-
1
-
-
0025946606
-
Control of ligand specificity in cyclic nucleotide-gated channels from rod photoreceptors and olfactory epithelium
-
Altenhofen, W., Ludwig, J., Eismann, E., Kraus, W., Bönigk, W. and Kaupp, U. B. (1991) Control of ligand specificity in cyclic nucleotide-gated channels from rod photoreceptors and olfactory epithelium. Proc. Natl. Acad. Sci. USA, 88, 9868-9872.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 9868-9872
-
-
Altenhofen, W.1
Ludwig, J.2
Eismann, E.3
Kraus, W.4
Bönigk, W.5
Kaupp, U.B.6
-
2
-
-
0028794022
-
A gene for autosomal dominant progressive cone dystrophy (CORDS) maps to chromosome 17p12-p13
-
Balciuniene, J., Johansson, K., Sandgren, O., Wachtmeister, L., Holmgren, G. and Forsman, K. (1995) A gene for autosomal dominant progressive cone dystrophy (CORDS) maps to chromosome 17p12-p13. Genomics, 30, 281-286.
-
(1995)
Genomics
, vol.30
, pp. 281-286
-
-
Balciuniene, J.1
Johansson, K.2
Sandgren, O.3
Wachtmeister, L.4
Holmgren, G.5
Forsman, K.6
-
3
-
-
0027138447
-
Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21. 1-p11. 3
-
Bergen, A. A. B., Meire, F., Ten-Brink, J., Schuurman, E. J. M., Van Ommen, G. J. B. and Delleman, J. W. (1993) Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21. 1-p11. 3. Genomics, 18, 463-464.
-
(1993)
Genomics
, vol.18
, pp. 463-464
-
-
Bergen, A.A.B.1
Meire, F.2
Ten-Brink, J.3
Schuurman, E.J.M.4
Van Ommen, G.J.B.5
Delleman, J.W.6
-
4
-
-
0027193853
-
Rod and cone photoreceptor cells express distinct genes for cGMP-gated channels
-
Bönigk, W., Altenhofen, W., Müller, F., Dose, A., Illing, M., Molday, R. S. and Kaupp, U. B. (1993) Rod and cone photoreceptor cells express distinct genes for cGMP-gated channels. Neuron, 10, 865-877.
-
(1993)
Neuron
, vol.10
, pp. 865-877
-
-
Bönigk, W.1
Altenhofen, W.2
Müller, F.3
Dose, A.4
Illing, M.5
Molday, R.S.6
Kaupp, U.B.7
-
5
-
-
0024990758
-
Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase
-
Bowes, C., Li, T., Danciger, M., Baxter, L. C., Applebury, M. L. and Farber, D. B. (1990) Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase. Nature, 347, 677-680.
-
(1990)
Nature
, vol.347
, pp. 677-680
-
-
Bowes, C.1
Li, T.2
Danciger, M.3
Baxter, L.C.4
Applebury, M.L.5
Farber, D.B.6
-
6
-
-
0029019342
-
Cyclic GMP contact points within the 63-kDa subunit and a 240-kDa associated protein of retinal rod cGMP-activated channels
-
Brown, R. L., Gramling, R., Bert, R. J. and Karpen, J. W. (1995) Cyclic GMP contact points within the 63-kDa subunit and a 240-kDa associated protein of retinal rod cGMP-activated channels. Biochemistry, 34, 8365-8370.
-
(1995)
Biochemistry
, vol.34
, pp. 8365-8370
-
-
Brown, R.L.1
Gramling, R.2
Bert, R.J.3
Karpen, J.W.4
-
7
-
-
0027158799
-
A new subunit of the cyclic nucleotide-gated cation channel in retinal rods
-
Chen, T. Y., Peng, Y. W., Dhallan, R. S., Ahamed, B., Reed, R. R. and Yau, K. W. (1993) A new subunit of the cyclic nucleotide-gated cation channel in retinal rods. Nature, 362, 764-767.
