-
1
-
-
78650515181
-
The diverse roles of ribbon synapses in sensory neurotransmission
-
Matthews, G. and Fuchs, P. (2010) The diverse roles of ribbon synapses in sensory neurotransmission. Nat. Rev. Neurosci., 11, 812-822.
-
(2010)
Nat. Rev. Neurosci.
, vol.11
, pp. 812-822
-
-
Matthews, G.1
Fuchs, P.2
-
2
-
-
24344454662
-
Synaptic transmission at retinal ribbon synapses
-
Heidelberger, R., Thoreson, W.B. and Witkovsky, P. (2005) Synaptic transmission at retinal ribbon synapses. Prog. Retin. Eye Res., 24, 682-720.
-
(2005)
Prog. Retin. Eye Res.
, vol.24
, pp. 682-720
-
-
Heidelberger, R.1
Thoreson, W.B.2
Witkovsky, P.3
-
3
-
-
0942287236
-
Functional characterization of the L-type Ca2+ channel Cav1.4alpha1 from mouse retina
-
Baumann, L., Gerstner, A., Zong, X., Biel, M. and Wahl-Schott, C. (2004) Functional characterization of the L-type Ca2+ channel Cav1.4alpha1 from mouse retina. Invest Ophthalmol. Vis. Sci., 45, 708-713.
-
(2004)
Invest Ophthalmol. Vis. Sci.
, vol.45
, pp. 708-713
-
-
Baumann, L.1
Gerstner, A.2
Zong, X.3
Biel, M.4
Wahl-Schott, C.5
-
4
-
-
33750293580
-
Switching offcalcium-dependent inactivation in L-type calcium channels by an autoinhibitory domain
-
Wahl-Schott, C., Baumann, L., Cuny, H., Eckert, C., Griessmeier, K. and Biel, M. (2006) Switching offcalcium-dependent inactivation in L-type calcium channels by an autoinhibitory domain. Proc. Natl Acad. Sci. USA, 103, 15657-15662.
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, pp. 15657-15662
-
-
Wahl-Schott, C.1
Baumann, L.2
Cuny, H.3
Eckert, C.4
Griessmeier, K.5
Biel, M.6
-
5
-
-
10744227075
-
The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution
-
McRory, J.E., Hamid, J., Doering, C.J., Garcia, E., Parker, R., Hamming, K., Chen, L., Hildebrand, M., Beedle, A.M., Feldcamp, L. et al. (2004) The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution. J. Neurosci., 24, 1707-1718.
-
(2004)
J. Neurosci.
, vol.24
, pp. 1707-1718
-
-
McRory, J.E.1
Hamid, J.2
Doering, C.J.3
Garcia, E.4
Parker, R.5
Hamming, K.6
Chen, L.7
Hildebrand, M.8
Beedle, A.M.9
Feldcamp, L.10
-
6
-
-
0037811332
-
Cav1.4alpha1 subunits can form slowly inactivating dihydropyridine-sensitive L-type Ca2+ channels lacking Ca2+-dependent inactivation
-
Koschak, A., Reimer, D., Walter, D., Hoda, J.C., Heinzle, T., Grabner, M. and Striessnig, J. (2003) Cav1.4alpha1 subunits can form slowly inactivating dihydropyridine-sensitive L-type Ca2+ channels lacking Ca2+-dependent inactivation. J. Neurosci., 23, 6041-6049.
-
(2003)
J. Neurosci.
, vol.23
, pp. 6041-6049
-
-
Koschak, A.1
Reimer, D.2
Walter, D.3
Hoda, J.C.4
Heinzle, T.5
Grabner, M.6
Striessnig, J.7
-
7
-
-
0036241136
-
Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer
-
Ball, S.L., Powers, P.A., Shin, H.S., Morgans, C.W., Peachey, N.S. and Gregg, R.G. (2002) Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer. Invest. Ophthalmol. Vis. Sci., 43, 1595-1603.
-
(2002)
Invest. Ophthalmol. Vis. Sci.
