BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

95 related articles for article (PubMed ID: 11836681)

  • 1. [The full sequence of intron 51 of dystrophin gene and its characteristic of sequence].
    Pan S; Zhang C; Liu Z; Chen G; Sheng W; Lu X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Feb; 19(1):26-9. PubMed ID: 11836681
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The 5' region of intron 11 of the dystrophin gene contains target sequences for mobile elements and three overlapping ORFs.
    Ferlini A; Muntoni F
    Biochem Biophys Res Commun; 1998 Jan; 242(2):401-6. PubMed ID: 9446807
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The evolution of an intron: analysis of a long, deletion-prone intron in the human dystrophin gene.
    McNaughton JC; Hughes G; Jones WA; Stockwell PA; Klamut HJ; Petersen GB
    Genomics; 1997 Mar; 40(2):294-304. PubMed ID: 9119397
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A cluster of transposon-like repetitive sequences in intron 7 of the human dystrophin gene.
    McNaughton JC; Broom JE; Hill DF; Jones WA; Marshall CJ; Renwick NM; Stockwell PA; Petersen GB
    J Mol Biol; 1993 Jul; 232(1):314-21. PubMed ID: 8392588
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Is the human dystrophin gene's intron structure related to its intron instability?
    Sheng W; Chen J; Zhu L; Liu Z
    Chin Med J (Engl); 2003 Nov; 116(11):1733-6. PubMed ID: 14642147
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cloning and sequencing of junction fragment with exons 45-54 deletion of dystrophin gene.
    Zhong M; Pan SY; Lu BX; Li W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Apr; 23(2):138-41. PubMed ID: 16604481
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Comparison and analysis of the molecular character of breakpoints in introns of deletion hotspots of dystrophin gene].
    Sheng WL; Chen JY; Pan SY; Zhang C; Liu ZL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct; 20(5):376-80. PubMed ID: 14556187
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Non-homologous recombination between Alu and LINE-1 repeats caused a 430-kb deletion in the dystrophin gene: a novel source of genomic instability.
    Suminaga R; Takeshima Y; Yasuda K; Shiga N; Nakamura H; Matsuo M
    J Hum Genet; 2000; 45(6):331-6. PubMed ID: 11185740
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Cloning and sequencing of junction fragment with exon 51 deletion of Dystrophin gene].
    Pan SY; Zhang C; Liu ZL; Chen GJ; Lu XL
    Yi Chuan Xue Bao; 2002 Feb; 29(2):105-10. PubMed ID: 11901990
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The goat alphas1-casein gene: gene structure and promoter analysis.
    Ramunno L; Cosenza G; Rando A; Illario R; Gallo D; Di Berardino D; Masina P
    Gene; 2004 Jun; 334():105-11. PubMed ID: 15256260
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Cloning and sequencing of the junction fragment of dystrophin gene with exons 3 to 5 deletion].
    Zhong M; Pan SY; Lu BX; Jiang L; Li W
    Nan Fang Yi Ke Da Xue Xue Bao; 2006 Jun; 26(6):757-9. PubMed ID: 16793593
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. [The sequences of intron 50 and 51 of DMD gene and the deletion mechanism of 51st exon].
    Sheng W; Chai J; Liu Z
    Zhonghua Yi Xue Za Zhi; 1996 Nov; 76(11):852-4. PubMed ID: 9275539
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genes within genes: multiple LAGLIDADG homing endonucleases target the ribosomal protein S3 gene encoded within an rnl group I intron of Ophiostoma and related taxa.
    Sethuraman J; Majer A; Friedrich NC; Edgell DR; Hausner G
    Mol Biol Evol; 2009 Oct; 26(10):2299-315. PubMed ID: 19597163
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene.
    Toffolatti L; Cardazzo B; Nobile C; Danieli GA; Gualandi F; Muntoni F; Abbs S; Zanetti P; Angelini C; Ferlini A; Fanin M; Patarnello T
    Genomics; 2002 Nov; 80(5):523-30. PubMed ID: 12408970
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sequencing and expression of the second allele of the interleukin-1beta1 gene in rainbow trout (Oncorhynchus mykiss): identification of a novel SINE in the third intron.
    Wang T; Johnson N; Zou J; Bols N; Secombes CJ
    Fish Shellfish Immunol; 2004 Mar; 16(3):335-58. PubMed ID: 15123302
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Isolation and molecular characterization of the porcine stearoyl-CoA desaturase gene.
    Ren J; Knorr C; Huang L; Brenig B
    Gene; 2004 Sep; 340(1):19-30. PubMed ID: 15556291
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5.
    Suminaga R; Takeshima Y; Adachi K; Yagi M; Nakamura H; Matsuo M
    J Hum Genet; 2002; 47(4):196-201. PubMed ID: 12166656
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A G-to-A transition at the fifth position of intron-32 of the dystrophin gene inactivates a splice-donor site both in vivo and in vitro.
    Thi Tran HT; Takeshima Y; Surono A; Yagi M; Wada H; Matsuo M
    Mol Genet Metab; 2005 Jul; 85(3):213-9. PubMed ID: 15979033
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.