-
1
-
-
0028819352
-
Modulation of in vitro splicing of the upstream intron by modifying an intra-exon sequence which is deleted from the dystrophin gene in dystrophin Kobe
-
10.1172/JCI117693, 295503, 7860733
-
Takeshima Y, Nishio H, Sakamoto H, Nakamura H, Matsuo M. Modulation of in vitro splicing of the upstream intron by modifying an intra-exon sequence which is deleted from the dystrophin gene in dystrophin Kobe. J Clin Invest 1995, 95:515-520. 10.1172/JCI117693, 295503, 7860733.
-
(1995)
J Clin Invest
, vol.95
, pp. 515-520
-
-
Takeshima, Y.1
Nishio, H.2
Sakamoto, H.3
Nakamura, H.4
Matsuo, M.5
-
2
-
-
77957322170
-
Antisense-mediated modulation of splicing: Therapeutic implications for duchenne muscular dystrophy
-
10.4161/rna.7.4.12264, 20523110
-
Aartsma-Rus A. Antisense-mediated modulation of splicing: Therapeutic implications for duchenne muscular dystrophy. RNA Biol 2010, 7(4):453-461. 10.4161/rna.7.4.12264, 20523110.
-
(2010)
RNA Biol
, vol.7
, Issue.4
, pp. 453-461
-
-
Aartsma-Rus, A.1
-
3
-
-
78650916689
-
The Status of Exon Skipping as a Therapeutic Approach to Duchenne Muscular Dystrophy
-
10.1038/mt.2010.219, 3017449, 20978473
-
Lu QL, Yokota T, Takeda S, Garcia L, Muntoni F, Partridge T. The Status of Exon Skipping as a Therapeutic Approach to Duchenne Muscular Dystrophy. Mol Ther 2011, 19:9-15. 10.1038/mt.2010.219, 3017449, 20978473.
-
(2011)
Mol Ther
, vol.19
, pp. 9-15
-
-
Lu, Q.L.1
Yokota, T.2
Takeda, S.3
Garcia, L.4
Muntoni, F.5
Partridge, T.6
-
4
-
-
0027470203
-
The structural and functional diversity of dystrophin
-
10.1038/ng0493-283, 7981747
-
Ahn AH, Kunkel LM. The structural and functional diversity of dystrophin. Nat Genet 1993, 3:283-291. 10.1038/ng0493-283, 7981747.
-
(1993)
Nat Genet
, vol.3
, pp. 283-291
-
-
Ahn, A.H.1
Kunkel, L.M.2
-
5
-
-
0027936780
-
Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter
-
10.1172/JCI117417, 295157, 8083345
-
Nishio H, Takeshima Y, Narita N, Yanagawa H, Suzuki Y, Ishikawa Y, Minami R, Nakamura H, Matsuo M. Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter. J Clin Invest 1994, 94:1037-1042. 10.1172/JCI117417, 295157, 8083345.
-
(1994)
J Clin Invest
, vol.94
, pp. 1037-1042
-
-
Nishio, H.1
Takeshima, Y.2
Narita, N.3
Yanagawa, H.4
Suzuki, Y.5
Ishikawa, Y.6
Minami, R.7
Nakamura, H.8
Matsuo, M.9
-
6
-
-
0024582731
-
Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus
-
10.1038/338509a0, 2648158
-
Feener CA, Koenig M, Kunkel LM. Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus. Nature 1989, 338:509-511. 10.1038/338509a0, 2648158.
-
(1989)
Nature
, vol.338
, pp. 509-511
-
-
Feener, C.A.1
Koenig, M.2
Kunkel, L.M.3
-
7
-
-
0037165639
-
The dystrophin gene is alternatively spliced throughout its coding sequence
-
10.1016/S0014-5793(02)02613-3, 12062429
-
Sironi M, Cagliani R, Pozzoli U, Bardoni A, Comi GP, Giorda R, Bresolin N. The dystrophin gene is alternatively spliced throughout its coding sequence. FEBS Lett 2002, 517:163-166. 10.1016/S0014-5793(02)02613-3, 12062429.
