322 related articles for article (PubMed ID: 14681464)
1. AluGene: a database of Alu elements incorporated within protein-coding genes.
Dagan T; Sorek R; Sharon E; Ast G; Graur D
Nucleic Acids Res; 2004 Jan; 32(Database issue):D489-92. PubMed ID: 14681464
[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. Xpro: database of eukaryotic protein-encoding genes.
Gopalan V; Tan TW; Lee BT; Ranganathan S
Nucleic Acids Res; 2004 Jan; 32(Database issue):D59-63. PubMed ID: 14681359
[TBL] [Abstract][Full Text] [Related]
4. Beyond DNA: RNA editing and steps toward Alu exonization in primates.
Möller-Krull M; Zemann A; Roos C; Brosius J; Schmitz J
J Mol Biol; 2008 Oct; 382(3):601-9. PubMed ID: 18680752
[TBL] [Abstract][Full Text] [Related]
5. RPG: the Ribosomal Protein Gene database.
Nakao A; Yoshihama M; Kenmochi N
Nucleic Acids Res; 2004 Jan; 32(Database issue):D168-70. PubMed ID: 14681386
[TBL] [Abstract][Full Text] [Related]
6. Information for the Coordinates of Exons (ICE): a human splice sites database.
Chong A; Zhang G; Bajic VB
Genomics; 2004 Oct; 84(4):762-6. PubMed ID: 15475254
[TBL] [Abstract][Full Text] [Related]
7. Disease-causing mutations improving the branch site and polypyrimidine tract: pseudoexon activation of LINE-2 and antisense Alu lacking the poly(T)-tail.
Meili D; Kralovicova J; Zagalak J; Bonafé L; Fiori L; Blau N; Thöny B; Vorechovsky I
Hum Mutat; 2009 May; 30(5):823-31. PubMed ID: 19280650
[TBL] [Abstract][Full Text] [Related]
8. A recurrent large Alu-mediated deletion in the hypoxanthine phosphoribosyltransferase (HPRT1) gene associated with Lesch-Nyhan syndrome.
Mizunuma M; Fujimori S; Ogino H; Ueno T; Inoue H; Kamatani N
Hum Mutat; 2001 Nov; 18(5):435-43. PubMed ID: 11668636
[TBL] [Abstract][Full Text] [Related]
9. Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs.
Abeysinghe SS; Chuzhanova N; Krawczak M; Ball EV; Cooper DN
Hum Mutat; 2003 Sep; 22(3):229-44. PubMed ID: 12938088
[TBL] [Abstract][Full Text] [Related]
10. Alu-SINE exonization: en route to protein-coding function.
Krull M; Brosius J; Schmitz J
Mol Biol Evol; 2005 Aug; 22(8):1702-11. PubMed ID: 15901843
[TBL] [Abstract][Full Text] [Related]
11. Advances in the Exon-Intron Database (EID).
Shepelev V; Fedorov A
Brief Bioinform; 2006 Jun; 7(2):178-85. PubMed ID: 16772261
[TBL] [Abstract][Full Text] [Related]
12. EuSplice: a unified resource for the analysis of splice signals and alternative splicing in eukaryotic genes.
Bhasi A; Pandey RV; Utharasamy SP; Senapathy P
Bioinformatics; 2007 Jul; 23(14):1815-23. PubMed ID: 17344236
[TBL] [Abstract][Full Text] [Related]
13. AthaMap: an online resource for in silico transcription factor binding sites in the Arabidopsis thaliana genome.
Steffens NO; Galuschka C; Schindler M; Bülow L; Hehl R
Nucleic Acids Res; 2004 Jan; 32(Database issue):D368-72. PubMed ID: 14681436
[TBL] [Abstract][Full Text] [Related]
14. Evidence of Alu and B1 expression in dbEST.
Umylny B; Presting G; Ward WS
Arch Androl; 2007; 53(4):207-18. PubMed ID: 17852045
[TBL] [Abstract][Full Text] [Related]
15. Alu repeats and human genomic diversity.
Batzer MA; Deininger PL
Nat Rev Genet; 2002 May; 3(5):370-9. PubMed ID: 11988762
[TBL] [Abstract][Full Text] [Related]
16. Functional persistence of exonized mammalian-wide interspersed repeat elements (MIRs).
Krull M; Petrusma M; Makalowski W; Brosius J; Schmitz J
Genome Res; 2007 Aug; 17(8):1139-45. PubMed ID: 17623809
[TBL] [Abstract][Full Text] [Related]
17. Tandem insertions of Alu elements.
El-Sawy M; Deininger P
Cytogenet Genome Res; 2005; 108(1-3):58-62. PubMed ID: 15545716
[TBL] [Abstract][Full Text] [Related]
18. ssSNPTarget: genome-wide splice-site Single Nucleotide Polymorphism database.
Yang JO; Kim WY; Bhak J
Hum Mutat; 2009 Dec; 30(12):E1010-20. PubMed ID: 19760752
[TBL] [Abstract][Full Text] [Related]
19. Nonrandom distribution of alu elements in genes of various functional categories: insight from analysis of human chromosomes 21 and 22.
Grover D; Majumder PP; B Rao C; Brahmachari SK; Mukerji M
Mol Biol Evol; 2003 Sep; 20(9):1420-4. PubMed ID: 12832639
[TBL] [Abstract][Full Text] [Related]
20. Homeologous recombination between AluSx-sequences as a cause of hemophilia.
Rossetti LC; Goodeve A; Larripa IB; De Brasi CD
Hum Mutat; 2004 Nov; 24(5):440. PubMed ID: 15459970
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
