-
1
-
-
0025779484
-
Atrial fibrillation as an independent risk factor for stroke: The Framingham Study
-
Wolf PA, Abott RD, Kannel WB. Atrial fibrillation as an independent risk factor for stroke: the Framingham Study. Stroke 1991;22:983-8.
-
(1991)
Stroke
, vol.22
, pp. 983-988
-
-
Wolf, P.A.1
Abott, R.D.2
Kannel, W.B.3
-
2
-
-
0032497292
-
Impact of atrial fibrillation on the risk of death: The Framingham Heart Study
-
Benjamin EJ, Wolf PA, D'Agostino RB, Silbershatz H, Kannel WB, Levy D. Impact of atrial fibrillation on the risk of death: the Framingham Heart Study. Circulation 1998;98:946-52.
-
(1998)
Circulation
, vol.98
, pp. 946-952
-
-
Benjamin, E.J.1
Wolf, P.A.2
D'Agostino, R.B.3
Silbershatz, H.4
Kannel, W.B.5
Levy, D.6
-
3
-
-
0028921708
-
Prevalence, age distribution, and gender of patients with atrial fibrillation analysis and implications
-
Feinberg WM, Blackshear JL, Laupacis A, Kronmal R, Hart RG. Prevalence, age distribution, and gender of patients with atrial fibrillation analysis and implications. Arch Intern Med 1995;155:469-73.
-
(1995)
Arch Intern Med
, vol.155
, pp. 469-473
-
-
Feinberg, W.M.1
Blackshear, J.L.2
Laupacis, A.3
Kronmal, R.4
Hart, R.G.5
-
4
-
-
0043164965
-
Increasing trends in hospitalization for atrial fibrillation in the United States, 1985 through 1999: Implications for primary prevention
-
Wattigney WA, Mensah GA, Croft JB. Increasing trends in hospitalization for atrial fibrillation in the United States, 1985 through 1999: implications for primary prevention. Circulation 2003;108:711-6.
-
(2003)
Circulation
, vol.108
, pp. 711-716
-
-
Wattigney, W.A.1
Mensah, G.A.2
Croft, J.B.3
-
5
-
-
0037428218
-
KCNQ1 gain-of-function mutation in familial atrial fibrillation
-
Chen YH, Xu SJ, Bendahhou S, et al. KCNQ1 gain-of-function mutation in familial atrial fibrillation. Science 2003;299:251-4.
-
(2003)
Science
, vol.299
, pp. 251-254
-
-
Chen, Y.H.1
Xu, S.J.2
Bendahhou, S.3
-
6
-
-
0031004845
-
Identification of a genetic locus for familial atrial fibrillation
-
Brugada R, Tapscott T, Czernuszewicz GZ, et al. Identification of a genetic locus for familial atrial fibrillation. N Engl J Med 1997;336:905-11.
-
(1997)
N Engl J Med
, vol.336
, pp. 905-911
-
-
Brugada, R.1
Tapscott, T.2
Czernuszewicz, G.Z.3
-
7
-
-
0037635439
-
Locus for atrial fibrillation maps to chromosome 6q14-16
-
Ellinor PT, Shin JT, Moore RK, Yoerger DM, MacRae CA. Locus for atrial fibrillation maps to chromosome 6q14-16. Circulation 2003;107:2880-3.
-
(2003)
Circulation
, vol.107
, pp. 2880-2883
-
-
Ellinor, P.T.1
Shin, J.T.2
Moore, R.K.3
Yoerger, D.M.4
MacRae, C.A.5
-
8
-
-
0037342752
-
Somatic gene mutation and human disease other than cancer
-
Erickson RP. Somatic gene mutation and human disease other than cancer. Mutat Res 2003;543:125-36.
-
(2003)
Mutat Res
, vol.543
, pp. 125-136
-
-
Erickson, R.P.1
-
9
-
-
4644298618
-
Somatic mutations - Not just for cancer anymore
-
Puck JM, Straus SE. Somatic mutations - not just for cancer anymore. N Engl J Med 2004;351:1388-90.
