-
1
-
-
0032751084
-
Channelopathies of inwardly rectifying potassium channels
-
Abraham M.R., Jahangir A., Alekseev A.E., and Terzic A. Channelopathies of inwardly rectifying potassium channels. FASEB J. 13 (1999) 1901-1910
-
(1999)
FASEB J.
, vol.13
, pp. 1901-1910
-
-
Abraham, M.R.1
Jahangir, A.2
Alekseev, A.E.3
Terzic, A.4
-
2
-
-
0034831138
-
Segmental duplications: organization and impact within the current human genome project assembly
-
Bailey J.A., Yavor A.M., Massa H.F., Trask B.J., and Eichler E.E. Segmental duplications: organization and impact within the current human genome project assembly. Genome Res. 11 (2001) 1005-1017
-
(2001)
Genome Res.
, vol.11
, pp. 1005-1017
-
-
Bailey, J.A.1
Yavor, A.M.2
Massa, H.F.3
Trask, B.J.4
Eichler, E.E.5
-
3
-
-
1242296273
-
Mechanisms of thyroid hormone receptor-specific nuclear and extra nuclear actions
-
Bassett J.H., Harvey C.B., and Williams G.R. Mechanisms of thyroid hormone receptor-specific nuclear and extra nuclear actions. Mol. Cell. Endocrinol. 213 (2003) 1-11
-
(2003)
Mol. Cell. Endocrinol.
, vol.213
, pp. 1-11
-
-
Bassett, J.H.1
Harvey, C.B.2
Williams, G.R.3
-
4
-
-
0032801833
-
A novel sodium channel mutation in a family with hypokalemic periodic paralysis
-
Bulman D.E., Scoggan K.A., van Oene M.D., Nicolle M.W., Hahn A.F., Tollar L.L., and Ebers G.C. A novel sodium channel mutation in a family with hypokalemic periodic paralysis. Neurology 53 (1999) 1932-1936
-
(1999)
Neurology
, vol.53
, pp. 1932-1936
-
-
Bulman, D.E.1
Scoggan, K.A.2
van Oene, M.D.3
Nicolle, M.W.4
Hahn, A.F.5
Tollar, L.L.6
Ebers, G.C.7
-
5
-
-
0037777713
-
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome
-
Donaldson M.R., Jensen J.L., Tristani-Firouzi M., Tawil R., Bendahhou S., Suarez W.A., Cobo A.M., Poza J.J., Behr E., Wagstaff J., et al. PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome. Neurology 60 (2003) 1811-1816
-
(2003)
Neurology
, vol.60
, pp. 1811-1816
-
-
Donaldson, M.R.1
Jensen, J.L.2
Tristani-Firouzi, M.3
Tawil, R.4
Bendahhou, S.5
Suarez, W.A.6
Cobo, A.M.7
Poza, J.J.8
Behr, E.9
Wagstaff, J.10
-
6
-
-
1942499458
-
An assessment of the sequence gaps: unfinished business in a finished human genome
-
Eichler E.E., Clark R.A., and She X. An assessment of the sequence gaps: unfinished business in a finished human genome. Nat. Rev. Genet. 5 (2004) 345-354
-
(2004)
Nat. Rev. Genet.
