-
1
-
-
79959676965
-
The tubby family proteins
-
10.1186/gb-2011-12-6-225, 3218838, 21722349
-
Mukhopadhyay S, Jackson PK. The tubby family proteins. Genome Biol 2011, 12:225. 10.1186/gb-2011-12-6-225, 3218838, 21722349.
-
(2011)
Genome Biol
, vol.12
, pp. 225
-
-
Mukhopadhyay, S.1
Jackson, P.K.2
-
3
-
-
0031004576
-
Molecular characterization of TUB, TULP1, and TULP2, members of the novel tubby gene family and their possible relation to ocular diseases
-
10.1073/pnas.94.7.3128, 20333, 9096357
-
North MA, Naggert JK, Yan Y, Noben-Trauth K, Nishina PM. Molecular characterization of TUB, TULP1, and TULP2, members of the novel tubby gene family and their possible relation to ocular diseases. Proc Natl Acad Sci U S A 1997, 94:3128-3133. 10.1073/pnas.94.7.3128, 20333, 9096357.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 3128-3133
-
-
North, M.A.1
Naggert, J.K.2
Yan, Y.3
Noben-Trauth, K.4
Nishina, P.M.5
-
4
-
-
0030006024
-
A candidate gene for the mouse mutation tubby
-
10.1038/380534a0, 8606774
-
Noben-Trauth K, Naggert JK, North MA, Nishina PM. A candidate gene for the mouse mutation tubby. Nature 1996, 380:534-538. 10.1038/380534a0, 8606774.
-
(1996)
Nature
, vol.380
, pp. 534-538
-
-
Noben-Trauth, K.1
Naggert, J.K.2
North, M.A.3
Nishina, P.M.4
-
5
-
-
0032884085
-
Cell-specific expression of tubby gene family members (tub, Tulp1,2, and 3) in the retina
-
Ikeda S, He W, Ikeda A, Naggert JK, North MA, Nishina PM. Cell-specific expression of tubby gene family members (tub, Tulp1,2, and 3) in the retina. Invest Ophthalmol Vis Sci 1999, 40:2706-2712.
-
(1999)
Invest Ophthalmol Vis Sci
, vol.40
, pp. 2706-2712
-
-
Ikeda, S.1
He, W.2
Ikeda, A.3
Naggert, J.K.4
North, M.A.5
Nishina, P.M.6
-
6
-
-
0031942582
-
Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa
-
10.1038/ng0298-174, 9462750
-
Hagstrom SA, North MA, Nishina PL, Berson EL, Dryja TP. Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa. Nat Genet 1998, 18:174-176. 10.1038/ng0298-174, 9462750.
-
(1998)
Nat Genet
, vol.18
, pp. 174-176
-
-
Hagstrom, S.A.1
North, M.A.2
Nishina, P.L.3
Berson, E.L.4
Dryja, T.P.5
-
7
-
-
0032759729
-
Retinal degeneration in tulp1-/- mice: vesiclular accumulation in the interphotoreceptor matrix
-
Hagstrom SA, Duyao M, North MA, Li T. Retinal degeneration in tulp1-/- mice: vesiclular accumulation in the interphotoreceptor matrix. Invest Ophthalmol Vis Sci 1999, 40:2795-2802.
-
(1999)
Invest Ophthalmol Vis Sci
, vol.40
, pp. 2795-2802
-
-
Hagstrom, S.A.1
Duyao, M.2
North, M.A.3
Li, T.4
-
8
-
-
0033978890
-
Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene
-
10.1093/hmg/9.2.155, 10607826
-
Ikeda S, Shiva N, Ikeda A, Smith RS, Nusinowitz S, Yan G, Lin TR, Chu S, Heckenlively JR, North MA, Naggert JK, Nishina PM, Duyao MP. Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene. Hum Mol Genet 2000, 9:155-163. 10.1093/hmg/9.2.155, 10607826.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 155-163
-
-
Ikeda, S.1
Shiva, N.2
Ikeda, A.3
Smith, R.S.4
Nusinowitz, S.5
Yan, G.6
Lin, T.R.7
Chu, S.8
Heckenlively, J.R.9
North, M.A.10
Naggert, J.K.11
Nishina, P.M.12
Duyao, M.P.13
-
9
-
-
0034907947
-
A role for the Tubby-like protein 1 in rhodopsin transport
-
Hagstrom SA, Adamian M, Scimeca M, Pawlyk BS, Yue G, Li T. A role for the Tubby-like protein 1 in rhodopsin transport. Invest Ophthalmol Vis Sci 2001, 42:1955-1962.