-
(1993)
Nature
, vol.362
, pp. 764-767
-
-
Chen, T.Y.1
Peng, Y.W.2
Dhallan, R.S.3
Ahamed, B.4
Reed, R.R.5
Yau, K.W.6
-
8
-
-
0026686171
-
Human rod photoreceptor cGMP-gated channel: Amino acid sequence, gene structure, and functional expression
-
Dhallan, R. S., Macke, J. P., Eddy, R. L., Shows, T. B., Reed, R. R., Yau, K. W. and Nathans, J. (1992) Human rod photoreceptor cGMP-gated channel: amino acid sequence, gene structure, and functional expression. J. Neurosci., 12, 3248-3256.
-
(1992)
J. Neurosci.
, vol.12
, pp. 3248-3256
-
-
Dhallan, R.S.1
Macke, J.P.2
Eddy, R.L.3
Shows, T.B.4
Reed, R.R.5
Yau, K.W.6
Nathans, J.7
-
9
-
-
0025105161
-
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
-
Dryja, T. P., McGee, T. L., Reichel, E., Hahn, L. B., Cowley, G. S., Yandell, D. W., Sandberg, M. A. and Berson, E. L. (1990) A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Nature, 343, 364-366.
-
(1990)
Nature
, vol.343
, pp. 364-366
-
-
Dryja, T.P.1
McGee, T.L.2
Reichel, E.3
Hahn, L.B.4
Cowley, G.S.5
Yandell, D.W.6
Sandberg, M.A.7
Berson, E.L.8
-
10
-
-
0027248024
-
Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness
-
Dryja, T. P., Berson, E. L., Rao, V. R. and Oprian, D. D. (1993) Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. Nature Genet., 4, 280-283.
-
(1993)
Nature Genet.
, vol.4
, pp. 280-283
-
-
Dryja, T.P.1
Berson, E.L.2
Rao, V.R.3
Oprian, D.D.4
-
11
-
-
0028820045
-
Mutations in the gene encoding the α-subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa
-
Dryja, T. P., Finn, J. T., Peng, Y. W., McGee, T. L., Berson, E. L. and Yau, K. W. (1995) Mutations in the gene encoding the α-subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa. Proc. Natl Acad. Sci. USA, 92, 10177-10181.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 10177-10181
-
-
Dryja, T.P.1
Finn, J.T.2
Peng, Y.W.3
McGee, T.L.4
Berson, E.L.5
Yau, K.W.6
-
12
-
-
0028047839
-
2+ blockage, and ionic selectivity
-
2+ blockage, and ionic selectivity. Proc. Natl Acad. Sci. USA, 91, 1109-1113.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 1109-1113
-
-
Eismann, E.1
Müller, F.2
Heinemann, S.H.3
Kaupp, U.B.4
-
13
-
-
0028244138
-
Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion
-
Evans, K., Fryer, A., Inglehearn, C., Duvall-Young, J., Whittaker, J. L., Gregory, C. Y., Butler, R., Ebenezer, N., Hunt, D. M. and Bhattacharya, S. (1994) Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion. Nature Genet., 6, 210-213.
-
(1994)
Nature 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
-
14
-
-
0025721075
-
A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa
-
Farrar, G. J., Kenna, P., Jordan, S. A., Kumar-Singh, R., Humphries, M. M., Sharp, E. M., Sheils, D. M. and Humphries, P. (1991) A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa. Nature, 354, 478-480.
-
(1991)
Nature
, vol.354
, pp. 478-480
-
-
Farrar, G.J.1
Kenna, P.2
Jordan, S.A.3
Kumar-Singh, R.4
Humphries, M.M.5
Sharp, E.M.6
Sheils, D.M.7
Humphries, P.8
-
15
-
-
0029117775
-
Profoundly different calcium permeation and blockage determine the specific function of distinct cyclic nucleotide-gated channels
-
Frings, S., Seifert, R., Godde, M. and Kaupp, U. B. (1995) Profoundly different calcium permeation and blockage determine the specific function of distinct cyclic nucleotide-gated channels. Neuron, 15, 169-179.
