APDS2 is caused by mutations in PIK3R1 gene resulting in constitutive PI3Kδ activation. PI3Kδ is predominantly expressed in leukocytes and plays critical roles in regulating immune responses. Here we first derived fibroblast primary cells from a skin biopsy of a patient carrying a heterozygous single T deletion in intron 11 of the PIK3R1 gene. We next present the derivation of an induced pluripotent stem cell (iPS) line using a non-integrative reprogramming technology. Pluripotent-related hallmarks are further shown, including: iPSCs self-renewal and expression of pluripotent and differentiation markers after in vitro differentiation towards embryonic germ layers, assessed by RT-PCR and immunofluorescence
A human induced pluripotent stem cell (hiPSC) line (UCLi013-A) was generated from fibroblast cells o...
An induced pluripotent stem cell (iPSC) line was generated from a 36-year-old patient with sporadic ...
Heterozygous mutations within Keratin 5 (KRT5) are common genetic causes of epidermolysis bullosa si...
The effects of genetic mutations on protein function can be studied in a physiologically relevant en...
Abstract Peripheral blood mononuclear cells (PBMCs) derived from a healthy 40-year-old female were s...
The human pluripotent stem cells are able to differentiate into all cell types of the three primary ...
We have generated UQACi001-A, a new induced pluripotent stem cell (iPSC) line derived from skin fibr...
We have generated two human induced pluripotent stem cell (iPSC) lines from CD133+ cells isolated fr...
Four disease-specific induced pluripotent stem cell (iPSC) lines were respectively derived from peri...
Patient-derived induced pluripotent stem cells (iPSC) are a valuable approach to model cardiovascula...
The use of induced pluripotent stem cells (iPSC) derived from independent patients and sources holds...
AbstractIn this work we describe for the first time the generation and characterization of human ind...
AbstractHere we describe the generation and characterization of the human induced pluripotent stem c...
One of the recent breakthroughs in stem cell research has been the reprogramming of human somatic ce...
Mosaic, activating mutations in PIK3CA, the gene encoding the catalytic p110α subunit of class IA ph...
A human induced pluripotent stem cell (hiPSC) line (UCLi013-A) was generated from fibroblast cells o...
An induced pluripotent stem cell (iPSC) line was generated from a 36-year-old patient with sporadic ...
Heterozygous mutations within Keratin 5 (KRT5) are common genetic causes of epidermolysis bullosa si...
The effects of genetic mutations on protein function can be studied in a physiologically relevant en...
Abstract Peripheral blood mononuclear cells (PBMCs) derived from a healthy 40-year-old female were s...
The human pluripotent stem cells are able to differentiate into all cell types of the three primary ...
We have generated UQACi001-A, a new induced pluripotent stem cell (iPSC) line derived from skin fibr...
We have generated two human induced pluripotent stem cell (iPSC) lines from CD133+ cells isolated fr...
Four disease-specific induced pluripotent stem cell (iPSC) lines were respectively derived from peri...
Patient-derived induced pluripotent stem cells (iPSC) are a valuable approach to model cardiovascula...
The use of induced pluripotent stem cells (iPSC) derived from independent patients and sources holds...
AbstractIn this work we describe for the first time the generation and characterization of human ind...
AbstractHere we describe the generation and characterization of the human induced pluripotent stem c...
One of the recent breakthroughs in stem cell research has been the reprogramming of human somatic ce...
Mosaic, activating mutations in PIK3CA, the gene encoding the catalytic p110α subunit of class IA ph...
A human induced pluripotent stem cell (hiPSC) line (UCLi013-A) was generated from fibroblast cells o...
An induced pluripotent stem cell (iPSC) line was generated from a 36-year-old patient with sporadic ...
Heterozygous mutations within Keratin 5 (KRT5) are common genetic causes of epidermolysis bullosa si...