-
(2002)
FEBS Lett
, vol.517
, pp. 163-166
-
-
Sironi, M.1
Cagliani, R.2
Pozzoli, U.3
Bardoni, A.4
Comi, G.P.5
Giorda, R.6
Bresolin, N.7
-
8
-
-
78650787882
-
Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activity
-
3000234, 21151598
-
Kubokawa I, Takeshima Y, Ota M, Enomoto M, Okizuka Y, Mori T, Nishimura N, Awano H, Yagi M, Matsuo M. Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activity. Mol Vis 2010, 16:2590-2597. 3000234, 21151598.
-
(2010)
Mol Vis
, vol.16
, pp. 2590-2597
-
-
Kubokawa, I.1
Takeshima, Y.2
Ota, M.3
Enomoto, M.4
Okizuka, Y.5
Mori, T.6
Nishimura, N.7
Awano, H.8
Yagi, M.9
Matsuo, M.10
-
9
-
-
0033846543
-
Multiple splicing defects in an intronic false exon
-
10.1128/MCB.20.17.6414-6425.2000, 86117, 10938119
-
Sun H, Chasin LA. Multiple splicing defects in an intronic false exon. Mol Cell Biol 2000, 20:6414-6425. 10.1128/MCB.20.17.6414-6425.2000, 86117, 10938119.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 6414-6425
-
-
Sun, H.1
Chasin, L.A.2
-
10
-
-
34347366205
-
Identification of seven novel cryptic exons embedded in the dystrophin gene and characterization of 14 cryptic dystrophin exons
-
10.1007/s10038-007-0163-0, 17579806
-
Zhang Z, Habara Y, Nishiyama A, Oyazato Y, Yagi M, Takeshima Y, Matsuo M. Identification of seven novel cryptic exons embedded in the dystrophin gene and characterization of 14 cryptic dystrophin exons. J Hum Genet 2007, 52:607-617. 10.1007/s10038-007-0163-0, 17579806.
-
(2007)
J Hum Genet
, vol.52
, pp. 607-617
-
-
Zhang, Z.1
Habara, Y.2
Nishiyama, A.3
Oyazato, Y.4
Yagi, M.5
Takeshima, Y.6
Matsuo, M.7
-
11
-
-
85011940677
-
Role of the snRNAs in spliceosomal active site
-
10.4161/rna.7.3.12089, 20458185
-
Valadkhan S. Role of the snRNAs in spliceosomal active site. RNA Biol 2010, 7:345-353. 10.4161/rna.7.3.12089, 20458185.
-
(2010)
RNA Biol
, vol.7
, pp. 345-353
-
-
Valadkhan, S.1
-
12
-
-
18344364099
-
Understanding alternative splicing: towards a cellular code
-
10.1038/nrm1645, 15956978
-
Matlin AJ, Clark F, Smith CW. Understanding alternative splicing: towards a cellular code. Nat Rev Mol Cell Biol 2005, 6:386-398. 10.1038/nrm1645, 15956978.
-
(2005)
Nat Rev Mol Cell Biol
, vol.6
, pp. 386-398
-
-
Matlin, A.J.1
Clark, F.2
Smith, C.W.3
-
13
-
-
79955823029
-
Chemical treatment enhances skipping of a mutated exon in the dystrophin gene
-
3113229, 21556062
-
Nishida A, Kataoka N, Takeshima Y, Yagi M, Awano H, Ota M, Itoh K, Hagiwara M, Matsuo M. Chemical treatment enhances skipping of a mutated exon in the dystrophin gene. Nat Commun 2011, 2:308. 3113229, 21556062.
-
(2011)
Nat Commun
, vol.2
, pp. 308
-
-
Nishida, A.1
Kataoka, N.2
Takeshima, Y.3
Yagi, M.4
Awano, H.5
Ota, M.6
Itoh, K.7
Hagiwara, M.8
Matsuo, M.9
-
14
-
-
51349111653
-
What are decision trees?
-
10.1038/nbt0908-1011, 2701298, 18779814
-
Kingsford C, Salzberg SL. What are decision trees?. Nat Biotechnol 2008, 26:1011-1013. 10.1038/nbt0908-1011, 2701298, 18779814.
