BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

236 related articles for article (PubMed ID: 28363916)

  • 1. Analysis of CTG repeat length variation in the
    Ambrose KK; Ishak T; Lian LH; Goh KJ; Wong KT; Ahmad-Annuar A; Thong MK
    BMJ Open; 2017 Mar; 7(3):e010711. PubMed ID: 28363916
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Myotonic Dystrophy Type 1 Clinical, Electrophysiological and Molecular Characterization: Experience at Tertiary Care Centre.
    Khadilkar S; Jagiasi K; Yadav J; Chavan SV; Soni G; Patel B
    J Assoc Physicians India; 2017 Jun; 65(6):32-37. PubMed ID: 28782311
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program.
    Johnson NE; Butterfield RJ; Mayne K; Newcomb T; Imburgia C; Dunn D; Duval B; Feldkamp ML; Weiss RB
    Neurology; 2021 Feb; 96(7):e1045-e1053. PubMed ID: 33472919
    [TBL] [Abstract][Full Text] [Related]  

  • 4.
    Visconti VV; Macrì E; D'Apice MR; Centofanti F; Massa R; Novelli G; Botta A
    Int J Mol Sci; 2023 Jun; 24(12):. PubMed ID: 37373276
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Triplet-primed PCR is more sensitive than southern blotting-long PCR for the diagnosis of myotonic dystrophy type1.
    Addis M; Serrenti M; Meloni C; Cau M; Melis MA
    Genet Test Mol Biomarkers; 2012 Dec; 16(12):1428-31. PubMed ID: 23030650
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Single-Tube Dodecaplex PCR Panel of Polymorphic Microsatellite Markers Closely Linked to the
    Lian M; Zhao M; Lee CG; Chong SS
    Clin Chem; 2017 Jun; 63(6):1127-1140. PubMed ID: 28428361
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Distribution of CTG repeats at the DMPK gene in myotonic dystrophy patients and healthy individuals from the Mexican population.
    Magaña JJ; Cortés-Reynosa P; Escobar-Cedillo R; Gómez R; Leyva-García N; Cisneros B
    Mol Biol Rep; 2011 Feb; 38(2):1341-6. PubMed ID: 20635151
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fuchs' Endothelial Corneal Dystrophy in Patients With Myotonic Dystrophy, Type 1.
    Winkler NS; Milone M; Martinez-Thompson JM; Raja H; Aleff RA; Patel SV; Fautsch MP; Wieben ED; Baratz KH
    Invest Ophthalmol Vis Sci; 2018 Jun; 59(7):3053-3057. PubMed ID: 30025114
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Modification of the triplet repeat primed polymerase chain reaction method for detection of the CTG repeat expansion in myotonic dystrophy type 1: application in preimplantation genetic diagnosis.
    Kakourou G; Dhanjal S; Mamas T; Serhal P; Delhanty JD; SenGupta SB
    Fertil Steril; 2010 Oct; 94(5):1674-9. PubMed ID: 20171614
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CTG repeat lengths of the DMPK gene in myotonic dystrophy patients compared to healthy controls in Thailand.
    Theerasasawat S; Papsing C; Pulkes T
    J Clin Neurosci; 2010 Dec; 17(12):1520-2. PubMed ID: 20801043
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Investigation of molecular diagnosis in Chinese patients with myotonic dystrophy type 1.
    Li M; Wang Z; Cui F; Yang F; Chen Z; Ling L; Pu C; Huang X
    Chin Med J (Engl); 2014; 127(6):1084-8. PubMed ID: 24622439
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fuchs' Endothelial Corneal Dystrophy and RNA Foci in Patients With Myotonic Dystrophy.
    Mootha VV; Hansen B; Rong Z; Mammen PP; Zhou Z; Xing C; Gong X
    Invest Ophthalmol Vis Sci; 2017 Sep; 58(11):4579-4585. PubMed ID: 28886202
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions.
    Pešović J; Perić S; Brkušanin M; Brajušković G; Rakočević-Stojanović V; Savić-Pavićević D
    Neurogenetics; 2017 Dec; 18(4):207-218. PubMed ID: 28942489
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in the Korean population.
    Kwon MJ; Lee ST; Kim BJ; Sung DH; Kim JW; Ki CS
    Ann Clin Lab Sci; 2010; 40(2):156-62. PubMed ID: 20421627
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1.
    Ballester-Lopez A; Linares-Pardo I; Koehorst E; Núñez-Manchón J; Pintos-Morell G; Coll-Cantí J; Almendrote M; Lucente G; Arbex A; Magaña JJ; Murillo-Melo NM; Lucia A; Monckton DG; Cumming SA; Ramos-Fransi A; Martínez-Piñeiro A; Nogales-Gadea G
    Genes (Basel); 2020 Jul; 11(7):. PubMed ID: 32645888
    [TBL] [Abstract][Full Text] [Related]  

  • 16. DM1 Phenotype Variability and Triplet Repeat Instability: Challenges in the Development of New Therapies.
    Tomé S; Gourdon G
    Int J Mol Sci; 2020 Jan; 21(2):. PubMed ID: 31936870
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Robust and accurate detection and sizing of repeats within the DMPK gene using a novel TP-PCR test.
    Leferink M; Wong DPW; Cai S; Yeo M; Ho J; Lian M; Kamsteeg EJ; Chong SS; Haer-Wigman L; Guan M
    Sci Rep; 2019 Jun; 9(1):8280. PubMed ID: 31164682
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution.
    Murillo-Melo NM; Márquez-Quiróz LC; Gómez R; Orozco L; Mendoza-Caamal E; Tapia-Guerrero YS; Camacho-Mejorado R; Cortés H; López-Reyes A; Santana C; Noris G; Hernández-Hernández O; Cisneros B; Magaña JJ
    Neuromuscul Disord; 2017 Dec; 27(12):1106-1114. PubMed ID: 29054426
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Non-radioactive PCR southern method for analysis of CTG repeat in myotonic dystrophy].
    Kozuka N; Tachi N; Ohya K; Uchida E; Kikuchi S; Sengoku Y
    No To Hattatsu; 2003 Sep; 35(5):380-7. PubMed ID: 13677946
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans.
    Kim SY; Kim JY; Kim GP; Sung JJ; Lim KS; Lee KW; Chae JH; Hong YH; Seong MW; Park SS
    Korean J Lab Med; 2008 Dec; 28(6):483-92. PubMed ID: 19127114
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.