-
(2001)
Invest Ophthalmol Vis Sci
, vol.42
, pp. 1955-1962
-
-
Hagstrom, S.A.1
Adamian, M.2
Scimeca, M.3
Pawlyk, B.S.4
Yue, G.5
Li, T.6
-
10
-
-
0032402244
-
Molecular characterization of a novel tubby gene family member, TULP3, in mouse and humans
-
10.1006/geno.1998.5567, 9828123
-
Nishina PM, North MA, Ikeda A, Yan Y, Naggert JK. Molecular characterization of a novel tubby gene family member, TULP3, in mouse and humans. Genomics 1998, 54:215-220. 10.1006/geno.1998.5567, 9828123.
-
(1998)
Genomics
, vol.54
, pp. 215-220
-
-
Nishina, P.M.1
North, M.A.2
Ikeda, A.3
Yan, Y.4
Naggert, J.K.5
-
11
-
-
65449124963
-
Tubby-like protein 3 (TULP3) regulates patterning in the mouse embryo through inhibition of Hedgehog signaling
-
10.1093/hmg/ddp113, 2671991, 19286674
-
Norman RX, Ko HW, Huang V, Eun CM, Abler LL, Zhang Z, Sun X, Eggenschwiler JT. Tubby-like protein 3 (TULP3) regulates patterning in the mouse embryo through inhibition of Hedgehog signaling. Hum Mol Genet 2009, 18:1740-1754. 10.1093/hmg/ddp113, 2671991, 19286674.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1740-1754
-
-
Norman, R.X.1
Ko, H.W.2
Huang, V.3
Eun, C.M.4
Abler, L.L.5
Zhang, Z.6
Sun, X.7
Eggenschwiler, J.T.8
-
12
-
-
14844346387
-
Genome-wide transcriptional analysis of flagellar regeneration in Chlamydomonas reinhardtii identifies orthologs of ciliary disease genes
-
10.1073/pnas.0408358102, 553310, 15738400
-
Stolc V, Samanta MP, Tongprasit W, Marshall WF. Genome-wide transcriptional analysis of flagellar regeneration in Chlamydomonas reinhardtii identifies orthologs of ciliary disease genes. Proc Natl Acad Sci U S A 2005, 102:3703-3707. 10.1073/pnas.0408358102, 553310, 15738400.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 3703-3707
-
-
Stolc, V.1
Samanta, M.P.2
Tongprasit, W.3
Marshall, W.F.4
-
13
-
-
3042742243
-
Genome-wide linkage analysis for severe obesity in French Caucasians finds significant susceptibility locus on chromosome 19q
-
10.2337/diabetes.53.7.1857, 15220211
-
Bell CG, Benzinou M, Siddiq A, Lecoeur C, Dina C, Lemainque A, Clement K, Basdevant A, Guy-Grand B, Mein CA, Meyre D, Froguel P. Genome-wide linkage analysis for severe obesity in French Caucasians finds significant susceptibility locus on chromosome 19q. Diabetes 2004, 53:1857-1865. 10.2337/diabetes.53.7.1857, 15220211.
-
(2004)
Diabetes
, vol.53
, pp. 1857-1865
-
-
Bell, C.G.1
Benzinou, M.2
Siddiq, A.3
Lecoeur, C.4
Dina, C.5
Lemainque, A.6
Clement, K.7
Basdevant, A.8
Guy-Grand, B.9
Mein, C.A.10
Meyre, D.11
Froguel, P.12
-
14
-
-
0035874921
-
G-protein signaling through tubby proteins
-
10.1126/science.1061233, 11375483
-
Santagata S, Boggon TJ, Baird CL, Gomez CA, Zhao J, Shan WS, Myszka DG, Shapiro L. G-protein signaling through tubby proteins. Science 2001, 292:2041-2050. 10.1126/science.1061233, 11375483.