-
(2008)
Nat Biotechnol
, vol.26
, pp. 1011-1013
-
-
Kingsford, C.1
Salzberg, S.L.2
-
15
-
-
33748641488
-
JIGSAW, GeneZilla, and GlimmerHMM: puzzling out the features of human genes in the ENCODE regions
-
1810558, 16925843
-
Allen JE, Majoros WH, Pertea M, Salzberg SL. JIGSAW, GeneZilla, and GlimmerHMM: puzzling out the features of human genes in the ENCODE regions. Genome Biol 2006, 7(Suppl 1:S9):1-13. 1810558, 16925843.
-
(2006)
Genome Biol
, vol.7
, Issue.SUPPL.1
, pp. 1-13
-
-
Allen, J.E.1
Majoros, W.H.2
Pertea, M.3
Salzberg, S.L.4
-
16
-
-
54049095232
-
Dystrophin nonsense mutations can generate alternative rescue transcripts in lymphocytes
-
10.1111/j.1469-1809.2008.00468.x, 18652600
-
Nishiyama A, Takeshima Y, Zhang Z, Habara Y, Tran TH, Yagi M, Matsuo M. Dystrophin nonsense mutations can generate alternative rescue transcripts in lymphocytes. Ann Hum Genet 2008, 72:717-724. 10.1111/j.1469-1809.2008.00468.x, 18652600.
-
(2008)
Ann Hum Genet
, vol.72
, pp. 717-724
-
-
Nishiyama, A.1
Takeshima, Y.2
Zhang, Z.3
Habara, Y.4
Tran, T.H.5
Yagi, M.6
Matsuo, M.7
-
17
-
-
36248977122
-
Global control of aberrant splice-site activation by auxiliary splicing sequences: evidence for a gradient in exon and intron definition
-
10.1093/nar/gkm680, 2095810, 17881373
-
Královicová J, Vorechovsky I. Global control of aberrant splice-site activation by auxiliary splicing sequences: evidence for a gradient in exon and intron definition. Nucleic Acids Res 2007, 35:6399-6413. 10.1093/nar/gkm680, 2095810, 17881373.
-
(2007)
Nucleic Acids Res
, vol.35
, pp. 6399-6413
-
-
Královicová, J.1
Vorechovsky, I.2
-
18
-
-
77949516611
-
Using simple artificial intelligence methods for predicting amyloidogenesis in antibodies
-
David MP, Concepcion GP, Padlan EA. Using simple artificial intelligence methods for predicting amyloidogenesis in antibodies. BMC Bioinforma 2010, 11:79.
-
(2010)
BMC Bioinforma
, vol.11
, pp. 79
-
-
David, M.P.1
Concepcion, G.P.2
Padlan, E.A.3
-
19
-
-
0030725216
-
Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy
-
10.1172/JCI119757, 508415, 9410897
-
Shiga N, Takeshima Y, Sakamoto H, Inoue K, Yokota Y, Yokoyama M, Matsuo M. Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy. J Clin Invest 1997, 100:2204-2210. 10.1172/JCI119757, 508415, 9410897.
-
(1997)
J Clin Invest
, vol.100
, pp. 2204-2210
-
-
Shiga, N.1
Takeshima, Y.2
Sakamoto, H.3
Inoue, K.4
Yokota, Y.5
Yokoyama, M.6
Matsuo, M.7
-
20
-
-
34547850647
-
Aberrant 5' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization
-
10.1093/nar/gkm402, 1934990, 17576681
-
Buratti E, Chivers M, Královicová J, Romano M, Baralle M, Krainer A, Vorechovsky I. Aberrant 5' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization. Nucleic Acids Res 2007, 35:4250-4263. 10.1093/nar/gkm402, 1934990, 17576681.
-
(2007)
Nucleic Acids Res
, vol.35
, pp. 4250-4263
-
-
Buratti, E.1
Chivers, M.2
Královicová, J.3
Romano, M.4
Baralle, M.5
Krainer, A.6
Vorechovsky, I.7
-
21
-
-
76149138842
-
Alternative splicing: role of pseudoexons in human disease and potential therapeutic strategies
-
10.1111/j.1742-4658.2009.07520.x, 20082636
-
Dhir A, Buratti E. Alternative splicing: role of pseudoexons in human disease and potential therapeutic strategies. FEBS J 2010, 277:841-855. 10.1111/j.1742-4658.2009.07520.x, 20082636.