, vol.43
, pp. 1595-1603
-
-
Ball, S.L.1
Powers, P.A.2
Shin, H.S.3
Morgans, C.W.4
Peachey, N.S.5
Gregg, R.G.6
-
8
-
-
17344366487
-
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
-
Strom, T.M., Nyakatura, G., Apfelstedt-Sylla, E., Hellebrand, H., Lorenz, B., Weber, B.H., Wutz, K., Gutwillinger, N., Ruther, K., Drescher, B. et al. (1998) An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nat. Genet., 19, 260-263.
-
(1998)
Nat. Genet.
, vol.19
, pp. 260-263
-
-
Strom, T.M.1
Nyakatura, G.2
Apfelstedt-Sylla, E.3
Hellebrand, H.4
Lorenz, B.5
Weber, B.H.6
Wutz, K.7
Gutwillinger, N.8
Ruther, K.9
Drescher, B.10
-
9
-
-
0041104621
-
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness
-
Bech-Hansen, N.T., Naylor, M.J., Maybaum, T.A., Pearce, W.G., Koop, B., Fishman, G.A., Mets, M., Musarella, M.A. and Boycott, K.M. (1998) Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Nat. Genet., 19, 264-267.
-
(1998)
Nat. Genet.
, vol.19
, pp. 264-267
-
-
Bech-Hansen, N.T.1
Naylor, M.J.2
Maybaum, T.A.3
Pearce, W.G.4
Koop, B.5
Fishman, G.A.6
Mets, M.7
Musarella, M.A.8
Boycott, K.M.9
-
10
-
-
34347251602
-
A novel CACNA1F gene mutation causes Aland Island eye disease
-
Jalkanen, R., Bech-Hansen, N.T., Tobias, R., Sankila, E.M., Mantyjarvi, M., Forsius, H., de la Chapelle, A. and Alitalo, T. (2007) A novel CACNA1F gene mutation causes Aland Island eye disease. Invest. Ophthalmol. Vis. Sci., 48, 2498-2502.
-
(2007)
Invest. Ophthalmol. Vis. Sci.
, vol.48
, pp. 2498-2502
-
-
Jalkanen, R.1
Bech-Hansen, N.T.2
Tobias, R.3
Sankila, E.M.4
Mantyjarvi, M.5
Forsius, H.6
de la Chapelle, A.7
Alitalo, T.8
-
11
-
-
84856153244
-
A novel p. Gly603Arg mutation in CACNA1F causes Aland island eye disease and incomplete congenital stationary night blindness phenotypes in a family
-
Vincent, A., Wright, T., Day, M.A., Westall, C.A. and Heon, E. (2011) A novel p. Gly603Arg mutation in CACNA1F causes Aland island eye disease and incomplete congenital stationary night blindness phenotypes in a family. Mol. Vis., 17, 3262-3270.
-
(2011)
Mol. Vis.
, vol.17
, pp. 3262-3270
-
-
Vincent, A.1
Wright, T.2
Day, M.A.3
Westall, C.A.4
Heon, E.5
-
12
-
-
33747047272
-
X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene
-
Jalkanen, R., Mantyjarvi, M., Tobias, R., Isosomppi, J., Sankila, E.M., Alitalo, T. and Bech-Hansen, N.T. (2006) X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene. J. Med. Genet., 43, 699-704.
-
(2006)
J. Med. Genet.
, vol.43
, pp. 699-704
-
-
Jalkanen, R.1
Mantyjarvi, M.2
Tobias, R.3
Isosomppi, J.4
Sankila, E.M.5
Alitalo, T.6
Bech-Hansen, N.T.7
-
13
-
-
27544503765
-
Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina
-
Mansergh, F., Orton, N.C., Vessey, J.P., Lalonde, M.R., Stell, W.K., Tremblay, F., Barnes, S., Rancourt, D.E. and Bech-Hansen, N.T. (2005) Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina. Hum. Mol. Genet., 14, 3035-3046.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 3035-3046
-
-
Mansergh, F.1
Orton, N.C.2
Vessey, J.P.3
Lalonde, M.R.4
Stell, W.K.5
Tremblay, F.6
Barnes, S.7
Rancourt, D.E.8
Bech-Hansen, N.T.9
-
14
-
-
59449084437
-
Effects of presynaptic mutations on a postsynaptic Cacna1s calcium channel colocalized with mGluR6 at mouse photoreceptor ribbon synapses
-
Specht, D., Wu, S.B., Turner, P., Dearden, P., Koentgen, F., Wolfrum, U., Maw, M., Brandstatter, J.H. and tom Dieck, S. (2009) Effects of presynaptic mutations on a postsynaptic Cacna1s calcium channel colocalized with mGluR6 at mouse photoreceptor ribbon synapses. Invest. Ophthalmol. Vis. Sci., 50, 505-515.
