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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 16834926)

  • 1. A different spectrum of DMD gene mutations in local Chinese patients with Duchenne/Becker muscular dystrophy.
    Lo IF; Lai KK; Tong TM; Lam ST
    Chin Med J (Engl); 2006 Jul; 119(13):1079-87. PubMed ID: 16834926
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Mutation screening of 433 families with Duchenne/Becker muscular dystrophy].
    Bai Y; Li S; Zong YN; Li XL; Zhao ZH; Kong XD
    Zhonghua Yi Xue Za Zhi; 2016 Apr; 96(16):1261-9. PubMed ID: 27122458
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exon deletion patterns of the dystrophin gene in 82 Vietnamese Duchenne/Becker muscular dystrophy patients.
    Tran VK; Ta VT; Vu DC; Nguyen ST; Do HN; Ta MH; Tran TH; Matsuo M
    J Neurogenet; 2013 Dec; 27(4):170-5. PubMed ID: 24099565
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients.
    Lee T; Takeshima Y; Kusunoki N; Awano H; Yagi M; Matsuo M; Iijima K
    J Hum Genet; 2014 Jan; 59(1):46-50. PubMed ID: 24225992
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic analysis of 1051 Chinese families with Duchenne/Becker Muscular Dystrophy.
    Kong X; Zhong X; Liu L; Cui S; Yang Y; Kong L
    BMC Med Genet; 2019 Aug; 20(1):139. PubMed ID: 31412794
    [TBL] [Abstract][Full Text] [Related]  

  • 6. MLPA Analyses Reveal a Spectrum of Dystrophin Gene Deletions/Duplications in Pakistani Patients Suspected of Having Duchenne/Becker Muscular Dystrophy: A Retrospective Study.
    Ansar Z; Nasir A; Moatter T; Khan S; Kirmani S; Ibrahim S; Imam K; Ather A; Samreen A; Hasan Z
    Genet Test Mol Biomarkers; 2019 Jul; 23(7):468-472. PubMed ID: 31157985
    [No Abstract]   [Full Text] [Related]  

  • 7. The X-linked Becker muscular dystrophy (bmx) mouse models Becker muscular dystrophy via deletion of murine dystrophin exons 45-47.
    Heier CR; McCormack NM; Tully CB; Novak JS; Newell-Stamper BL; Russell AJ; Fiorillo AA
    J Cachexia Sarcopenia Muscle; 2023 Apr; 14(2):940-954. PubMed ID: 36628607
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials.
    Anthony K; Cirak S; Torelli S; Tasca G; Feng L; Arechavala-Gomeza V; Armaroli A; Guglieri M; Straathof CS; Verschuuren JJ; Aartsma-Rus A; Helderman-van den Enden P; Bushby K; Straub V; Sewry C; Ferlini A; Ricci E; Morgan JE; Muntoni F
    Brain; 2011 Dec; 134(Pt 12):3547-59. PubMed ID: 22102647
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to exon 44 or 45 skipping.
    Anthony K; Arechavala-Gomeza V; Ricotti V; Torelli S; Feng L; Janghra N; Tasca G; Guglieri M; Barresi R; Armaroli A; Ferlini A; Bushby K; Straub V; Ricci E; Sewry C; Morgan J; Muntoni F
    JAMA Neurol; 2014 Jan; 71(1):32-40. PubMed ID: 24217213
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multiplex ligation-dependent probe amplification identification of deletions and duplications of the Duchenne muscular dystrophy gene in Taiwanese subjects.
    Hwa HL; Chang YY; Chen CH; Kao YS; Jong YJ; Chao MC; Ko TM
    J Formos Med Assoc; 2007 May; 106(5):339-46. PubMed ID: 17561468
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach.
    Freund AA; Scola RH; Arndt RC; Lorenzoni PJ; Kay CK; Werneck LC
    Arq Neuropsiquiatr; 2007 Mar; 65(1):73-6. PubMed ID: 17420831
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patients.
    Todorova A; Todorov T; Georgieva B; Lukova M; Guergueltcheva V; Kremensky I; Mitev V
    Neuromuscul Disord; 2008 Aug; 18(8):667-70. PubMed ID: 18653336
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comprehensive genetic characteristics of dystrophinopathies in China.
    Ma P; Zhang S; Zhang H; Fang S; Dong Y; Zhang Y; Hao W; Wu S; Zhao Y
    Orphanet J Rare Dis; 2018 Jul; 13(1):109. PubMed ID: 29973226
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular Analysis-Based Genetic Characterization of a Cohort of Patients with Duchenne and Becker Muscular Dystrophy in Eastern China.
    Zhao HH; Sun XP; Shi MC; Yi YX; Cheng H; Wang XX; Xu QC; Ma HM; Wu HQ; Jin QW; Niu Q
    Chin Med J (Engl); 2018 Apr; 131(7):770-775. PubMed ID: 29578119
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic analysis of dystrophin gene for affected male and female carriers with Duchenne/Becker muscular dystrophy in Korea.
    Lee BL; Nam SH; Lee JH; Ki CS; Lee M; Lee J
    J Korean Med Sci; 2012 Mar; 27(3):274-80. PubMed ID: 22379338
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MLPA based detection of mutations in the dystrophin gene of 180 Polish families with Duchenne/Becker muscular dystrophy.
    Zimowski JG; Massalska D; Holding M; Jadczak S; Fidziańska E; Lusakowska A; Kostera-Pruszczyk A; Kamińska A; Zaremba J
    Neurol Neurochir Pol; 2014; 48(6):416-22. PubMed ID: 25482253
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiplex Ligation-Dependent Probe Amplification in X-linked Recessive Muscular Dystrophy in Korean Subjects.
    Suh MR; Lee KA; Kim EY; Jung J; Choi WA; Kang SW
    Yonsei Med J; 2017 May; 58(3):613-618. PubMed ID: 28332368
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Causes of clinical variability in Duchenne and Becker muscular dystrophies and implications for exon skipping therapies.
    Hoffman EP
    Acta Myol; 2020 Dec; 39(4):179-186. PubMed ID: 33458572
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Central nervous system involvements in Duchenne/Becker muscular dystrophy].
    Kumagai T; Miura K; Ohki T; Matsumoto A; Miyazaki S; Nakamura M; Ochi N; Takahashi O
    No To Hattatsu; 2001 Nov; 33(6):480-6. PubMed ID: 11725514
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis.
    Murugan S; Chandramohan A; Lakshmi BR
    Indian J Med Res; 2010 Sep; 132():303-11. PubMed ID: 20847377
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.