BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 31333208)

  • 1. Molecular and Histopathological Characterization of Patients Presenting with the Duchenne Muscular Dystrophy Phenotype in a Tertiary Care Center in Southern India.
    Tallapaka K; Ranganath P; Ramachandran A; Uppin MS; Perala S; Aggarwal S; Lakshmi D; Meena AK; Dalal AB
    Indian Pediatr; 2019 Jul; 56(7):556-559. PubMed ID: 31333208
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A comparative study of mPCR, MLPA, and muscle biopsy results in a cohort of children with Duchenne muscular dystrophy: a first study.
    Manjunath M; Kiran P; Preethish-Kumar V; Nalini A; Singh RJ; Gayathri N
    Neurol India; 2015; 63(1):58-62. PubMed ID: 25751470
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Targeted sequencing of the
    Aravind S; Ashley B; Mannan A; Ganapathy A; Ramesh K; Ramachandran A; Nongthomba U; Shastry A
    Indian J Med Res; 2019 Sep; 150(3):282-289. PubMed ID: 31719299
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A resolved discrepancy between multiplex PCR and multiplex ligation-dependent probe amplification by targeted next-generation sequencing discloses a novel partial exonic deletion in the Duchenne muscular dystrophy gene.
    Liu C; Deng H; Yang C; Li X; Zhu Y; Chen X; Li H; Li S; Cui H; Zhang X; Tan X; Li D; Zhang Z
    J Clin Lab Anal; 2018 Oct; 32(8):e22575. PubMed ID: 29802662
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification.
    Dastur RS; Kachwala MY; Khadilkar SV; Hegde MR; Gaitonde PS
    Neurol India; 2011; 59(6):803-9. PubMed ID: 22234189
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community.
    Elhawary NA; Jiffri EH; Jambi S; Mufti AH; Dannoun A; Kordi H; Khogeer A; Jiffri OH; Elhawary AN; Tayeb MT
    Hum Genomics; 2018 Apr; 12(1):18. PubMed ID: 29631625
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic profile of Brazilian patients with dystrophinopathies.
    de Almeida PAD; Machado-Costa MC; Manzoli GN; Ferreira LS; Rodrigues MCS; Bueno LSM; Saute JAM; Pinto Vairo F; Matte US; Siebert M; Cossio SL; Macedo GS; Winckler PB; Becker MM; Magalhães LVB; Gonçalves MVM; Marrone CD; Nucci A; França MC
    Clin Genet; 2017 Aug; 92(2):199-203. PubMed ID: 28116794
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutation pattern in 606 Duchenne muscular dystrophy children with a comparison between familial and non-familial forms: a study in an Indian large single-center cohort.
    Polavarapu K; Preethish-Kumar V; Sekar D; Vengalil S; Nashi S; Mahajan NP; Thomas PT; Sadasivan A; Warrier M; Gupta A; Arunachal G; Debnath M; Keerthipriya MS; Pradeep-Chandra-Reddy C; Puttegowda A; John AP; Tavvala A; Gunasekaran S; Sathyaprabha TN; Chandra SR; Kramer B; Delhaas T; Nalini A
    J Neurol; 2019 Sep; 266(9):2177-2185. PubMed ID: 31139960
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Predominance of Dystrophinopathy Genotypes in Mexican Male Patients Presenting as Muscular Dystrophy with A Normal Multiplex Polymerase Chain Reaction
    Alcántara-Ortigoza MA; Reyna-Fabián ME; González-Del Angel A; Estandia-Ortega B; Bermúdez-López C; Cruz-Miranda GM; Ruíz-García M
    Genes (Basel); 2019 Oct; 10(11):. PubMed ID: 31671740
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic diagnosis of Duchenne and Becker muscular dystrophy using multiplex ligation-dependent probe amplification in Rwandan patients.
    Uwineza A; Hitayezu J; Murorunkwere S; Ndinkabandi J; Kalala Malu CK; Caberg JH; Dideberg V; Bours V; Mutesa L
    J Trop Pediatr; 2014 Apr; 60(2):112-7. PubMed ID: 24213305
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Genetic diagnosis of Duchenne/Becker muscular dystrophy by MLPA].
    Zhang Y; Liu X; He R; Ma H; Zhao Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):338-43. PubMed ID: 24928015
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Improved detection of deletions and duplications in the DMD gene using the multiplex ligation-dependent probe amplification (MLPA) method.
    Sansović I; Barišić I; Dumić K
    Biochem Genet; 2013 Apr; 51(3-4):189-201. PubMed ID: 23224783
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation Spectrum of Dystrophinopathies in India: Implications for Therapy.
    Kohli S; Saxena R; Thomas E; Singh K; Bijarnia Mahay S; Puri RD; Verma IC
    Indian J Pediatr; 2020 Jul; 87(7):495-504. PubMed ID: 32358784
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic analysis of the dystrophin gene in children with Duchenne and Becker muscular dystrophies.
    Zhong J; Xu T; Chen G; Liao H; Zhang J; Lan D
    Muscle Nerve; 2017 Jul; 56(1):117-121. PubMed ID: 27750387
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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; 26(3):318-22. PubMed ID: 19504448
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India.
    Deepha S; Vengalil S; Preethish-Kumar V; Polavarapu K; Nalini A; Gayathri N; Purushottam M
    BMC Med Genet; 2017 Jun; 18(1):67. PubMed ID: 28610567
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.