-
(2009)
Invest. Ophthalmol. Vis. Sci.
, vol.50
, pp. 505-515
-
-
Specht, D.1
Wu, S.B.2
Turner, P.3
Dearden, P.4
Koentgen, F.5
Wolfrum, U.6
Maw, M.7
Brandstatter, J.H.8
tom Dieck, S.9
-
15
-
-
33644872908
-
The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses
-
Chang, B., Heckenlively, J.R., Bayley, P.R., Brecha, N.C., Davisson, M.T., Hawes, N.L., Hirano, A.A., Hurd, R.E., Ikeda, A., Johnson, B.A. et al. (2006) The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses. Vis. Neurosci., 23, 11-24.
-
(2006)
Vis. Neurosci.
, vol.23
, pp. 11-24
-
-
Chang, B.1
Heckenlively, J.R.2
Bayley, P.R.3
Brecha, N.C.4
Davisson, M.T.5
Hawes, N.L.6
Hirano, A.A.7
Hurd, R.E.8
Ikeda, A.9
Johnson, B.A.10
-
16
-
-
49749143330
-
ModifiedCa(v)1.4 expression in the Cacna1f(nob2) mouse due to alternative splicing of an ETn inserted in exon 2
-
Doering, C.J., Rehak, R., Bonfield, S., Peloquin, J.B., Stell, W.K., Mema, S.C., Sauve, Y. and McRory, J.E. (2008) ModifiedCa(v)1.4 expression in the Cacna1f(nob2) mouse due to alternative splicing of an ETn inserted in exon 2. PLoS One, 3, e2538.
-
(2008)
PLoS One
, vol.3
-
-
Doering, C.J.1
Rehak, R.2
Bonfield, S.3
Peloquin, J.B.4
Stell, W.K.5
Mema, S.C.6
Sauve, Y.7
McRory, J.E.8
-
17
-
-
21144457360
-
A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation
-
Hemara-Wahanui, A., Berjukow, S., Hope, C.I., Dearden, P.K., Wu, S.B., Wilson-Wheeler, J., Sharp, D.M., Lundon-Treweek, P., Clover, G.M., Hoda, J.C. et al. (2005) A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation. Proc. Natl Acad. Sci. USA, 102, 7553-7558.
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 7553-7558
-
-
Hemara-Wahanui, A.1
Berjukow, S.2
Hope, C.I.3
Dearden, P.K.4
Wu, S.B.5
Wilson-Wheeler, J.6
Sharp, D.M.7
Lundon-Treweek, P.8
Clover, G.M.9
Hoda, J.C.10
-
18
-
-
0344037111
-
ERGs in female carriers of incomplete congenital stationary night blindness (I-CSNB).Afamily report
-
Rigaudiere, F., Roux, C., Lachapelle, P., Rosolen, S.G., Bitoun, P., Gay-Duval, A. and Le Gargasson, J.F. (2003) ERGs in female carriers of incomplete congenital stationary night blindness (I-CSNB).Afamily report. Doc. Ophthalmol., 107, 203-212.
-
(2003)
Doc. Ophthalmol.
, vol.107
, pp. 203-212
-
-
Rigaudiere, F.1
Roux, C.2
Lachapelle, P.3
Rosolen, S.G.4
Bitoun, P.5
Gay-Duval, A.6
Le Gargasson, J.F.7
-
19
-
-
18644364692
-
Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2
-
Hope, C.I., Sharp, D.M., Hemara-Wahanui, A., Sissingh, J.I., Lundon, P., Mitchell, E.A., Maw, M.A. and Clover, G.M. (2005) Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2. Clin. Exp. Ophthalmol., 33, 129-136.
-
(2005)
Clin. Exp. Ophthalmol.
