| SKIP000839 |
| SKIP ID |
SKIP000839 |
| Organism(En) |
- |
| Organism(Ja) |
- |
| Cell Type(En) |
- |
| Cell Type(Ja) |
- |
| Cell Tissue(En) |
- |
| Cell Tissue(Ja) |
- |
| Cell Origin |
Normal |
| Cell Name 1(En) |
eTKA4 |
| Cell Name 1(Ja) |
eTKA4 |
| Cell Name 2(En) |
- |
| Cell Name 2(Ja) |
- |
| Disease Name 1(Ja) |
- |
| ICD Code 1 |
- |
| Disease Name 1(En) |
- |
| OMIM1 |
- |
| Disease Name 2(Ja) |
- |
| ICD Code 2 |
- |
| Disease Name 2(En) |
- |
| OMIM 2 |
- |
| Disease Name 3(Ja) |
- |
| ICD Code 3 |
- |
| Disease Name 3(En) |
- |
| OMIM 3 |
- |
| Age |
40 |
| Age Range |
40-49 |
| Sex |
Male |
| Race(En) |
Japanese |
| Race(Ja) |
Japanese |
| Genetic Diagnosis |
-- |
| Not Detected |
No |
| Description(En) |
Healthy control iPSCs derived from T cells.
|
| Description(Ja) |
健常人T細胞由来iPS細胞 |
| Cell Morphology |
human ES-like |
| Grade |
Research Grade |
| Vector |
Plasmid |
| Transgene |
episomal plasmid vectors (containing OCT4, SOX2, KLF4, L-MYC, LIN28, EBNA1, and dominant-negative p53) |
| Adhesiveness |
- |
| Feeder |
Yes |
| Feeder Cell |
SNL |
| Medium |
Primate ES Cell Medium+4ng/mL human basic FGF |
| Genome Editing |
- |
| CO2 |
- |
| Mycoplasma |
- |
| Detection of Contaminants Mycoplasma |
- |
| Pluripotent Markers |
Yes |
| Pluripotent Markers Assay |
Immunocytochemical analysis |
| in vitro Differentiation |
Yes |
| in vitro Differentiation Assay |
neural differentiation |
| in vivo Differentiation |
- |
| in vivo Differentiation Assay |
- |
| Other 1 Assay |
Yes |
| Other 1 Assay Method |
qPCR |
| Other 2 Assay |
- |
| Other 2 Assay Method |
- |
| Other 3 Assay |
- |
| Other 3 Assay Method |
- |
| Karyotype |
- |
| Karyotype Assay |
- |
| Remaining Vector Detection |
- |
| Remaining Vector Detection Assay |
- |
| STR |
- |
| HLA |
- |
| Stem Cell Transcriptome analysis |
- |
| Stem Cell Transcriptome analysis Assay |
- |
| Author Name(En) |
Hideyuki Okano |
| Author Name(Ja) |
岡野栄之 |
| Author Organization(En) |
Keio University, School of Medicine, Department of Physiology |
| Author Organization(Ja) |
慶應義塾大学 医学部 生理学教室 |
| Author Contact Email |
hidokano[at]a2[dot]keio[dot]jp |
| PI Organization(En) |
Keio University, School of Medicine, Department of Physiology |
| PI Organization(Ja) |
慶應義塾大学 医学部 生理学教室 |
| PI Name(En) |
Hideyuki Okano |
| PI Name(Ja) |
岡野栄之 |
| PI Contact Email |
hidokano[at]a2[dot]keio[dot]jp |
| Availability |
Information Only |
| Provider Organization(En) |
Keio University, School of Medicine, Department of Physiology |
| Provider Organization(Ja) |
慶應義塾大学 医学部 生理学教室 |
| Provider Email |
- |
| Provider URL |
- |
| Ethical Statement(En) |
- |
| Ethical Statement(Ja) |
- |
| Terms of Use(En) |
- |
| Terms of Use(Ja) |
- |
| PubMed ID |
26905201 |
| DOI |
10.1016/j.stemcr.2016.01.010 |
| Title |
Functional Neurons Generated from T Cell-Derived Induced Pluripotent Stem Cells for Neurological Disease Modeling. |
| Authors |
Matsumoto T, Fujimori K, Andoh-Noda T, Ando T, Kuzumaki N, Toyoshima M, Tada H, Imaizumi K, Ishikawa M, Yamaguchi R, Isoda M, Zhou Z, Sato S, Kobayashi T, Ohtaka M, Nishimura K, Kurosawa H, Yoshikawa T, Takahashi T, Nakanishi M, Ohyama M, Hattori N, Akamatsu W, Okano H |
| Journal |
Stem Cell Reports |
| Year |
2016 |
| Volume |
6 |
| Issue |
3 |
| Pages |
422-35 |
| URL |
http://www.ncbi.nlm.nih.gov/pubmed/26905201 |
| Free input |
- |
| Note |
- |