-
1
-
-
33748769378
-
The ciliopathies: an emerging class of human genetic disorders
-
Badano JL, Mitsuma N, Beales PL, Katsanis N, (2006) The ciliopathies: an emerging class of human genetic disorders. Annu Rev Genomics Hum Genet 7: 125-48.
-
(2006)
Annu Rev Genomics Hum Genet
, vol.7
, pp. 125-148
-
-
Badano, J.L.1
Mitsuma, N.2
Beales, P.L.3
Katsanis, N.4
-
2
-
-
84856030268
-
Scrutinizing ciliopathies by unraveling ciliary interaction networks
-
van Reeuwijk J, Arts HH, Roepman R, (2011) Scrutinizing ciliopathies by unraveling ciliary interaction networks. Hum Mol Genet 15 20(R2): R149-57.
-
(2011)
Hum Mol Genet 15
, vol.20
, Issue.R2
-
-
van Reeuwijk, J.1
Arts, H.H.2
Roepman, R.3
-
3
-
-
79959951978
-
An update on the genetics of usher syndrome
-
Millán JM, Aller E, Jaijo T, Blanco-Kelly F, Gimenez-Pardo A, et al. (2011) An update on the genetics of usher syndrome. J Ophthalmol 2011: 417217.
-
(2011)
J Ophthalmol
, vol.2011
, pp. 417217
-
-
Millán, J.M.1
Aller, E.2
Jaijo, T.3
Blanco-Kelly, F.4
Gimenez-Pardo, A.5
-
4
-
-
0032511101
-
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa. Science
-
Eudy JD, Weston MD, Yao S, Hoover DM, Rehm HL, et al. (1998) Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa. Science. 12 280(5370): 1753-7.
-
(1998)
12
, vol.280
, Issue.5370
, pp. 1753-1757
-
-
Eudy, J.D.1
Weston, M.D.2
Yao, S.3
Hoover, D.M.4
Rehm, H.L.5
-
5
-
-
1842592042
-
Identification of 51 novel exons of the Ushersyndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II
-
vanWijk E, Pennings RJ, te Brinke H, Claassen A, Yntema HG, et al. (2004) Identification of 51 novel exons of the Ushersyndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II. Am J Hum Genet 74(4): 738-44.
-
(2004)
Am J Hum Genet
, vol.74
, Issue.4
, pp. 738-744
-
-
vanWijk, E.1
Pennings, R.J.2
te Brinke, H.3
Claassen, A.4
Yntema, H.G.5
-
6
-
-
0842328857
-
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II
-
74(2): 357-66. Erratum in: Am J Hum Genet
-
Weston MD, Luijendijk MW, Humphrey KD, Möller C, Kimberling WJ, (2004) Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II. Am J Hum Genet 74(2): 357-66. Erratum in: Am J Hum Genet. 2004 74(5): 1080.
-
(2004)
Am J Hum Genet
, vol.74
, Issue.5
, pp. 1080
-
-
Weston, M.D.1
Luijendijk, M.W.2
Humphrey, K.D.3
Möller, C.4
Kimberling, W.J.5
-
7
-
-
33947148611
-
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
-
Ebermann I, Scholl HP, CharbelIssa P, Becirovic E, Lamprecht J, et al. (2007) A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss. Hum Genet 121(2): 203-11.
-
(2007)
Hum Genet
, vol.121
, Issue.2
, pp. 203-211
-
-
Ebermann, I.1
Scholl, H.P.2
CharbelIssa, P.3
Becirovic, E.4
Lamprecht, J.5
-
8
-
-
34548014988
-
Molecular and in silico analyses of the full-length isoform of usherin identify new pathogenic alleles in Usher type II patients
-
Baux D, Larrieu L, Blanchet C, Hamel C, Ben Salah S, et al. (2007) Molecular and in silico analyses of the full-length isoform of usherin identify new pathogenic alleles in Usher type II patients. Hum Mutat 28(8): 781-9.
