These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

291 related items for PubMed ID: 16793593

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

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. [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
    [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
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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 Nov; 45(6):331-6. PubMed ID: 11185740
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Southern blot and PCR analyses of dystrophin gene deletions in Japanese patients with Duchenne muscular dystrophy.
    Nakajima T, Matsuo M, Nakamura H, Fujiwara Y.
    Kobe J Med Sci; 1991 Feb; 37(1):21-33. PubMed ID: 1921260
    [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
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. [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 02; 76(11):852-4. PubMed ID: 9275539
    [Abstract] [Full Text] [Related]

  • 15. 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 02; 54(8):466-73. PubMed ID: 19609279
    [Abstract] [Full Text] [Related]

  • 16. Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation.
    Wilton SD, Johnsen RD, Pedretti JR, Laing NG.
    Am J Med Genet; 1993 Jun 15; 46(5):563-9. PubMed ID: 8322822
    [Abstract] [Full Text] [Related]

  • 17. Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. Online.
    Ikezawa M, Nishino I, Goto Y, Miike T, Nonaka I.
    Hum Mutat; 1999 Jun 15; 13(2):170. PubMed ID: 10094556
    [Abstract] [Full Text] [Related]

  • 18. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
    Li H, Ding J, Wang W, Chen Y, Lu W, Shao H, Wu BL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun 15; 26(3):318-22. PubMed ID: 19504448
    [Abstract] [Full Text] [Related]

  • 19. [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 15; 32(10):1392-5. PubMed ID: 9091412
    [Abstract] [Full Text] [Related]

  • 20. [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 15; 18(3):191-4. PubMed ID: 11402447
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.