-
1
-
-
0037062982
-
Alternative pre-mRNA splicing and proteome expansion in metazoans
-
PMID:12110900
-
Maniatis T, Tasic B. Alternative pre-mRNA splicing and proteome expansion in metazoans. Nature 2002; 418:236-43; PMID:12110900; http://dx.doi.org/10.1038/418236a
-
(2002)
Nature
, vol.418
, pp. 236-243
-
-
Maniatis, T.1
Tasic, B.2
-
2
-
-
0042671357
-
Pre-mRNA splicing: Awash in a sea of proteins
-
PMID: 12887888
-
Jurica MS, Moore MJ. Pre-mRNA splicing: awash in a sea of proteins. Mol Cell 2003; 12:5-14; PMID: 12887888; http://dx.doi.org/10.1016/S1097-2765(03)00270-3
-
(2003)
Mol Cell
, vol.12
, pp. 5-14
-
-
Jurica, M.S.1
Moore, M.J.2
-
3
-
-
60149093432
-
RNA and disease
-
PMID:19239895
-
Cooper TA, Wan L, Dreyfuss G. RNA and disease. Cell 2009; 136:777-93; PMID:19239895; http://dx.doi.org/10.1016/j.cell.2009.02.011
-
(2009)
Cell
, vol.136
, pp. 777-793
-
-
Cooper, T.A.1
Wan, L.2
Dreyfuss, G.3
-
4
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophy-determining gene
-
PMID:7813012
-
Lefebvre S, Burglen L, Reboullet S, Clermont O, Burlet P, Viollet L, Benichou B, Cruaud C, Millasseau P, Zeviani M, et al. Identification and characterization of a spinal muscular atrophy-determining gene. Cell 1995; 80:155-65; PMID:7813012; http://dx.doi.org/10.1016/0092-8674(95)90460-3
-
(1995)
Cell
, vol.80
, pp. 155-165
-
-
Lefebvre, S.1
Burglen, L.2
Reboullet, S.3
Clermont, O.4
Burlet, P.5
Viollet, L.6
Benichou, B.7
Cruaud, C.8
Millasseau, P.9
Zeviani, M.10
-
5
-
-
0343267780
-
Structure and organization of the human survival motor neurone (SMN) gene
-
PMID:8838816
-
Burglen L, Lefebvre S, Clermont O, Burlet P, Viollet L, Cruaud C, Munnich A, Melki J. Structure and organization of the human survival motor neurone (SMN) gene. Genomics 1996; 32:479-82; PMID:8838816; http://dx.doi.org/10.1006/geno.1996.0147
-
(1996)
Genomics
, vol.32
, pp. 479-482
-
-
Burglen, L.1
Lefebvre, S.2
Clermont, O.3
Burlet, P.4
Viollet, L.5
Cruaud, C.6
Munnich, A.7
Melki, J.8
-
6
-
-
0036207384
-
Listening to silence and understanding nonsense: Exonic mutations that affect splicing
-
PMID:11967553
-
Cartegni L, Chew SL, Krainer AR. Listening to silence and understanding nonsense: exonic mutations that affect splicing. Nat Rev Genet 2002; 3:285-98; PMID:11967553; http://dx.doi.org/10.1038/nrg775
-
(2002)
Nat Rev Genet
, vol.3
, pp. 285-298
-
-
Cartegni, L.1
Chew, S.L.2
Krainer, A.R.3
-
7
-
-
29244490598
-
Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2
-
PMID:16385450
-
Cartegni L, Hastings ML, Calarco JA, de Stanchina E, Krainer AR. Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2. Am J Hum Genet 2006; 78:63-77; PMID:16385450; http://dx.doi.org/10.1086/498853
-
(2006)
Am J Hum Genet
, vol.78
, pp. 63-77
-
-
Cartegni, L.1
Hastings, M.L.2
Calarco, J.A.3
De Stanchina, E.4
Krainer, A.R.5
-
8
-
-
0041665176
-
A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy
-
PMID:12833158
-
Kashima T, Manley JL. A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy. Nat Genet 2003; 34:460-3; PMID:12833158; http://dx.doi.org/10.1038/ng1207
-
(2003)
Nat Genet
, vol.34
, pp. 460-463
-
-
Kashima, T.1
Manley, J.L.2
-
9
-
-
0030928716
-
The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis
-