-
(2001)
Science
, vol.292
, pp. 2041-2050
-
-
Santagata, S.1
Boggon, T.J.2
Baird, C.L.3
Gomez, C.A.4
Zhao, J.5
Shan, W.S.6
Myszka, D.G.7
Shapiro, L.8
-
15
-
-
77957682469
-
TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia
-
10.1101/gad.1966210, 2947770, 20889716
-
Mukhopadhyay S, Wen X, Chih B, Nelson CD, Lane WS, Scales SJ, Jackson PK. TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia. Genes Dev 2010, 24:2180-2193. 10.1101/gad.1966210, 2947770, 20889716.
-
(2010)
Genes Dev
, vol.24
, pp. 2180-2193
-
-
Mukhopadhyay, S.1
Wen, X.2
Chih, B.3
Nelson, C.D.4
Lane, W.S.5
Scales, S.J.6
Jackson, P.K.7
-
16
-
-
0028972472
-
Mouse model for Usher syndrome: Linkage mapping suggests homology to Usher type I reported at human chromosome 11p15
-
10.1073/pnas.92.24.11100, 40579, 7479945
-
Heckenlively JR, Chang B, Erway LC, Peng C, Hawes NL, Hageman GS, Roderick TH. Mouse model for Usher syndrome: Linkage mapping suggests homology to Usher type I reported at human chromosome 11p15. Proc Natl Acad Sci U S A 1995, 92:11100-11104. 10.1073/pnas.92.24.11100, 40579, 7479945.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 11100-11104
-
-
Heckenlively, J.R.1
Chang, B.2
Erway, L.C.3
Peng, C.4
Hawes, N.L.5
Hageman, G.S.6
Roderick, T.H.7
-
17
-
-
84862908687
-
Bardet-Biedl syndrome 3 (BBs3) knockout mouse model reveals common BBS-associated phenotypes and BBs3 unique phenotypes
-
10.1073/pnas.1113220108, 3251145, 22139371
-
Zhang Q, Nishimura D, Seo S, Vogel T, Morgan DA, Searby C, Bugge K, Stone EM, Rahmouni K, Sheffield VC. Bardet-Biedl syndrome 3 (BBs3) knockout mouse model reveals common BBS-associated phenotypes and BBs3 unique phenotypes. Proc Natl Acad Sci U S A 2011, 108:20678-20683. 10.1073/pnas.1113220108, 3251145, 22139371.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 20678-20683
-
-
Zhang, Q.1
Nishimura, D.2
Seo, S.3
Vogel, T.4
Morgan, D.A.5
Searby, C.6
Bugge, K.7
Stone, E.M.8
Rahmouni, K.9
Sheffield, V.C.10
-
18
-
-
79551718744
-
The blind leading the obese: the molecular pathophysiology of a human obesity syndrome
-
discussion 181-182, 2917141, 20697559
-
Sheffield VC. The blind leading the obese: the molecular pathophysiology of a human obesity syndrome. Trans Am Clin Climatol Assoc 2010, 121:172-181. discussion 181-182, 2917141, 20697559.
-
(2010)
Trans Am Clin Climatol Assoc
, vol.121
, pp. 172-181
-
-
Sheffield, V.C.1
-
19
-
-
15844372440
-
Identification and characterization of the mouse obesity gene tubby: a member of a novel gene family
-
10.1016/S0092-8674(00)81104-6, 8612280
-
Kleyn PW, Fan W, Kovats SG, Lee JJ, Pulido JC, Wu Y, Berkemeier LR, Misumi DJ, Holmgren L, Charlat O, Woolf EA, Tayber O, Brody T, Shu P, Hawkins F, Kennedy B, Baldini L, Ebeling C, Alperin GD, Deeds J, Lakey ND, Culpepper J, Chen H, Glücksmann-Kuis MA, Carlson GA, Duyk GM, Moore KJ. Identification and characterization of the mouse obesity gene tubby: a member of a novel gene family. Cell 1996, 85:281-290. 10.1016/S0092-8674(00)81104-6, 8612280.