-
(2007)
Hum Mutat
, vol.28
, Issue.8
, pp. 781-789
-
-
Baux, D.1
Larrieu, L.2
Blanchet, C.3
Hamel, C.4
Ben Salah, S.5
-
9
-
-
41449108355
-
Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II
-
Dreyer B, Brox V, Tranebjaerg L, Rosenberg T, Sadeghi AM, et al. (2008) Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II. Hum Mutat 29(3): 451.
-
(2008)
Hum Mutat
, vol.29
, Issue.3
, pp. 451
-
-
Dreyer, B.1
Brox, V.2
Tranebjaerg, L.3
Rosenberg, T.4
Sadeghi, A.M.5
-
10
-
-
80054064728
-
Mutational screening of the USH2A gene in Spanish USH patients reveals 23 novel pathogenic mutations
-
Garcia-Garcia G, Aparisi MJ, Jaijo T, Rodrigo R, Leon AM, et al. (2011) Mutational screening of the USH2A gene in Spanish USH patients reveals 23 novel pathogenic mutations. Orphanet J Rare Dis 17 6: 65.
-
(2011)
Orphanet J Rare Dis 17
, vol.6
, pp. 65
-
-
Garcia-Garcia, G.1
Aparisi, M.J.2
Jaijo, T.3
Rodrigo, R.4
Leon, A.M.5
-
11
-
-
0033927821
-
Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss
-
Rivolta C, Sweklo EA, Berson EL, Dryja TP, (2000) Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss. Am J Hum Genet 66: 1975-1978.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1975-1978
-
-
Rivolta, C.1
Sweklo, E.A.2
Berson, E.L.3
Dryja, T.P.4
-
12
-
-
2442656582
-
Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments
-
Aller E, Najera C, Millan JM, Oltra JS, Perez-Garrigues H, et al. (2004) Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments. Eur J Hum Genet 12: 407-10.
-
(2004)
Eur J Hum Genet
, vol.12
, pp. 407-410
-
-
Aller, E.1
Najera, C.2
Millan, J.M.3
Oltra, J.S.4
Perez-Garrigues, H.5
-
13
-
-
66749156456
-
Linking genes underlying deafness to hair-bundle development and function
-
Petit C, Richardson GP, (2009) Linking genes underlying deafness to hair-bundle development and function. Nat Neurosci 12(6): 703-10.
-
(2009)
Nat Neurosci
, vol.12
, Issue.6
, pp. 703-710
-
-
Petit, C.1
Richardson, G.P.2
-
14
-
-
34248353947
-
Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells
-
Liu X, Bulgakov OV, Darrow KN, Pawlyk B, Adamian M, et al. (2007) Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells. Proc Natl Acad Sci 13 104(11): 4413-8.
-
(2007)
Proc Natl Acad Sci 13
, vol.104
, Issue.11
, pp. 4413-4418
-
-
Liu, X.1
Bulgakov, O.V.2
Darrow, K.N.3
Pawlyk, B.4
Adamian, M.5
-
15
-
-
37549042393
-
A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells
-
Maerker T, van Wijk E, Overlack N, Kersten FF, McGee J, et al. (2008) A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells. Hum Mol Genet 1 17(1): 71-86.
-
(2008)
Hum Mol Genet 1
, vol.17
, Issue.1
, pp. 71-86
-
-
Maerker, T.1
van Wijk, E.2
Overlack, N.3
Kersten, F.F.4
McGee, J.5
-
16
-
-
38749124706
-
Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy
-
Williams DS, (2008) Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy. Vision Res 48(3): 433-41.
-
(2008)
Vision Res
, vol.48
, Issue.3
, pp. 433-441
-
-
Williams, D.S.1
-
17
-
-
77951209789
-
Cell transplantation to arrest early changes in an ush2a animal model
-
Lu B, Wang S, Francis PJ, Li T, Gamm DM, et al. (2010) Cell transplantation to arrest early changes in an ush2a animal model. Invest Ophthalmol Vis Sci 51(4): 2269-76.