-
(2004)
N Engl J Med
, vol.351
, pp. 1388-1390
-
-
Puck, J.M.1
Straus, S.E.2
-
10
-
-
15944422499
-
Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia
-
Yamaguchi H, Calado RT, Ly H, et al. Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia. N Engl J Med 2005;352:1413-24.
-
(2005)
N Engl J Med
, vol.352
, pp. 1413-1424
-
-
Yamaguchi, H.1
Calado, R.T.2
Ly, H.3
-
11
-
-
3042856300
-
Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease
-
Beck JA, Poulter M, Campbell TA, et al. Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease. Hum Mol Genet 2004;13:1219-24.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1219-1224
-
-
Beck, J.A.1
Poulter, M.2
Campbell, T.A.3
-
12
-
-
0034812869
-
The role of myocardial gap junctions in electrical conduction and arrhythmogenesis
-
Kanno S, Saffitz JE. The role of myocardial gap junctions in electrical conduction and arrhythmogenesis. Cardiovasc Pathol 2001;10:169-77.
-
(2001)
Cardiovasc Pathol
, vol.10
, pp. 169-177
-
-
Kanno, S.1
Saffitz, J.E.2
-
13
-
-
0033596919
-
Conduction disturbances and increased atrial vulnerability in connexin40-deficient mice analyzed by transesophageal stimulation
-
Hagendorff A, Schumacher B, Kirchhoff S, Luderitz B, Willecke K. Conduction disturbances and increased atrial vulnerability in connexin40-deficient mice analyzed by transesophageal stimulation. Circulation 1999;99:1508-15.
-
(1999)
Circulation
, vol.99
, pp. 1508-1515
-
-
Hagendorff, A.1
Schumacher, B.2
Kirchhoff, S.3
Luderitz, B.4
Willecke, K.5
-
14
-
-
16644398147
-
Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation
-
Firouzi M, Ramanna H, Kok B, et al. Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation. Circ Res 2004;95:e29-e33.
-
(2004)
Circ Res
, vol.95
-
-
Firouzi, M.1
Ramanna, H.2
Kok, B.3
-
15
-
-
0033000913
-
Molecular mechanism underlying a Cx50-linked congenital cataract
-
Pal JD, Berthoud VM, Beyer EC, Mackay D, Shiels A, Ebihara L. Molecular mechanism underlying a Cx50-linked congenital cataract. Am J Physiol 1999;276:C1443-C1446.
-
(1999)
Am J Physiol
, vol.276
-
-
Pal, J.D.1
Berthoud, V.M.2
Beyer, E.C.3
Mackay, D.4
Shiels, A.5
Ebihara, L.6
-
16
-
-
0031021107
-
Mutation analysis of the connexin32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: Identification of five new mutations
-
Nelis E, Simokovic S, Timmerman V, et al. Mutation analysis of the connexin32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutations. Hum Mutat 1997;9:47-52.
-
(1997)
Hum Mutat
, vol.9
, pp. 47-52
-
-
Nelis, E.1
Simokovic, S.2
Timmerman, V.3
-
17
-
-
0030896412
-
Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)
-
Janssen EA, Kemp S, Hensels GW, et al. Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1). Hum Genet 1997;99:501-5.
-
(1997)
Hum Genet
, vol.99
, pp. 501-505
-
-
Janssen, E.A.1
Kemp, S.2
Hensels, G.W.3
-
18
-
-
0030919434
-
Mutational analysis of the MPZ, PMP22, and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies
-
Bort S, Nelis E, Timmerman V, et al. Mutational analysis of the MPZ, PMP22, and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies. Hum Genet 1997;99:746-54.