PMID:9323130
-
Fischer U, Liu Q, Dreyfuss G. The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis. Cell 1997; 90:1023-9; PMID:9323130; http://dx.doi.org/10.1016/S0092-8674(00)80368-2
-
(1997)
Cell
, vol.90
, pp. 1023-1029
-
-
Fischer, U.1
Liu, Q.2
Dreyfuss, G.3
-
10
-
-
0030931727
-
The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins
-
PMID:9323129
-
Liu Q, Fischer U, Wang F, Dreyfuss G. The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins. Cell 1997; 90:1013-21; PMID:9323129; http://dx.doi.org/10.1016/S0092-8674(00)80367-0
-
(1997)
Cell
, vol.90
, pp. 1013-1021
-
-
Liu, Q.1
Fischer, U.2
Wang, F.3
Dreyfuss, G.4
-
11
-
-
0034069505
-
Mechanisms of fidelity in pre-mRNA splicing
-
PMID:10801464
-
Reed R. Mechanisms of fidelity in pre-mRNA splicing. Curr Opin Cell Biol 2000; 12:340-5; PMID:10801464; http://dx.doi.org/10.1016/S0955-0674(00)00097-1
-
(2000)
Curr Opin Cell Biol
, vol.12
, pp. 340-345
-
-
Reed, R.1
-
12
-
-
25844461744
-
Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy
-
PMID:16204184
-
Winkler C, Eggert C, Gradl D, Meister G, Giegerich M, Wedlich D, Laggerbauer B, Fischer U. Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy. Genes Dev 2005; 19:2320-30; PMID:16204184; http://dx.doi.org/10.1101/gad.342005
-
(2005)
Genes Dev
, vol.19
, pp. 2320-2330
-
-
Winkler, C.1
Eggert, C.2
Gradl, D.3
Meister, G.4
Giegerich, M.5
Wedlich, D.6
Laggerbauer, B.7
Fischer, U.8
-
13
-
-
77953122127
-
Specific splicing defects in S. pombe carrying a degron allele of the Survival of Motor Neuron gene
-
PMID:20400941
-
Campion Y, Neel H, Gostan T, Soret J, Bordonné R. Specific splicing defects in S. pombe carrying a degron allele of the Survival of Motor Neuron gene. Embo J 2010; 29:1817-29; PMID:20400941; http://dx.doi.org/10.1038/emboj.2010.70
-
(2010)
Embo J
, vol.29
, pp. 1817-1829
-
-
Campion, Y.1
Neel, H.2
Gostan, T.3
Soret, J.4
Bordonné, R.5
-
14
-
-
84867555865
-
An SMN-dependent U12 splicing event essential for motor circuit function
-
PMID: 23063131
-
Lotti F, Imlach WL, Saieva L, Beck ES, Hao le T, Li DK, Jiao W, Mentis GZ, Beattie CE, McCabe BD, et al. An SMN-dependent U12 splicing event essential for motor circuit function. Cell 2012; 151:440-54; PMID: 23063131; http://dx.doi.org/10.1016/j.cell.2012.09.012
-
(2012)
Cell
, vol.151
, pp. 440-454
-
-
Lotti, F.1
Imlach, W.L.2
Saieva, L.3
Beck, E.S.4
Hao Le, T.5
Li, D.K.6
Jiao, W.7
Mentis, G.Z.8
Beattie, C.E.9
McCabe, B.D.10
-
15
-
-
84863114222
-
A Drosophila model of spinal muscular atrophy uncouples snRNP biogenesis functions of survival motor neuron from locomotion and viability defects
-
PMID: 22813737
-
Praveen K, Wen Y, Matera AG. A Drosophila model of spinal muscular atrophy uncouples snRNP biogenesis functions of survival motor neuron from locomotion and viability defects. Cell Rep 2012; 1:624-31; PMID: 22813737; http://dx.doi.org/10.1016/j.celrep.2012.05.014
-
(2012)
Cell Rep
, vol.1
, pp. 624-631
-
-
Praveen, K.1
Wen, Y.2
Matera, A.G.3
-
16
-
-
84901822168
-
SMN deficiency alters Nrxn2 expression and splicing in zebrafish and mouse models of spinal muscular atrophy
-
PMID: 24218366
-
