000			nab a22 7a 4500
999			_c17852 _d17852
003			PC17852
005			20240527123046.0
008			240527b xxu||||| |||| 00| 0 eng d
040			_cH12O
041			_aeng
100			_93406 _aZurita, Francisco _eInstituto de Investigación imas12
100			_93407 _aGalera, Teresa _eInstituto de Investigación imas12
100			_93408 _aGonzález Páramos, Cristina _eInstituto de Investigación imas12
100			_92421 _aMoreno Izquierdo, Ana _eGenética
100			_9862 _aGaresse, Rafael _eInstituto de Investigación i+12
100			_92795 _aGallardo, María Esther _eInstituto de Investigación i+12
245	0	0	_aGeneration of a human iPSC line from a patient with a defect of intergenomic communication. _h[artículo]
260			_bStem cell research, _c2016
300			_a16(1):120-3.
500			_aFormato 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.
501			_aPMID: 27345795
504			_aContiene 3 referencias
520			_aHuman 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.
710			_9625 _aInstituto de Investigación imas12
856			_uhttp://pc-h12o-es.m-hdoct.a17.csinet.es/pdf/pc/1/pc17852.pdf _ySolicitar documento
942			_2ddc _cART _n0