-
(1997)
Hum Genet
, vol.99
, pp. 746-754
-
-
Bort, S.1
Nelis, E.2
Timmerman, V.3
-
19
-
-
0031959735
-
A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q
-
Shiels A, Mackay D, Ionides A, Berry V, Moore A, Bhattacharya SA. A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q. Am J Hum Genet 1998;62:526-32.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 526-532
-
-
Shiels, A.1
Mackay, D.2
Ionides, A.3
Berry, V.4
Moore, A.5
Bhattacharya, S.A.6
-
20
-
-
12244278266
-
Phenotypic expression of a Pro 87 to Leu mutation in the connexin 32 gene in a large Swiss family with Charcot-Marie-Tooth neuropathy
-
Kuntzer T, Dunand M, Schorderet DF, Vallat JM, Hahn AF, Bogousslavsky J. Phenotypic expression of a Pro 87 to Leu mutation in the connexin 32 gene in a large Swiss family with Charcot-Marie-Tooth neuropathy. J Neurol Sci 2003;207:77-86.
-
(2003)
J Neurol Sci
, vol.207
, pp. 77-86
-
-
Kuntzer, T.1
Dunand, M.2
Schorderet, D.F.3
Vallat, J.M.4
Hahn, A.F.5
Bogousslavsky, J.6
-
22
-
-
0034080924
-
Connexin gene mutations in human genetic diseases
-
Krutovskikh V, Yamasaki H. Connexin gene mutations in human genetic diseases. Mutat Res 2000;462:197-207.
-
(2000)
Mutat Res
, vol.462
, pp. 197-207
-
-
Krutovskikh, V.1
Yamasaki, H.2
-
23
-
-
0031836722
-
Simple electrocardiographic markers for the prediction of paroxysmal idiopathic atrial fibrillation
-
Dilaveris PE, Gialafos EJ, Sideris SK, et al. Simple electrocardiographic markers for the prediction of paroxysmal idiopathic atrial fibrillation. Am Heart J 1998;135:733-8.
-
(1998)
Am Heart J
, vol.135
, pp. 733-738
-
-
Dilaveris, P.E.1
Gialafos, E.J.2
Sideris, S.K.3
-
24
-
-
0032526065
-
Right ventricular outflow tract tachycardia due to a somatic cell mutation in G protein subunit αai2
-
Lerman BB, Dong B, Stein KM, Markowitz SM, Linden J, Catanzaro DF. Right ventricular outflow tract tachycardia due to a somatic cell mutation in G protein subunit αai2. J Clin Invest 1998;101:2862-8.
-
(1998)
J Clin Invest
, vol.101
, pp. 2862-2868
-
-
Lerman, B.B.1
Dong, B.2
Stein, K.M.3
Markowitz, S.M.4
Linden, J.5
Catanzaro, D.F.6
-
25
-
-
0035806899
-
Heterogeneous expression of gap junction channels in the heart leads to conduction defects and ventricular dysfunction
-
Gutstein DE, Morely GE, Vaidya D, et al. Heterogeneous expression of gap junction channels in the heart leads to conduction defects and ventricular dysfunction. Circulation 2001;104:1194-9.
-
(2001)
Circulation
, vol.104
, pp. 1194-1199
-
-
Gutstein, D.E.1
Morely, G.E.2
Vaidya, D.3
-
27
-
-
0035012765
-
Innexins get into the gap
-
Phelan P, Starich TA. Innexins get into the gap. Bioessays 2001;23:388-96.
-
(2001)
Bioessays
, vol.23
, pp. 388-396
-
-
Phelan, P.1
Starich, T.A.2
-
28
-
-
0030686435
-
The Caenorhabditis elegans avermectin resistance and anesthetic response gene unc-9 encodes a member of a protein family implicated in electrical coupling of excitable cells
-
Barnes TM, Hekimi S. The Caenorhabditis elegans avermectin resistance and anesthetic response gene unc-9 encodes a member of a protein family implicated in electrical coupling of excitable cells. J Neurochem 1997;69:2251-60.
