-
1
-
-
57649234553
-
An ankyrin-based mechanism for functional organization of dystrophin and dystroglycan
-
Ayalon G., Davis J.Q., Scotland P.B., and Bennett V. An ankyrin-based mechanism for functional organization of dystrophin and dystroglycan. Cell 135 7 (2008) 1189-1200
-
(2008)
Cell
, vol.135
, Issue.7
, pp. 1189-1200
-
-
Ayalon, G.1
Davis, J.Q.2
Scotland, P.B.3
Bennett, V.4
-
2
-
-
62849099990
-
Ankyrin-G promotes cyclic nucleotide-gated channel transport to rod photoreceptor sensory cilia
-
Kizhatil K., Baker S.A., Arshavsky V.Y., and Bennett V. Ankyrin-G promotes cyclic nucleotide-gated channel transport to rod photoreceptor sensory cilia. Science 323 5921 (2009) 1614-1617
-
(2009)
Science
, vol.323
, Issue.5921
, pp. 1614-1617
-
-
Kizhatil, K.1
Baker, S.A.2
Arshavsky, V.Y.3
Bennett, V.4
-
3
-
-
57649130788
-
Ankyrin-B is required for coordinated expression of beta-2-spectrin, the Na/K-ATPase and the Na/Ca exchanger in the inner segment of rod photoreceptors
-
Kizhatil K., Sandhu N.K., Peachey N.S., and Bennett V. Ankyrin-B is required for coordinated expression of beta-2-spectrin, the Na/K-ATPase and the Na/Ca exchanger in the inner segment of rod photoreceptors. Exp. Eye Res. 88 1 (2009) 57-64
-
(2009)
Exp. Eye Res.
, vol.88
, Issue.1
, pp. 57-64
-
-
Kizhatil, K.1
Sandhu, N.K.2
Peachey, N.S.3
Bennett, V.4
-
4
-
-
0034958883
-
Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues
-
Bennett V., and Baines A.J. Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues. Physiol. Rev. 81 3 (2001) 1353-1392
-
(2001)
Physiol. Rev.
, vol.81
, Issue.3
, pp. 1353-1392
-
-
Bennett, V.1
Baines, A.J.2
-
5
-
-
0017853463
-
Purification of an active proteolytic fragment of the membrane attachment site for human erythrocyte spectrin
-
Bennett V. Purification of an active proteolytic fragment of the membrane attachment site for human erythrocyte spectrin. J. Biol. Chem. 253 7 (1978) 2292-2299
-
(1978)
J. Biol. Chem.
, vol.253
, Issue.7
, pp. 2292-2299
-
-
Bennett, V.1
-
6
-
-
9044220232
-
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis
-
Eber S.W., Gonzalez J.M., Lux M.L., Scarpa A.L., Tse W.T., Dornwell M., et al. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Nat. Genet. 13 2 (1996) 214-218
-
(1996)
Nat. Genet.
, vol.13
, Issue.2
, pp. 214-218
-
-
Eber, S.W.1
Gonzalez, J.M.2
Lux, M.L.3
Scarpa, A.L.4
Tse, W.T.5
Dornwell, M.6
-
8
-
-
0037155903
-
The ankyrin-B C-terminal domain determines activity of ankyrin-B/G chimeras in rescue of abnormal inositol 1,4,5-trisphosphate and ryanodine receptor distribution in ankyrin-B (-/-) neonatal cardiomyocytes
-
Mohler P.J., Gramolini A.O., and Bennett V. The ankyrin-B C-terminal domain determines activity of ankyrin-B/G chimeras in rescue of abnormal inositol 1,4,5-trisphosphate and ryanodine receptor distribution in ankyrin-B (-/-) neonatal cardiomyocytes. J. Biol. Chem. 277 12 (2002) 10599-10607
-
(2002)
J. Biol. Chem.
, vol.277
, Issue.12
, pp. 10599-10607
-
-
Mohler, P.J.1
Gramolini, A.O.2
Bennett, V.3
-
10
-
-
0242464931
-
Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death
-
Mohler P.J., Schott J.J., Gramolini A.O., Dilly K.W., Guatimosim S., duBell W.H., et al. Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death. Nature 421 6923 (2003) 634-639
-
(2003)
Nature
, vol.421
, Issue.6923
, pp. 634-639
-
-
Mohler, P.J.1
Schott, J.J.2
Gramolini, A.O.3
Dilly, K.W.4
Guatimosim, S.5
duBell, W.H.6
-
11
-
-
1842477215
-
Inositol 1,4,5-trisphosphate receptor localization and stability in neonatal cardiomyocytes requires interaction with ankyrin-B
-
Mohler P.J., Davis J.Q., Davis L.H., Hoffman J.A., Michaely P., and Bennett V. Inositol 1,4,5-trisphosphate receptor localization and stability in neonatal cardiomyocytes requires interaction with ankyrin-B. J. Biol. Chem. 279 13 (2004) 12980-12987
-
(2004)
J. Biol. Chem.
, vol.279
, Issue.13
, pp. 12980-12987
-
-
Mohler, P.J.1
Davis, J.Q.2
Davis, L.H.3
Hoffman, J.A.4
Michaely, P.5
Bennett, V.6
-
13
-
-
29144509561
-
Ankyrin-B coordinates the Na/K ATPase, Na/Ca exchanger, and InsP(3) receptor in a cardiac T-tubule/SR microdomain
-
Mohler P.J., Davis J.Q., and Bennett V. Ankyrin-B coordinates the Na/K ATPase, Na/Ca exchanger, and InsP(3) receptor in a cardiac T-tubule/SR microdomain. PLoS Biol. 3 12 (2005) e423
-
(2005)
PLoS Biol.
, vol.3
, Issue.12
-
-
Mohler, P.J.1
Davis, J.Q.2
Bennett, V.3
-
14
-
-
34547131050
-
Molecular basis for PP2A regulatory subunit B56{alpha} targeting in cardiomyocytes
-
Bhasin N., Cunha S.R., Mudannayake M., Gigena M.S., Rogers T.B., and Mohler P.J. Molecular basis for PP2A regulatory subunit B56{alpha} targeting in cardiomyocytes. Am. J. Physiol., Heart Circ. Physiol. 293 1 (2007) H109-H119
-
(2007)
Am. J. Physiol., Heart Circ. Physiol.