, vol.33
, pp. 129-136
-
-
Hope, C.I.1
Sharp, D.M.2
Hemara-Wahanui, A.3
Sissingh, J.I.4
Lundon, P.5
Mitchell, E.A.6
Maw, M.A.7
Clover, G.M.8
-
20
-
-
0037421994
-
The presynaptic active zone protein bassoon is essential for photoreceptor ribbon synapse formation in the retina
-
Dick, O., tom Dieck, S., Altrock, W.D., Ammermuller, J., Weiler, R., Garner, C.C., Gundelfinger, E.D. and Brandstatter, J.H. (2003) The presynaptic active zone protein bassoon is essential for photoreceptor ribbon synapse formation in the retina. Neuron, 37, 775-786.
-
(2003)
Neuron
, vol.37
, pp. 775-786
-
-
Dick, O.1
tom Dieck, S.2
Altrock, W.D.3
Ammermuller, J.4
Weiler, R.5
Garner, C.C.6
Gundelfinger, E.D.7
Brandstatter, J.H.8
-
21
-
-
19944428767
-
Impaired channel targeting and retinal degeneration in mice lacking the cyclic nucleotide-gated channel subunit CNGB1
-
Huttl, S., Michalakis, S., Seeliger, M., Luo, D.G., Acar, N., Geiger, H., Hudl, K., Mader, R., Haverkamp, S., Moser, M. et al. (2005) Impaired channel targeting and retinal degeneration in mice lacking the cyclic nucleotide-gated channel subunit CNGB1. J. Neurosci., 25, 130-138.
-
(2005)
J. Neurosci.
, vol.25
, pp. 130-138
-
-
Huttl, S.1
Michalakis, S.2
Seeliger, M.3
Luo, D.G.4
Acar, N.5
Geiger, H.6
Hudl, K.7
Mader, R.8
Haverkamp, S.9
Moser, M.10
-
22
-
-
0031941610
-
Neurite outgrowth from bipolar and horizontal cells after experimental retinal detachment
-
Lewis, G.P., Linberg, K.A. and Fisher, S.K. (1998) Neurite outgrowth from bipolar and horizontal cells after experimental retinal detachment. Invest. Ophthalmol. Vis. Sci., 39, 424-434.
-
(1998)
Invest. Ophthalmol. Vis. Sci.
, vol.39
, pp. 424-434
-
-
Lewis, G.P.1
Linberg, K.A.2
Fisher, S.K.3
-
23
-
-
84867122079
-
Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosa
-
Koch, S., Sothilingam, V., Garcia Garrido, M., Tanimoto, N., Becirovic, E., Koch, F., Seide, C., Beck, S.C., Seeliger, M.W., Biel, M. et al. (2012) Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosa. Hum. Mol. Genet., 21, 4486-4496.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 4486-4496
-
-
Koch, S.1
Sothilingam, V.2
Garcia Garrido, M.3
Tanimoto, N.4
Becirovic, E.5
Koch, F.6
Seide, C.7
Beck, S.C.8
Seeliger, M.W.9
Biel, M.10
-
24
-
-
0037454611
-
Immunocytochemical description of five bipolar cell types of the mouse retina
-
Haverkamp, S., Ghosh, K.K., Hirano, A.A. and Wassle, H. (2003) Immunocytochemical description of five bipolar cell types of the mouse retina. J. Comp. Neurol., 455, 463-476.
-
(2003)
J. Comp. Neurol.
, vol.455
, pp. 463-476
-
-
Haverkamp, S.1
Ghosh, K.K.2
Hirano, A.A.3
Wassle, H.4
-
25
-
-
84865332357
-
The absence of Complexin 3 and Complexin 4 differentially impacts the ON and OFF pathways in mouse retina
-
Landgraf, I., Muhlhans, J., Dedek, K., Reim, K., Brandstatter, J.H. and Ammermuller, J. (2012) The absence of Complexin 3 and Complexin 4 differentially impacts the ON and OFF pathways in mouse retina. Eur. J. Neurosci., 36, 2470-2481.
-
(2012)
Eur. J. Neurosci.
, vol.36
, pp. 2470-2481
-
-
Landgraf, I.1
Muhlhans, J.2
Dedek, K.3
Reim, K.4
Brandstatter, J.H.5
Ammermuller, J.6
-
26
-
-
18244390994
-
Impaired opsin targeting and cone photoreceptor migration in the retina of mice lacking the cyclic nucleotide-gated channel CNGA3
-
Michalakis, S., Geiger, H., Haverkamp, S., Hofmann, F., Gerstner, A. and Biel, M. (2005) Impaired opsin targeting and cone photoreceptor migration in the retina of mice lacking the cyclic nucleotide-gated channel CNGA3. Invest. Ophthalmol. Vis. Sci., 46, 1516-1524.
