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Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage
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- المؤلفون: Bidollari, E; Rotundo, G; Ferrari, D; Candido, O; Bernardini, L; Consoli, F; De Luca, A; Santimone, I; Lamorte, G; Ilari, A; Squitieri, F; Vescovi, A; Rosati, J; Bidollari, Eris; Rotundo, Giovannina; Ferrari, Daniela; Candido, Ornella; Bernardini, Laura; Consoli, Federica; De Luca, Alessandro; Santimone, Iolanda; Lamorte, Giuseppe; Ilari, Andrea; Squitieri, Ferdinando; Vescovi, Angelo Luigi; ROSATI, JESSICA
- نوع التسجيلة:
Electronic Resource
- الدخول الالكتروني :
http://hdl.handle.net/10281/191628
http://www.elsevier.com/wps/find/journaldescription.cws_home/711630/description#description
info:eu-repo/semantics/altIdentifier/pmid/29486399
info:eu-repo/semantics/altIdentifier/wos/WOS:000428799700026
volume:28
firstpage:145
lastpage:148
numberofpages:4
journal:STEM CELL RESEARCH
- معلومة اضافية
- Publisher Information:
Elsevier B.V. 2018
- نبذة مختصرة :
Huntington's disease (HD) is an incurable, autosomal dominant, hereditary neurodegenerative disorder that typically manifests itself in midlife. This pathology is linked to the deregulation of multiple, as yet unknown, cellular processes starting before HD onset. A human iPS cell line was generated from skin fibroblasts of a subject at the presymptomatic life stage, carrying a polyglutamine expansion in HTT gene codifying Huntingtin protein. The iPSC line contained the expected CAG expansion, expressed the expected pluripotency markers, displayed in vivo differentiation potential to the three germ layers and had a normal karyotype.
- الموضوع:
- Note:
English
- Other Numbers:
ITBAO oai:boa.unimib.it:10281/191628
10.1016/j.scr.2018.02.014
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85042460767
1308924542
- Contributing Source:
BICOCCA OPEN ARCH
From OAIster®, provided by the OCLC Cooperative.
- الرقم المعرف:
edsoai.on1308924542
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