, vol.293
, Issue.1
-
-
Bhasin, N.1
Cunha, S.R.2
Mudannayake, M.3
Gigena, M.S.4
Rogers, T.B.5
Mohler, P.J.6
-
15
-
-
33947521401
-
Targeting and stability of Na/Ca exchanger 1 in cardiomyocytes requires direct interaction with the membrane adaptor ankyrin-B
-
Cunha S.R., Bhasin N., and Mohler P.J. Targeting and stability of Na/Ca exchanger 1 in cardiomyocytes requires direct interaction with the membrane adaptor ankyrin-B. J. Biol. Chem. 282 7 (2007) 4875-4883
-
(2007)
J. Biol. Chem.
, vol.282
, Issue.7
, pp. 4875-4883
-
-
Cunha, S.R.1
Bhasin, N.2
Mohler, P.J.3
-
16
-
-
38349080944
-
Voltage-gated Nav channel targeting in the heart requires an ankyrin-G dependent cellular pathway
-
Lowe J.S., Palygin O., Bhasin N., Hund T.J., Boyden P.A., Shibata E., et al. Voltage-gated Nav channel targeting in the heart requires an ankyrin-G dependent cellular pathway. J. Cell Biol. 180 1 (2008) 173-186
-
(2008)
J. Cell Biol.
, vol.180
, Issue.1
, pp. 173-186
-
-
Lowe, J.S.1
Palygin, O.2
Bhasin, N.3
Hund, T.J.4
Boyden, P.A.5
Shibata, E.6
-
17
-
-
55749103406
-
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease
-
Le Scouarnec S., Bhasin N., Vieyres C., Hund T.J., Cunha S.R., Koval O., et al. Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease. Proc. Natl. Acad. Sci. U. S. A. 105 40 (2008) 15617-15622
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, Issue.40
, pp. 15617-15622
-
-
Le Scouarnec, S.1
Bhasin, N.2
Vieyres, C.3
Hund, T.J.4
Cunha, S.R.5
Koval, O.6
-
18
-
-
33744902323
-
Cardiac ankyrins: essential components for development and maintenance of excitable membrane domains in heart
-
Cunha S.R., and Mohler P.J. Cardiac ankyrins: essential components for development and maintenance of excitable membrane domains in heart. Cardiovasc. Res. 71 1 (2006) 22-29
-
(2006)
Cardiovasc. Res.
, vol.71
, Issue.1
, pp. 22-29
-
-
Cunha, S.R.1
Mohler, P.J.2
-
19
-
-
55649115607
-
Exon organization and novel alternative splicing of the human ANK2 gene: implications for cardiac function and human cardiac disease
-
Cunha S.R., Le Scouarnec S., Schott J.J., and Mohler P.J. Exon organization and novel alternative splicing of the human ANK2 gene: implications for cardiac function and human cardiac disease. J. Mol. Cell. Cardiol. 45 6 (2008) 724-734
-
(2008)
J. Mol. Cell. Cardiol.
, vol.45
, Issue.6
, pp. 724-734
-
-
Cunha, S.R.1
Le Scouarnec, S.2
Schott, J.J.3
Mohler, P.J.4
-
20
-
-
0029558546
-
A neuron-specific isoform of brain ankyrin, 440-kD ankyrinB, is targeted to the axons of rat cerebellar neurons
-
Kunimoto M. A neuron-specific isoform of brain ankyrin, 440-kD ankyrinB, is targeted to the axons of rat cerebellar neurons. J. Cell Biol. 131 6 Pt 2 (1995) 1821-1829
-
(1995)
J. Cell Biol.
, vol.131
, Issue.6 PART 2
, pp. 1821-1829
-
-
Kunimoto, M.1
-
21
-
-
0037343054
-
Obscurin is a ligand for small ankyrin 1 in skeletal muscle
-
Kontrogianni-Konstantopoulos A., Jones E.M., Van Rossum D.B., and Bloch R.J. Obscurin is a ligand for small ankyrin 1 in skeletal muscle. Mol. Biol. Cell 14 3 (2003) 1138-1148
-
(2003)
Mol. Biol. Cell
, vol.14
, Issue.3
, pp. 1138-1148
-
-
Kontrogianni-Konstantopoulos, A.1
Jones, E.M.2
Van Rossum, D.B.3
Bloch, R.J.4
-
22
-
-
0037423366
-
The hydrophilic domain of small ankyrin-1 interacts with the two N-terminal immunoglobulin domains of titin
-
Kontrogianni-Konstantopoulos A., and Bloch R.J. The hydrophilic domain of small ankyrin-1 interacts with the two N-terminal immunoglobulin domains of titin. J. Biol. Chem. 278 6 (2003) 3985-3991
-
(2003)
J. Biol. Chem.
, vol.278
, Issue.6
, pp. 3985-3991
-
-
Kontrogianni-Konstantopoulos, A.1
Bloch, R.J.2
-
23
-
-
0037455559
-
Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles
-
Bagnato P., Barone V., Giacomello E., Rossi D., and Sorrentino V. Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles. J. Cell Biol. 160 2 (2003) 245-253
-
(2003)
J. Cell Biol.
, vol.160
, Issue.2
, pp. 245-253
-
-
Bagnato, P.1
Barone, V.2
Giacomello, E.3
Rossi, D.4
Sorrentino, V.5
-
24
-
-
0031049612
-
Small, membrane-bound, alternatively spliced forms of ankyrin 1 associated with the sarcoplasmic reticulum of mammalian skeletal muscle
-
Zhou D., Birkenmeier C.S., Williams M.W., Sharp J.J., Barker J.E., and Bloch R.J. Small, membrane-bound, alternatively spliced forms of ankyrin 1 associated with the sarcoplasmic reticulum of mammalian skeletal muscle. J. Cell Biol. 136 3 (1997) 621-631
-
(1997)
J. Cell Biol.
, vol.136
, Issue.3
, pp. 621-631
-
-
Zhou, D.1
Birkenmeier, C.S.2
Williams, M.W.3
Sharp, J.J.4
Barker, J.E.5
Bloch, R.J.6
-
25
-
-
0032524295
-
An alternative first exon in the distal end of the erythroid ankyrin gene leads to production of a small isoform containing an NH2-terminal membrane anchor
-
Birkenmeier C.S., Sharp J.J., Gifford E.J., Deveau S.A., and Barker J.E. An alternative first exon in the distal end of the erythroid ankyrin gene leads to production of a small isoform containing an NH2-terminal membrane anchor. Genomics 50 1 (1998) 79-88
-
(1998)
Genomics
, vol.50
, Issue.1
, pp. 79-88
-
-
Birkenmeier, C.S.1
Sharp, J.J.2
Gifford, E.J.3
Deveau, S.A.4
Barker, J.E.5
-
26
-
-
0031915372
-
An alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin 1 gene
-
Gallagher P.G., and Forget B.G. An alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin 1 gene. J. Biol. Chem. 273 3 (1998) 1339-1348
-
(1998)
J. Biol. Chem.
, vol.273
, Issue.3
, pp. 1339-1348
-
-
Gallagher, P.G.1
Forget, B.G.2
-
27
-
-
57649129419
-
Obscurin targets ankyrin-B and protein phosphatase 2A to the cardiac M-line
-
Cunha S.R., and Mohler P.J. Obscurin targets ankyrin-B and protein phosphatase 2A to the cardiac M-line. J. Biol. Chem. 283 46 (2008) 31968-31980
-
(2008)
J. Biol. Chem.
, vol.283
, Issue.46
, pp. 31968-31980
-
-
Cunha, S.R.1
Mohler, P.J.2
-
28
-
-
2942695712
-
A cardiac arrhythmia syndrome caused by loss of ankyrin-B function
-
Mohler P.J., Splawski I., Napolitano C., Bottelli G., Sharpe L., Timothy K., et al. A cardiac arrhythmia syndrome caused by loss of ankyrin-B function. Proc. Natl. Acad. Sci. U. S. A. 101 24 (2004) 9137-9142
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, Issue.24
, pp. 9137-9142
-
-
Mohler, P.J.1
Splawski, I.2
Napolitano, C.3
Bottelli, G.4
Sharpe, L.5
Timothy, K.6
-
30
-
-
0023262074
-
+) ATPase and implications for the organization of membrane domains in polarized cells
-
+) ATPase and implications for the organization of membrane domains in polarized cells. Nature 328 6130 (1987) 533-536
-
(1987)
Nature
, vol.328
, Issue.6130
, pp. 533-536
-
-
Nelson, W.J.1
Veshnock, P.J.2
-
31
-
-
0023954085
-
Colocalization and coprecipitation of ankyrin and Na+,K+-ATPase in kidney epithelial cells
-
Koob R., Zimmermann M., Schoner W., and Drenckhahn D. Colocalization and coprecipitation of ankyrin and Na+,K+-ATPase in kidney epithelial cells. Eur. J. Cell Biol. 45 2 (1988) 230-237
-
(1988)
Eur. J. Cell Biol.