-
(2010)
Invest Ophthalmol Vis Sci
, vol.51
, Issue.4
, pp. 2269-2276
-
-
Lu, B.1
Wang, S.2
Francis, P.J.3
Li, T.4
Gamm, D.M.5
-
18
-
-
0034284683
-
Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness
-
Ernest S, Rauch GJ, Haffter P, Geisler R, Petit C, et al. (2000) Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness. Hum Mol Genet 1 9(14): 2189-96.
-
(2000)
Hum Mol Genet 1
, vol.9
, Issue.14
, pp. 2189-2196
-
-
Ernest, S.1
Rauch, G.J.2
Haffter, P.3
Geisler, R.4
Petit, C.5
-
19
-
-
84905556082
-
Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells
-
Söllner C, Rauch GJ, Siemens J, Geisler R, Schuster SC, et al. (2004) Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells. Nature 29 428(6986): 955-9.
-
(2004)
Nature 29
, vol.428
, Issue.6986
, pp. 955-959
-
-
Söllner, C.1
Rauch, G.J.2
Siemens, J.3
Geisler, R.4
Schuster, S.C.5
-
20
-
-
84866700980
-
The Usher gene cadherin 23 is expressed in the zebrafish brain and a subset of retinal amacrine cells
-
Glover G, Mueller KP, Söllner C, Neuhauss SC, Nicolson T, (2012) The Usher gene cadherin 23 is expressed in the zebrafish brain and a subset of retinal amacrine cells. Mol Vis 18: 2309-2322.
-
(2012)
Mol Vis
, vol.18
, pp. 2309-2322
-
-
Glover, G.1
Mueller, K.P.2
Söllner, C.3
Neuhauss, S.C.4
Nicolson, T.5
-
21
-
-
14044258529
-
Duplicated genes with split functions: independent roles of protocadherin15 orthologues in zebrafish hearing and vision
-
Seiler C, Finger-Baier KC, Rinner O, Makhankov YV, Schwarz H, et al. (2005) Duplicated genes with split functions: independent roles of protocadherin15 orthologues in zebrafish hearing and vision. Development 132(3): 615-23.
-
(2005)
Development
, vol.132
, Issue.3
, pp. 615-623
-
-
Seiler, C.1
Finger-Baier, K.C.2
Rinner, O.3
Makhankov, Y.V.4
Schwarz, H.5
-
22
-
-
81455136716
-
Harmonin (Ush1c) is required in zebrafish Müller glial cells forphotoreceptor synaptic development and function
-
Phillips JB, Blanco-Sanchez B, Lentz JJ, Tallafuss A, Khanobdee K, et al. (2011) Harmonin (Ush1c) is required in zebrafish Müller glial cells forphotoreceptor synaptic development and function. Dis Model Mech 4(6): 786-800.
-
(2011)
Dis Model Mech
, vol.4
, Issue.6
, pp. 786-800
-
-
Phillips, J.B.1
Blanco-Sanchez, B.2
Lentz, J.J.3
Tallafuss, A.4
Khanobdee, K.5
-
23
-
-
77953207481
-
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome
-
Ebermann I, Phillips JB, Liebau MC, Koenekoop RK, Schermer B, et al. (2010) PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome. J Clin Invest 120(6): 1812-23.
-
(2010)
J Clin Invest
, vol.120
, Issue.6
, pp. 1812-1823
-
-
Ebermann, I.1
Phillips, J.B.2
Liebau, M.C.3
Koenekoop, R.K.4
Schermer, B.5
-
24
-
-
21744448333
-
Analysis of the very large G-protein coupled receptor gene (Vlgr1/Mass1/USH2C) in zebrafish
-
Gibert Y, McMillan DR, Kayes-Wandover K, Meyer A, Begemann G, et al. (2005) Analysis of the very large G-protein coupled receptor gene (Vlgr1/Mass1/USH2C) in zebrafish. Gene 4 353(2): 200-6.