See K, Yadav P, Giegerich M, Cheong PS, Graf M, Vyas H, Lee SG, Mathavan S, Fischer U, Sendtner M, et al. SMN deficiency alters Nrxn2 expression and splicing in zebrafish and mouse models of spinal muscular atrophy. Hum Mol Genet 2014; 23:1754-70; PMID: 24218366; http://dx.doi.org/10.1093/hmg/ddt567
-
(2014)
Hum Mol Genet
, vol.23
, pp. 1754-1770
-
-
See, K.1
Yadav, P.2
Giegerich, M.3
Cheong, P.S.4
Graf, M.5
Vyas, H.6
Lee, S.G.7
Mathavan, S.8
Fischer, U.9
Sendtner, M.10
-
17
-
-
74249094999
-
Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy
-
PMID:20019802
-
Baumer D, Lee S, Nicholson G, Davies JL, Parkinson NJ, Murray LM, Gillingwater TH, Ansorge O, Davies KE, Talbot K. Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy. PLoS Genet 2009; 5:e1000773; PMID:20019802; http://dx.doi.org/10.1371/journal.pgen.1000773
-
(2009)
PLoS Genet
, vol.5
, pp. e1000773
-
-
Baumer, D.1
Lee, S.2
Nicholson, G.3
Davies, J.L.4
Parkinson, N.J.5
Murray, L.M.6
Gillingwater, T.H.7
Ansorge, O.8
Davies, K.E.9
Talbot, K.10
-
18
-
-
84892981582
-
Chondrolectin affects cell survival and neuronal outgrowth in in vitro and in vivo models of spinal muscular atrophy
-
PMID:24067532
-
Sleigh JN, Barreiro-Iglesias A, Oliver PL, Biba A, Becker T, Davies KE, Becker CG, Talbot K. Chondrolectin affects cell survival and neuronal outgrowth in in vitro and in vivo models of spinal muscular atrophy. Hum Mol Genet 2014; 23:855-69; PMID:24067532; http://dx.doi.org/10.1093/hmg/ddt477
-
(2014)
Hum Mol Genet
, vol.23
, pp. 855-869
-
-
Sleigh, J.N.1
Barreiro-Iglesias, A.2
Oliver, P.L.3
Biba, A.4
Becker, T.5
Davies, K.E.6
Becker, C.G.7
Talbot, K.8
-
19
-
-
43049168361
-
SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing
-
PMID: 18485868
-
Zhang Z, Lotti F, Dittmar K, Younis I, Wan L, Kasim M, Dreyfuss G. SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing. Cell 2008; 133:585-600; PMID: 18485868; http://dx.doi.org/10.1016/j.cell.2008.03.031
-
(2008)
Cell
, vol.133
, pp. 585-600
-
-
Zhang, Z.1
Lotti, F.2
Dittmar, K.3
Younis, I.4
Wan, L.5
Kasim, M.6
Dreyfuss, G.7
-
20
-
-
84888375636
-
Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy
-
PMID:24191055
-
Zhang Z, Pinto AM, Wan L, Wang W, Berg MG, Oliva I, Singh LN, Dengler C, Wei Z, Dreyfuss G. Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy. Proc Natl Acad Sci U S A 2013; 110:19348-53; PMID:24191055; http://dx.doi.org/10.1073/pnas.1319280110
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. 19348-19353
-
-
Zhang, Z.1
Pinto, A.M.2
Wan, L.3
Wang, W.4
Berg, M.G.5
Oliva, I.6
Singh, L.N.7
Dengler, C.8
Wei, Z.9
Dreyfuss, G.10
-
21
-
-
78751685185
-
Impaired minor tri-snRNP assembly generates differential splicing defects of U12-type introns in lymphoblasts derived from a type I SMA patient
-
PMID:21098506
-
Boulisfane N, Choleza M, Rage F, Neel H, Soret J, Bordonné R. Impaired minor tri-snRNP assembly generates differential splicing defects of U12-type introns in lymphoblasts derived from a type I SMA patient. Hum Mol Genet 2011; 20:641-8; PMID:21098506; http://dx.doi.org/10.1093/hmg/ddq508
-
(2011)
Hum Mol Genet
, vol.20
, pp. 641-648
-
-
Boulisfane, N.1
Choleza, M.2
Rage, F.3
Neel, H.4
Soret, J.5
Bordonné, R.6
-
22
-
-
67651083390
-
Spinal muscular atrophy: Why do low levels of survival motor neuron protein make motor neurons sick?