, vol.45
, Issue.2
, pp. 230-237
-
-
Koob, R.1
Zimmermann, M.2
Schoner, W.3
Drenckhahn, D.4
-
32
-
-
0024571516
-
Ankyrin links fodrin to the alpha subunit of Na,K-ATPase in Madin-Darby canine kidney cells and in intact renal tubule cells
-
Morrow J.S., Cianci C.D., Ardito T., Mann A.S., and Kashgarian M. Ankyrin links fodrin to the alpha subunit of Na,K-ATPase in Madin-Darby canine kidney cells and in intact renal tubule cells. J. Cell Biol. 108 2 (1989) 455-465
-
(1989)
J. Cell Biol.
, vol.108
, Issue.2
, pp. 455-465
-
-
Morrow, J.S.1
Cianci, C.D.2
Ardito, T.3
Mann, A.S.4
Kashgarian, M.5
-
33
-
-
0037780537
-
Kv3.1b is a novel component of CNS nodes
-
Devaux J., Alcaraz G., Grinspan J., Bennett V., Joho R., Crest M., et al. Kv3.1b is a novel component of CNS nodes. J. Neurosci. 23 11 (2003) 4509-4518
-
(2003)
J. Neurosci.
, vol.23
, Issue.11
, pp. 4509-4518
-
-
Devaux, J.1
Alcaraz, G.2
Grinspan, J.3
Bennett, V.4
Joho, R.5
Crest, M.6
-
34
-
-
20044369520
-
The ammonium transporter RhBG: requirement of a tyrosine-based signal and ankyrin-G for basolateral targeting and membrane anchorage in polarized kidney epithelial cells
-
Lopez C., Metral S., Eladari D., Drevensek S., Gane P., Chambrey R., et al. The ammonium transporter RhBG: requirement of a tyrosine-based signal and ankyrin-G for basolateral targeting and membrane anchorage in polarized kidney epithelial cells. J. Biol. Chem. 280 9 (2005) 8221-8228
-
(2005)
J. Biol. Chem.
, vol.280
, Issue.9
, pp. 8221-8228
-
-
Lopez, C.1
Metral, S.2
Eladari, D.3
Drevensek, S.4
Gane, P.5
Chambrey, R.6
-
36
-
-
0029150191
-
The ANK repeats of erythrocyte ankyrin form two distinct but cooperative binding sites for the erythrocyte anion exchanger
-
Michaely P., and Bennett V. The ANK repeats of erythrocyte ankyrin form two distinct but cooperative binding sites for the erythrocyte anion exchanger. J. Biol. Chem. 270 37 (1995) 22050-22057
-
(1995)
J. Biol. Chem.
, vol.270
, Issue.37
, pp. 22050-22057
-
-
Michaely, P.1
Bennett, V.2
-
37
-
-
0018397366
-
Identification and partial purification of ankyrin, the high affinity membrane attachment site for human erythrocyte spectrin
-
Bennett V., and Stenbuck P.J. Identification and partial purification of ankyrin, the high affinity membrane attachment site for human erythrocyte spectrin. J. Biol. Chem. 254 7 (1979) 2533-2541
-
(1979)
J. Biol. Chem.
, vol.254
, Issue.7
, pp. 2533-2541
-
-
Bennett, V.1
Stenbuck, P.J.2
-
38
-
-
0021704597
-
Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes
-
Bodine D.M.t., Birkenmeier C.S., and Barker J.E. Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes. Cell 37 3 (1984) 721-729
-
(1984)
Cell
, vol.37
, Issue.3
, pp. 721-729
-
-
Bodine, D.M.t.1
Birkenmeier, C.S.2
Barker, J.E.3
-
39
-
-
0025369182
-
Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis
-
Liu S.C., Derick L.H., Agre P., and Palek J. Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis. Blood 76 1 (1990) 198-205
-
(1990)
Blood
, vol.76
, Issue.1
, pp. 198-205
-
-
Liu, S.C.1
Derick, L.H.2
Agre, P.3
Palek, J.4
-
40
-
-
0026083898
-
Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin
-
Hanspal M., Yoon S.H., Yu H., Hanspal J.S., Lambert S., Palek J., et al. Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin. Blood 77 1 (1991) 165-173
-
(1991)
Blood
, vol.77
, Issue.1
, pp. 165-173
-
-
Hanspal, M.1
Yoon, S.H.2
Yu, H.3
Hanspal, J.S.4
Lambert, S.5
Palek, J.6
-
41
-
-
0035956420
-
Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments
-
Jenkins S.M., and Bennett V. Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments. J. Cell Biol. 155 5 (2001) 739-746
-
(2001)
J. Cell Biol.
, vol.155
, Issue.5
, pp. 739-746
-
-
Jenkins, S.M.1
Bennett, V.2
-
42
-
-
1942533405
-
Lateral membrane biogenesis in human bronchial epithelial cells requires 190-kDa ankyrin-G
-
Kizhatil K., and Bennett V. Lateral membrane biogenesis in human bronchial epithelial cells requires 190-kDa ankyrin-G. J. Biol. Chem. 279 16 (2004) 16706-16714
-
(2004)
J. Biol. Chem.
, vol.279
, Issue.16
, pp. 16706-16714
-
-
Kizhatil, K.1
Bennett, V.2
-
43
-
-
33846962133
-
betaIV spectrin is recruited to axon initial segments and nodes of Ranvier by ankyrinG
-
Yang Y., Ogawa Y., Hedstrom K.L., and Rasband M.N. betaIV spectrin is recruited to axon initial segments and nodes of Ranvier by ankyrinG. J. Cell Biol. 176 4 (2007) 509-519
-
(2007)
J. Cell Biol.
, vol.176
, Issue.4
, pp. 509-519
-
-
Yang, Y.1
Ogawa, Y.2
Hedstrom, K.L.3
Rasband, M.N.4
-
44
-
-
7244258884
-
BetaIV spectrins are essential for membrane stability and the molecular organization of nodes of Ranvier
-
Yang Y., Lacas-Gervais S., Morest D.K., Solimena M., and Rasband M.N. BetaIV spectrins are essential for membrane stability and the molecular organization of nodes of Ranvier. J. Neurosci. 24 33 (2004) 7230-7240
-
(2004)