-
(1995)
Neuron
, vol.15
, pp. 169-179
-
-
Frings, S.1
Seifert, R.2
Godde, M.3
Kaupp, U.B.4
-
16
-
-
0024212067
-
Rapid production of full length cDNAs from rare transcripts: Amplification using a single gene specific oligonucleotide primer
-
Frohman, M. A., Dush, M. K. and Martin, G. R. (1988) Rapid production of full length cDNAs from rare transcripts: amplification using a single gene specific oligonucleotide primer. Proc. Natl Acad. Sci. USA, 85, 8998-9002.
-
(1988)
Proc. Natl Acad. Sci. USA
, vol.85
, pp. 8998-9002
-
-
Frohman, M.A.1
Dush, M.K.2
Martin, G.R.3
-
17
-
-
0029067542
-
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese
-
Fuchs, S., Nakazawa, M., Maw, M., Tamai, M., Oguchi, Y. and Gal, A. (1995) A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese. Nature Genet., 10, 360-362.
-
(1995)
Nature Genet.
, vol.10
, pp. 360-362
-
-
Fuchs, S.1
Nakazawa, M.2
Maw, M.3
Tamai, M.4
Oguchi, Y.5
Gal, A.6
-
18
-
-
0028128535
-
Heterozygous missense mutation in the rod cGMP phosphodiesterase β-subunit gene in autosomal dominant stationary night blindness
-
Gal, A., Orth, U., Baehr, W., Schwinger, E. and Rosenberg, T. (1994) Heterozygous missense mutation in the rod cGMP phosphodiesterase β-subunit gene in autosomal dominant stationary night blindness. Nature Genet., 7, 64-67.
-
(1994)
Nature Genet.
, vol.7
, pp. 64-67
-
-
Gal, A.1
Orth, U.2
Baehr, W.3
Schwinger, E.4
Rosenberg, T.5
-
19
-
-
0025328952
-
A phosphodiesterase inhibitor specific to a subset of bovine retinal cones
-
Hamilton, S. E. and Hurley, J. B. (1990) A phosphodiesterase inhibitor specific to a subset of bovine retinal cones. J. Biol. Chem., 265, 11259-11264.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 11259-11264
-
-
Hamilton, S.E.1
Hurley, J.B.2
-
20
-
-
0027473894
-
Affinities of bovine photoreceptor cGMP phosphodiesterases for rod and cone inhibitory subunits
-
Hamilton, S. E., Prusti, R. K., Bentley, J. K., Beavo, J. A. and Hurley, J. B. (1993) Affinities of bovine photoreceptor cGMP phosphodiesterases for rod and cone inhibitory subunits. FEBS Lett., 318, 157-161.
-
(1993)
FEBS Lett.
, vol.318
, pp. 157-161
-
-
Hamilton, S.E.1
Prusti, R.K.2
Bentley, J.K.3
Beavo, J.A.4
Hurley, J.B.5
-
21
-
-
0028789921
-
Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase
-
Huang, S. H., Pittler, S. J., Huang, X., Oliveira, L., Berson, E. L. and Dryja, T. P. (1995) Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase. Nature Genet., 11, 468-471.
-
(1995)
Nature Genet.
, vol.11
, pp. 468-471
-
-
Huang, S.H.1
Pittler, S.J.2
Huang, X.3
Oliveira, L.4
Berson, E.L.5
Dryja, T.P.6
-
22
-
-
0025720710
-
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa
-
Kajiwara, K., Hahn, L. B., Mukai, S., Travis, G. H., Berson, E. L. and Dryja, T. P. (1991) Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. Nature, 354, 480-483.