-
(2005)
Gene 4
, vol.353
, Issue.2
, pp. 200-206
-
-
Gibert, Y.1
McMillan, D.R.2
Kayes-Wandover, K.3
Meyer, A.4
Begemann, G.5
-
25
-
-
0036245348
-
Medaka - a model organism from the Far East
-
Genet3
-
Wittbrodt J, Shima A, Schartl M, (2002) Medaka- a model organism from the Far East. Nat Rev Genet3: 53-64.
-
(2002)
Nat Rev
, pp. 53-64
-
-
Wittbrodt, J.1
Shima, A.2
Schartl, M.3
-
26
-
-
3042569659
-
Medaka and zebrafish, an evolutionary twin study
-
Dev121
-
Furutani-Seiki M, Wittbrodt J, (2004) Medaka and zebrafish, an evolutionary twin study. Mech Dev121: 629-637.
-
(2004)
Mech
, pp. 629-637
-
-
Furutani-Seiki, M.1
Wittbrodt, J.2
-
27
-
-
2142756448
-
Inbred strains of the medaka (Oryzias latipes)
-
Hyodo-Taguchi Y, (1996) Inbred strains of the medaka (Oryzias latipes). Fish Biol J Medaka 8: 29-30.30.
-
(1996)
Fish Biol J Medaka
, vol.8
, pp. 29-30
-
-
Hyodo-Taguchi, Y.1
-
29
-
-
3042631471
-
Stages of normal development in the medaka Oryzias latipes
-
Iwamatsu T, (2004) Stages of normal development in the medaka Oryzias latipes. Mech Dev 121: 605-618.
-
(2004)
Mech Dev
, vol.121
, pp. 605-618
-
-
Iwamatsu, T.1
-
30
-
-
70349868349
-
Nanog regulates proliferation during early fish development
-
Camp E, Sánchez-Sánchez AV, García-España A, Desalle R, Odqvist L, et al. (2009) Nanog regulates proliferation during early fish development. Stem Cells 27: 2081-2091.
-
(2009)
Stem Cells
, vol.27
, pp. 2081-2091
-
-
Camp, E.1
Sánchez-Sánchez, A.V.2
García-España, A.3
Desalle, R.4
Odqvist, L.5
-
31
-
-
61849175945
-
Intron evolution: testing hypotheses of intron evolution using the phylogenomics of tetraspanins
-
Garcia-España A, Mares R, Sun TT, Desalle R, (2009) Intron evolution: testing hypotheses of intron evolution using the phylogenomics of tetraspanins. PLoS One 4: e4680.
-
(2009)
PLoS One
, vol.4
-
-
Garcia-España, A.1
Mares, R.2
Sun, T.T.3
Desalle, R.4
-
32
-
-
0034161321
-
TIBS 25
-
Combet C, Blanchet C, Geourjon C, Deléage G, (2000) NPS@: Network Protein Sequence Analysis. TIBS 25. 3(291): 147-150.
-
(2000)
, vol.3
, Issue.291
, pp. 147-150
-
-
Combet, C.1
Blanchet, C.2
Geourjon, C.3
Deléage, G.4
-
33
-
-
80053345905
-
SignalP 4.0: discriminating signal peptides from transmembrane regions
-
Petersen TN, Brunak S, von Heijne G, Nielsen H, (2011) SignalP 4.0: discriminating signal peptides from transmembrane regions. Nature Methods 8: 785-786.
