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Cellosaurus HEL46.11 (CVCL_UL37)

[Text version]
Cell line name HEL46.11
Synonyms ULBi003-A
Accession CVCL_UL37
Resource Identification Initiative To cite this cell line use: HEL46.11 (RRID:CVCL_UL37)
Comments From: University of Helsinki; Helsinki; Finland.
Population: Caucasian.
Derived from site: In situ; Foreskin, skin; UBERON=UBERON_0001471.
Cell type: Fibroblast of foreskin; CL=CL_1001608.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_2769 (CCD-1112Sk)
Sex of cell Male
Age at sampling <1M
Category Induced pluripotent stem cell
Publications

PubMed=27411166; DOI=10.1002/dneu.22419
Achuta V.S., Grym H., Putkonen N., Louhivuori V., Karkkainen V., Koistinaho J., Roybon L., Castren M.L.
Metabotropic glutamate receptor 5 responses dictate differentiation of neural progenitors to NMDA-responsive cells in fragile X syndrome.
Dev. Neurobiol. 77:438-453(2017)

PubMed=28402852; DOI=10.1016/j.celrep.2017.03.055
Saarimaki-Vire J., Balboa D., Russell M.A., Saarikettu J., Kinnunen M., Keskitalo S., Malhi A., Valensisi C., Andrus C., Eurola S., Grym H., Ustinov J., Wartiovaara K., Hawkins R.D., Silvennoinen O., Varjosalo M., Morgan N.G., Otonkoski T.
An activating STAT3 mutation causes neonatal diabetes through premature induction of pancreatic differentiation.
Cell Rep. 19:281-294(2017)

PubMed=29339535; DOI=10.1126/scisignal.aan8784
Achuta V.S., Moykkynen T., Peteri U.-K., Turconi G., Rivera C., Keinanen K.P., Castren M.L.
Functional changes of AMPA responses in human induced pluripotent stem cell-derived neural progenitors in fragile X syndrome.
Sci. Signal. 11:eaan8784.1-eaan8784.11(2018)

PubMed=30247717; DOI=10.1093/nar/gky839; PMCID=PMC6212784
Cosentino C., Toivonen S., Diaz Villamil E., Atta M., Ravanat J.-L., Demine S., Schiavo A.A., Pachera N., Deglasse J.-P., Jonas J.-C., Balboa D., Otonkoski T., Pearson E.R., Marchetti P., Eizirik D.L., Cnop M., Igoillo-Esteve M.
Pancreatic beta-cell tRNA hypomethylation and fragmentation link TRMT10A deficiency with diabetes.
Nucleic Acids Res. 46:10302-10318(2018)

PubMed=30503263; DOI=10.1016/j.stemcr.2018.11.003; PMCID=PMC6294261
Danesi C., Achuta V.S., Corcoran P., Peteri U.-K., Turconi G., Matsui N., Albayrak I., Rezov V., Isaksson A., Castren M.L.
Increased calcium influx through L-type calcium channels in human and mouse neural progenitors lacking fragile X mental retardation protein.
Stem Cell Reports 11:1449-1461(2018)

Cross-references
Cell line databases/resources hPSCreg; ULBi003-A
Biological sample resources BioSamples; SAMEA5573418
Encyclopedic resources Wikidata; Q94096136
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number8