-
(2005)
Invest. Ophthalmol. Vis. Sci.
, vol.46
, pp. 1516-1524
-
-
Michalakis, S.1
Geiger, H.2
Haverkamp, S.3
Hofmann, F.4
Gerstner, A.5
Biel, M.6
-
27
-
-
20044363287
-
Molecular dissection of the photoreceptor ribbon synapse: physical interaction of Bassoon and RIBEYE is essential for the assembly of the ribbon complex
-
tom Dieck, S., Altrock, W.D., Kessels, M.M., Qualmann, B., Regus, H., Brauner, D., Fejtova, A., Bracko, O., Gundelfinger, E.D. and Brandstatter, J.H. (2005) Molecular dissection of the photoreceptor ribbon synapse: physical interaction of Bassoon and RIBEYE is essential for the assembly of the ribbon complex. J. Cell Biol., 168, 825-836.
-
(2005)
J. Cell Biol.
, vol.168
, pp. 825-836
-
-
tom Dieck, S.1
Altrock, W.D.2
Kessels, M.M.3
Qualmann, B.4
Regus, H.5
Brauner, D.6
Fejtova, A.7
Bracko, O.8
Gundelfinger, E.D.9
Brandstatter, J.H.10
-
28
-
-
17744371655
-
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
-
Boycott, K.M., Maybaum, T.A., Naylor, M.J., Weleber, R.G., Robitaille, J., Miyake, Y., Bergen, A.A., Pierpont, M.E., Pearce, W.G. and Bech-Hansen, N.T. (2001)Asummary of 20CACNA1Fmutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants. Hum. Genet., 108, 91-97.
-
(2001)
Hum. Genet.
, vol.108
, pp. 91-97
-
-
Boycott, K.M.1
Maybaum, T.A.2
Naylor, M.J.3
Weleber, R.G.4
Robitaille, J.5
Miyake, Y.6
Bergen, A.A.7
Pierpont, M.E.8
Pearce, W.G.9
Bech-Hansen, N.T.10
-
29
-
-
38549152316
-
Early afferent signaling in the outer plexiform layer regulates development of horizontal cell morphology
-
Raven, M.A., Orton, N.C., Nassar, H., Williams, G.A., Stell, W.K., Jacobs, G.H., Bech-Hansen, N.T. and Reese, B.E. (2008) Early afferent signaling in the outer plexiform layer regulates development of horizontal cell morphology. J. Comp. Neurol., 506, 745-758.
-
(2008)
J. Comp. Neurol.
, vol.506
, pp. 745-758
-
-
Raven, M.A.1
Orton, N.C.2
Nassar, H.3
Williams, G.A.4
Stell, W.K.5
Jacobs, G.H.6
Bech-Hansen, N.T.7
Reese, B.E.8
-
30
-
-
0036015952
-
The role of tangential dispersion in retinal mosaic formation
-
Reese, B.E. and Galli-Resta, L. (2002) The role of tangential dispersion in retinal mosaic formation. Prog. Retin. Eye Res., 21, 153-168.
-
(2002)
Prog. Retin. Eye Res.
, vol.21
, pp. 153-168
-
-
Reese, B.E.1
Galli-Resta, L.2
-
31
-
-
0028946298
-
Radial and tangential dispersion patterns in the mouse retina are cell-class specific
-
Reese, B.E., Harvey, A.R. and Tan, S.S. (1995) Radial and tangential dispersion patterns in the mouse retina are cell-class specific. Proc. Natl Acad. Sci. USA, 92, 2494-2498.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 2494-2498
-
-
Reese, B.E.1
Harvey, A.R.2
Tan, S.S.3
-
32
-
-
0032084321
-
Clonal boundary analysis in the developing retina using X-inactivation transgenic mosaic mice
-
Reese, B.E. and Tan, S.S. (1998) Clonal boundary analysis in the developing retina using X-inactivation transgenic mosaic mice. Semin. Cell Dev. Biol., 9, 285-292.