-
(2011)
Nature Methods
, vol.8
, pp. 785-786
-
-
Petersen, T.N.1
Brunak, S.2
von Heijne, G.3
Nielsen, H.4
-
34
-
-
78651285748
-
CDD: a Conserved Domain Database for the functional annotation of proteins
-
Marchler-Bauer A, Lu S, Anderson JB, Chitsaz F, Derbyshire MK, et al. (2011) CDD: a Conserved Domain Database for the functional annotation of proteins. Nucleic Acids Res 39: D225-9.
-
(2011)
Nucleic Acids Res
, vol.39
-
-
Marchler-Bauer, A.1
Lu, S.2
Anderson, J.B.3
Chitsaz, F.4
Derbyshire, M.K.5
-
35
-
-
0035910270
-
Predicting transmembrane protein topology with a hidden Markov model: Application to complete genomes
-
Krogh A, Larsson B, von Heijne G, Sonnhammer ELL, (2001) Predicting transmembrane protein topology with a hidden Markov model: Application to complete genomes. Journal of Molecular Biology 305(3): 567-580.
-
(2001)
Journal of Molecular Biology
, vol.305
, Issue.3
, pp. 567-580
-
-
Krogh, A.1
Larsson, B.2
von Heijne, G.3
Sonnhammer, E.L.L.4
-
36
-
-
73949148203
-
Wnt signaling has different temporal roles during retinal development
-
Sánchez-Sánchez AV, Camp E, Leal-Tassias A, Mullor JL, (2010) Wnt signaling has different temporal roles during retinal development. 239(1): 297-310.
-
(2010)
, vol.239
, Issue.1
, pp. 297-310
-
-
Sánchez-Sánchez, A.V.1
Camp, E.2
Leal-Tassias, A.3
Mullor, J.L.4
-
37
-
-
77954586448
-
Expression of usherin in the anthozoan Nematostella vectensis. Biol Bull
-
Tucker RP, (2010) Expression of usherin in the anthozoan Nematostella vectensis. Biol Bull. 218(2): 105-12.
-
(2010)
, vol.218
, Issue.2
, pp. 105-112
-
-
Tucker, R.P.1
-
38
-
-
34447300950
-
Sea anemone genome reveals ancestral eumetazoan gene repertoire and genomic organization
-
Putnam NH, Srivastava M, Hellsten U, Dirks B, Chapman J, et al. (2007) Sea anemone genome reveals ancestral eumetazoan gene repertoire and genomic organization. Science 317: 86-94.
-
(2007)
Science
, vol.317
, pp. 86-94
-
-
Putnam, N.H.1
Srivastava, M.2
Hellsten, U.3
Dirks, B.4
Chapman, J.5
-
39
-
-
29644441618
-
Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells
-
Adato A, Lefèvre G, Delprat B, Michel V, Michalski N, et al. (2005) Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells. Hum Mol Genet 15 14(24): 3921-32.
-
(2005)
Hum Mol Genet 15
, vol.14
, Issue.24
, pp. 3921-3932
-
-
Adato, A.1
Lefèvre, G.2
Delprat, B.3
Michel, V.4
Michalski, N.5
-
40
-
-
0036888465
-
Usherin expression is highly conserved in mouse and human tissues
-
Pearsall N, Bhattacharya G, Wisecarver J, Adams J, Cosgrove D, et al. (2002) Usherin expression is highly conserved in mouse and human tissues. Hear Res 174(1-2): 55-63.
-
(2002)
Hear Res
, vol.174
, Issue.1-2
, pp. 55-63
-
-
Pearsall, N.1
Bhattacharya, G.2
Wisecarver, J.3
Adams, J.4
Cosgrove, D.5
-
41
-
-
67349141319
-
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies
-
Khanna H, Davis EE, Murga-Zamalloa CA, Estrada-Cuzcano A, Lopez I, et al. (2009) A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies. Nat Genet 41(6): 739-45.
