI98
Resource Identification Initiative To cite this cell line use: NUIGi022-B (RRID:CVCL_XI98)
Comments From: National University of Ireland Galway; Galway; Ireland.
Population: Caucasian.
Derived from sampling site: Skin.
Sequence variations Heterozygous for NRXN1 Ex1-5del (PubMed=31759289).
Disease Autism spectrum disorder (NCIt: C88412)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_WT08 ! NUIGi022-A
Sex of cell Male
Age at sampling 14Y
Category Induced pluripotent stem cell
Publications

PubMed=31759289; DOI=10.1016/j.scr.2019.101653
Ding Y., Marco de la Cruz B., Xia Y., Liu M., Lu Y., McInerney V., Krawczyk J., Lynch S.A., Howard L., O'Brien T., Gallagher L., Shen S.
Derivation of familial iPSC lines from three ASD patients carrying NRXN1alpha(+/-) and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B NUIGi026-A, NUIGi026-B).
Stem Cell Res. 41:101653-101653(2019)

Cross-references
Cell line databases/resources hPSCreg; NUIGi022-B
Biological sample resources BioSamples; SAMEA6032107
Entry history
Entry creation19-Dec-2019
Last entry updated19-Dec-2019
Version number1