Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1
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Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1. / Tubsuwan, Alisa; Pires, Carlota; Rasmussen, Mikkel A.; Schmid, Benjamin; Nielsen, Jørgen Erik; Hjermind, Lena Elisabeth; Hall, Vanessa Jane; Nielsen, Troels Tolstrup; Waldemar, Gunhild; Hyttel, Poul; Clausen, Christian; Kitiyanant, Narisorn; Freude, Kristine; Holst, Bjørn.
I: Stem Cell Research, Bind 16, Nr. 1, 01.2016, s. 110-112.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1
AU - Tubsuwan, Alisa
AU - Pires, Carlota
AU - Rasmussen, Mikkel A.
AU - Schmid, Benjamin
AU - Nielsen, Jørgen Erik
AU - Hjermind, Lena Elisabeth
AU - Hall, Vanessa Jane
AU - Nielsen, Troels Tolstrup
AU - Waldemar, Gunhild
AU - Hyttel, Poul
AU - Clausen, Christian
AU - Kitiyanant, Narisorn
AU - Freude, Kristine
AU - Holst, Bjørn
PY - 2016/1
Y1 - 2016/1
N2 - Induced pluripotent stem cells (iPSCs) were generated from skin fibroblasts isolated from a 58-year old male with a L150P mutation in the presenilin 1 (PSEN-1) gene, which is responsible for the majority of familial cases of Alzheimer's disease (AD). The iPSC swere established by co-electroporation with episomal plasmids containing hOCT4, hSOX2, hL-MYC, hKLF4, hNANOG, hLIN28, and short hairpin RNA against TP53. The iPSCs contained the specific heterozygous mutation c.449C>T, had normal karyotype, expressed the expected pluripotency genes and displayed in vitro differentiation potential to the three germ layers. The iPSCsmay be useful for studying familialAD pathology in vitro.
AB - Induced pluripotent stem cells (iPSCs) were generated from skin fibroblasts isolated from a 58-year old male with a L150P mutation in the presenilin 1 (PSEN-1) gene, which is responsible for the majority of familial cases of Alzheimer's disease (AD). The iPSC swere established by co-electroporation with episomal plasmids containing hOCT4, hSOX2, hL-MYC, hKLF4, hNANOG, hLIN28, and short hairpin RNA against TP53. The iPSCs contained the specific heterozygous mutation c.449C>T, had normal karyotype, expressed the expected pluripotency genes and displayed in vitro differentiation potential to the three germ layers. The iPSCsmay be useful for studying familialAD pathology in vitro.
U2 - 10.1016/j.scr.2015.12.015
DO - 10.1016/j.scr.2015.12.015
M3 - Journal article
C2 - 27345792
VL - 16
SP - 110
EP - 112
JO - Stem Cell Research
JF - Stem Cell Research
SN - 1873-5061
IS - 1
ER -
ID: 162605874