-
PMID:19584893
-
Burghes AH, Beattie CE. Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? Nat Rev Neurosci 2009; 10:597-609; PMID:19584893; http://dx.doi.org/10.1038/nrn2670
-
(2009)
Nat Rev Neurosci
, vol.10
, pp. 597-609
-
-
Burghes, A.H.1
Beattie, C.E.2
-
23
-
-
0345599021
-
Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons
-
PMID: 14623865
-
Rossoll W, Jablonka S, Andreassi C, Kroning AK, Karle K, Monani UR, Sendtner M. Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons. J Cell Biol 2003; 163:801-12; PMID: 14623865; http://dx.doi.org/10.1083/jcb.200304128
-
(2003)
J Cell Biol
, vol.163
, pp. 801-812
-
-
Rossoll, W.1
Jablonka, S.2
Andreassi, C.3
Kroning, A.K.4
Karle, K.5
Monani, U.R.6
Sendtner, M.7
-
24
-
-
0042887389
-
Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding
-
PMID: 12952942
-
McWhorter ML, Monani UR, Burghes AH, Beattie CE. Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding. J Cell Biol 2003; 162:919-31; PMID: 12952942; http://dx.doi.org/10.1083/jcb.200303168
-
(2003)
J Cell Biol
, vol.162
, pp. 919-931
-
-
McWhorter, M.L.1
Monani, U.R.2
Burghes, A.H.3
Beattie, C.E.4
-
25
-
-
33947217787
-
A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle
-
PMID: 17353360
-
Rajendra TK, Gonsalvez GB, Walker MP, Shpargel KB, Salz HK, Matera AG. A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle. J Cell Biol 2007; 176:831-41; PMID: 17353360; http://dx.doi.org/10.1083/jcb.200610053
-
(2007)
J Cell Biol
, vol.176
, pp. 831-841
-
-
Rajendra, T.K.1
Gonsalvez, G.B.2
Walker, M.P.3
Shpargel, K.B.4
Salz, H.K.5
Matera, A.G.6
-
26
-
-
42549088649
-
Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy
-
PMID: 18440926
-
Oprea GE, Krober S, McWhorter ML, Rossoll W, Muller S, Krawczak M, Bassell GJ, Beattie CE, Wirth B. Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy. Science 2008; 320:524-7; PMID: 18440926; http://dx.doi.org/10.1126/science.1155085
-
(2008)
Science
, vol.320
, pp. 524-527
-
-
Oprea, G.E.1
Krober, S.2
McWhorter, M.L.3
Rossoll, W.4
Muller, S.5
Krawczak, M.6
Bassell, G.J.7
Beattie, C.E.8
Wirth, B.9
-
27
-
-
84875236246
-
Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality
-
PMID:23263861
-
Ackermann B, Krober S, Torres-Benito L, Borgmann A, Peters M, Barkooie SM, Tejero R, Jakubik M, Schreml J, Milbradt J, et al. Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality. Hum Mol Genet 2013; 22:1328-47; PMID:23263861; http://dx.doi.org/10.1093/hmg/dds540
-
(2013)
Hum Mol Genet
, vol.22
, pp. 1328-1347
-
-
Ackermann, B.1
Krober, S.2
Torres-Benito, L.3
Borgmann, A.4
Peters, M.5
Barkooie, S.M.6
Tejero, R.7
Jakubik, M.8
Schreml, J.9
Milbradt, J.10
-
28
-
-
52449095571
-
Modeling spinal muscular atrophy in Drosophila
-
PMID:18791638
-
Chang HC, Dimlich DN, Yokokura T, Mukherjee A, Kankel MW, Sen A, Sridhar V, Fulga TA, Hart AC, Van Vactor D, et al. Modeling spinal muscular atrophy in Drosophila. PloS One 2008; 3:e3209; PMID:18791638; http://dx.doi.org/10.1371/journal.pone.0003209
-
(2008)
PloS One
, vol.3
, pp. e3209
-
-
Chang, H.C.1
Dimlich, D.N.2
Yokokura, T.3
