000 | 01920 a2200565 4500 | ||
---|---|---|---|
005 | 20250516180905.0 | ||
264 | 0 | _c20140210 | |
008 | 201402s 0 0 eng d | ||
022 | _a1460-2075 | ||
024 | 7 |
_a10.1038/emboj.2013.240 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aBellin, Milena | |
245 | 0 | 0 |
_aIsogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndrome. _h[electronic resource] |
260 |
_bThe EMBO journal _cDec 2013 |
||
300 |
_a3161-75 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAction Potentials _xgenetics |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aCells, Cultured |
650 | 0 | 4 | _aERG1 Potassium Channel |
650 | 0 | 4 |
_aEmbryonic Stem Cells _xphysiology |
650 | 0 | 4 |
_aEther-A-Go-Go Potassium Channels _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHomeobox Protein Nkx-2.5 |
650 | 0 | 4 |
_aHomeodomain Proteins _xgenetics |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInduced Pluripotent Stem Cells |
650 | 0 | 4 |
_aLong QT Syndrome _xgenetics |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 |
_aMyocytes, Cardiac _xpathology |
650 | 0 | 4 | _aPatch-Clamp Techniques |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 |
_aPluripotent Stem Cells _xphysiology |
650 | 0 | 4 |
_aProtein Transport _xgenetics |
650 | 0 | 4 |
_aTranscription Factors _xgenetics |
700 | 1 | _aCasini, Simona | |
700 | 1 | _aDavis, Richard P | |
700 | 1 | _aD'Aniello, Cristina | |
700 | 1 | _aHaas, Jessica | |
700 | 1 | _aWard-van Oostwaard, Dorien | |
700 | 1 | _aTertoolen, Leon G J | |
700 | 1 | _aJung, Christian B | |
700 | 1 | _aElliott, David A | |
700 | 1 | _aWelling, Andrea | |
700 | 1 | _aLaugwitz, Karl-Ludwig | |
700 | 1 | _aMoretti, Alessandra | |
700 | 1 | _aMummery, Christine L | |
773 | 0 |
_tThe EMBO journal _gvol. 32 _gno. 24 _gp. 3161-75 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1038/emboj.2013.240 _zAvailable from publisher's website |
999 |
_c23249518 _d23249518 |