BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 11901990)

  • 1. [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]  

  • 2. [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]  

  • 3. 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]  

  • 4. [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]  

  • 5. Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy.
    Narita N; Nishio H; Kitoh Y; Ishikawa Y; Ishikawa Y; Minami R; Nakamura H; Matsuo M
    J Clin Invest; 1993 May; 91(5):1862-7. PubMed ID: 8387534
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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.
    Nishio H; Takeshima Y; Narita N; Yanagawa H; Suzuki Y; Ishikawa Y; Ishikawa Y; Minami R; Nakamura H; Matsuo M
    J Clin Invest; 1994 Sep; 94(3):1037-42. PubMed ID: 8083345
    [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. Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.
    Matsuo M; Masumura T; Nishio H; Nakajima T; Kitoh Y; Takumi T; Koga J; Nakamura H
    J Clin Invest; 1991 Jun; 87(6):2127-31. PubMed ID: 2040695
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Severe haemophilia B due to a 6 kb factor IX gene deletion including exon 4: non-homologous recombination associated with a shortened transcript from whole blood.
    Hsu TC; Nakaya SM; Thompson AR
    Thromb Haemost; 2007 Feb; 97(2):176-80. PubMed ID: 17264943
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation.
    Patria SY; Alimsardjono H; Nishio H; Takeshima Y; Nakamura H; Matsuo M
    Proc Assoc Am Physicians; 1996 Jul; 108(4):308-14. PubMed ID: 8863344
    [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. [Deletion analysis of the dystrophin gene in patients with Duchenne's muscular dystrophy in Tajikistan].
    Odinokova ON; Puzyrev VP; Radzhabaliev ShF; Rakhmonov RA
    Genetika; 1996 Oct; 32(10):1392-5. PubMed ID: 9091412
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Studying dystrophin gene deletion in the northeast of China and applicating].
    Lu Y; Jin CL; Lin CK; Wu YY; Liu LY; Sun KL
    Yi Chuan Xue Bao; 2004 May; 31(5):449-53. PubMed ID: 15478603
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Insertion of the IL1RAPL1 gene into the duplication junction of the dystrophin gene.
    Zhang Z; Yagi M; Okizuka Y; Awano H; Takeshima Y; Matsuo M
    J Hum Genet; 2009 Aug; 54(8):466-73. PubMed ID: 19609279
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Problems found in genetic diagnosis of DMD/BMD].
    Matsuo M
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1413-5. PubMed ID: 8752414
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Intron 44 is not the most unstable intron in the "central deletion hot spot" of dystrophin gene].
    Pan S; Xie Y; Zhang C; Liu Z; Chen G; Lu X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun; 18(3):191-4. PubMed ID: 11402447
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45-55 of the Duchenne muscular dystrophy (DMD) gene.
    Miyazaki D; Yoshida K; Fukushima K; Nakamura A; Suzuki K; Sato T; Takeda S; Ikeda S
    J Hum Genet; 2009 Feb; 54(2):127-30. PubMed ID: 19158820
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A transposon-like element in the deletion-prone region of the dystrophin gene.
    Pizzuti A; Pieretti M; Fenwick RG; Gibbs RA; Caskey CT
    Genomics; 1992 Jul; 13(3):594-600. PubMed ID: 1322353
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.