J. Neurosci.
, vol.24
, Issue.33
, pp. 7230-7240
-
-
Yang, Y.1
Lacas-Gervais, S.2
Morest, D.K.3
Solimena, M.4
Rasband, M.N.5
-
45
-
-
0026722207
-
Ankyrin regulation: an alternatively spliced segment of the regulatory domain functions as an intramolecular modulator
-
Davis L.H., Davis J.Q., and Bennett V. Ankyrin regulation: an alternatively spliced segment of the regulatory domain functions as an intramolecular modulator. J. Biol. Chem. 267 26 (1992) 18966-18972
-
(1992)
J. Biol. Chem.
, vol.267
, Issue.26
, pp. 18966-18972
-
-
Davis, L.H.1
Davis, J.Q.2
Bennett, V.3
-
46
-
-
0023196746
-
Regulatory domains of erythrocyte ankyrin
-
Hall T.G., and Bennett V. Regulatory domains of erythrocyte ankyrin. J. Biol. Chem. 262 22 (1987) 10537-10545
-
(1987)
J. Biol. Chem.
, vol.262
, Issue.22
, pp. 10537-10545
-
-
Hall, T.G.1
Bennett, V.2
-
47
-
-
2942533956
-
Isoform specificity among ankyrins: an amphipathic alpha-helix in the divergent regulatory domain of ankyrin-B interacts with the molecular co-chaperone Hdj1/Hsp40
-
Mohler P.J., Hoffman J.A., Davis J.Q., Abdi K.M., Kim C.R., Jones S.K., et al. Isoform specificity among ankyrins: an amphipathic alpha-helix in the divergent regulatory domain of ankyrin-B interacts with the molecular co-chaperone Hdj1/Hsp40. J. Biol. Chem. 279 24 (2004) 25798-25804
-
(2004)
J. Biol. Chem.
, vol.279
, Issue.24
, pp. 25798-25804
-
-
Mohler, P.J.1
Hoffman, J.A.2
Davis, J.Q.3
Abdi, K.M.4
Kim, C.R.5
Jones, S.K.6
-
48
-
-
33646830169
-
Isoform specificity of ankyrin-B: a site in the divergent c-terminal domain is required for intramolecular association
-
Abdi K.M., Mohler P.J., Davis J.Q., and Bennett V. Isoform specificity of ankyrin-B: a site in the divergent c-terminal domain is required for intramolecular association. J. Biol. Chem. 281 9 (2006) 5741-5749
-
(2006)
J. Biol. Chem.
, vol.281
, Issue.9
, pp. 5741-5749
-
-
Abdi, K.M.1
Mohler, P.J.2
Davis, J.Q.3
Bennett, V.4
-
49
-
-
33846562077
-
Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes
-
Mohler P.J., Le Scouarnec S., Denjoy I., Lowe J.S., Guicheney P., Caron L., et al. Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes. Circulation 115 4 (2007) 432-441
-
(2007)
Circulation
, vol.115
, Issue.4
, pp. 432-441
-
-
Mohler, P.J.1
Le Scouarnec, S.2
Denjoy, I.3
Lowe, J.S.4
Guicheney, P.5
Caron, L.6
-
50
-
-
36148952130
-
Mapping the binding site on small ankyrin 1 for obscurin
-
Borzok M.A., Catino D.H., Nicholson J.D., Kontrogianni-Konstantopoulos A., and Bloch R.J. Mapping the binding site on small ankyrin 1 for obscurin. J. Biol. Chem. 282 44 (2007) 32384-32396
-
(2007)
J. Biol. Chem.
, vol.282
, Issue.44
, pp. 32384-32396
-
-
Borzok, M.A.1
Catino, D.H.2
Nicholson, J.D.3
Kontrogianni-Konstantopoulos, A.4
Bloch, R.J.5
-
51
-
-
0347364671
-
The death domain of kidney ankyrin interacts with Fas and promotes Fas-mediated cell death in renal epithelia
-
Del Rio M., Imam A., DeLeon M., Gomez G., Mishra J., Ma Q., et al. The death domain of kidney ankyrin interacts with Fas and promotes Fas-mediated cell death in renal epithelia. J. Am. Soc. Nephrol. 15 1 (2004) 41-51
-
(2004)
J. Am. Soc. Nephrol.
, vol.15
, Issue.1
, pp. 41-51
-
-
Del Rio, M.1
Imam, A.2
DeLeon, M.3
Gomez, G.4
Mishra, J.5
Ma, Q.6
-
52
-
-
34548827681
-
Ankyrin-G is a molecular partner of E-cadherin in epithelial cells and early embryos
-
Kizhatil K., Davis J.Q., Davis L., Hoffman J., Hogan B.L., and Bennett V. Ankyrin-G is a molecular partner of E-cadherin in epithelial cells and early embryos. J Biol Chem 282 36 (2007) 26552-26561
-
(2007)
J Biol Chem
, vol.282
, Issue.36
, pp. 26552-26561
-
-
Kizhatil, K.1
Davis, J.Q.2
Davis, L.3
Hoffman, J.4
Hogan, B.L.5
Bennett, V.6
-
53
-
-
0034609531
-
Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2
-
Splawski I., Shen J., Timothy K.W., Lehmann M.H., Priori S., Robinson J.L., et al. Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation 102 10 (2000) 1178-1185
-
(2000)
Circulation
, vol.102
, Issue.10
, pp. 1178-1185
-
-
Splawski, I.1
Shen, J.2
Timothy, K.W.3
Lehmann, M.H.4
Priori, S.5
Robinson, J.L.6
-
55
-
-
0028914969
-
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
-
Curran M.E., Splawski I., Timothy K.W., Vincent G.M., Green E.D., and Keating M.T. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell 80 5 (1995) 795-803
-
(1995)
Cell
, vol.80
, Issue.5
, pp. 795-803
-
-
Curran, M.E.1
Splawski, I.2
Timothy, K.W.3
Vincent, G.M.4
Green, E.D.5
Keating, M.T.6
-
56
-
-
9044240040
-
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
-
Wang Q., Curran M.E., Splawski I., Burn T.C., Millholland J.M., VanRaay T.J., et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat. Genet. 12 1 (1996) 17-23
-
(1996)
Nat. Genet.
, vol.12
, Issue.1
, pp. 17-23
-
-
Wang, Q.1
Curran, M.E.2
Splawski, I.3
Burn, T.C.4
Millholland, J.M.5
VanRaay, T.J.6
-
57
-
-
0029116230
-
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia
-
Wang Q., Shen J., Li Z., Timothy K., Vincent G.M., Priori S.G., et al. Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia. Hum. Mol. Genet. 4 9 (1995) 1603-1607
-
(1995)
Hum. Mol. Genet.
, vol.4
, Issue.9
, pp. 1603-1607
-
-
Wang, Q.1
Shen, J.2
Li, Z.3
Timothy, K.4
Vincent, G.M.5
Priori, S.G.6
-
58
-
-
0028819671
-
Mapping of a gene for long QT syndrome to chromosome 4q25-27
-
Schott J.J., Charpentier F., Peltier S., Foley P., Drouin E., Bouhour J.B., et al. Mapping of a gene for long QT syndrome to chromosome 4q25-27. Am. J. Hum. Genet. 57 5 (1995) 1114-1122
-
(1995)
Am. J. Hum. Genet.