-
(1991)
Nature
, vol.354
, pp. 480-483
-
-
Kajiwara, K.1
Hahn, L.B.2
Mukai, S.3
Travis, G.H.4
Berson, E.L.5
Dryja, T.P.6
-
23
-
-
0029080926
-
Family of nucleotide gated ion channels
-
Kaupp, U. B. (1995) Family of nucleotide gated ion channels. Curr. Opin. Neurobiol., 5, 434-442.
-
(1995)
Curr. Opin. Neurobiol.
, vol.5
, pp. 434-442
-
-
Kaupp, U.B.1
-
24
-
-
0029160032
-
A 240 kDA protein represents the complete β-subunit of the cyclic nucleotide-gated channel from rod photoreceptor
-
Körschen, H. G., Illing, M., Seifert, R., Sesti, F., Williams, A., Gotzes, S., Colville, C., Müller, F., Dose, A., Godde, M., Molday, L., Kaupp, U. B. and Molday, R. S. (1995) A 240 kDA protein represents the complete β-subunit of the cyclic nucleotide-gated channel from rod photoreceptor. Neuron, 15, 627-636.
-
(1995)
Neuron
, vol.15
, pp. 627-636
-
-
Körschen, H.G.1
Illing, M.2
Seifert, R.3
Sesti, F.4
Williams, A.5
Gotzes, S.6
Colville, C.7
Müller, F.8
Dose, A.9
Godde, M.10
Molday, L.11
Kaupp, U.B.12
Molday, R.S.13
-
25
-
-
0022993799
-
Identification of specific transducin α subunits in retinal rod and cone photoreceptors
-
Lerea, C. L., Somers, D. E., Hurley, J. B., Klock, I. B. and Bunt-Milan, A. H. (1986) Identification of specific transducin α subunits in retinal rod and cone photoreceptors. Science, 234, 77-80.
-
(1986)
Science
, vol.234
, pp. 77-80
-
-
Lerea, C.L.1
Somers, D.E.2
Hurley, J.B.3
Klock, I.B.4
Bunt-Milan, A.H.5
-
26
-
-
0023692635
-
Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using chromosome specific library probes
-
Lichter, P., Cremer, T., Borden, J., Manuelidis, L. and Ward, D. C. (1988) Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using chromosome specific library probes. Hum. Genet., 80, 224-234.
-
(1988)
Hum. Genet.
, vol.80
, pp. 224-234
-
-
Lichter, P.1
Cremer, T.2
Borden, J.3
Manuelidis, L.4
Ward, D.C.5
-
27
-
-
0026485457
-
+ channel determined by construction of multimeric cDNAs
-
+ channel determined by construction of multimeric cDNAs. Neuron, 9, 861-871.
-
(1992)
Neuron
, vol.9
, pp. 861-871
-
-
Liman, E.R.1
Tytgat, J.2
Hess, P.3
-
28
-
-
0027270053
-
Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa
-
McLaughlin, M. E., Sandberg, M. A., Berson, E. L. and Dryja, T. P. (1993) Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa. Nature Genet., 4, 130-134.
-
(1993)
Nature Genet.
, vol.4
, pp. 130-134
-
-
McLaughlin, M.E.1
Sandberg, M.A.2
Berson, E.L.3
Dryja, T.P.4
-
29
-
-
0028130058
-
Differences in transduction between rod and cone photoreceptors and exploration of the role of calcium homeostasis
-
Miller, L., Picones, A. and Korenbrot, J. I. (1994) Differences in transduction between rod and cone photoreceptors and exploration of the role of calcium homeostasis. Curr. Opin. Neurobiol., 4, 488-495.
-
(1994)
Curr. Opin. Neurobiol.
, vol.4
, pp. 488-495
-
-
Miller, L.1
Picones, A.2
Korenbrot, J.I.3
-
30
-
-
0001877802
-
Splicing of precursors to mRNA by the spliceosome
-
Gesteland, R. F. and Atkins, J. K. (eds), Cold Spring Harbor Laboratory Press, Cold Spring Harbor
-
Moore, M. J., Query, C. C. and Sharp, P. A. (1993) Splicing of precursors to mRNA by the spliceosome. In Gesteland, R. F. and Atkins, J. K. (eds), The RNA World. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, pp. 303-357.