Mukherjee, A.4
Kankel, M.W.5
Sen, A.6
Sridhar, V.7
Fulga, T.A.8
Hart, A.C.9
Van Vactor, D.10
-
29
-
-
78449265215
-
Conserved genes act as modifiers of invertebrate SMN loss of function defects
-
PMID:NOT-FOUND
-
Dimitriadi M, Sleigh JN, Walker A, Chang HC, Sen A, Kalloo G, Harris J, Barsby T, Walsh MB, Satterlee JS, et al. Conserved genes act as modifiers of invertebrate SMN loss of function defects. PLoS Genet 2010; 6: e1001172; PMID:NOT-FOUND
-
(2010)
PLoS Genet
, vol.6
, pp. e1001172
-
-
Dimitriadi, M.1
Sleigh, J.N.2
Walker, A.3
Chang, H.C.4
Sen, A.5
Kalloo, G.6
Harris, J.7
Barsby, T.8
Walsh, M.B.9
Satterlee, J.S.10
-
30
-
-
84879524441
-
Genetic circuitry of Survival motor neuron, the gene underlying spinal muscular atrophy
-
PMID:23757500
-
Sen A, Dimlich DN, Guruharsha KG, Kankel MW, Hori K, Yokokura T, Brachat S, Richardson D, Loureiro J, Sivasankaran R, et al. Genetic circuitry of Survival motor neuron, the gene underlying spinal muscular atrophy. Proc Natl Acad Sci U S A 2013; 110:E2371-80; PMID:23757500; http://dx.doi.org/10.1073/pnas.1301738110
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. E2371-E2380
-
-
Sen, A.1
Dimlich, D.N.2
Guruharsha, K.G.3
Kankel, M.W.4
Hori, K.5
Yokokura, T.6
Brachat, S.7
Richardson, D.8
Loureiro, J.9
Sivasankaran, R.10
-
31
-
-
73649087945
-
Mutations in the Caenorhabditis elegans U2AF large subunit UAF-1 alter the choice of a 30 splice site in vivo
-
PMID:19893607
-
Ma L, Horvitz HR. Mutations in the Caenorhabditis elegans U2AF large subunit UAF-1 alter the choice of a 30 splice site in vivo. PLoS Genet 2009; 5:e1000708; PMID:19893607; http://dx.doi.org/10.1371/journal.pgen.1000708
-
(2009)
PLoS Genet
, vol.5
, pp. e1000708
-
-
Ma, L.1
Horvitz, H.R.2
-
32
-
-
81755161587
-
In vivo effects on intron retention and exon skipping by the U2AF large subunit and SF1/BBP in the nematode Caenorhabditis elegans
-
PMID: 22033331
-
Ma L, Tan Z, Teng Y, Hoersch S, Horvitz HR. In vivo effects on intron retention and exon skipping by the U2AF large subunit and SF1/BBP in the nematode Caenorhabditis elegans. RNA 2011; 17:2201-11; PMID: 22033331; http://dx.doi.org/10.1261/rna.027458.111
-
(2011)
RNA
, vol.17
, pp. 2201-2211
-
-
Ma, L.1
Tan, Z.2
Teng, Y.3
Hoersch, S.4
Horvitz, H.R.5
-
33
-
-
84864580596
-
The Caenorhabditis elegans gene mfap-1 encodes a nuclear protein that affects alternative splicing
-
PMID:22829783
-
Ma L, Gao X, Luo J, Huang L, Teng Y, Horvitz HR. The Caenorhabditis elegans gene mfap-1 encodes a nuclear protein that affects alternative splicing. PLoS Genet 2012; 8:e1002827; PMID:22829783; http://dx.doi.org/10.1371/journal.pgen.1002827
-
(2012)
PLoS Genet
, vol.8
, pp. e1002827
-
-
Ma, L.1
Gao, X.2
Luo, J.3
Huang, L.4
Teng, Y.5
Horvitz, H.R.6
-
34
-
-
0032718045
-
The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability
-
PMID:10545592
-
Miguel-Aliaga I, Culetto E, Walker DS, Baylis HA, Sattelle DB, Davies KE. The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability. Hum Mol Genet 1999; 8:2133-43; PMID:10545592; http://dx.doi.org/10.1093/hmg/8.12.2133
-
(1999)
