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90 related items for PubMed ID: 14642147

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. [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
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  • 4. [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
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  • 5. 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
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  • 7. 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 01; 40(2):294-304. PubMed ID: 9119397
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  • 8. 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 01; 80(5):523-30. PubMed ID: 12408970
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  • 9. 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 05; 232(1):314-21. PubMed ID: 8392588
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  • 10. [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 05; 18(3):191-4. PubMed ID: 11402447
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  • 11. [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 05; 76(11):852-4. PubMed ID: 9275539
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  • 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 05; 31(5):431-43. PubMed ID: 15478601
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  • 13. 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 May 05; 45(6):331-6. PubMed ID: 11185740
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  • 14. Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends.
    Chuzhanova N, Abeysinghe SS, Krawczak M, Cooper DN.
    Hum Mutat; 2003 Sep 05; 22(3):245-51. PubMed ID: 12938089
    [Abstract] [Full Text] [Related]

  • 15. In vitro splicing analysis showed that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G-->A mutations in introns of the dystrophin gene.
    Habara Y, Takeshima Y, Awano H, Okizuka Y, Zhang Z, Saiki K, Yagi M, Matsuo M.
    J Med Genet; 2009 Aug 05; 46(8):542-7. PubMed ID: 19001018
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  • 16. Patterns of deletions and the distribution of breakpoints in the dystrophin gene in Czech patients with Duchenne and Becker muscular dystrophy (statistical comparison with results from several other countries).
    Hrdlicka I, Zadina J, Krejcí R, Srbová A, Kucerová M.
    Folia Biol (Praha); 2001 Aug 05; 47(3):81-7. PubMed ID: 11409318
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  • 17. Mutation analysis in Duchenne and Becker muscular dystrophy patients from Bulgaria shows a peculiar distribution of breakpoints by intron.
    Todoroya A, Bronzova J, Miorin M, Rosa M, Kremensky I, Danieli GA.
    Am J Med Genet; 1996 Oct 02; 65(1):40-3. PubMed ID: 8914739
    [Abstract] [Full Text] [Related]

  • 18. 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 14; 242(2):401-6. PubMed ID: 9446807
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  • 19. Non Random Distribution of DMD Deletion Breakpoints and Implication of Double Strand Breaks Repair and Replication Error Repair Mechanisms.
    Marey I, Ben Yaou R, Deburgrave N, Vasson A, Nectoux J, Leturcq F, Eymard B, Laforet P, Behin A, Stojkovic T, Mayer M, Tiffreau V, Desguerre I, Boyer FC, Nadaj-Pakleza A, Ferrer X, Wahbi K, Becane HM, Claustres M, Chelly J, Cossee M.
    J Neuromuscul Dis; 2016 May 27; 3(2):227-245. PubMed ID: 27854212
    [Abstract] [Full Text] [Related]

  • 20. [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 27; 31(5):449-53. PubMed ID: 15478603
    [Abstract] [Full Text] [Related]

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