-
(1993)
The RNA World
, pp. 303-357
-
-
Moore, M.J.1
Query, C.C.2
Sharp, P.A.3
-
31
-
-
0023840568
-
Calcium and magnesium fluxes across the plasma membrane of toad rod outer segment
-
Nakatani, K. and Yau, K. W. (1988) Calcium and magnesium fluxes across the plasma membrane of toad rod outer segment. J. Physiol. (Lond.), 395, 695-729.
-
(1988)
J. Physiol. (Lond.)
, vol.395
, pp. 695-729
-
-
Nakatani, K.1
Yau, K.W.2
-
32
-
-
0027054292
-
Molecular genetics of human visual pigments
-
Nathans, J., Merbs, S. L., Sung, C. H., Weitz, C. J. and Wang, Y. (1992) Molecular genetics of human visual pigments. Annu. Rev. Genet., 26, 403-424.
-
(1992)
Annu. Rev. Genet.
, vol.26
, pp. 403-424
-
-
Nathans, J.1
Merbs, S.L.2
Sung, C.H.3
Weitz, C.J.4
Wang, Y.5
-
33
-
-
0025972460
-
Response properties of cones from the retina of tiger salamander
-
Perry, R. J. and McNaughton, P. A. (1991) Response properties of cones from the retina of tiger salamander. J. Physiol. (Lond.), 433, 561-587.
-
(1991)
J. Physiol. (Lond.)
, vol.433
, pp. 561-587
-
-
Perry, R.J.1
McNaughton, P.A.2
-
34
-
-
0028980230
-
2+ with cGMP-gated ion channels differ in retinal rod and cone photoreceptors
-
2+ with cGMP-gated ion channels differ in retinal rod and cone photoreceptors. Biophys. J., 69, 120-127.
-
(1995)
Biophys. J.
, vol.69
, pp. 120-127
-
-
Picones, A.1
Korenbrot, J.I.2
-
35
-
-
0029098705
-
Gene structure and amino acid sequence of the human cone photoreceptor cGMP-phosphodiesterase α′ subunit (PDEA2) and its chromosomal localization to 10q24
-
Piriev, N. I., Viczian, A. S., Ye, J., Kerner, B., Korenberg, J. R. and Farber, D. B. (1995) Gene structure and amino acid sequence of the human cone photoreceptor cGMP-phosphodiesterase α′ subunit (PDEA2) and its chromosomal localization to 10q24. Genomics, 28, 429-435.
-
(1995)
Genomics
, vol.28
, pp. 429-435
-
-
Piriev, N.I.1
Viczian, A.S.2
Ye, J.3
Kerner, B.4
Korenberg, J.R.5
Farber, D.B.6
-
36
-
-
0028053664
-
A cGMP-gated current can control exocytosis at cone synapses
-
Rieke, F. and Schwartz, E. A. (1994) A cGMP-gated current can control exocytosis at cone synapses. Neuron, 13, 863-873.
-
(1994)
Neuron
, vol.13
, pp. 863-873
-
-
Rieke, F.1
Schwartz, E.A.2
-
37
-
-
0027424793
-
Identification of an external divalent cation-binding site in the pore of the cGMP-activated channel
-
Root, M. J. and MacKinnon, R. (1993) Identification of an external divalent cation-binding site in the pore of the cGMP-activated channel. Neuron, 11, 459-466.
-
(1993)
Neuron
, vol.11
, pp. 459-466
-
-
Root, M.J.1
MacKinnon, R.2
-
38
-
-
0026878962
-
A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa
-
Rosenfeld, P. J., Cowley, G. S., McGee, T. L., Sandberg, M. A., Berson, E. L. and Dryja, T. P. (1992) A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa. Nature Genet., 1, 209-213.