Hum Mol Genet
, vol.8
, pp. 2133-2143
-
-
Miguel-Aliaga, I.1
Culetto, E.2
Walker, D.S.3
Baylis, H.A.4
Sattelle, D.B.5
Davies, K.E.6
-
35
-
-
57649207934
-
Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan
-
PMID:18829666
-
Briese M, Esmaeili B, Fraboulet S, Burt EC, Christodoulou S, Towers PR, Davies KE, Sattelle DB. Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan. Hum Mol Genet 2009; 18:97-104; PMID:18829666; http://dx.doi.org/10.1093/hmg/ddn320
-
(2009)
Hum Mol Genet
, vol.18
, pp. 97-104
-
-
Briese, M.1
Esmaeili, B.2
Fraboulet, S.3
Burt, E.C.4
Christodoulou, S.5
Towers, P.R.6
Davies, K.E.7
Sattelle, D.B.8
-
36
-
-
75849145292
-
Expansion of the eukaryotic proteome by alternative splicing
-
PMID:20110989
-
Nilsen TW, Graveley BR. Expansion of the eukaryotic proteome by alternative splicing. Nature 2010; 463:457-63; PMID:20110989; http://dx.doi.org/10.1038/nature08909
-
(2010)
Nature
, vol.463
, pp. 457-463
-
-
Nilsen, T.W.1
Graveley, B.R.2
-
37
-
-
0027451263
-
Sequence requirements for myosin gene expression and regulation in Caenorhabditis elegans
-
PMID:8244003
-
Okkema PG, Harrison SW, Plunger V, Aryana A, Fire A. Sequence requirements for myosin gene expression and regulation in Caenorhabditis elegans. Genetics 1993; 135:385-404; PMID:8244003
-
(1993)
Genetics
, vol.135
, pp. 385-404
-
-
Okkema, P.G.1
Harrison, S.W.2
Plunger, V.3
Aryana, A.4
Fire, A.5
-
38
-
-
0037448540
-
Systematic functional analysis of the Caenorhabditis elegans genome using RNAi
-
PMID:12529635
-
Kamath RS, Fraser AG, Dong Y, Poulin G, Durbin R, Gotta M, Kanapin A, Le Bot N, Moreno S, Sohrmann M, et al. Systematic functional analysis of the Caenorhabditis elegans genome using RNAi. Nature 2003; 421:231-7; PMID:12529635; http://dx.doi.org/10.1038/nature01278
-
(2003)
Nature
, vol.421
, pp. 231-237
-
-
Kamath, R.S.1
Fraser, A.G.2
Dong, Y.3
Poulin, G.4
Durbin, R.5
Gotta, M.6
Kanapin, A.7
Le Bot, N.8
Moreno, S.9
Sohrmann, M.10
-
39
-
-
7444270371
-
Toward improving Caenorhabditis elegans phenome mapping with an ORFeome-based RNAi library
-
PMID: 15489339
-
Rual JF, Ceron J, Koreth J, Hao T, Nicot AS, Hirozane-Kishikawa T, Vandenhaute J, Orkin SH, Hill DE, van den Heuvel S, et al. Toward improving Caenorhabditis elegans phenome mapping with an ORFeome-based RNAi library. Genome Res 2004; 14:2162-8; PMID: 15489339; http://dx.doi.org/10.1101/gr.2505604
-
(2004)
Genome Res
, vol.14
, pp. 2162-2168
-
-
Rual, J.F.1
Ceron, J.2
Koreth, J.3
Hao, T.4
Nicot, A.S.5
Hirozane-Kishikawa, T.6
Vandenhaute, J.7
Orkin, S.H.8
Hill, D.E.9
Van Den Heuvel, S.10
-
40
-
-
0030614546
-
Cloning of Caenorhabditis U2AF65: An alternatively spliced RNA containing a novel exon
-
PMID:9001248
-
Zorio DA, Lea K, Blumenthal T. Cloning of Caenorhabditis U2AF65: an alternatively spliced RNA containing a novel exon. Mol Cell Biol 1997; 17:946-53; PMID:9001248
-
(1997)
Mol Cell Biol
, vol.17
, pp. 946-953
-
-
Zorio, D.A.1
Lea, K.2
Blumenthal, T.3
-
41
-
-
13944280200
-
U2AF binding selects for the high conservation of the C. elegans 30 splice site
-
PMID: 15661845
-