-
(1996)
Cell
, vol.85
, pp. 281-290
-
-
Kleyn, P.W.1
Fan, W.2
Kovats, S.G.3
Lee, J.J.4
Pulido, J.C.5
Wu, Y.6
Berkemeier, L.R.7
Misumi, D.J.8
Holmgren, L.9
Charlat, O.10
Woolf, E.A.11
Tayber, O.12
Brody, T.13
Shu, P.14
Hawkins, F.15
Kennedy, B.16
Baldini, L.17
Ebeling, C.18
Alperin, G.D.19
Deeds, J.20
Lakey, N.D.21
Culpepper, J.22
Chen, H.23
Glücksmann-Kuis, M.A.24
Carlson, G.A.25
Duyk, G.M.26
Moore, K.J.27
more..
-
20
-
-
0033971939
-
Targeted deletion of the tub mouse obesity gene reveals that tubby is a loss-of-function mutation
-
10.1128/MCB.20.3.878-882.2000, 85204, 10629044
-
Stubdal H, Lynch CA, Moriarty A, Fang Q, Chickering T, Deeds JD, Fairchild-Huntress V, Charlat O, Dunmore JH, Kleyn P, Huszar D, Kapeller R. Targeted deletion of the tub mouse obesity gene reveals that tubby is a loss-of-function mutation. Mol Cell Biol 2000, 20:878-882. 10.1128/MCB.20.3.878-882.2000, 85204, 10629044.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 878-882
-
-
Stubdal, H.1
Lynch, C.A.2
Moriarty, A.3
Fang, Q.4
Chickering, T.5
Deeds, J.D.6
Fairchild-Huntress, V.7
Charlat, O.8
Dunmore, J.H.9
Kleyn, P.10
Huszar, D.11
Kapeller, R.12
-
21
-
-
0036544659
-
Microtubule-associated protein 1A is a modifier of tubby hearing (moth1)
-
10.1038/ng838, 2862212, 11925566
-
Ikeda A, Zheng QY, Zuberi AR, Johnson KR, Naggert JK, Nishina PM. Microtubule-associated protein 1A is a modifier of tubby hearing (moth1). Nat Genet 2002, 30:401-405. 10.1038/ng838, 2862212, 11925566.
-
(2002)
Nat Genet
, vol.30
, pp. 401-405
-
-
Ikeda, A.1
Zheng, Q.Y.2
Zuberi, A.R.3
Johnson, K.R.4
Naggert, J.K.5
Nishina, P.M.6
-
22
-
-
84860652401
-
An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub mutant mice
-
10.1167/iovs.11-8871, 3339923, 22323461
-
Maddox DM, Ikeda S, Ikeda A, Zhang W, Krebs MP, Nishina PM, Naggert JK. An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub mutant mice. Invest Ophthalmol Vis Sci 2012, 53:1663-1669. 10.1167/iovs.11-8871, 3339923, 22323461.
-
(2012)
Invest Ophthalmol Vis Sci
, vol.53
, pp. 1663-1669
-
-
Maddox, D.M.1
Ikeda, S.2
Ikeda, A.3
Zhang, W.4
Krebs, M.P.5
Nishina, P.M.6
Naggert, J.K.7
-
23
-
-
0030475229
-
Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments
-
10.1073/pnas.93.24.14176, 19513, 8943080
-
Li T, Snyder WK, Olsson JE, Dryja TP. Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments. Proc Natl Acad Sci U S A 1996, 93:14176-14181. 10.1073/pnas.93.24.14176, 19513, 8943080.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 14176-14181
-
-
Li, T.1
Snyder, W.K.2
Olsson, J.E.3
Dryja, T.P.4
-
24
-
-
0032787396
-
Implication of tubby proteins as transcription factors by structure-based functional analysis
-
Boggon TJ, Shan WS, Santagata S, Myers SC, Shapiro L. Implication of tubby proteins as transcription factors by structure-based functional analysis. Science 286:2119-2125.