, vol.57
, Issue.5
, pp. 1114-1122
-
-
Schott, J.J.1
Charpentier, F.2
Peltier, S.3
Foley, P.4
Drouin, E.5
Bouhour, J.B.6
-
59
-
-
0024324830
-
Cellular origins of the transient inward current in cardiac myocytes. Role of fluctuations and waves of elevated intracellular calcium
-
Berlin J.R., Cannell M.B., and Lederer W.J. Cellular origins of the transient inward current in cardiac myocytes. Role of fluctuations and waves of elevated intracellular calcium. Circ. Res. 65 1 (1989) 115-126
-
(1989)
Circ. Res.
, vol.65
, Issue.1
, pp. 115-126
-
-
Berlin, J.R.1
Cannell, M.B.2
Lederer, W.J.3
-
60
-
-
0034721607
-
Sarcoplasmic reticulum Ca(2+) release causes myocyte depolarization. Underlying mechanism and threshold for triggered action potentials
-
Schlotthauer K., and Bers D.M. Sarcoplasmic reticulum Ca(2+) release causes myocyte depolarization. Underlying mechanism and threshold for triggered action potentials. Circ. Res. 87 9 (2000) 774-780
-
(2000)
Circ. Res.
, vol.87
, Issue.9
, pp. 774-780
-
-
Schlotthauer, K.1
Bers, D.M.2
-
61
-
-
0033847506
-
Relative importance of SR load and cytoplasmic calcium concentration in the genesis of aftercontractions in cardiac myocytes
-
Egdell R.M., De Souza A.I., and Macleod K.T. Relative importance of SR load and cytoplasmic calcium concentration in the genesis of aftercontractions in cardiac myocytes. Cardiovasc. Res. 47 4 (2000) 769-777
-
(2000)
Cardiovasc. Res.
, vol.47
, Issue.4
, pp. 769-777
-
-
Egdell, R.M.1
De Souza, A.I.2
Macleod, K.T.3
-
62
-
-
33845206599
-
Association of torsades de pointes with novel and known single nucleotide polymorphisms in long QT syndrome genes
-
Mank-Seymour A.R., Richmond J.L., Wood L.S., Reynolds J.M., Fan Y.T., Warnes G.R., et al. Association of torsades de pointes with novel and known single nucleotide polymorphisms in long QT syndrome genes. Am. Heart J. 152 6 (2006) 1116-1122
-
(2006)
Am. Heart J.
, vol.152
, Issue.6
, pp. 1116-1122
-
-
Mank-Seymour, A.R.1
Richmond, J.L.2
Wood, L.S.3
Reynolds, J.M.4
Fan, Y.T.5
Warnes, G.R.6
-
63
-
-
27744480028
-
Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects
-
Sherman J., Tester D.J., and Ackerman M.J. Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects. Heart Rhythm 2 11 (2005) 1218-1223
-
(2005)
Heart Rhythm
, vol.2
, Issue.11
, pp. 1218-1223
-
-
Sherman, J.1
Tester, D.J.2
Ackerman, M.J.3
-
64
-
-
0034624502
-
The evaluation and management of bradycardia
-
Mangrum J.M., and DiMarco J.P. The evaluation and management of bradycardia. N. Engl. J. Med. 342 10 (2000) 703-709
-
(2000)
N. Engl. J. Med.
, vol.342
, Issue.10
, pp. 703-709
-
-
Mangrum, J.M.1
DiMarco, J.P.2
-
65
-
-
0001895396
-
Aging changes in the human sinoatrial node
-
Lev M. Aging changes in the human sinoatrial node. J. Gerontol. 9 1 (1954) 1-9
-
(1954)
J. Gerontol.
, vol.9
, Issue.1
, pp. 1-9
-
-
Lev, M.1
-
66
-
-
0026537455
-
Survey of cardiac pacing in the United States in 1989
-
Bernstein A.D., and Parsonnet V. Survey of cardiac pacing in the United States in 1989. Am. J. Cardiol. 69 4 (1992) 331-338
-
(1992)
Am. J. Cardiol.
, vol.69
, Issue.4
, pp. 331-338
-
-
Bernstein, A.D.1
Parsonnet, V.2
-
67
-
-
0018220461
-
Histopathological correlates of sinoatrial disease
-
Demoulin J.C., and Kulbertus H.E. Histopathological correlates of sinoatrial disease. Br. Heart J. 40 12 (1978) 1384-1389
-
(1978)
Br. Heart J.
, vol.40
, Issue.12
, pp. 1384-1389
-
-
Demoulin, J.C.1
Kulbertus, H.E.2
-
68
-
-
0242317397
-
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)
-
Benson D.W., Wang D.W., Dyment M., Knilans T.K., Fish F.A., Strieper M.J., et al. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A). J. Clin. Invest. 112 7 (2003) 1019-1028
-
(2003)
J. Clin. Invest.
, vol.112
, Issue.7
, pp. 1019-1028
-
-
Benson, D.W.1
Wang, D.W.2
Dyment, M.3
Knilans, T.K.4
Fish, F.A.5
Strieper, M.J.6
-
69
-
-
21144438184
-
A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families
-
Smits J.P., Koopmann T.T., Wilders R., Veldkamp M.W., Opthof T., Bhuiyan Z.A., et al. A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families. J. Mol. Cell. Cardiol. 38 6 (2005) 969-981
-
(2005)
J. Mol. Cell. Cardiol.
, vol.38
, Issue.6
, pp. 969-981
-
-
Smits, J.P.1
Koopmann, T.T.2
Wilders, R.3
Veldkamp, M.W.4
Opthof, T.5
Bhuiyan, Z.A.6
-
70
-
-
3042549234
-
Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia
-
Ueda K., Nakamura K., Hayashi T., Inagaki N., Takahashi M., Arimura T., et al. Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia. J. Biol. Chem. 279 26 (2004) 27194-27198
-
(2004)
J. Biol. Chem.
, vol.279
, Issue.26
, pp. 27194-27198
-
-
Ueda, K.1
Nakamura, K.2
Hayashi, T.3
Inagaki, N.4
Takahashi, M.5
Arimura, T.6
-
71
-
-
0038434034
-
Increased open probability of single cardiac L-type calcium channels in patients with chronic atrial fibrillation. role of phosphatase 2A
-
Klein G., Schroder F., Vogler D., Schaefer A., Haverich A., Schieffer B., et al. Increased open probability of single cardiac L-type calcium channels in patients with chronic atrial fibrillation. role of phosphatase 2A. Cardiovasc. Res. 59 1 (2003) 37-45
-
(2003)
Cardiovasc. Res.
, vol.59
, Issue.1
, pp. 37-45
-
-
Klein, G.1
Schroder, F.2
Vogler, D.3
Schaefer, A.4
Haverich, A.5
Schieffer, B.6
-
72
-
-
54349116992
-
Phosphodiesterase 4 and phosphatase 2A differentially regulate cAMP/protein kinase a signaling for cardiac myocyte contraction under stimulation of beta1 adrenergic receptor
-
De Arcangelis V., Soto D., and Xiang Y. Phosphodiesterase 4 and phosphatase 2A differentially regulate cAMP/protein kinase a signaling for cardiac myocyte contraction under stimulation of beta1 adrenergic receptor. Mol. Pharmacol. 74 5 (2008) 1453-1462
-
(2008)
Mol. Pharmacol.