-
(1998)
Semin. Cell Dev. Biol.
, vol.9
, pp. 285-292
-
-
Reese, B.E.1
Tan, S.S.2
-
33
-
-
33645082502
-
The role of X inactivation and cellular mosaicism in women's health and sex-specific diseases
-
Migeon, B.R. (2006) The role of X inactivation and cellular mosaicism in women's health and sex-specific diseases. JAMA, 295, 1428-1433.
-
(2006)
JAMA
, vol.295
, pp. 1428-1433
-
-
Migeon, B.R.1
-
34
-
-
3543044979
-
Fundus autofluorescence in carriers of X-linked recessive retinitis pigmentosa associated with mutations in RPGR, and correlation with electrophysiological and psychophysical data
-
Wegscheider, E., Preising, M.N. and Lorenz, B. (2004) Fundus autofluorescence in carriers of X-linked recessive retinitis pigmentosa associated with mutations in RPGR, and correlation with electrophysiological and psychophysical data. Graefes Arch. Clin. Exp. Ophthalmol., 242, 501-511.
-
(2004)
Graefes Arch. Clin. Exp. Ophthalmol.
, vol.242
, pp. 501-511
-
-
Wegscheider, E.1
Preising, M.N.2
Lorenz, B.3
-
35
-
-
67349105082
-
Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical data
-
1201-1209+e1201-e1202
-
Preising, M.N., Wegscheider, E., Friedburg, C., Poloschek, C.M., Wabbels, B.K. and Lorenz, B. (2009) Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical data. Ophthalmology, 116, 1201-1209 e1201-1202.
-
(2009)
Ophthalmology
, vol.116
-
-
Preising, M.N.1
Wegscheider, E.2
Friedburg, C.3
Poloschek, C.M.4
Wabbels, B.K.5
Lorenz, B.6
-
36
-
-
84861973365
-
Chemical chaperone TUDCA preserves cone photoreceptors in a mouse model of Leber congenital amaurosis
-
Zhang, T., Baehr, W. and Fu, Y. (2012) Chemical chaperone TUDCA preserves cone photoreceptors in a mouse model of Leber congenital amaurosis. Invest. Ophthalmol. Vis. Sci., 53, 3349-3356.
-
(2012)
Invest. Ophthalmol. Vis. Sci.
, vol.53
, pp. 3349-3356
-
-
Zhang, T.1
Baehr, W.2
Fu, Y.3
-
37
-
-
0020713543
-
Monoclonal antibodies to rhodopsin: characterization, cross-reactivity, and application as structural probes
-
Molday, R.S. and MacKenzie, D. (1983) Monoclonal antibodies to rhodopsin: characterization, cross-reactivity, and application as structural probes. Biochemistry, 22, 653-660.
-
(1983)
Biochemistry
, vol.22
, pp. 653-660
-
-
Molday, R.S.1
MacKenzie, D.2
-
38
-
-
17944379443
-
New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis
-
Seeliger, M.W., Grimm, C., Stahlberg, F., Friedburg, C., Jaissle, G., Zrenner, E., Guo, H., Reme, C.E., Humphries, P., Hofmann, F. et al. (2001) New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis. Nat. Genet., 29, 70-74.
-
(2001)
Nat. Genet.
, vol.29
, pp. 70-74
-
-
Seeliger, M.W.1
Grimm, C.2
Stahlberg, F.3
Friedburg, C.4
Jaissle, G.5
Zrenner, E.6
Guo, H.7
Reme, C.E.8
Humphries, P.9
Hofmann, F.10
-
39
-
-
63149183620
-
Vision tests in the mouse: Functional phenotyping with electroretinography
-
Tanimoto, N., Muehlfriedel, R.L., Fischer, M.D., Fahl, E., Humphries, P., Biel, M. and Seeliger, M.W. (2009) Vision tests in the mouse: Functional phenotyping with electroretinography. Front. Biosci. (Landmark Ed), 14, 2730-2737.
-
(2009)
Front. Biosci. (Landmark Ed)
, vol.14
, pp. 2730-2737
-
-
Tanimoto, N.1
Muehlfriedel, R.L.2
Fischer, M.D.3
Fahl, E.4
Humphries, P.5
Biel, M.6
Seeliger, M.W.7
|