-
Science
, vol.286
, pp. 2119-2125
-
-
Boggon, T.J.1
Shan, W.S.2
Santagata, S.3
Myers, S.C.4
Shapiro, L.5
-
25
-
-
45249112609
-
Monitoring changes in membrane phosphatidylinositol 4,5-bisphosphate in living cells using a domain from the transcription factor tubby
-
10.1113/jphysiol.2008.153791, 2517197, 18420701
-
Quinn KV, Behe P, Tinker A. Monitoring changes in membrane phosphatidylinositol 4,5-bisphosphate in living cells using a domain from the transcription factor tubby. J Physiol 2008, 586:2855-2871. 10.1113/jphysiol.2008.153791, 2517197, 18420701.
-
(2008)
J Physiol
, vol.586
, pp. 2855-2871
-
-
Quinn, K.V.1
Behe, P.2
Tinker, A.3
-
26
-
-
78649714537
-
Tubby and tubby-like protein 1 are new MerTK ligands for phagocytosis
-
10.1038/emboj.2010.265, 3020645, 20978472
-
Caberoy NB, Zhou Y, Li W. Tubby and tubby-like protein 1 are new MerTK ligands for phagocytosis. EMBO J 2010, 29:3898-3910. 10.1038/emboj.2010.265, 3020645, 20978472.
-
(2010)
EMBO J
, vol.29
, pp. 3898-3910
-
-
Caberoy, N.B.1
Zhou, Y.2
Li, W.3
-
27
-
-
0030781737
-
Allele-specific PCR assays for the tub and cpefat mutations
-
10.1007/s003359900594, 9337402
-
Maddatu T, Naggert JK. Allele-specific PCR assays for the tub and cpefat mutations. Mamm Genome 1997, 8:857-858. 10.1007/s003359900594, 9337402.
-
(1997)
Mamm Genome
, vol.8
, pp. 857-858
-
-
Maddatu, T.1
Naggert, J.K.2
-
28
-
-
0037064591
-
Rootletin, a novel coiled-coil protein, is a structural component of the ciliary rootlet
-
10.1083/jcb.200207153, 2173070, 12427867
-
Yang J, Liu X, Yue G, Adamian M, Bulgakov O, Li T. Rootletin, a novel coiled-coil protein, is a structural component of the ciliary rootlet. J Cell Biol 2002, 159:431-440. 10.1083/jcb.200207153, 2173070, 12427867.
-
(2002)
J Cell Biol
, vol.159
, pp. 431-440
-
-
Yang, J.1
Liu, X.2
Yue, G.3
Adamian, M.4
Bulgakov, O.5
Li, T.6
-
29
-
-
0037129827
-
Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
-
RESEARCH0034, 126239, 12184808
-
Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, Speleman F. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 2002, 3:RESEARCH0034. 126239, 12184808.
-
(2002)
Genome Biol
, vol.3
-
-
Vandesompele, J.1
De Preter, K.2
Pattyn, F.3
Poppe, B.4
Van Roy, N.5
De Paepe, A.6
Speleman, F.7
-
30
-
-
44949231424
-
Analyzing real-time PCR data by the comparative C(T) method
-
10.1038/nprot.2008.73, 18546601
-
Schmittgen TD, Livak KJ. Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc 2008, 3:1101-1108. 10.1038/nprot.2008.73, 18546601.
-
(2008)
Nat Protoc
, vol.3
, pp. 1101-1108
-
-
Schmittgen, T.D.1
Livak, K.J.2
-
32
-
-
44449106038
-
Identification of ciliary localization sequences within the third intracellular loop of G protein-coupled receptors
-
10.1091/mbc.E07-09-0942, 2291422, 18256283
-
Berbari NF, Johnson AD, Lewis JS, Askwith CC, Mykytyn K. Identification of ciliary localization sequences within the third intracellular loop of G protein-coupled receptors. Mol Biol Cell 2008, 19:1540-1547. 10.1091/mbc.E07-09-0942, 2291422, 18256283.
