Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Blake C. Wu"'
Autor:
Gema Mondéjar-Parreño, James W.S. Jahng, Nadjet Belbachir, Blake C. Wu, Xiaolan Zhang, Marco V. Perez, Nitish Badhwar, Joseph C. Wu
Publikováno v:
Stem Cell Research, Vol 54, Iss , Pp 102402- (2021)
Congenital long QT syndrome type 2 (LQT2) results from KCNH2 mutations that cause loss of Kv11.1 channel function which can lead to arrhythmias, syncope, and sudden death. Here, we generated three human-induced pluripotent stem cell (iPSC) lines from
Externí odkaz:
https://doaj.org/article/d87f8252619345a6b2908e70912149e9
Autor:
James W.S. Jahng, Xiaolan Zhang, Marco V Perez, Nitish Badhwar, Gema Mondéjar-Parreño, Nadjet Belbachir, Blake C. Wu, Joseph C. Wu
Publikováno v:
Stem Cell Research, Vol 54, Iss, Pp 102402-(2021)
Congenital long QT syndrome type 2 (LQT2) results from KCNH2 mutations that cause loss of Kv11.1 channel function which can lead to arrhythmias, syncope, and sudden death. Here, we generated three human-induced pluripotent stem cell (iPSC) lines from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0adbde458d245b0243e2e376cceb7e8
http://www.sciencedirect.com/science/article/pii/S1873506121002488
http://www.sciencedirect.com/science/article/pii/S1873506121002488