Generation of human induced pluripotent stem cell lines derived from four DiGeorge syndrome patients with 22q11.2 deletion

DiGeorge syndrome (22q11.2 deletion syndrome, or CATCH22 syndrome), caused by hemizygous deletion of chromosome 22q11.2, results in the poor development of multiple organs. Here we have generated DiGeorge syndrome-specific human induced pluripotsnt stem cells (hiPSCs) derived from four patients. The...

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Hlavní autoři: Tomoya Shimizu, Mami Matsuo-Takasaki, Dorian Luijkx, Miho Takami, Yutaka Arai, Michiya Noguchi, Yukio Nakamura, Tadayoshi Hayata, Megumu K. Saito, Yohei Hayashi
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2022-05-01
Edice:Stem Cell Research
On-line přístup:http://www.sciencedirect.com/science/article/pii/S1873506122000939
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