Zurita, Francisco Galera, Teresa González Páramos, Cristina Moreno Izquierdo, Ana Garesse, Rafael Gallardo, María Esther
Generation of a human iPSC line from a patient with a defect of intergenomic communication. [artículo] - Stem cell research, 2016 - 16(1):120-3.
Formato Vancouver:
Zurita F, Galera T, González Páramos C, Moreno Izquierdo A, Schneiderat P, Fraga MF et al. Generation of a human iPSC line from a patient with a defect of intergenomic communication. Stem Cell Res. 2016 Jan;16(1):120-3.
PMID: 27345795
Contiene 3 referencias
Human iPSC line PG64SV.2 was generated from fibroblasts of a patient with a defect of intergenomic communication. This patient harbored a homozygous mutation (c.2243G>C; p.Trp748Ser) in the gene encoding the catalytic subunit of the mitochondrial DNA polymerase gamma gene (POLG). Reprogramming factors Oct3/4, Sox2, Klf4, and cMyc were delivered using a non integrative methodology that involves the use of Sendai virus.
Generation of a human iPSC line from a patient with a defect of intergenomic communication. [artículo] - Stem cell research, 2016 - 16(1):120-3.
Formato Vancouver:
Zurita F, Galera T, González Páramos C, Moreno Izquierdo A, Schneiderat P, Fraga MF et al. Generation of a human iPSC line from a patient with a defect of intergenomic communication. Stem Cell Res. 2016 Jan;16(1):120-3.
PMID: 27345795
Contiene 3 referencias
Human iPSC line PG64SV.2 was generated from fibroblasts of a patient with a defect of intergenomic communication. This patient harbored a homozygous mutation (c.2243G>C; p.Trp748Ser) in the gene encoding the catalytic subunit of the mitochondrial DNA polymerase gamma gene (POLG). Reprogramming factors Oct3/4, Sox2, Klf4, and cMyc were delivered using a non integrative methodology that involves the use of Sendai virus.