Hollins C, Zorio DA, MacMorris M, Blumenthal T. U2AF binding selects for the high conservation of the C. elegans 30 splice site. RNA 2005; 11:248-53; PMID: 15661845; http://dx.doi.org/10.1261/rna.7221605
-
(2005)
RNA
, vol.11
, pp. 248-253
-
-
Hollins, C.1
Zorio, D.A.2
MacMorris, M.3
Blumenthal, T.4
-
42
-
-
0033832676
-
Conservation, regulation, synteny, and introns in a large-scale C. briggsae-C. elegans genomic alignment
-
PMID: 10958630
-
Kent WJ, Zahler AM. Conservation, regulation, synteny, and introns in a large-scale C. briggsae-C. elegans genomic alignment. Genome Res 2000; 10:1115-25; PMID: 10958630; http://dx.doi.org/10.1101/gr.10.8.1115
-
(2000)
Genome Res
, vol.10
, pp. 1115-1125
-
-
Kent, W.J.1
Zahler, A.M.2
-
43
-
-
0033714116
-
C. elegans locomotory rate is modulated by the environment through a dopaminergic pathway and by experience through a serotonergic pathway
-
PMID:10896158
-
Sawin ER, Ranganathan R, Horvitz HR. C. elegans locomotory rate is modulated by the environment through a dopaminergic pathway and by experience through a serotonergic pathway. Neuron 2000; 26:619-31; PMID:10896158; http://dx.doi.org/10.1016/S0896-6273(00)81199-X
-
(2000)
Neuron
, vol.26
, pp. 619-631
-
-
Sawin, E.R.1
Ranganathan, R.2
Horvitz, H.R.3
-
44
-
-
41549119007
-
Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs
-
PMID:17895963
-
Gabanella F, Butchbach ME, Saieva L, Carissimi C, Burghes AH, Pellizzoni L. Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs. PloS One 2007; 2:e921; PMID:17895963; http://dx.doi.org/10.1371/journal.pone.0000921
-
(2007)
PloS One
, vol.2
, pp. e921
-
-
Gabanella, F.1
Butchbach, M.E.2
Saieva, L.3
Carissimi, C.4
Burghes, A.H.5
Pellizzoni, L.6
-
45
-
-
84876005922
-
2+-activated K+ channels to ameliorate defects in spinal muscular atrophy models
-
PMID:23575853
-
2+-activated K+ channels to ameliorate defects in spinal muscular atrophy models. J Neurosci 2013; 33:6557-62; PMID:23575853; http://dx.doi.org/10.1523/JNEUROSCI.1536-12.2013
-
(2013)
J Neurosci
, vol.33
, pp. 6557-6562
-
-
Dimitriadi, M.1
Kye, M.J.2
Kalloo, G.3
Yersak, J.M.4
Sahin, M.5
Hart, A.C.6
-
46
-
-
35148880587
-
A conditional role of U2AF in splicing of introns with unconventional polypyrimidine tracts
-
PMID: 17709389
-
Sridharan V, Singh R. A conditional role of U2AF in splicing of introns with unconventional polypyrimidine tracts. Mol Cell Biol 2007; 27:7334-44; PMID: 17709389; http://dx.doi.org/10.1128/MCB.00627-07
-
(2007)
Mol Cell Biol
, vol.27
, pp. 7334-7344
-
-
Sridharan, V.1
Singh, R.2
-
47
-
-
33846071878
-
U12DB: A database of orthologous U12-type spliceosomal introns
-
PMID:17082203
-
Alioto TS. U12DB: a database of orthologous U12-type spliceosomal introns. Nucleic Acids Res 2007; 35:D110-5; PMID:17082203; http://dx.doi.org/10.1093/nar/gkl796
-
(2007)
Nucleic Acids Res
, vol.35
, pp. D110-D115
-
-
Alioto, T.S.1
-
48
-
-
84886048721
-
Developmental arrest of Drosophila survival motor neuron (Smn) mutants accounts for differences in expression of minor intron-containing genes
-
PMID:24006466
-
