Induced pluripotent stem cells (iPSCs) derived from a symptomatic carrier of a S305I mutation in the microtubule-associated protein tau (MAPT)-gene causing frontotemporal dementia
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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Induced pluripotent stem cells (iPSCs) derived from a symptomatic carrier of a S305I mutation in the microtubule-associated protein tau (MAPT)-gene causing frontotemporal dementia. / Nimsanor, Natakarn; Jørring, Ida; Rasmussen, Mikkel A.; Clausen, Christian; Mau-Holzmann, Ulrike A; Kitiyanant, Narisorn; Nielsen, Jørgen E; Nielsen, Troels T; Hyttel, Poul; Holst, Bjørn; Schmid, Benjamin.
I: Stem Cell Research, Bind 17, Nr. 3, 11.2016, s. 564-567.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Induced pluripotent stem cells (iPSCs) derived from a symptomatic carrier of a S305I mutation in the microtubule-associated protein tau (MAPT)-gene causing frontotemporal dementia
AU - Nimsanor, Natakarn
AU - Jørring, Ida
AU - Rasmussen, Mikkel A.
AU - Clausen, Christian
AU - Mau-Holzmann, Ulrike A
AU - Kitiyanant, Narisorn
AU - Nielsen, Jørgen E
AU - Nielsen, Troels T
AU - Hyttel, Poul
AU - Holst, Bjørn
AU - Schmid, Benjamin
N1 - Copyright © 2016. Published by Elsevier B.V.
PY - 2016/11
Y1 - 2016/11
N2 - Frontotemporal dementia with parkinsonism linked to chromosome 17q21.2 (FTDP-17) is an autosomal-dominant neurodegenerative disorder. Mutations in the gene coding the microtubule-associated protein tau (MAPT) can cause FTDP-17 but the underlying mechanisms of the disease are still unknown. Induced pluripotent stem cells (iPSCs) hold great promise to model FTDP-17 as such cells can be differentiated in vitro to the required neuronal cell type. Here, we report the generation of iPSCs from a 44-year-old symptomatic woman carrying a S305I mutation in the MAPT-gene.
AB - Frontotemporal dementia with parkinsonism linked to chromosome 17q21.2 (FTDP-17) is an autosomal-dominant neurodegenerative disorder. Mutations in the gene coding the microtubule-associated protein tau (MAPT) can cause FTDP-17 but the underlying mechanisms of the disease are still unknown. Induced pluripotent stem cells (iPSCs) hold great promise to model FTDP-17 as such cells can be differentiated in vitro to the required neuronal cell type. Here, we report the generation of iPSCs from a 44-year-old symptomatic woman carrying a S305I mutation in the MAPT-gene.
U2 - 10.1016/j.scr.2016.10.006
DO - 10.1016/j.scr.2016.10.006
M3 - Journal article
C2 - 27789411
VL - 17
SP - 564
EP - 567
JO - Stem Cell Research
JF - Stem Cell Research
SN - 1873-5061
IS - 3
ER -
ID: 172816652