160 related articles for article (PubMed ID: 11691849)
1. The contribution of exon-skipping events on chromosome 22 to protein coding diversity.
Hide WA; Babenko VN; van Heusden PA; Seoighe C; Kelso JF
Genome Res; 2001 Nov; 11(11):1848-53. PubMed ID: 11691849
[TBL] [Abstract][Full Text] [Related]
2. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
3. The role of common single-nucleotide polymorphisms on exon 9 and exon 12 skipping in nonmutated CFTR alleles.
Steiner B; Truninger K; Sanz J; Schaller A; Gallati S
Hum Mutat; 2004 Aug; 24(2):120-9. PubMed ID: 15241793
[TBL] [Abstract][Full Text] [Related]
4. Sequence conservation, relative isoform frequencies, and nonsense-mediated decay in evolutionarily conserved alternative splicing.
Baek D; Green P
Proc Natl Acad Sci U S A; 2005 Sep; 102(36):12813-8. PubMed ID: 16123126
[TBL] [Abstract][Full Text] [Related]
5. Structural analysis of the genes for human arylamine N-acetyltransferases and characterisation of alternative transcripts.
Boukouvala S; Sim E
Basic Clin Pharmacol Toxicol; 2005 May; 96(5):343-51. PubMed ID: 15853926
[TBL] [Abstract][Full Text] [Related]
6. Genome-wide analysis of transcript isoform variation in humans.
Kwan T; Benovoy D; Dias C; Gurd S; Provencher C; Beaulieu P; Hudson TJ; Sladek R; Majewski J
Nat Genet; 2008 Feb; 40(2):225-31. PubMed ID: 18193047
[TBL] [Abstract][Full Text] [Related]
7. Multiple transcription initiation sites, alternative splicing, and differential polyadenylation contribute to the complexity of human neurofibromatosis 2 transcripts.
Chang LS; Akhmametyeva EM; Wu Y; Zhu L; Welling DB
Genomics; 2002 Jan; 79(1):63-76. PubMed ID: 11827459
[TBL] [Abstract][Full Text] [Related]
8. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
Lee PL; Gelbart T; West C; Halloran C; Beutler E
Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
[TBL] [Abstract][Full Text] [Related]
9. Alternatively spliced human genes by exon skipping--a database (ASHESdb).
Sakharkar MK; Perumal BS; Lim YP; Chern LP; Yu Y; Kangueane P
In Silico Biol; 2005; 5(3):221-5. PubMed ID: 15984933
[TBL] [Abstract][Full Text] [Related]
10. Alternative splicing and differential gene expression in colon cancer detected by a whole genome exon array.
Gardina PJ; Clark TA; Shimada B; Staples MK; Yang Q; Veitch J; Schweitzer A; Awad T; Sugnet C; Dee S; Davies C; Williams A; Turpaz Y
BMC Genomics; 2006 Dec; 7():325. PubMed ID: 17192196
[TBL] [Abstract][Full Text] [Related]
11. Changes in alternative splicing of human and mouse genes are accompanied by faster evolution of constitutive exons.
Cusack BP; Wolfe KH
Mol Biol Evol; 2005 Nov; 22(11):2198-208. PubMed ID: 16049198
[TBL] [Abstract][Full Text] [Related]
12. Human gene MOB: structure specification and aspects of transcriptional activity.
Vladychenskaya IP; Dergunova LV; Dmitrieva VG; Limborska SA
Gene; 2004 Sep; 338(2):257-65. PubMed ID: 15315829
[TBL] [Abstract][Full Text] [Related]
13. Human transcription factor Sp3: genomic structure, identification of a processed pseudogene, and transcript analysis.
Moran KM; Crusio RH; Chan CH; Grekova MC; Richert JR
Gene; 2004 Oct; 341():235-47. PubMed ID: 15474306
[TBL] [Abstract][Full Text] [Related]
14. A new advance in alternative splicing databases: from catalogue to detailed analysis of regulation of expression and function of human alternative splicing variants.
de la Grange P; Dutertre M; Correa M; Auboeuf D
BMC Bioinformatics; 2007 Jun; 8():180. PubMed ID: 17547750
[TBL] [Abstract][Full Text] [Related]
15. Conserved modularity and potential for alternate splicing in mouse and human Slit genes.
Little M; Rumballe B; Georgas K; Yamada T; Teasdale RD
Int J Dev Biol; 2002; 46(4):385-91. PubMed ID: 12141424
[TBL] [Abstract][Full Text] [Related]
16. Variation in alternative splicing across human tissues.
Yeo G; Holste D; Kreiman G; Burge CB
Genome Biol; 2004; 5(10):R74. PubMed ID: 15461793
[TBL] [Abstract][Full Text] [Related]
17. Multiple sequence variants of BRCA2 exon 7 alter splicing regulation.
Gaildrat P; Krieger S; Di Giacomo D; Abdat J; Révillion F; Caputo S; Vaur D; Jamard E; Bohers E; Ledemeney D; Peyrat JP; Houdayer C; Rouleau E; Lidereau R; Frébourg T; Hardouin A; Tosi M; Martins A
J Med Genet; 2012 Oct; 49(10):609-17. PubMed ID: 22962691
[TBL] [Abstract][Full Text] [Related]
18. Gene expression and isoform variation analysis using Affymetrix Exon Arrays.
Bemmo A; Benovoy D; Kwan T; Gaffney DJ; Jensen RV; Majewski J
BMC Genomics; 2008 Nov; 9():529. PubMed ID: 18990248
[TBL] [Abstract][Full Text] [Related]
19. Alternative splicing of the human estrogen receptor alpha primary transcript: mechanisms of exon skipping.
Ferro P; Forlani A; Muselli M; Pfeffer U
Int J Mol Med; 2003 Sep; 12(3):355-63. PubMed ID: 12883652
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide detection and analysis of alternative splicing for nucleotide binding site-leucine-rich repeats sequences in rice.
Gu L; Guo R
J Genet Genomics; 2007 Mar; 34(3):247-57. PubMed ID: 17498622
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]