-
(1992)
Nature Genet.
, vol.1
, pp. 209-213
-
-
Rosenfeld, P.J.1
Cowley, G.S.2
McGee, T.L.3
Sandberg, M.A.4
Berson, E.L.5
Dryja, T.P.6
-
39
-
-
0025822625
-
Visual excitation and recovery
-
Stryer, L. (1991) Visual excitation and recovery. J. Biol. Chem., 266, 10711-10714.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 10711-10714
-
-
Stryer, L.1
-
40
-
-
0027262347
-
Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase β-subunit gene
-
Suber, M. L., Pittler, S. J., Qin, N., Wright, G. C., Holcombe, V., Lee, R. H., Craft, C. M., Lolley, R. N., Baehr, W. and Hurwitz, R. L. (1993) Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase β-subunit gene. Proc. Natl Acad. Sci. USA, 90, 3968-3972.
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, pp. 3968-3972
-
-
Suber, M.L.1
Pittler, S.J.2
Qin, N.3
Wright, G.C.4
Holcombe, V.5
Lee, R.H.6
Craft, C.M.7
Lolley, R.N.8
Baehr, W.9
Hurwitz, R.L.10
-
41
-
-
0024571803
-
Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)
-
Travis, G. H., Brennan, M. B., Danielson, P. E., Kozak, C. A. and Sutcliffe, J. G. (1989) Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds). Nature, 338, 70-73.
-
(1989)
Nature
, vol.338
, pp. 70-73
-
-
Travis, G.H.1
Brennan, M.B.2
Danielson, P.E.3
Kozak, C.A.4
Sutcliffe, J.G.5
-
42
-
-
0028230414
-
Cloning and functional expression of a cyclic nucleotide-gated channel from mammalian sperm
-
Weyand, I., Godde, M., Frings, S., Weiner, J., Müller, F., Altenhofen, W., Hatt, H. and Kaupp, U. B. (1994) Cloning and functional expression of a cyclic nucleotide-gated channel from mammalian sperm. Nature, 368, 859-863.
-
(1994)
Nature
, vol.368
, pp. 859-863
-
-
Weyand, I.1
Godde, M.2
Frings, S.3
Weiner, J.4
Müller, F.5
Altenhofen, W.6
Hatt, H.7
Kaupp, U.B.8
-
43
-
-
0026569779
-
Antibodies against synthetic peptides used to determine the topology and site of glycosylation of the cGMP-gated channel from bovine rod photoreceptors
-
Wohlfart, P., Haase, W., Molday, R. S. and Cook, N. J. (1992) Antibodies against synthetic peptides used to determine the topology and site of glycosylation of the cGMP-gated channel from bovine rod photoreceptors. J. Biol. Chem., 267, 644-648.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 644-648
-
-
Wohlfart, P.1
Haase, W.2
Molday, R.S.3
Cook, N.J.4
-
44
-
-
0024564964
-
Cyclic GMP-activated conductance of retinal photoreceptor cells
-
Yau, K. W. and Baylor, D. A. (1989) Cyclic GMP-activated conductance of retinal photoreceptor cells. Annu. Rev. Neurosci., 12, 289-327.
-
(1989)
Annu. Rev. Neurosci.
, vol.12
, pp. 289-327
-
-
Yau, K.W.1
Baylor, D.A.2
-
45
-
-
0030590488
-
Molecular cloning, functional expression and chromosomal localization of a human homolog of the cyclic nucleotide-gated ion channel of retinal cone photoreceptors
-
Yu, W. P., Grunwald, M. E. and Yau, K. W. (1996) Molecular cloning, functional expression and chromosomal localization of a human homolog of the cyclic nucleotide-gated ion channel of retinal cone photoreceptors. FEBS Lett., 393, 211-215.
-
(1996)
FEBS Lett.
, vol.393
, pp. 211-215
-
-
Yu, W.P.1
Grunwald, M.E.2
Yau, K.W.3
|