, vol.5
, pp. 345-354
-
-
Eichler, E.E.1
Clark, R.A.2
She, X.3
-
7
-
-
0031033619
-
The human inward rectifying K+ channel Kir 2.2 (KCNJ12) gene: gene structure, assignment to chromosome 17p11.1, and identification of a simple tandem repeat polymorphism
-
Hugnot J.P., Pedeutour F., Le Calvez C., Grosgeorge J., Passage E., Fontes M., and Lazdunski M. The human inward rectifying K+ channel Kir 2.2 (KCNJ12) gene: gene structure, assignment to chromosome 17p11.1, and identification of a simple tandem repeat polymorphism. Genomics 39 (1997) 113-116
-
(1997)
Genomics
, vol.39
, pp. 113-116
-
-
Hugnot, J.P.1
Pedeutour, F.2
Le Calvez, C.3
Grosgeorge, J.4
Passage, E.5
Fontes, M.6
Lazdunski, M.7
-
8
-
-
0037126016
-
Human cardiac inwardly-rectifying K+ channel Kir(2.1b) is inhibited by direct protein kinase C-dependent regulation in human isolated cardiomyocytes and in an expression system
-
Karle C.A., Zitron E., Zhang W., Wendt-Nordahl G., Kathöfer S., Thomas D., Gut B., Scholz E., Vahl C.F., Katus H.A., and Kiehn J. Human cardiac inwardly-rectifying K+ channel Kir(2.1b) is inhibited by direct protein kinase C-dependent regulation in human isolated cardiomyocytes and in an expression system. Circulation 106 (2002) 1493-1499
-
(2002)
Circulation
, vol.106
, pp. 1493-1499
-
-
Karle, C.A.1
Zitron, E.2
Zhang, W.3
Wendt-Nordahl, G.4
Kathöfer, S.5
Thomas, D.6
Gut, B.7
Scholz, E.8
Vahl, C.F.9
Katus, H.A.10
Kiehn, J.11
-
9
-
-
0035752485
-
Thyroxine signal transduction in liver cells involves phospholipase C and phospholipase D activation. Genomic independent action of thyroid hormone
-
Kavok N.S., Krasilnikova O.A., and Babenko N.A. Thyroxine signal transduction in liver cells involves phospholipase C and phospholipase D activation. Genomic independent action of thyroid hormone. BMC Cell Biol. 2 (2001) 5
-
(2001)
BMC Cell Biol.
, vol.2
, pp. 5
-
-
Kavok, N.S.1
Krasilnikova, O.A.2
Babenko, N.A.3
-
10
-
-
0024458585
-
Thyrotoxic periodic paralysis. Report of 10 cases and review of electromyographic findings
-
Kelley D.E., Gharib H., Kennedy F.P., Duda Jr. R.J., and McManis P.G. Thyrotoxic periodic paralysis. Report of 10 cases and review of electromyographic findings. Arch. Intern. Med. 149 (1989) 2597-2600
-
(1989)
Arch. Intern. Med.
, vol.149
, pp. 2597-2600
-
-
Kelley, D.E.1
Gharib, H.2
Kennedy, F.P.3
Duda Jr., R.J.4
McManis, P.G.5
-
11
-
-
0032077277
-
A novel inward rectifier K+ channel with unique pore properties
-
Krapivinsky G., Medina I., Eng L., Krapivinsky L., Yang Y., and Clapham D.E. A novel inward rectifier K+ channel with unique pore properties. Neuron 20 (1998) 995-1005
-
(1998)
Neuron
, vol.20
, pp. 995-1005
-
-
Krapivinsky, G.1
Medina, I.2
Eng, L.3
Krapivinsky, L.4
Yang, Y.5
Clapham, D.E.6
-
12
-
-
1642280895
-
Thyrotoxic Periodic Paralysis
-
Wass J.A.H., Shalet S.M., and Gale E.A.M. (Eds), Oxford University Press, Oxford
-
Kung A.W. Thyrotoxic Periodic Paralysis. In: Wass J.A.H., Shalet S.M., and Gale E.A.M. (Eds). Oxford Textbook of Endocrinology and Diabetes (2002), Oxford University Press, Oxford 427-429
-
(2002)
Oxford Textbook of Endocrinology and Diabetes
, pp. 427-429
-
-
Kung, A.W.1
-
13
-
-
33745786609
-
Clinical review: thyrotoxic periodic paralysis: a diagnostic challenge
-
Kung A.W. Clinical review: thyrotoxic periodic paralysis: a diagnostic challenge. J. Clin. Endocrinol. Metab. 91 (2006) 2490-2495
-
(2006)
J. Clin. Endocrinol. Metab.
, vol.91
, pp. 2490-2495
-
-
Kung, A.W.1
-
14
-
-
0037423665
-
Microarray analysis reveals complex remodeling of cardiac ion channel expression with altered thyroid status: relation to cellular and integrated electrophysiology
-
Le Bouter S., Demolombe S., Chambellan A., Bellocq C., Aimond F., Toumaniantz G., Lande G., Siavoshian S., Baró I., Pond A.L., et al. Microarray analysis reveals complex remodeling of cardiac ion channel expression with altered thyroid status: relation to cellular and integrated electrophysiology. Circ. Res. 92 (2003) 234-242
-
(2003)
Circ. Res.