Garcia EL, Lu Z, Meers MP, Praveen K, Matera AG. Developmental arrest of Drosophila survival motor neuron (Smn) mutants accounts for differences in expression of minor intron-containing genes. RNA 2013; 19:1510-6; PMID:24006466; http://dx.doi.org/10.1261/rna.038919.113
-
(2013)
RNA
, vol.19
, pp. 1510-1516
-
-
Garcia, E.L.1
Lu, Z.2
Meers, M.P.3
Praveen, K.4
Matera, A.G.5
-
49
-
-
63049135125
-
Gemin3 is an essential gene required for larval motor function and pupation in Drosophila
-
PMID:18923150
-
Shpargel KB, Praveen K, Rajendra TK, Matera AG. Gemin3 is an essential gene required for larval motor function and pupation in Drosophila. Mol Biol Cell 2009; 20:90-101; PMID:18923150; http://dx.doi.org/10.1091/mbc.E08-01-0024
-
(2009)
Mol Biol Cell
, vol.20
, pp. 90-101
-
-
Shpargel, K.B.1
Praveen, K.2
Rajendra, T.K.3
Matera, A.G.4
-
50
-
-
0028950419
-
Mutations in the clk-1 gene of Caenorhabditis elegans affect developmental and behavioral timing
-
PMID:7768437
-
Wong A, Boutis P, Hekimi S. Mutations in the clk-1 gene of Caenorhabditis elegans affect developmental and behavioral timing. Genetics 1995; 139:1247-59; PMID:7768437
-
(1995)
Genetics
, vol.139
, pp. 1247-1259
-
-
Wong, A.1
Boutis, P.2
Hekimi, S.3
-
51
-
-
20744455958
-
The survival of motor neurons protein determines the capacity for snRNP assembly: Biochemical deficiency in spinal muscular atrophy
-
PMID:15964810
-
Wan L, Battle DJ, Yong J, Gubitz AK, Kolb SJ, Wang J, Dreyfuss G. The survival of motor neurons protein determines the capacity for snRNP assembly: biochemical deficiency in spinal muscular atrophy. Mol Cell Biol 2005; 25:5543-51; PMID:15964810; http://dx.doi.org/10.1128/MCB.25.13.5543-5551.2005
-
(2005)
Mol Cell Biol
, vol.25
, pp. 5543-5551
-
-
Wan, L.1
Battle, D.J.2
Yong, J.3
Gubitz, A.K.4
Kolb, S.J.5
Wang, J.6
Dreyfuss, G.7
-
52
-
-
0016063911
-
The genetics of Caenorhabditis elegans
-
PMID:4366476
-
Brenner S. The genetics of Caenorhabditis elegans. Genetics 1974; 77:71-94; PMID:4366476
-
(1974)
Genetics
, vol.77
, pp. 71-94
-
-
Brenner, S.1
-
53
-
-
17344392308
-
A new mathematical model for relative quantification in real-time RT-PCR
-
PMID:11328886
-
Pfaffl MW. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 2001; 29:e45; PMID:11328886; http://dx.doi.org/10.1093/nar/29.9.e45
-
(2001)
Nucleic Acids Res
, vol.29
, pp. e45
-
-
Pfaffl, M.W.1
-
54
-
-
0035941485
-
Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans
-
PMID:11223248
-
Timmons L, Court DL, Fire A. Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans. Gene 2001; 263:103-12; PMID:11223248; http://dx.doi.org/10.1016/S0378-1119(00)00579-5
-
(2001)
Gene
, vol.263
, pp. 103-112
-
-
Timmons, L.1
Court, D.L.2
Fire, A.3
-
55
-
-
0025942107
-
Efficient gene transfer in C.elegans: Extrachromosomal maintenance and integration of transforming sequences
-
PMID:1935914
-
Mello CC, Kramer JM, Stinchcomb D, Ambros V. Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences. EMBO J 1991; 10:3959-70; PMID:1935914
-
(1991)
EMBO J
, vol.10
, pp. 3959-3970
-
-
Mello, C.C.1
Kramer, J.M.2
Stinchcomb, D.3
Ambros, V.4
|