-
1
-
-
0028123295
-
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19
-
(1994)
Hum Mol Genet
, vol.3
, pp. 351-354
-
-
Al-Maghtheh, M.1
Inglehearn, C.F.2
Keen, T.J.3
Evans, K.4
Moore, A.T.5
Jay, M.6
Bird, A.C.7
Bhattacharya, S.S.8
-
4
-
-
0027332435
-
Subcellular localization of tubulin and opsin mRNA in the goldfish retina using digoxigenin-labeled cRNA probes detected by alkaline phosphatase and HRP histochemistry
-
(1993)
J Neurosci Methods
, vol.50
, pp. 145-152
-
-
Barthel, L.K.1
Raymond, P.A.2
-
5
-
-
0028812435
-
+ channel. II. Cloning and distribution of alternative forms
-
(1995)
Am J Physiol Renal Fluid Electrolyte Physiol
, vol.268
-
-
Boim, M.A.1
Ho, K.2
Shuck, M.E.3
Bienkowski, M.J.4
Block, J.H.5
Slightom, J.L.6
Yang, Y.7
Brenner, B.M.8
Hebert, S.C.9
-
6
-
-
0028124225
-
Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
-
(1994)
Nat Genet
, vol.8
, pp. 136-140
-
-
Browne, D.L.1
Gancher, S.T.2
Nutt, J.G.3
Brunt, E.R.4
Smith, E.A.5
Kramer, P.6
Litt, M.7
-
9
-
-
0030054399
-
+ and intracellular pH allosterically regulate renal K(ir)1.1 channels
-
(1996)
J Biol Chem
, vol.271
, pp. 17261-17266
-
-
Doi, T.1
Fakler, B.2
Schultz, J.H.3
Schulte, U.4
Brandle, U.5
Weidemann, S.6
Zenner, H.P.7
Lang, F.8
Ruppersberg, J.P.9
-
11
-
-
0028244138
-
Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion
-
(1994)
Nat Genet
, vol.6
, pp. 210-213
-
-
Evans, K.1
Fryer, A.2
Inglehearn, C.3
Duvall-Young, J.4
Whittaker, J.L.5
Gregory, C.Y.6
Butler, R.7
Ebenezer, N.8
Hunt, D.M.9
Bhattacharya, S.10
-
15
-
-
0030669568
-
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
-
(1997)
Cell
, vol.91
, pp. 543-553
-
-
Freund, C.L.1
Gregory-Evans, C.Y.2
Furukawa, T.3
Papaioannou, M.4
Looser, J.5
Ploder, L.6
Bellingham, J.7
Ng, D.8
Herbrick, J.A.9
Duncan, A.10
Scherer, S.W.11
Tsui, L.C.12
Loutradis-Anagnostou, A.13
Jacobson, S.G.14
Cepko, C.L.15
Bhattacharya, S.S.16
McInnes, R.R.17
-
18
-
-
0023270313
-
The properties and function of inward rectification in rod photoreceptors of the tiger salamander
-
(1987)
J Physiol (Lond)
, vol.390
, pp. 319-333
-
-
Hestrin, S.1
-
19
-
-
0008083116
-
-
Ionic Channels in Excitable Membranes. Sunderland, MA: Sinauer
-
(1992)
-
-
Hille, B.1
-
21
-
-
0030831943
-
Expression and clustered distribution of an inwardly rectifying potassium channel, Kir 4.1, on mammalian retinal Mueller cell membrane: Their regulation by insulin and laminin signals
-
(1997)
J Neurosci
, vol.17
, pp. 7725-7735
-
-
Ishii, M.1
Horio, Y.2
Tada, Y.3
Hibino, H.4
Inanobe, A.5
Ito, M.6
Yamada, M.7
Gotow, T.8
Uchiyama, Y.9
Kurachi, Y.10
-
27
-
-
0033569584
-
+ channel, Kir4.1, in rat retinal pigment epithelium
-
(1999)
J Physiol (Lond)
, vol.520
, pp. 373-381
-
-
Kusaka, S.1
Horio, Y.2
Fujita, A.3