-
(2008)
Mol Biol Cell
, vol.19
, pp. 1540-1547
-
-
Berbari, N.F.1
Johnson, A.D.2
Lewis, J.S.3
Askwith, C.C.4
Mykytyn, K.5
-
33
-
-
0034725792
-
Localization of 5-HT(6) receptors at the plasma membrane of neuronal cilia in the rat brain
-
10.1016/S0006-8993(00)02519-1, 10924708
-
Brailov I, Bancila M, Brisorgueil MJ, Miquel MC, Hamon M, Verge D. Localization of 5-HT(6) receptors at the plasma membrane of neuronal cilia in the rat brain. Brain Res 2000, 872:271-275. 10.1016/S0006-8993(00)02519-1, 10924708.
-
(2000)
Brain Res
, vol.872
, pp. 271-275
-
-
Brailov, I.1
Bancila, M.2
Brisorgueil, M.J.3
Miquel, M.C.4
Hamon, M.5
Verge, D.6
-
34
-
-
0345561551
-
Selective targeting of somatostatin receptor 3 to neuronal cilia
-
10.1016/S0306-4522(98)00354-6, 10199624
-
Handel M, Schulz S, Stanarius A, Schreff M, Erdtmann-Vourliotis M, Schmidt H, Wolf G, Hollt V. Selective targeting of somatostatin receptor 3 to neuronal cilia. Neuroscience 1999, 89:909-926. 10.1016/S0306-4522(98)00354-6, 10199624.
-
(1999)
Neuroscience
, vol.89
, pp. 909-926
-
-
Handel, M.1
Schulz, S.2
Stanarius, A.3
Schreff, M.4
Erdtmann-Vourliotis, M.5
Schmidt, H.6
Wolf, G.7
Hollt, V.8
-
35
-
-
33646869042
-
Focus on molecules: rootletin
-
10.1016/j.exer.2005.10.013, 16318850
-
Yang J, Li T. Focus on molecules: rootletin. Exp Eye Res 2006, 83:1-2. 10.1016/j.exer.2005.10.013, 16318850.
-
(2006)
Exp Eye Res
, vol.83
, pp. 1-2
-
-
Yang, J.1
Li, T.2
-
36
-
-
38049092146
-
Type III adenylyl cyclase localizes to primary cilia throughout the adult mouse brain
-
10.1002/cne.21510, 17924533
-
Bishop GA, Berbari NF, Lewis J, Mykytyn K. Type III adenylyl cyclase localizes to primary cilia throughout the adult mouse brain. J Comp Neurol 2007, 505:562-571. 10.1002/cne.21510, 17924533.
-
(2007)
J Comp Neurol
, vol.505
, pp. 562-571
-
-
Bishop, G.A.1
Berbari, N.F.2
Lewis, J.3
Mykytyn, K.4
-
37
-
-
41949116864
-
Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia
-
10.1073/pnas.0711027105, 2393805, 18334641
-
Berbari NF, Lewis JS, Bishop GA, Askwith CC, Mykytyn K. Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia. Proc Natl Acad Sci U S A 2008, 105:4242-4246. 10.1073/pnas.0711027105, 2393805, 18334641.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 4242-4246
-
-
Berbari, N.F.1
Lewis, J.S.2
Bishop, G.A.3
Askwith, C.C.4
Mykytyn, K.5
-
38
-
-
0026463972
-
Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa
-
10.1016/0896-6273(92)90236-7, 1418997
-
Olsson JE, Gordon JW, Pawlyk BS, Roof D, Hayes A, Molday RS, Mukai S, Cowley GS, Berson EL, Dryja TP. Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa. Neuron 1992, 9:815-830. 10.1016/0896-6273(92)90236-7, 1418997.
-
(1992)
Neuron
, vol.9
, pp. 815-830
-
-
Olsson, J.E.1
Gordon, J.W.2
Pawlyk, B.S.3
Roof, D.4
Hayes, A.5
Molday, R.S.6
Mukai, S.7
Cowley, G.S.8
Berson, E.L.9
Dryja, T.P.10
-
39
-
-
0030729168
-
Defective phototransductive disk membrane morphogenesis in transgenic mice expressing opsin with a mutated N-terminal domain
-
Liu X, Wu T-H, Stowe S, Matsushita A, Arikawa K, Naash MI, Williams DS. Defective phototransductive disk membrane morphogenesis in transgenic mice expressing opsin with a mutated N-terminal domain. J Cell Sci 1997, 110:2589-2597.