, vol.92
, pp. 234-242
-
-
Le Bouter, S.1
Demolombe, S.2
Chambellan, A.3
Bellocq, C.4
Aimond, F.5
Toumaniantz, G.6
Lande, G.7
Siavoshian, S.8
Baró, I.9
Pond, A.L.10
-
15
-
-
2542470459
-
Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins
-
Leonoudakis D., Conti L.R., Anderson S., Radeke C.M., McGuire L.M., Adams M.E., Froehner S.C., Yates III J.R., and Vandenberg C.A. Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins. J. Biol. Chem. 279 (2004) 22331-22346
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 22331-22346
-
-
Leonoudakis, D.1
Conti, L.R.2
Anderson, S.3
Radeke, C.M.4
McGuire, L.M.5
Adams, M.E.6
Froehner, S.C.7
Yates III, J.R.8
Vandenberg, C.A.9
-
16
-
-
2442515348
-
A multiprotein trafficking complex composed of SAP97, CASK, Veli, and Mint1 is associated with inward rectifier Kir2 potassium channels
-
Leonoudakis D., Conti L.R., Radeke C.M., McGuire L.M., and Vandenberg C.A. A multiprotein trafficking complex composed of SAP97, CASK, Veli, and Mint1 is associated with inward rectifier Kir2 potassium channels. J. Biol. Chem. 279 (2004) 19051-19063
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 19051-19063
-
-
Leonoudakis, D.1
Conti, L.R.2
Radeke, C.M.3
McGuire, L.M.4
Vandenberg, C.A.5
-
17
-
-
0033022440
-
Thyroid hormone induces activation of mitogen-activated protein kinase in cultured cells
-
Lin H.Y., Davis F.B., Gordinier J.K., Martino L.J., and Davis P.J. Thyroid hormone induces activation of mitogen-activated protein kinase in cultured cells. Am. J. Physiol. 276 (1999) C1014-C1024
-
(1999)
Am. J. Physiol.
, vol.276
-
-
Lin, H.Y.1
Davis, F.B.2
Gordinier, J.K.3
Martino, L.J.4
Davis, P.J.5
-
18
-
-
0037071897
-
Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies
-
Lopes C.M., Zhang H., Rohacs T., Jin T., Yang J., and Logothetis D.E. Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies. Neuron 34 (2002) 933-944
-
(2002)
Neuron
, vol.34
, pp. 933-944
-
-
Lopes, C.M.1
Zhang, H.2
Rohacs, T.3
Jin, T.4
Yang, J.5
Logothetis, D.E.6
-
19
-
-
2342652379
-
Mechanism of rectification in inward-rectifier K+ channels
-
Lu Z. Mechanism of rectification in inward-rectifier K+ channels. Annu. Rev. Physiol. 66 (2004) 103-129
-
(2004)
Annu. Rev. Physiol.
, vol.66
, pp. 103-129
-
-
Lu, Z.1
-
20
-
-
0029896262
-
Kir2.2v: a possible negative regulator of the inwardly rectifying K+ channel Kir2.2
-
Namba N., Inagaki N., Gonoi T., Seino Y., and Seino S. Kir2.2v: a possible negative regulator of the inwardly rectifying K+ channel Kir2.2. FEBS Lett. 386 (1996) 211-214
-
(1996)
FEBS Lett.
, vol.386
, pp. 211-214
-
-
Namba, N.1
Inagaki, N.2
Gonoi, T.3
Seino, Y.4
Seino, S.5
-
21
-
-
0031424251
-
The inwardly rectifying potassium channel subunit Kir2.2v (KCNJN1) maps to 17p11.2->p11.1
-
Namba N., Mori R., Tanaka H., Kondo I., Narahara K., and Seino Y. The inwardly rectifying potassium channel subunit Kir2.2v (KCNJN1) maps to 17p11.2->p11.1. Cytogenet. Cell Genet. 79 (1997) 85-87
-
(1997)
Cytogenet. Cell Genet.