-
(2010)
FEBS J
, vol.277
, pp. 841-855
-
-
Dhir, A.1
Buratti, E.2
-
22
-
-
76249097319
-
Transposable elements in disease-associated cryptic exons
-
10.1007/s00439-009-0752-4, 19823873
-
Vorechovsky I. Transposable elements in disease-associated cryptic exons. Hum Genet 2010, 127:135-154. 10.1007/s00439-009-0752-4, 19823873.
-
(2010)
Hum Genet
, vol.127
, pp. 135-154
-
-
Vorechovsky, I.1
-
23
-
-
77149153689
-
The intronic splicing code: multiple factors involved in ATM pseudoexon definition
-
10.1038/emboj.2009.397, 2829169, 20094034
-
Dhir A, Buratti E, van Santen MA, Luhrmann R, Baralle FE. The intronic splicing code: multiple factors involved in ATM pseudoexon definition. EMBO J 2010, 29:749-760. 10.1038/emboj.2009.397, 2829169, 20094034.
-
(2010)
EMBO J
, vol.29
, pp. 749-760
-
-
Dhir, A.1
Buratti, E.2
van Santen, M.A.3
Luhrmann, R.4
Baralle, F.E.5
-
24
-
-
78651248717
-
Troponin T isoforms and posttranscriptional modifications: Evolution, regulation and function
-
10.1016/j.abb.2010.10.013, 3018564, 20965144
-
Wei B, Jin JP. Troponin T isoforms and posttranscriptional modifications: Evolution, regulation and function. Arch Biochem Biophys 2011, 505:144-154. 10.1016/j.abb.2010.10.013, 3018564, 20965144.
-
(2011)
Arch Biochem Biophys
, vol.505
, pp. 144-154
-
-
Wei, B.1
Jin, J.P.2
-
25
-
-
0026046262
-
Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy Kobe
-
10.1172/JCI115244, 296970, 2040695
-
Matsuo M, Masumura T, Nishio H, Nakajima T, Kitoh Y, Takumi T, Koga J, Nakamura H. Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy Kobe. J Clin Invest 1991, 87:2127-2131. 10.1172/JCI115244, 296970, 2040695.
-
(1991)
J Clin Invest
, vol.87
, pp. 2127-2131
-
-
Matsuo, M.1
Masumura, T.2
Nishio, H.3
Nakajima, T.4
Kitoh, Y.5
Takumi, T.6
Koga, J.7
Nakamura, H.8
-
26
-
-
0030582315
-
Induction of exon skipping of the dystrophin transcript in lymphoblastoid cells by transfecting an antisense oligodeoxynucleotide complementary to an exon recognition sequence
-
10.1006/bbrc.1996.1375, 8806654
-
Pramono ZA, Takeshima Y, Alimsardjono H, Ishii A, Takeda S, Matsuo M. Induction of exon skipping of the dystrophin transcript in lymphoblastoid cells by transfecting an antisense oligodeoxynucleotide complementary to an exon recognition sequence. Biochem Biophys Res Commun 1996, 226:445-449. 10.1006/bbrc.1996.1375, 8806654.
-
(1996)
Biochem Biophys Res Commun
, vol.226
, pp. 445-449
-
-
Pramono, Z.A.1
Takeshima, Y.2
Alimsardjono, H.3
Ishii, A.4
Takeda, S.5
Matsuo, M.6
-
27
-
-
33646671717
-
Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophy
-
10.1203/01.pdr.0000215047.51278.7c, 16627883
-
Takeshima Y, Yagi M, Wada H, Ishibashi K, Nishiyama A, Kakumoto M, Sakaeda T, Saura R, Okumura K, Matsuo M. Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophy. Pediatr Res 2006, 59:690-694. 10.1203/01.pdr.0000215047.51278.7c, 16627883.
-
(2006)
Pediatr Res
, vol.59
, pp. 690-694
-
-
Takeshima, Y.1
Yagi, M.2
Wada, H.3
Ishibashi, K.4
Nishiyama, A.5
Kakumoto, M.6
Sakaeda, T.7
Saura, R.8
Okumura, K.9
Matsuo, M.10
-
28
-
-
77954158696
-
Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center
-
10.1038/jhg.2010.49, 20485447
-
Takeshima Y, Yagi M, Okizuka Y, Awano H, Zhang Z, Yamauchi Y, Nishio H, Matsuo M. Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center. J Hum Genet 2010, 55:379-388. 10.1038/jhg.2010.49, 20485447.