-
(1997)
J Cell Sci
, vol.110
, pp. 2589-2597
-
-
Liu, X.1
Wu, T.-H.2
Stowe, S.3
Matsushita, A.4
Arikawa, K.5
Naash, M.I.6
Williams, D.S.7
-
40
-
-
0034015064
-
Characterization of rhodopsin mis-sorting and constitutive activation in a transgenic rat model of retinitis pigmentosa
-
Green ES, Menz MD, LaVail MM, Flannery JG. Characterization of rhodopsin mis-sorting and constitutive activation in a transgenic rat model of retinitis pigmentosa. Invest Ophthalmol Vis Sci 2000, 41:1546-1553.
-
(2000)
Invest Ophthalmol Vis Sci
, vol.41
, pp. 1546-1553
-
-
Green, E.S.1
Menz, M.D.2
LaVail, M.M.3
Flannery, J.G.4
-
41
-
-
0030022944
-
Cytoplasmic domain of rhodopsin is essential for post-Golgi vesicle formation in a retinal cell-free system
-
10.1074/jbc.271.4.2279, 8567690
-
Deretic D, Puleo-Scheppke B, Trippe C. Cytoplasmic domain of rhodopsin is essential for post-Golgi vesicle formation in a retinal cell-free system. J Biol Chem 1996, 271:2279-2286. 10.1074/jbc.271.4.2279, 8567690.
-
(1996)
J Biol Chem
, vol.271
, pp. 2279-2286
-
-
Deretic, D.1
Puleo-Scheppke, B.2
Trippe, C.3
-
42
-
-
0027935666
-
A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment
-
Sung CH, Makino C, Baylor D, Nathans J. A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment. J Neurosci 1994, 14:5818-5833.
-
(1994)
J Neurosci
, vol.14
, pp. 5818-5833
-
-
Sung, C.H.1
Makino, C.2
Baylor, D.3
Nathans, J.4
-
43
-
-
18444375866
-
Targeted disruption of the melanin-concentrating hormone receptor-1 results in hyperphagia and resistance to diet-induced obesity
-
10.1210/en.143.7.2469, 12072376
-
Chen Y, Hu C, Hsu CK, Zhang Q, Bi C, Asnicar M, Hsiung HM, Fox N, Slieker LJ, Yang DD, Heiman ML, Shi Y. Targeted disruption of the melanin-concentrating hormone receptor-1 results in hyperphagia and resistance to diet-induced obesity. Endocrinology 2002, 143:2469-2477. 10.1210/en.143.7.2469, 12072376.
-
(2002)
Endocrinology
, vol.143
, pp. 2469-2477
-
-
Chen, Y.1
Hu, C.2
Hsu, C.K.3
Zhang, Q.4
Bi, C.5
Asnicar, M.6
Hsiung, H.M.7
Fox, N.8
Slieker, L.J.9
Yang, D.D.10
Heiman, M.L.11
Shi, Y.12
-
44
-
-
77949816722
-
Somatostatin signaling in neuronal cilia is critical for object recognition memory
-
10.1523/JNEUROSCI.5295-09.2010, 20335466
-
Einstein EB, Patterson CA, Hon BJ, Regan KA, Reddi J, Melnikoff DE, Mateer MJ, Schulz S, Johnson BN, Tallent MK. Somatostatin signaling in neuronal cilia is critical for object recognition memory. J Neurosci 2010, 30:4306-4314. 10.1523/JNEUROSCI.5295-09.2010, 20335466.
-
(2010)
J Neurosci
, vol.30
, pp. 4306-4314
-
-
Einstein, E.B.1
Patterson, C.A.2
Hon, B.J.3
Regan, K.A.4
Reddi, J.5
Melnikoff, D.E.6
Mateer, M.J.7
Schulz, S.8
Johnson, B.N.9
Tallent, M.K.10
-
45
-
-
79955765994
-
The type 3 adenylyl cyclase is required for novel object learning and extinction of contextual memory: role of cAMP signaling in primary cilia
-
10.1523/JNEUROSCI.6561-10.2011, 3091825, 21490195
-
Wang Z, Phan T, Storm DR. The type 3 adenylyl cyclase is required for novel object learning and extinction of contextual memory: role of cAMP signaling in primary cilia. J Neurosci 2011, 31:5557-5561. 10.1523/JNEUROSCI.6561-10.2011, 3091825, 21490195.