, vol.79
, pp. 85-87
-
-
Namba, N.1
Mori, R.2
Tanaka, H.3
Kondo, I.4
Narahara, K.5
Seino, Y.6
-
24
-
-
0035907032
-
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
-
Plaster N.M., Tawil R., Tristani-Firouzi M., Canún S., Bendahhou S., Tsunoda A., Donaldson M.R., Iannaccone S.T., Brunt E., Barohn R., et al. Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. Cell 105 (2001) 511-519
-
(2001)
Cell
, vol.105
, pp. 511-519
-
-
Plaster, N.M.1
Tawil, R.2
Tristani-Firouzi, M.3
Canún, S.4
Bendahhou, S.5
Tsunoda, A.6
Donaldson, M.R.7
Iannaccone, S.T.8
Brunt, E.9
Barohn, R.10
-
25
-
-
0037188493
-
Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome
-
Preisig-Müller R., Schlichthörl G., Goerge T., Heinen S., Brüggemann A., Rajan S., Derst C., Veh R.W., and Daut J. Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome. Proc. Natl. Acad. Sci. USA 99 (2002) 7774-7779
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 7774-7779
-
-
Preisig-Müller, R.1
Schlichthörl, G.2
Goerge, T.3
Heinen, S.4
Brüggemann, A.5
Rajan, S.6
Derst, C.7
Veh, R.W.8
Daut, J.9
-
26
-
-
0028234647
-
Dihydropyridine receptor mutations cause hypokalemic periodic paralysis
-
Ptácek L.J., Tawil R., Griggs R.C., Engel A.G., Layzer R.B., Kwieciński H., McManis P.G., Santiago L., Moore M., Fouad G., et al. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Cell 77 (1994) 863-868
-
(1994)
Cell
, vol.77
, pp. 863-868
-
-
Ptácek, L.J.1
Tawil, R.2
Griggs, R.C.3
Engel, A.G.4
Layzer, R.B.5
Kwieciński, H.6
McManis, P.G.7
Santiago, L.8
Moore, M.9
Fouad, G.10
-
27
-
-
73349127367
-
Ion channel disorders
-
Rosenberg R.N., DiMauro S., Paulson H.L., Ptácek L.J., and Nestler E.J. (Eds), Lippincott Williams & Wilkins, Philadelphia
-
Ryan D.P., and Ptácek L.J. Ion channel disorders. In: Rosenberg R.N., DiMauro S., Paulson H.L., Ptácek L.J., and Nestler E.J. (Eds). The Molecular and Genetic Basis of Neurologic and Psychiatric Disease (2007), Lippincott Williams & Wilkins, Philadelphia 550-568
-
(2007)
The Molecular and Genetic Basis of Neurologic and Psychiatric Disease
, pp. 550-568
-
-
Ryan, D.P.1
Ptácek, L.J.2
-
28
-
-
22044444137
-
Thyrotoxic hypokalemic periodic paralysis, an endocrine emergency: clinical and genetic features in 25 patients
-
Silva M.R., Chiamolera M.I., Kasamatsu T.S., Cerutti J.M., and Maciel R.M. Thyrotoxic hypokalemic periodic paralysis, an endocrine emergency: clinical and genetic features in 25 patients. Arq. Bras. Endocrinol. Metabol. 48 (2004) 196-215
-
(2004)
Arq. Bras. Endocrinol. Metabol.
, vol.48
, pp. 196-215
-
-
Silva, M.R.1
Chiamolera, M.I.2
Kasamatsu, T.S.3
Cerutti, J.M.4
Maciel, R.M.5
-
29
-
-
0035830482
-
Multiple PIP2 binding sites in Kir2.1 inwardly rectifying potassium channels
-
Soom M., Schönherr R., Kubo Y., Kirsch C., Klinger R., and Heinemann S.H. Multiple PIP2 binding sites in Kir2.1 inwardly rectifying potassium channels. FEBS Lett. 490 (2001) 49-53
-
(2001)
FEBS Lett.