-
(2010)
J Hum Genet
, vol.55
, pp. 379-388
-
-
Takeshima, Y.1
Yagi, M.2
Okizuka, Y.3
Awano, H.4
Zhang, Z.5
Yamauchi, Y.6
Nishio, H.7
Matsuo, M.8
-
29
-
-
0037318192
-
Two alternative exons can result from activation of the cryptic splice acceptor site deep within intron 2 of the dystrophin gene in a patient with as yet asymptomatic dystrophinopathy
-
Yagi M, Takeshima Y, Wada H, Nakamura H, Matsuo M. Two alternative exons can result from activation of the cryptic splice acceptor site deep within intron 2 of the dystrophin gene in a patient with as yet asymptomatic dystrophinopathy. Hum Genet 2003, 112:164-170.
-
(2003)
Hum Genet
, vol.112
, pp. 164-170
-
-
Yagi, M.1
Takeshima, Y.2
Wada, H.3
Nakamura, H.4
Matsuo, M.5
-
30
-
-
10744219888
-
Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene
-
10.1016/S0960-8966(03)00169-X, 14659407
-
Beroud C, Carrie A, Beldjord C, Deburgrave N, Llense S, Carelle N, Peccate C, Cuisset JM, Pandit F, Carre-Pigeon F, et al. Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene. Neuromuscul Disord 2004, 14:10-18. 10.1016/S0960-8966(03)00169-X, 14659407.
-
(2004)
Neuromuscul Disord
, vol.14
, pp. 10-18
-
-
Beroud, C.1
Carrie, A.2
Beldjord, C.3
Deburgrave, N.4
Llense, S.5
Carelle, N.6
Peccate, C.7
Cuisset, J.M.8
Pandit, F.9
Carre-Pigeon, F.10
-
31
-
-
0023651307
-
RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression
-
10.1093/nar/15.17.7155, 306199, 3658675
-
Shapiro MB, Senapathy P. RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression. Nucleic Acids Res 1987, 15:7155-7174. 10.1093/nar/15.17.7155, 306199, 3658675.
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 7155-7174
-
-
Shapiro, M.B.1
Senapathy, P.2
-
32
-
-
2442441507
-
Maximum entrophy modeling of short sequence motifs with applications to RNA splicing signals
-
Yeo G, Burge CB. Maximum entrophy modeling of short sequence motifs with applications to RNA splicing signals. J Comput Biol 2003, 11:377-394.
-
(2003)
J Comput Biol
, vol.11
, pp. 377-394
-
-
Yeo, G.1
Burge, C.B.2
-
33
-
-
17144362174
-
Automated splicing mutation analysis by information theory
-
10.1002/humu.20151, 15776446
-
Nalla VK, Rogan PK. Automated splicing mutation analysis by information theory. Hum Mutat 2005, 25:334-342. 10.1002/humu.20151, 15776446.
-
(2005)
Hum Mutat
, vol.25
, pp. 334-342
-
-
Nalla, V.K.1
Rogan, P.K.2
-
34
-
-
5044222204
-
How did alternative splicing evolve?
-
Ast G. How did alternative splicing evolve?. Nat Rev Genet 2004, 5:773-782.
-
(2004)
Nat Rev Genet
, vol.5
, pp. 773-782
-
-
Ast, G.1
-
35
-
-
67849092454
-
SROOGLE: webserver for integrative, user-friendly visualization of splicing signals
-
10.1093/nar/gkp320, 2703896, 19429896, Web Server
-
Schwartz S, Hall E, Ast G. SROOGLE: webserver for integrative, user-friendly visualization of splicing signals. Nucleic Acids Res 2009, 37(Web Server):W189-192. 10.1093/nar/gkp320, 2703896, 19429896.
-
(2009)
Nucleic Acids Res
, vol.37
-
-
Schwartz, S.1
Hall, E.2
Ast, G.3
-
36
-
-
0037047644
-
Predictive identification of exonic splicing enhancers in human genes
-
10.1126/science.1073774, 12114529
-
Fairbrother WG, Yeh RF, Sharp PA, Burge CB. Predictive identification of exonic splicing enhancers in human genes. Science 2002, 297:1007-1013. 10.1126/science.1073774, 12114529.