, vol.74
, Issue.5
, pp. 1453-1462
-
-
De Arcangelis, V.1
Soto, D.2
Xiang, Y.3
-
74
-
-
0034671738
-
Protein phosphatase 2A is associated with class C L-type calcium channels (Cav1.2) and antagonizes channel phosphorylation by cAMP-dependent protein kinase
-
Davare M.A., Horne M.C., and Hell J.W. Protein phosphatase 2A is associated with class C L-type calcium channels (Cav1.2) and antagonizes channel phosphorylation by cAMP-dependent protein kinase. J. Biol. Chem. 275 50 (2000) 39710-39717
-
(2000)
J. Biol. Chem.
, vol.275
, Issue.50
, pp. 39710-39717
-
-
Davare, M.A.1
Horne, M.C.2
Hell, J.W.3
-
75
-
-
0034640113
-
PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts
-
Marx S.O., Reiken S., Hisamatsu Y., Jayaraman T., Burkhoff D., Rosemblit N., et al. PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts. Cell 101 4 (2000) 365-376
-
(2000)
Cell
, vol.101
, Issue.4
, pp. 365-376
-
-
Marx, S.O.1
Reiken, S.2
Hisamatsu, Y.3
Jayaraman, T.4
Burkhoff, D.5
Rosemblit, N.6
-
76
-
-
0037131261
-
Protein kinase A and two phosphatases are components of the inositol 1,4,5-trisphosphate receptor macromolecular signaling complex
-
DeSouza N., Reiken S., Ondrias K., Yang Y.M., Matkovich S., and Marks A.R. Protein kinase A and two phosphatases are components of the inositol 1,4,5-trisphosphate receptor macromolecular signaling complex. J. Biol. Chem. 277 42 (2002) 39397-39400
-
(2002)
J. Biol. Chem.
, vol.277
, Issue.42
, pp. 39397-39400
-
-
DeSouza, N.1
Reiken, S.2
Ondrias, K.3
Yang, Y.M.4
Matkovich, S.5
Marks, A.R.6
-
77
-
-
33845625148
-
Na,K-ATPase alpha1-subunit dephosphorylation by protein phosphatase 2A is necessary for its recruitment to the plasma membrane
-
Lecuona E., Dada L.A., Sun H., Butti M.L., Zhou G., Chew T.L., et al. Na,K-ATPase alpha1-subunit dephosphorylation by protein phosphatase 2A is necessary for its recruitment to the plasma membrane. FASEB J. 20 14 (2006) 2618-2620
-
(2006)
FASEB J.
, vol.20
, Issue.14
, pp. 2618-2620
-
-
Lecuona, E.1
Dada, L.A.2
Sun, H.3
Butti, M.L.4
Zhou, G.5
Chew, T.L.6
-
78
-
-
0141868811
-
Rapid response of cardiac obscurin gene cluster to aortic stenosis: differential activation of Rho-GEF and MLCK and involvement in hypertrophic growth
-
Borisov A.B., Raeker M.O., Kontrogianni-Konstantopoulos A., Yang K., Kurnit D.M., Bloch R.J., et al. Rapid response of cardiac obscurin gene cluster to aortic stenosis: differential activation of Rho-GEF and MLCK and involvement in hypertrophic growth. Biochem. Biophys. Res. Commun. 310 3 (2003) 910-918
-
(2003)
Biochem. Biophys. Res. Commun.
, vol.310
, Issue.3
, pp. 910-918
-
-
Borisov, A.B.1
Raeker, M.O.2
Kontrogianni-Konstantopoulos, A.3
Yang, K.4
Kurnit, D.M.5
Bloch, R.J.6
-
79
-
-
32444435668
-
Essential role of obscurin in cardiac myofibrillogenesis and hypertrophic response: evidence from small interfering RNA-mediated gene silencing
-
Borisov A.B., Sutter S.B., Kontrogianni-Konstantopoulos A., Bloch R.J., Westfall M.V., and Russell M.W. Essential role of obscurin in cardiac myofibrillogenesis and hypertrophic response: evidence from small interfering RNA-mediated gene silencing. Histochem. Cell Biol. 125 3 (2006) 227-238
-
(2006)
Histochem. Cell Biol.
, vol.125
, Issue.3
, pp. 227-238
-
-
Borisov, A.B.1
Sutter, S.B.2
Kontrogianni-Konstantopoulos, A.3
Bloch, R.J.4
Westfall, M.V.5
Russell, M.W.6
-
80
-
-
61949226650
-
2+ release and promotes cardiac arrhythmogenesis by targeting PP2A regulatory subunit B56{alpha} and causing CaMKII-dependent hyperphosphorylation of RyR2
-
2+ release and promotes cardiac arrhythmogenesis by targeting PP2A regulatory subunit B56{alpha} and causing CaMKII-dependent hyperphosphorylation of RyR2. Circ. Res. 104 (2009) 514-521
-
(2009)
Circ. Res.
, vol.104
, pp. 514-521
-
-
Terentyev, D.1
Belevych, A.E.2
Terentyeva, R.3
Martin, M.M.4
Malana, G.E.5
Kuhn, D.E.6
-
81
-
-
60149094801
-
Regulation of the ankyrin-B-based targeting pathway following myocardial infarction
-
Hund T.J., Wright P.J., Dun W., Snyder J.S., Boyden P.A., and Mohler P.J. Regulation of the ankyrin-B-based targeting pathway following myocardial infarction. Cardiovasc. Res. 81 4 (2009) 742-749
-
(2009)
Cardiovasc. Res.
, vol.81
, Issue.4
, pp. 742-749
-
-
Hund, T.J.1
Wright, P.J.2
Dun, W.3
Snyder, J.S.4
Boyden, P.A.5
Mohler, P.J.6
-
82
-
-
0024325322
-
Electrophysiological mechanisms of ventricular arrhythmias resulting from myocardial ischemia and infarction
-
Janse M.J., and Wit A.L. Electrophysiological mechanisms of ventricular arrhythmias resulting from myocardial ischemia and infarction. Physiol. Rev. 69 4 (1989) 1049-1169
-
(1989)
Physiol. Rev.
, vol.69
, Issue.4
, pp. 1049-1169
-
-
Janse, M.J.1
Wit, A.L.2
-
83
-
-
0032979165
-
Electrical remodeling in ischemia and infarction
-
Pinto J.M., and Boyden P.A. Electrical remodeling in ischemia and infarction. Cardiovasc. Res. 42 2 (1999) 284-297
-
(1999)
Cardiovasc. Res.
