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Publication
PropertyValue
Working Groups AG Cyganek
SubprojectS01
Open AccessOpen Access Yes
Publication TypeJournal Article
Peer ReviewedYes
DOIDOI 10.1016/j.scr.2023.103108
Publication Year2023
TitleGeneration of a genetically-modified induced pluripotent stem cell line harboring a Noonan syndrome-associated gene variant MRAS p.G23V
JournalStem Cell Research
ISSN1873-5061
eISSN1876-7753
URL http://dx.doi.org/10.1016/j.scr.2023.103108
Pages103108
Journal AbbreviationStem Cell Res
AuthorsBusley AV, Cyganek L
First AuthorBusley AV
Last AuthorCyganek L

 External Resources

 scienced...in.pdf  Article fulltext

 VCV000635781.3  NCBI clinvar (VCV000635781.3)

 NM_001085049.3  NCBI nucleotide (NM_001085049.3, reused)

 0000-0002-5036-0093  ORCID identifier (Alexandra Viktoria Busley)

 0000-0001-9120-1382  ORCID identifier (Lukas Cyganek)

 693  Published Data Registry entry (MBExC)

 031t5w623  ROR identifier (031t5w623, German Centre for Cardiovascular Research)

 05xy1nn52  ROR identifier (05xy1nn52, Multiscale Bioimaging)

 021ft0n22  ROR identifier (021ft0n22, University Medical Center Göttingen)

 AB_1645318  SciCrunch identifier (RRID:AB_1645318)

 AB_2784442  SciCrunch identifier (RRID:AB_2784442)

 AB_2536677  SciCrunch identifier (RRID:AB_2536677)

 AB_778563  SciCrunch identifier (RRID:AB_778563)

 AB_1645379  SciCrunch identifier (RRID:AB_1645379)

 AB_2650473  SciCrunch identifier (RRID:AB_2650473)

 AB_476701  SciCrunch identifier (RRID:AB_476701)

 AB_2728521  SciCrunch identifier (RRID:AB_2728521)

 AB_476766  SciCrunch identifier (RRID:AB_476766)

 AB_2147453  SciCrunch identifier (RRID:AB_2147453)

 AB_10950895  SciCrunch identifier (RRID:AB_10950895)

 AB_477629  SciCrunch identifier (RRID:AB_477629)

 AB_143165  SciCrunch identifier (RRID:AB_143165)

 AB_2536180  SciCrunch identifier (RRID:AB_2536180)

 AB_2722659  SciCrunch identifier (RRID:AB_2722659)

 AB_772210  SciCrunch identifier (RRID:AB_772210)

 CVCL_A4ZE  SciCrunch identifier (RRID:CVCL_A4ZE, UMGi014-C)

Linked Cellmodels

hPSCreg NameCell TypeICD CodeDiseaseSourceReprogrammingGrade
UMGi014-C-17iPSCResearch