Page 22 - CBAC Newsletter 2016

Reference List (Continued)

57. Giustetto C, Di Monte F, Wolpert C, Borggrefe M, Schimpf R, Sbragia P, Leone G, Maury P, Anttonen O,
Haissaguerre M, Gaita F. Short QT syndrome: clinical findings and diagnostic-therapeutic implications.
Eur Heart J. 27, 2440-2447, 2006.

58. Hong K, Piper DR, Diaz-Valdecantos A, Brugada J, Oliva A, Burashnikov E., Santos-de-Soto J,
Grueso-Montero J, Diaz-Enfante E, Brugada P, Sachse F, Sanguinetti MC, Brugada R. De novo KCNQ1
mutation responsible for atrial fibrillation and short QT syndrome in utero. Cardiovasc Res.
68, 433-440, 2005.

59. Chen YH, Xu SJ, Bendahhou S, Wang XL, Wang Y, Xu WY, Jin HW, Sun H, Su XY, Zhuang QN, Yang YQ, Li YB,
Liu Y, Xu HJ, Li XF, Ma N, Mou CP, Chen Z, Barhanin J, Huang W. KCNQ1 gain-of-function mutation in
familial atrial fibrillation. Science. 299, 251-254, 2003.

60. Neyroud N, Tesson F, Denjoy I, Leibovici M, Donger C, Barhanin J, Faure S, Gary F, Coumel P, Petit C,
Schwartz K, Guicheney P. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell
and Lange-Nielsen cardioauditory syndrome. Nat Genet. 15, 186-189, 1997.

61. Tinel N, Diochot S, Borsotto M, Lazdunski M, Barhanin J. KCNE2 confers background current characteristics to
the cardiac KCNQ1 potassium channel. EMBO J. 19, 6326-6330, 2000.

62. Roepke TK, Anantharam A, Kirchhoff P, Busque SM, Young JB, Geibel JP, Lerner DJ, Abbott GW. The KCNE2
potassium channel ancillary subunit is essential for gastric acid secretion. J Biol Chem. 281,
23740-23747, 2006.

63. Roepke TK, Kanda VA, Purtell K, King EC, Lerner DJ, Abbott GW. KCNE2 forms potassium channels with
KCNA3 and KCNQ1 in the choroid plexus epithelium. FASEB J. 25, 4264-4273, 2011.

64. Roepke TK, King EC, Reyna-Neyra A, Paroder M, Purtell K, Koba W, Fine E, Lerner DJ, Carrasco N, Abbott GW.
Kcne2 deletion uncovers its crucial role in thyroid hormone biosynthesis. Nat. Med. 15,
1186-1194, 2009.

65. Grahammer F, Herling AW, Lang HJ, Schmitt-Graff A, Wittekindt OH, Nitschke R, Bleich M, Barhanin J, Warth R.
The cardiac K+ channel KCNQ1 is essential for gastric acid secretion. Gastroenterology.
120, 1363-1371, 2001.

66. Lee MP, Ravenel JD, Hu RJ, Lustig LR, Tomaselli G, Berger RD, Brandenburg SA, Litzi TJ, Bunton TE, Limb C,
Francis H, Gorelikow M, Gu H, Washington K, Argani P, Goldenring JR, Coffey RJ, Feinberg AP. Targeted
disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice. J. Clin. Invest.
106, 1447-1455, 2000.

67. Frohlich H, Boini KM, Seebohm G, Strutz-Seebohm N, Ureche ON, Foller M, Eichenmuller M, Shumilina E,
Pathare G, Singh AK, Seidler U, Pfeifer KE, Lang F. Hypothyroidism of gene-targeted mice lacking Kcnq1.
Pflugers Arch. 461, 45-52, 2011.

68. Lohrmann E, Burhoff I, Nitschke RB, Lang HJ, Mania D, Englert HC, Hropot M, Warth R, Rohm W, Bleich M,
et al. A new class of inhibitors of cAMP-mediated Cl- secretion in rabbit colon, acting by the reduction of
cAMP-activated K+ conductance. Pflugers Arch. 429, 517-530, 1995.

69. Shah M, Mistry M, Marsh SJ, Brown DA., Delmas P. Molecular correlates of the M-current in cultured rat
hippocampal neurons. J Physiol. 544, 29-37, 2002.
70. Tatulian L, and Brown, D. A. Effect of the KCNQ potassium channel opener retigabine on single

KCNQ2/3 channels expressed in CHO cells. J Physiol. 549, 57-63, 2003.
71. Selyanko AA, Hadley JK, Wood IC, Abogadie FC, Jentsch TJ, Brown DA. Inhibition of KCNQ1-4 potassium

channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors. J Physiol. 522 Pt 3,
349-355, 2000.
72. Wladyka CL, Kunze DL. KCNQ/M-currents contribute to the resting membrane potential in rat visceral sensory
neurons. J Physiol. 575, 175-189, 2006.

18 | CBAC Center Heartbeat