, vol.490
, pp. 49-53
-
-
Soom, M.1
Schönherr, R.2
Kubo, Y.3
Kirsch, C.4
Klinger, R.5
Heinemann, S.H.6
-
30
-
-
0027933564
-
Molecular cloning and functional expression of cDNA encoding a second class of inward rectifier potassium channels in the mouse brain
-
Takahashi N., Morishige K., Jahangir A., Yamada M., Findlay I., Koyama H., and Kurachi Y. Molecular cloning and functional expression of cDNA encoding a second class of inward rectifier potassium channels in the mouse brain. J. Biol. Chem. 269 (1994) 23274-23279
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 23274-23279
-
-
Takahashi, N.1
Morishige, K.2
Jahangir, A.3
Yamada, M.4
Findlay, I.5
Koyama, H.6
Kurachi, Y.7
-
31
-
-
0030606298
-
Regions responsible for the assembly of inwardly rectifying potassium channels
-
Tinker A., Jan Y.N., and Jan L.Y. Regions responsible for the assembly of inwardly rectifying potassium channels. Cell 87 (1996) 857-868
-
(1996)
Cell
, vol.87
, pp. 857-868
-
-
Tinker, A.1
Jan, Y.N.2
Jan, L.Y.3
-
32
-
-
0028815414
-
Cloning and functional expression of an inwardly rectifying K+ channel from human atrium
-
Wible B.A., De Biasi M., Majumder K., Taglialatela M., and Brown A.M. Cloning and functional expression of an inwardly rectifying K+ channel from human atrium. Circ. Res. 76 (1995) 343-350
-
(1995)
Circ. Res.
, vol.76
, pp. 343-350
-
-
Wible, B.A.1
De Biasi, M.2
Majumder, K.3
Taglialatela, M.4
Brown, A.M.5
-
33
-
-
0034698084
-
Targeted disruption of Kir2.1 and Kir2.2 genes reveals the essential role of the inwardly rectifying K(+) current in K(+)-mediated vasodilation
-
Zaritsky J.J., Eckman D.M., Wellman G.C., Nelson M.T., and Schwarz T.L. Targeted disruption of Kir2.1 and Kir2.2 genes reveals the essential role of the inwardly rectifying K(+) current in K(+)-mediated vasodilation. Circ. Res. 87 (2000) 160-166
-
(2000)
Circ. Res.
, vol.87
, pp. 160-166
-
-
Zaritsky, J.J.1
Eckman, D.M.2
Wellman, G.C.3
Nelson, M.T.4
Schwarz, T.L.5
-
34
-
-
0035875149
-
The consequences of disrupting cardiac inwardly rectifying K(+) current (I(K1)) as revealed by the targeted deletion of the murine Kir2.1 and Kir2.2 genes
-
Zaritsky J.J., Redell J.B., Tempel B.L., and Schwarz T.L. The consequences of disrupting cardiac inwardly rectifying K(+) current (I(K1)) as revealed by the targeted deletion of the murine Kir2.1 and Kir2.2 genes. J. Physiol. 533 (2001) 697-710
-
(2001)
J. Physiol.
, vol.533
, pp. 697-710
-
-
Zaritsky, J.J.1
Redell, J.B.2
Tempel, B.L.3
Schwarz, T.L.4
-
35
-
-
0038116653
-
Molecular dissection of the inward rectifier potassium current (IK1) in rabbit cardiomyocytes: evidence for heteromeric co-assembly of Kir2.1 and Kir2.2
-
Zobel C., Cho H.C., Nguyen T.T., Pekhletski R., Diaz R.J., Wilson G.J., and Backx P.H. Molecular dissection of the inward rectifier potassium current (IK1) in rabbit cardiomyocytes: evidence for heteromeric co-assembly of Kir2.1 and Kir2.2. J. Physiol. 550 (2003) 365-372
-
(2003)
J. Physiol.
, vol.550
, pp. 365-372
-
-
Zobel, C.1
Cho, H.C.2
Nguyen, T.T.3
Pekhletski, R.4
Diaz, R.J.5
Wilson, G.J.6
Backx, P.H.7
|