-
(2009)
Nat Genet
, vol.41
, Issue.6
, pp. 739-745
-
-
Khanna, H.1
Davis, E.E.2
Murga-Zamalloa, C.A.3
Estrada-Cuzcano, A.4
Lopez, I.5
-
42
-
-
77950343938
-
Zebrafish Rpgr is required for normal retinal development and plays a role in dynein-based retrograde transport processes
-
Shu X, Zeng Z, Gautier P, Lennon A, Gakovic M, et al. (2010) Zebrafish Rpgr is required for normal retinal development and plays a role in dynein-based retrograde transport processes. Hum Mol Genet 15 19(4): 657-70.
-
(2010)
Hum Mol Genet 15
, vol.19
, Issue.4
, pp. 657-670
-
-
Shu, X.1
Zeng, Z.2
Gautier, P.3
Lennon, A.4
Gakovic, M.5
-
43
-
-
79955966762
-
Knockdown of the zebrafish ortholog of the retinitis pigmentosa 2 (RP2) gene results in retinal degeneration
-
Shu X, Zeng Z, Gautier P, Lennon A, Gakovic M, et al. (2011) Knockdown of the zebrafish ortholog of the retinitis pigmentosa 2 (RP2) gene results in retinal degeneration. Invest Ophthalmol Vis Sci5 52(6): 2960-6.
-
(2011)
Invest Ophthalmol Vis Sci5
, vol.52
, Issue.6
, pp. 2960-2966
-
-
Shu, X.1
Zeng, Z.2
Gautier, P.3
Lennon, A.4
Gakovic, M.5
-
44
-
-
84868207944
-
Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48
-
Riazuddin S, Belyantseva IA, Giese AP, Lee K, Indzhykulian AA, et al. (2012) Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48. Nat Genet 44(11): 1265-71.
-
(2012)
Nat Genet
, vol.44
, Issue.11
, pp. 1265-1271
-
-
Riazuddin, S.1
Belyantseva, I.A.2
Giese, A.P.3
Lee, K.4
Indzhykulian, A.A.5
-
45
-
-
33947228840
-
Mutant analyses reveal different functions of fgfr1 in medaka and zebrafish despite conserved ligand-receptor relationships
-
Yokoi H, Shimada A, Carl M, Takashima S, Kobayashi D, et al. (2007) Mutant analyses reveal different functions of fgfr1 in medaka and zebrafish despite conserved ligand-receptor relationships. Dev Biol 1 304(1): 326-37.
-
(2007)
Dev Biol 1
, vol.304
, Issue.1
, pp. 326-337
-
-
Yokoi, H.1
Shimada, A.2
Carl, M.3
Takashima, S.4
Kobayashi, D.5
-
46
-
-
27144460671
-
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates
-
Ross AJ, May-Simera H, Eichers ER, Kai M, Hill J, et al. (2005) Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates. Nat Genet 37(10): 1135-40.
-
(2005)
Nat Genet
, vol.37
, Issue.10
, pp. 1135-1140
-
-
Ross, A.J.1
May-Simera, H.2
Eichers, E.R.3
Kai, M.4
Hill, J.5
-
47
-
-
84855433919
-
Wnt/β-catenin signaling directly regulates Foxj1 expression and ciliogenesis in zebrafish Kupffer's vesicle
-
Caron A, Xu X, Lin X, (2012) Wnt/β-catenin signaling directly regulates Foxj1 expression and ciliogenesis in zebrafish Kupffer's vesicle. Development 139(3): 514-24.
-
(2012)
Development
, vol.139
, Issue.3
, pp. 514-524
-
-
Caron, A.1
Xu, X.2
Lin, X.3
-
48
-
-
25844471118
-
RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins
-
Khanna H, Hurd TW, Lillo C, Shu X, Parapuram SK, et al. (2005) RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins. J Biol Chem 30 280(39): 33580-7.
-
(2005)
J Biol Chem 30
, vol.280
, Issue.39
, pp. 33580-33587
-
-
Khanna, H.1
Hurd, T.W.2
Lillo, C.3
Shu, X.4
Parapuram, S.K.5
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