-
(1997)
J Neurochem
, vol.69
, pp. 2251-2260
-
-
Barnes, T.M.1
Hekimi, S.2
-
29
-
-
0027442575
-
Identification of a proline residue as a transduction element involved in voltage gating of gap junctions
-
Suchyna TM, Xu LX, Gao F, Fourtner CR, Nicholson BJ. Identification of a proline residue as a transduction element involved in voltage gating of gap junctions. Nature 1993;365:847-9.
-
(1993)
Nature
, vol.365
, pp. 847-849
-
-
Suchyna, T.M.1
Xu, L.X.2
Gao, F.3
Fourtner, C.R.4
Nicholson, B.J.5
-
30
-
-
0033063884
-
The role of a conserved proline in mediating conformational changes associated with voltage gating of Cx32 gap junctions
-
Ri Y, Ballesteros JA, Abrams CK, et al. The role of a conserved proline in mediating conformational changes associated with voltage gating of Cx32 gap junctions. Biophys J 1999;76:2887-98.
-
(1999)
Biophys J
, vol.76
, pp. 2887-2898
-
-
Ri, Y.1
Ballesteros, J.A.2
Abrams, C.K.3
-
31
-
-
0025856242
-
The surgical treatment of atrial fibrillation. II. Intraoperative electrophysiologic mapping and description of the electrophysiologic basis of atrial flutter and fibrillation
-
Cox JL, Canavan TE, Schuessler RB, et al. The surgical treatment of atrial fibrillation. II. Intraoperative electrophysiologic mapping and description of the electrophysiologic basis of atrial flutter and fibrillation. J Thorac Cardiovasc Surg 1991;101:406-26.
-
(1991)
J Thorac Cardiovasc Surg
, vol.101
, pp. 406-426
-
-
Cox, J.L.1
Canavan, T.E.2
Schuessler, R.B.3
-
32
-
-
0028280031
-
Highdensity mapping of electrically induced atrial fibrillation in humans
-
Konings KT, Kirchhof CJ, Smeets JR, Wellens HJ, Penn OC, Allessie MA. Highdensity mapping of electrically induced atrial fibrillation in humans. Circulation 1994;89:1665-80.
-
(1994)
Circulation
, vol.89
, pp. 1665-1680
-
-
Konings, K.T.1
Kirchhof, C.J.2
Smeets, J.R.3
Wellens, H.J.4
Penn, O.C.5
Allessie, M.A.6
-
33
-
-
0028047257
-
Initiating reentry: The role of nonuniform anisotropy in small circuits
-
Spach MS, Josephson ME. Initiating reentry: the role of nonuniform anisotropy in small circuits. J Cardiovasc Electrophysiol 1994;5:182-209.
-
(1994)
J Cardiovasc Electrophysiol
, vol.5
, pp. 182-209
-
-
Spach, M.S.1
Josephson, M.E.2
-
34
-
-
0002938412
-
Role of the autonomic nervous system in paroxysmal atrial fibrillation
-
Waldo AL, Touboul T, eds. Armonk, N.Y.: Futura Publishing
-
Coumel P. Role of the autonomic nervous system in paroxysmal atrial fibrillation. In: Waldo AL, Touboul T, eds. Atrial flutter: advances in mechanisms and management. Armonk, N.Y.: Futura Publishing, 1996:248-61.
-
(1996)
Atrial Flutter: Advances in Mechanisms and Management
, pp. 248-261
-
-
Coumel, P.1
-
35
-
-
0036959866
-
Muscarinic receptors in human luteinized granulosa cells: Activation blocks gap junctions and induces the transcription factor early growth response factor-1
-
Fritz S, Kunz L, Dimitrijevic N, Grunert R, Heiss C, Mayerhofer A. Muscarinic receptors in human luteinized granulosa cells: activation blocks gap junctions and induces the transcription factor early growth response factor-1. J Clin Endocrinol Metab 2002;87:1362-7.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 1362-1367
-
-
Fritz, S.1
Kunz, L.2
Dimitrijevic, N.3
Grunert, R.4
Heiss, C.5
Mayerhofer, A.6
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