, vol.42
, Issue.2
, pp. 284-297
-
-
Pinto, J.M.1
Boyden, P.A.2
-
84
-
-
27144523810
-
Remodeling in cells from different regions of the reentrant circuit during ventricular tachycardia
-
Baba S., Dun W., Cabo C., and Boyden P.A. Remodeling in cells from different regions of the reentrant circuit during ventricular tachycardia. Circulation 112 16 (2005) 2386-2396
-
(2005)
Circulation
, vol.112
, Issue.16
, pp. 2386-2396
-
-
Baba, S.1
Dun, W.2
Cabo, C.3
Boyden, P.A.4
-
85
-
-
0030969591
-
+ currents in myocytes from epicardial border zone of the infarcted heart. A possible ionic mechanism for reduced excitability and postrepolarization refractoriness
-
+ currents in myocytes from epicardial border zone of the infarcted heart. A possible ionic mechanism for reduced excitability and postrepolarization refractoriness. Circ. Res. 81 1 (1997) 110-119
-
(1997)
Circ. Res.
, vol.81
, Issue.1
, pp. 110-119
-
-
Pu, J.1
Boyden, P.A.2
-
88
-
-
0042859880
-
Short QT syndrome: a familial cause of sudden death
-
Gaita F., Giustetto C., Bianchi F., Wolpert C., Schimpf R., Riccardi R., et al. Short QT syndrome: a familial cause of sudden death. Circulation 108 8 (2003) 965-970
-
(2003)
Circulation
, vol.108
, Issue.8
, pp. 965-970
-
-
Gaita, F.1
Giustetto, C.2
Bianchi, F.3
Wolpert, C.4
Schimpf, R.5
Riccardi, R.6
-
89
-
-
0035936798
-
Molecular and cellular mechanisms of cardiac arrhythmias
-
Keating M.T., and Sanguinetti M.C. Molecular and cellular mechanisms of cardiac arrhythmias. Cell 104 4 (2001) 569-580
-
(2001)
Cell
, vol.104
, Issue.4
, pp. 569-580
-
-
Keating, M.T.1
Sanguinetti, M.C.2
-
90
-
-
0028905566
-
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
-
Wang Q., Shen J., Splawski I., Atkinson D., Li Z., Robinson J.L., et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 80 5 (1995) 805-811
-
(1995)
Cell
, vol.80
, Issue.5
, pp. 805-811
-
-
Wang, Q.1
Shen, J.2
Splawski, I.3
Atkinson, D.4
Li, Z.5
Robinson, J.L.6
-
91
-
-
20144386917
-
Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study
-
Pfeufer A., Jalilzadeh S., Perz S., Mueller J.C., Hinterseer M., Illig T., et al. Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study. Circ. Res. 96 6 (2005) 693-701
-
(2005)
Circ. Res.
, vol.96
, Issue.6
, pp. 693-701
-
-
Pfeufer, A.1
Jalilzadeh, S.2
Perz, S.3
Mueller, J.C.4
Hinterseer, M.5
Illig, T.6
-
92
-
-
67649104059
-
Common genetic variants in ANK2 modulate QT interval: results from the KORA study
-
Sedlacek K., Stark K., Cunha S.R., Pfeufer A., Weber S., Berger I., et al. Common genetic variants in ANK2 modulate QT interval: results from the KORA study. Circulation: Cardiovasc. Genet. 1 2 (2008) 93-99
-
(2008)
Circulation: Cardiovasc. Genet.
, vol.1
, Issue.2
, pp. 93-99
-
-
Sedlacek, K.1
Stark, K.2
Cunha, S.R.3
Pfeufer, A.4
Weber, S.5
Berger, I.6
-
93
-
-
33846941214
-
The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study
-
Akyol M., Jalilzadeh S., Sinner M.F., Perz S., Beckmann B.M., Gieger C., et al. The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study. Eur. Heart J. 28 3 (2007) 305-309
-
(2007)
Eur. Heart J.
, vol.28
, Issue.3
, pp. 305-309
-
-
Akyol, M.1
Jalilzadeh, S.2
Sinner, M.F.3
Perz, S.4
Beckmann, B.M.5
Gieger, C.6
-
94
-
-
33745237158
-
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
-
Arking D.E., Pfeufer A., Post W., Kao W.H., Newton-Cheh C., Ikeda M., et al. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat. Genet. 38 6 (2006) 644-651
-
(2006)
Nat. Genet.
, vol.38
, Issue.6
, pp. 644-651
-
-
Arking, D.E.1
Pfeufer, A.2
Post, W.3
Kao, W.H.4
Newton-Cheh, C.5
Ikeda, M.6
-
95
-
-
0029097799
-
Molecular mechanism for an inherited cardiac arrhythmia
-
Bennett P.B., Yazawa K., Makita N., and George Jr. A.L. Molecular mechanism for an inherited cardiac arrhythmia. Nature 376 6542 (1995) 683-685
-
(1995)
Nature
, vol.376
, Issue.6542
, pp. 683-685
-
-
Bennett, P.B.1
Yazawa, K.2
Makita, N.3
George Jr., A.L.4
-
96
-
-
0032546384
-
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
-
Chen Q., Kirsch G.E., Zhang D., Brugada R., Brugada J., Brugada P., et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature 392 6673 (1998) 293-296
-
(1998)
Nature
, vol.392
, Issue.6673
, pp. 293-296
-
-
Chen, Q.1
Kirsch, G.E.2
Zhang, D.3
Brugada, R.4
Brugada, J.5
Brugada, P.6
-
97
-
-
0003096674
-
Cardiac conduction defects associate with mutations in SCN5A
-
Schott J.J., Alshinawi C., Kyndt F., Probst V., Hoorntje T.M., Hulsbeek M., et al. Cardiac conduction defects associate with mutations in SCN5A. Nat. Genet. 23 1 (1999) 20-21
-
(1999)
Nat. Genet.
, vol.23
, Issue.1
, pp. 20-21
-
-
Schott, J.J.1
Alshinawi, C.2
Kyndt, F.3
Probst, V.4
Hoorntje, T.M.5
Hulsbeek, M.6
-
98
-
-
0032582909
-
AnkyrinG is required for clustering of voltage-gated Na channels at axon initial segments and for normal action potential firing
-
Zhou D., Lambert S., Malen P.L., Carpenter S., Boland L.M., and Bennett V. AnkyrinG is required for clustering of voltage-gated Na channels at axon initial segments and for normal action potential firing. J. Cell Biol. 143 5 (1998) 1295-1304
-
(1998)
J. Cell Biol.
, vol.143
, Issue.5
, pp. 1295-1304
-
-
Zhou, D.1
Lambert, S.2
Malen, P.L.3
Carpenter, S.4
Boland, L.M.5
Bennett, V.6
-
99
-
-
0037133171
-
Developing nodes of Ranvier are defined by ankyrin-G clustering and are independent of paranodal axoglial adhesion
-
Jenkins S.M., and Bennett V. Developing nodes of Ranvier are defined by ankyrin-G clustering and are independent of paranodal axoglial adhesion. Proc. Natl. Acad. Sci. U. S. A. 99 4 (2002) 2303-2308
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, Issue.4
, pp. 2303-2308
-
-
Jenkins, S.M.1
Bennett, V.2
-
100
-
-
0024708031
-
+ channels and ankyrin in neuromuscular junctions is complementary to that of acetylcholine receptors and the 43 kD protein
-
+ channels and ankyrin in neuromuscular junctions is complementary to that of acetylcholine receptors and the 43 kD protein. Neuron 3 2 (1989) 163-175
-
(1989)
Neuron
, vol.3
, Issue.2
, pp. 163-175
-
-
Flucher, B.E.1
Daniels, M.P.2
-
101
-
-
0031711226
-
AnkyrinG is associated with the postsynaptic membrane and the sarcoplasmic reticulum in the skeletal muscle fiber
-
Kordeli E., Ludosky M.A., Deprette C., Frappier T., and Cartaud J. AnkyrinG is associated with the postsynaptic membrane and the sarcoplasmic reticulum in the skeletal muscle fiber. J. Cell. Sci. 111 Pt 15 (1998) 2197-2207
-
(1998)
