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 *

122 related articles for article (PubMed ID: 25449077)

  • 21. Splicing mutation of a gene within the Duchenne muscular dystrophy family.
    Zhu YB; Gan JH; Luo JW; Zheng XY; Wei SC; Hu D
    Genet Mol Res; 2016 Jul; 15(2):. PubMed ID: 27421007
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Novel mutation in exon 56 of the dystrophin gene in a child with Duchenne muscular dystrophy.
    Zhu JF; Liu HH; Zhou T; Tian L
    Int J Mol Med; 2013 Nov; 32(5):1166-70. PubMed ID: 24065205
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Coexistence of two distinct intragenic dystrophin deletions in two maternal cousins with Duchenne Muscular Dystrophy.
    Balci-Hayta B; Talim B; Dinçer P; Topaloğlu H
    Neuromuscul Disord; 2013 Jan; 23(1):15-8. PubMed ID: 22985905
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Study on Duchenne muscular dystrophy gene mutation and prenatal diagnosis].
    Feng SW; Liang YY; Cao JQ; Song XM; Zhang C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):36-9. PubMed ID: 23450476
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries.
    Nouri N; Fazel-Najafabadi E; Behnam M; Nouri N; Aryani O; Ghasemi M; Nasiri J; Sedghi M
    Gene; 2014 Feb; 535(2):250-4. PubMed ID: 24274981
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Paternal inheritance or a de novo mutation in a Duchenne Muscular Dystrophy pedigree from South India.
    Purushottam M; Murthy AR; Shubha GN; Gayathri N; Nalini A
    J Neurol Sci; 2008 May; 268(1-2):179-82. PubMed ID: 18031759
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing.
    Chen WJ; Lin QF; Zhang QJ; He J; Liu XY; Lin MT; Murong SX; Liou CW; Wang N
    Clin Chim Acta; 2013 Aug; 423():35-8. PubMed ID: 23588064
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation.
    Wibawa T; Takeshima Y; Mitsuyoshi I; Wada H; Surono A; Nakamura H; Matsuo M
    Brain Dev; 2000 Mar; 22(2):107-12. PubMed ID: 10722962
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Duchenne muscular dystrophy in a female patient with a karyotype of 46,X,i(X)(q10).
    Ou Z; Li S; Li Q; Chen X; Liu W; Sun X
    Tohoku J Exp Med; 2010 Oct; 222(2):149-53. PubMed ID: 20944443
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Identification of two novel insertion abnormal transcripts in two Chinese families affected with Dystrophinopathy.
    Xu Y; Song T; Li Y; Guo F; Jin X; Cheng L; Zheng J; Li C; Zhang Y; Chen B; Zhang J
    J Clin Lab Anal; 2020 Apr; 34(4):e23142. PubMed ID: 31793735
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center.
    Cho A; Seong MW; Lim BC; Lee HJ; Byeon JH; Kim SS; Kim SY; Choi SA; Wong AL; Lee J; Kim JS; Ryu HW; Lee JS; Kim H; Hwang H; Choi JE; Kim KJ; Hwang YS; Hong KH; Park S; Cho SI; Lee SJ; Park H; Seo SH; Park SS; Chae JH
    Muscle Nerve; 2017 May; 55(5):727-734. PubMed ID: 27593222
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Phenotype-genotype analysis of dystrophinopathy caused by duplication mutation in Dystrophin gene in an African patient.
    Peddareddygari LR; Pillai BH; Nochlin D; Sharer LR; Grewal RP
    Afr Health Sci; 2011 Dec; 11(4):607-9. PubMed ID: 22649443
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Diagnostic strategy for the detection of dystrophin gene mutations in asian patients and carriers using immortalized cell lines.
    Tay SK; Khng HH; Low PS; Lai PS
    J Child Neurol; 2006 Feb; 21(2):150-5. PubMed ID: 16566881
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.
    Zhang J; Ma D; Liu G; Wang Y; Liu A; Li L; Luo C; Hu P; Xu Z
    BMC Med Genet; 2019 Nov; 20(1):180. PubMed ID: 31727011
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine.
    Mohammed F; Elshafey A; Al-Balool H; Alaboud H; Al Ben Ali M; Baqer A; Bastaki L
    PLoS One; 2018; 13(5):e0197205. PubMed ID: 29847600
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Evaluation of point mutations in dystrophin gene in Iranian Duchenne and Becker muscular dystrophy patients: introducing three novel variants.
    Haghshenas M; Akbari MT; Karizi SZ; Deilamani FK; Nafissi S; Salehi Z
    J Genet; 2016 Jun; 95(2):325-9. PubMed ID: 27350676
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The First Comprehensive Cohort of the Duchenne Muscular Dystrophy in Iranian Population: Mutation Spectrum of 314 Patients and Identifying Two Novel Nonsense Mutations.
    Zamani G; Hosseini Bereshneh A; Azizi Malamiri R; Bagheri S; Moradi K; Ashrafi MR; Tavasoli AR; Mohammadi M; Badv RS; Ghahvechi Akbari M; Heidari M
    J Mol Neurosci; 2020 Oct; 70(10):1565-1573. PubMed ID: 32436198
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Application whole exome sequencing for the clinical molecular diagnosis of patients with Duchenne muscular dystrophy; identification of four novel nonsense mutations in four unrelated Chinese DMD patients.
    Zhang Y; Yang W; Wen G; Wu Y; Jing Z; Li D; Tang M; Liu G; Wei X; Zhong Y; Li Y; Deng Y
    Mol Genet Genomic Med; 2019 May; 7(5):e622. PubMed ID: 30938079
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Targeted exon skipping as a potential gene correction therapy for Duchenne muscular dystrophy.
    Aartsma-Rus A; Bremmer-Bout M; Janson AA; den Dunnen JT; van Ommen GJ; van Deutekom JC
    Neuromuscul Disord; 2002 Oct; 12 Suppl 1():S71-7. PubMed ID: 12206800
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.