-
(2011)
J Neurosci
, vol.31
, pp. 5557-5561
-
-
Wang, Z.1
Phan, T.2
Storm, D.R.3
-
46
-
-
69349094765
-
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies
-
10.1038/ng.423, 2746682, 19668216
-
Bielas SL, Silhavy JL, Brancati F, Kisseleva MV, Al-Gazali L, Sztriha L, Bayoumi RA, Zaki MS, Abdel-Aleem A, Rosti RO, Kayserili H, Swistun D, Scott LC, Bertini E, Boltshauser E, Fazzi E, Travaglini L, Field SJ, Gayral S, Jacoby M, Schurmans S, Dallapiccola B, Majerus PW, Valente EM, Gleeson JG. Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies. Nat Genet 2009, 41:1032-1036. 10.1038/ng.423, 2746682, 19668216.
-
(2009)
Nat Genet
, vol.41
, pp. 1032-1036
-
-
Bielas, S.L.1
Silhavy, J.L.2
Brancati, F.3
Kisseleva, M.V.4
Al-Gazali, L.5
Sztriha, L.6
Bayoumi, R.A.7
Zaki, M.S.8
Abdel-Aleem, A.9
Rosti, R.O.10
Kayserili, H.11
Swistun, D.12
Scott, L.C.13
Bertini, E.14
Boltshauser, E.15
Fazzi, E.16
Travaglini, L.17
Field, S.J.18
Gayral, S.19
Jacoby, M.20
Schurmans, S.21
Dallapiccola, B.22
Majerus, P.W.23
Valente, E.M.24
Gleeson, J.G.25
more..
-
47
-
-
69349095810
-
INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse
-
10.1038/ng.427, 19668215
-
Jacoby M, Cox JJ, Gayral S, Hampshire DJ, Ayub M, Blockmans M, Pernot E, Kisseleva MV, Compere P, Schiffmann SN, Gergely F, Riley JH, Pérez-Morga D, Woods CG, Schurmans S. INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse. Nat Genet 2009, 41:1027-1031. 10.1038/ng.427, 19668215.
-
(2009)
Nat Genet
, vol.41
, pp. 1027-1031
-
-
Jacoby, M.1
Cox, J.J.2
Gayral, S.3
Hampshire, D.J.4
Ayub, M.5
Blockmans, M.6
Pernot, E.7
Kisseleva, M.V.8
Compere, P.9
Schiffmann, S.N.10
Gergely, F.11
Riley, J.H.12
Pérez-Morga, D.13
Woods, C.G.14
Schurmans, S.15
-
48
-
-
84863403706
-
Proteomic analysis of mammalian primary cilia
-
10.1016/j.cub.2012.01.031, 3298568, 22326026
-
Ishikawa H, Thompson J, Yates JR, Marshall WF. Proteomic analysis of mammalian primary cilia. Curr Biol 2012, 22:414-419. 10.1016/j.cub.2012.01.031, 3298568, 22326026.
-
(2012)
Curr Biol
, vol.22
, pp. 414-419
-
-
Ishikawa, H.1
Thompson, J.2
Yates, J.R.3
Marshall, W.F.4
-
49
-
-
84864509829
-
OCRL localizes to the primary cilium: a new role for cilia in Lowe syndrome
-
10.1093/hmg/dds163, 3392109, 22543976
-
Luo N, West C, Murga-Zamalloa C, Sun L, Anderson RM, Wells C, Weinreb RN, Travers JB, Khanna H, Sun Y. OCRL localizes to the primary cilium: a new role for cilia in Lowe syndrome. Hum Mol Genet 2012, 21:3333-3344. 10.1093/hmg/dds163, 3392109, 22543976.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 3333-3344
-
-
Luo, N.1
West, C.2
Murga-Zamalloa, C.3
Sun, L.4
Anderson, R.M.5
Wells, C.6
Weinreb, R.N.7
Travers, J.B.8
Khanna, H.9
Sun, Y.10
|