Matsushita, K.4
Inanobe, A.5
Gotow, T.6
Uchiyama, Y.7
Tano, Y.8
Kurachi, Y.9
-
30
-
-
0027184270
-
Inward-rectifying potassium channels in retinal glial (Muller) cells
-
(1993)
J Neurosci
, vol.13
, pp. 3333-3345
-
-
Newman, E.A.1
-
31
-
-
0030969280
-
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene
-
(1997)
Hum Mol Genet
, vol.6
, pp. 563-569
-
-
Nystuen, A.1
Costeff, H.2
Elpeleg, O.N.3
Apter, N.4
Bonne-Tamir, B.5
Mohrenweiser, H.6
Haider, N.7
Stone, E.M.8
Sheffield, V.C.9
-
34
-
-
0033553431
-
Identification of a critical motif responsible for gating of Kir2.3 channel by intracellular protons
-
(1999)
J Biol Chem
, vol.274
, pp. 13783-13789
-
-
Qu, Z.1
Zhu, G.2
Yang, S.3
Cui, N.4
Li, Y.5
Chanchenvalap, S.6
Sulaiman, S.7
Haynie, H.8
Jiang, C.9
-
38
-
-
0029794875
-
+ channel, ROMK
-
(1996)
Nat Genet
, vol.14
, pp. 152-156
-
-
Simon, D.B.1
Karet, F.E.2
Rodriguez-Soriano, J.3
Hamdan, J.H.4
DiPietro, A.5
Trachtman, H.6
Sanjad, S.A.7
Lifton, R.P.8
-
40
-
-
0031447030
-
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration
-
(1997)
Neuron
, vol.19
, pp. 1329-1336
-
-
Swain, P.K.1
Chen, S.2
Wang, Q.L.3
Affatigato, L.M.4
Coats, C.L.5
Brady, K.D.6
Fishman, G.A.7
Jacobson, S.G.8
Swaroop, A.9
Stone, E.10
Sieving, P.A.11
Zack, D.J.12
-
41
-
-
0032929074
-
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: Direct evidence for the involvement of CRX in the development of photoreceptor function
-
(1999)
Hum Mol Genet
, vol.8
, pp. 299-305
-
-
Swaroop, A.1
Wang, Q.L.2
Wu, W.3
Cook, J.4
Coats, C.5
Xu, S.6
Chen, S.7
Zack, D.J.8
Sieving, P.A.9
-
45
-
-
0029024248
-
A novel ATP-dependent inward rectifier potassium channel expressed predominately in glial cells
-
(1995)
J Biol Chem
, vol.270
, pp. 16339-16346
-
-
Takumi, T.1
Ishii, T.2
Horio, Y.3
Morishige, K.I.4
Takahashi, N.5
Yamada, M.6
Yamashita, T.7
Kiyama, H.8
Sohmiya, K.9
Nakanishi, S.10
Kurachi, Y.11
-
46
-
-
0343815823
-
+ inward rectifier channel associated with motoneurons of cranial nerve nuclei
-
(1998)
J Neurosci
, vol.18
, pp. 4096-4105
-
-
Topert, C.1
Doring, F.2
Wischmeyer, E.3
Karschin, C.4
Brockhaus, J.5
Ballanyi, K.6
Derest, C.7
Karschin, A.8
-
48
-
-
9044240040
-
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
-
(1996)
Nat Genet
, vol.12
, 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
Shen, J.7
Timothy, K.W.8
Vincent, G.M.9
De Jager, T.10
Schwartz, P.J.11
Toubin, J.A.12
Moss, A.J.13
Atkinson, D.L.14
Landes, G.M.15
Connors, T.D.16
Keating, M.T.17
-
49
-
-
0028905566
-
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
-
(1995)
Cell
, vol.80
, pp. 805-811
-
-
Wang, Q.1
Shen, J.2
Splawski, I.3
Atkinson, D.4
Li, Z.5
Robinson, J.L.6
Moss, A.J.7
Towbin, J.A.8
Keating, M.T.9
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