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Treatment of the amyotrophic lateral sclerosis using of genetically modified umbilical cord blood mononuclear cells in the preclinical studies fraction of umbilical cord blood cells (UCBC) by dual cassette plasmid vectors is observed. Based on our

Treatment of the amyotrophic lateral sclerosis using of genetically modified umbilical cord blood mononuclear cells in the preclinical studies fraction of umbilical cord blood cells (UCBC) by dual cassette plasmid vectors is observed. Based on our

Human umbilical cord blood mononuclear cells transfected with dual cassette plasmids (VEGF + neurotrophic factor) for the treatment of amyotrophic lateral sclerosis genes - human umbilical cord blood mononuclear cells genetically modified by dual cassette plasmids

Human umbilical cord blood mononuclear cells transfected with dual cassette plasmids (VEGF + neurotrophic factor) for the treatment of amyotrophic lateral sclerosis genes - human umbilical cord blood mononuclear cells genetically modified by dual cassette plasmids

Influence of recombinant codon‐optimized plasmid dna encoding vegf and fgf2 on co‐induction of angiogenesis plasmid to enhance healing of full thickness skin wounds in rats. The dual expression cassette plasmid p

Generation of Plasmid DNA Expressing Species-Specific Horse VEGF164 and FGF2 Factors for Gene Therapy cassette plasmid DNA (pDNA) construct containing the species-specific horse (Equus caballus) codon

Generation of Plasmid DNA Expressing Species-Specific Horse VEGF164 and FGF2 Factors for Gene Therapy cassette plasmid DNA (pDNA) construct containing the species-specific horse (Equus caballus) codon

Expression of pluripotency transcription factors in human third molar tooth germ derived multipotent mesenchymal stromal cells transfected by plasmid pBud-Sox2-Oct4In this study, the double expression cassette plasmid, based on pBudCE4.1 vector encoding

High-level expression of the monomeric SARS-CoV-2 S protein RBD 320-537 in stably transfected CHO cells by the EEF1A1-based plasmid vector pattern similar to the native S protein. Based on the previously developed p1.1 vector, containing

Expression of pluripotency transcription factors in human third molar tooth germ derived multipotent mesenchymal stromal cells transfected by plasmid pBud-Sox2-Oct4In this study, the double expression cassette plasmid, based on pBudCE4.1 vector encoding

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