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Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patientsAARTSMA-RUS, Annemieke; JANSON, Anneke A. M; KAMAN, Wendy E et al.Human molecular genetics (Print). 2003, Vol 12, Num 8, pp 907-914, issn 0964-6906, 8 p.Article

JETTA: junction and exon toolkits for transcriptome analysisSEOK, Junhee; WEIHONG XU; HONG GAO et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 9, pp 1274-1275, issn 1367-4803, 2 p.Article

A splice form of polycystin-2, lacking exon 7, does not interact with polycystin-1HACKMANN, Karl; MARKOFF, Arseni; FENG QIAN et al.Human molecular genetics (Print). 2005, Vol 14, Num 21, pp 3249-3262, issn 0964-6906, 14 p.Article

A frameshifting mutation in CHRNE unmasks skipping of the preceding exonOHNO, Kinji; MILONE, Margherita; SHEN, Xin-Ming et al.Human molecular genetics (Print). 2003, Vol 12, Num 23, pp 3055-3066, issn 0964-6906, 12 p.Article

Overlap of the gene encoding the novel poly(ADP-ribose) polymerase Parp10 with the plectin 1 gene and common use of exon sequencesLESNIEWICZ, Krzysztof; LÜSCHER-FIRZLAFF, Juliane; POREBA, Elzbieta et al.Genomics (San Diego, Calif.). 2005, Vol 86, Num 1, pp 38-46, issn 0888-7543, 9 p.Article

Antisense-mediated exon skipping to correct IL-12Rβ1 deficiency in T cellsVAN DE VOSSE, Esther; VERHARD, Els M; DE PAUS, Roelof A et al.Blood. 2009, Vol 113, Num 19, pp 4548-4555, issn 0006-4971, 8 p.Article

Combined Use of MS2 and PP7 Coat Fusions Shows that TIA-1 Dominates hnRNP A1 for K-SAM Exon Splicing ControlGESNEL, Marie-Claude; DEL GATTO-KONCZAK, Fabienne; BREATHNACH, Richard et al.Journal of Biomedicine and Biotechnology (Print). 2009, Vol 2009, issn 1110-7243, 104853.1-104853.6, 3Article

Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approachDENG, Han-Xiang; JIANG HUJUN; FU RONGGEN et al.Human molecular genetics (Print). 2008, Vol 17, Num 15, pp 2310-2319, issn 0964-6906, 10 p.Article

Association of attentional network function with exon 5 variations of the CHRNA4 geneWINTERER, Georg; MUSSO, Francesco; KONRAD, Andreas et al.Human molecular genetics (Print). 2007, Vol 16, Num 18, pp 2165-2174, issn 0964-6906, 10 p.Article

Origins of introns based on the definition of exon modules and their conserved interfacesDE ROOS, Albert D. G.Bioinformatics (Oxford. Print). 2005, Vol 21, Num 1, pp 2-9, issn 1367-4803, 8 p.Article

A novel PHF6 mutation results in enhanced exon skipping and mild Börjeson-Forssman-Lehmann syndromeVALLEE, D; CHEVRIER, E; GRAHAM, G. E et al.Journal of medical genetics. 2004, Vol 41, Num 10, pp 778-783, issn 0022-2593, 6 p.Article

Identification of a novel A4GALT exon reveals the genetic basis of the P₁/P₂ histo-blood groupsTHURESSON, Britt; WESTMAN, Julia S; OLSSON, Martin L et al.Blood. 2011, Vol 117, Num 2, pp 678-687, issn 0006-4971, 10 p.Article

Disperse-a software system for design of selector probes for exon resequencing applicationsSTENBERG, J; ZHANG, M; JI, H et al.Bioinformatics (Oxford. Print). 2009, Vol 25, Num 5, pp 666-667, issn 1367-4803, 2 p.Article

Functional consequences of new exon acquisition in mammalian chromodomain Y-like (CDYL) genesXIN LI; JING LIANG; HAIJING YU et al.Trends in genetics (Regular ed.). 2007, Vol 23, Num 9, pp 427-431, issn 0168-9525, 5 p.Article

Protein domains correlate strongly with exons in multiple eukaryotic genomes: evidence of exon shuffling?MINGYI LIU; GRIGORIEV, Andrei.Trends in genetics (Regular ed.). 2004, Vol 20, Num 9, pp 399-403, issn 0168-9525, 5 p.Article

In-Frame Mutations in Exon 1 of SKI Cause Dominant Shprintzen-Goldberg SyndromeCARMIGNAC, Virginie; THEVENON, Julien; RENARD, Marjolijn et al.American journal of human genetics. 2012, Vol 91, Num 5, pp 950-957, issn 0002-9297, 8 p.Article

Exon Array Analyzer: a web interface for Affymetrix exon array analysisGELLERT, Pascal; UCHIDA, Shizuka; BRAUN, Thomas et al.Bioinformatics (Oxford. Print). 2009, Vol 25, Num 24, pp 3323-3324, issn 1367-4803, 2 p.Article

Cross-hybridization modeling on Affymetrix exon arraysKAPUR, Karen; HUI JIANG; YI XING et al.Bioinformatics (Oxford. Print). 2008, Vol 24, Num 24, pp 2887-2893, issn 1367-4803, 7 p.Article

A Novel Exon 3 Mutation (P66S) in the SOD1 Gene in Familial ALSBAEK, Wonki; KOH, Seong-Ho; YOUNG SEO KIM et al.Canadian journal of neurological sciences. 2012, Vol 39, Num 2, pp 245-246, issn 0317-1671, 2 p.Article

Computational identification of promoters and first exons in the human genomeDAVULURI, Ramana V; GROSSE, Ivo; ZHANG, Michael Q et al.Nature genetics. 2001, Vol 29, Num 4, pp 412-417, issn 1061-4036Article

Therapeutic exon skipping for dysferlinopathies?AARTSMA-RUS, Annemieke; SINGH, Kavita Hk; FOKKEMA, Ivo Fac et al.European journal of human genetics. 2010, Vol 18, Num 8, pp 889-894, issn 1018-4813, 6 p.Article

Novel Promoter 1.8 and Promoter Usage in the CYP19 (Aromatase) GeneDEMURA, Masashi; REIERSTAD, Scott; INNES, Joy E et al.Reproductive sciences (Thousand Oaks, Calif.). 2008, Vol 15, Num 10, pp 1044-1053, issn 1933-7191, 10 p.Article

The length of the downstream exon and the substitution of specific sequences affect pre-mRNA splicing in vitroFURDON, P. J; KOLE, R.Molecular and cellular biology (Print). 1988, Vol 8, Num 2, pp 860-866, issn 0270-7306Article

New statistical approach to discriminate between protein coding and non-coding regions in DNA sequences and its evaluationMICHEL, C. J.Journal of theoretical biology. 1986, Vol 120, Num 2, pp 223-236, issn 0022-5193Article