-
(2002)
Science
, vol.297
, pp. 1007-1013
-
-
Fairbrother, W.G.1
Yeh, R.F.2
Sharp, P.A.3
Burge, C.B.4
-
37
-
-
10944256767
-
Systematic identification and analysis of exonic splicing silencers
-
10.1016/j.cell.2004.11.010, 15607979
-
Wang Z, Rolish ME, Yeo G, Tung V, Mawson M, Burge CB. Systematic identification and analysis of exonic splicing silencers. Cell 2004, 119:831-845. 10.1016/j.cell.2004.11.010, 15607979.
-
(2004)
Cell
, vol.119
, pp. 831-845
-
-
Wang, Z.1
Rolish, M.E.2
Yeo, G.3
Tung, V.4
Mawson, M.5
Burge, C.B.6
-
38
-
-
2642525438
-
Computational definition of sequence motifs governing constitutive exon splicing
-
10.1101/gad.1195304, 420350, 15145827
-
Zhang XH, Chasin LA. Computational definition of sequence motifs governing constitutive exon splicing. Genes Dev 2004, 18:1241-1250. 10.1101/gad.1195304, 420350, 15145827.
-
(2004)
Genes Dev
, vol.18
, pp. 1241-1250
-
-
Zhang, X.H.1
Chasin, L.A.2
-
39
-
-
0042242582
-
ESEfinder: A web resource to identify exonic splicing enhancers
-
10.1093/nar/gkg616, 169022, 12824367
-
Cartegni L, Wang J, Zhu Z, Zhang MQ, Krainer AR. ESEfinder: A web resource to identify exonic splicing enhancers. Nucleic Acids Res 2003, 31:3568-3571. 10.1093/nar/gkg616, 169022, 12824367.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 3568-3571
-
-
Cartegni, L.1
Wang, J.2
Zhu, Z.3
Zhang, M.Q.4
Krainer, A.R.5
-
40
-
-
79251564926
-
GC content around splice sites affects splicing through pre-mRNA secondary structures
-
10.1186/1471-2164-12-90, 3041747, 21281513
-
Zhang J, Kuo CC, Chen L. GC content around splice sites affects splicing through pre-mRNA secondary structures. BMC Genomics 2011, 12:90. 10.1186/1471-2164-12-90, 3041747, 21281513.
-
(2011)
BMC Genomics
, vol.12
, pp. 90
-
-
Zhang, J.1
Kuo, C.C.2
Chen, L.3
-
41
-
-
48449095385
-
The Vienna RNA websuite
-
10.1093/nar/gkn188, 2447809, 18424795, Web Server
-
Gruber AR, Lorenz R, Bernhart SH, Neubock R, Hofacker IL. The Vienna RNA websuite. Nucleic Acids Res 2008, 36(Web Server):W70-74. 10.1093/nar/gkn188, 2447809, 18424795.
-
(2008)
Nucleic Acids Res
, vol.36
-
-
Gruber, A.R.1
Lorenz, R.2
Bernhart, S.H.3
Neubock, R.4
Hofacker, I.L.5
-
45
-
-
0029678894
-
Improved Use of Continuous Attributes in C
-
Quinlan JR. Improved Use of Continuous Attributes in C. J Artif Intell Res 1996, 4:77-90.
-
(1996)
J Artif Intell Res
, vol.4
, pp. 77-90
-
-
Quinlan, J.R.1
-
46
-
-
0032976697
-
Circular dystrophin RNAs consisting of exons that were skipped by alternative splicing
-
10.1093/hmg/8.3.493, 9949208
-
Surono A, Takeshima Y, Wibawa T, Ikezawa M, Nonaka I, Matsuo M. Circular dystrophin RNAs consisting of exons that were skipped by alternative splicing. Hum Mol Genet 1999, 8:493-500. 10.1093/hmg/8.3.493, 9949208.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 493-500
-
-
Surono, A.1
Takeshima, Y.2
Wibawa, T.3
Ikezawa, M.4
Nonaka, I.5
Matsuo, M.6
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