J. Cell. Sci.
, vol.111
, Issue.PART 15
, pp. 2197-2207
-
-
Kordeli, E.1
Ludosky, M.A.2
Deprette, C.3
Frappier, T.4
Cartaud, J.5
-
102
-
-
0032498588
-
beta-Spectrin is colocalized with both voltage-gated sodium channels and ankyrinG at the adult rat neuromuscular junction
-
Wood S.J., and Slater C.R. beta-Spectrin is colocalized with both voltage-gated sodium channels and ankyrinG at the adult rat neuromuscular junction. J. Cell Biol. 140 3 (1998) 675-684
-
(1998)
J. Cell Biol.
, vol.140
, Issue.3
, pp. 675-684
-
-
Wood, S.J.1
Slater, C.R.2
-
103
-
-
0028985712
-
AnkyrinG. A new ankyrin gene with neural-specific isoforms localized at the axonal initial segment and node of Ranvier
-
Kordeli E., Lambert S., and Bennett V. AnkyrinG. A new ankyrin gene with neural-specific isoforms localized at the axonal initial segment and node of Ranvier. J. Biol. Chem. 270 5 (1995) 2352-2359
-
(1995)
J. Biol. Chem.
, vol.270
, Issue.5
, pp. 2352-2359
-
-
Kordeli, E.1
Lambert, S.2
Bennett, V.3
-
104
-
-
0030443956
-
Molecular composition of the node of Ranvier: identification of ankyrin-binding cell adhesion molecules neurofascin (mucin+/third FNIII domain-) and NrCAM at nodal axon segments
-
Davis J.Q., Lambert S., and Bennett V. Molecular composition of the node of Ranvier: identification of ankyrin-binding cell adhesion molecules neurofascin (mucin+/third FNIII domain-) and NrCAM at nodal axon segments. J. Cell Biol. 135 5 (1996) 1355-1367
-
(1996)
J. Cell Biol.
, vol.135
, Issue.5
, pp. 1355-1367
-
-
Davis, J.Q.1
Lambert, S.2
Bennett, V.3
-
105
-
-
33644819526
-
A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon
-
Pan Z., Kao T., Horvath Z., Lemos J., Sul J.Y., Cranstoun S.D., et al. A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon. J. Neurosci. 26 10 (2006) 2599-2613
-
(2006)
J. Neurosci.
, vol.26
, Issue.10
, pp. 2599-2613
-
-
Pan, Z.1
Kao, T.2
Horvath, Z.3
Lemos, J.4
Sul, J.Y.5
Cranstoun, S.D.6
-
106
-
-
58149144729
-
Ion channel clustering at the axon initial segment and node of Ranvier evolved sequentially in early chordates
-
Hill A.S., Nishino A., Nakajo K., Zhang G., Fineman J.R., Selzer M.E., et al. Ion channel clustering at the axon initial segment and node of Ranvier evolved sequentially in early chordates. PLoS Genet. 4 12 (2008) e1000317
-
(2008)
PLoS Genet.
, vol.4
, Issue.12
-
-
Hill, A.S.1
Nishino, A.2
Nakajo, K.3
Zhang, G.4
Fineman, J.R.5
Selzer, M.E.6
-
107
-
-
0038270765
-
A targeting motif involved in sodium channel clustering at the axonal initial segment
-
Garrido J.J., Giraud P., Carlier E., Fernandes F., Moussif A., Fache M.P., et al. A targeting motif involved in sodium channel clustering at the axonal initial segment. Science 300 5628 (2003) 2091-2094
-
(2003)
Science
, vol.300
, Issue.5628
, pp. 2091-2094
-
-
Garrido, J.J.1
Giraud, P.2
Carlier, E.3
Fernandes, F.4
Moussif, A.5
Fache, M.P.6
-
108
-
-
0041345748
-
Identification of a conserved ankyrin-binding motif in the family of sodium channel alpha subunits
-
Lemaillet G., Walker B., and Lambert S. Identification of a conserved ankyrin-binding motif in the family of sodium channel alpha subunits. J. Biol. Chem. 278 30 (2003) 27333-27339
-
(2003)
J. Biol. Chem.
, vol.278
, Issue.30
, pp. 27333-27339
-
-
Lemaillet, G.1
Walker, B.2
Lambert, S.3
-
109
-
-
20144388932
-
Brugada syndrome: report of the second consensus conference
-
Antzelevitch C., Brugada P., Borggrefe M., Brugada J., Brugada R., Corrado D., et al. Brugada syndrome: report of the second consensus conference. Heart Rhythm 2 4 (2005) 429-440
-
(2005)
Heart Rhythm
, vol.2
, Issue.4
, pp. 429-440
-
-
Antzelevitch, C.1
Brugada, P.2
Borggrefe, M.3
Brugada, J.4
Brugada, R.5
Corrado, D.6
-
110
-
-
1042268063
-
Inherited arrhythmogenic diseases: the complexity beyond monogenic disorders
-
Priori S.G. Inherited arrhythmogenic diseases: the complexity beyond monogenic disorders. Circ. Res. 94 2 (2004) 140-145
-
(2004)
Circ. Res.
, vol.94
, Issue.2
, pp. 140-145
-
-
Priori, S.G.1
-
111
-
-
3042800339
-
Genetics of cardiac arrhythmias and sudden cardiac death
-
Priori S.G., and Napolitano C. Genetics of cardiac arrhythmias and sudden cardiac death. Ann. N.Y. Acad. Sci. 1015 (2004) 96-110
-
(2004)
Ann. N.Y. Acad. Sci.
, vol.1015
, pp. 96-110
-
-
Priori, S.G.1
Napolitano, C.2
-
112
-
-
0037125369
-
Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients
-
Smits J.P., Eckardt L., Probst V., Bezzina C.R., Schott J.J., Remme C.A., et al. Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients. J. Am. Coll. Cardiol. 40 2 (2002) 350-356
-
(2002)
J. Am. Coll. Cardiol.
, vol.40
, Issue.2
, pp. 350-356
-
-
Smits, J.P.1
Eckardt, L.2
Probst, V.3
Bezzina, C.R.4
Schott, J.J.5
Remme, C.A.6
-
113
-
-
0037133593
-
Natural history of Brugada syndrome: insights for risk stratification and management
-
Priori S.G., Napolitano C., Gasparini M., Pappone C., Della Bella P., Giordano U., et al. Natural history of Brugada syndrome: insights for risk stratification and management. Circulation 105 11 (2002) 1342-1347
-
(2002)
Circulation
, vol.105
, Issue.11
, pp. 1342-1347
-
-
Priori, S.G.1
Napolitano, C.2
Gasparini, M.3
Pappone, C.4
Della Bella, P.5
Giordano, U.6
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