163 related articles for article (PubMed ID: 16792511)
1. Simple procedure for automatic detection of unstable alleles in the myotonic dystrophy and Huntington's disease loci.
Falk M; Vojtísková M; Lukás Z; Kroupová I; Froster U
Genet Test; 2006; 10(2):85-97. PubMed ID: 16792511
[TBL] [Abstract][Full Text] [Related]
2. [Methods of determination of the number of CTG/CAG repeats in trinucleotide repeats in the human genome].
Falk M; Froster U; Vojtísková M
Cas Lek Cesk; 2003; 142(10):609-14. PubMed ID: 14635426
[TBL] [Abstract][Full Text] [Related]
3. A simple and rapid analysis of triplet repeat diseases by expand long PCR.
Hećimović S; Vlasić J; Barisić L; Marković D; Culić V; Pavelić K
Clin Chem Lab Med; 2001 Dec; 39(12):1259-62. PubMed ID: 11798087
[TBL] [Abstract][Full Text] [Related]
4. No association of the SCA1 (CAG)31 allele with Huntington's disease, myotonic dystrophy type 1 and spinocerebellar ataxia type 3.
Hellenbroich Y; Kaulich M; Opitz S; Schwinger E; Zühlke C
Psychiatr Genet; 2004 Jun; 14(2):61-3. PubMed ID: 15167689
[TBL] [Abstract][Full Text] [Related]
5. Huntington Disease: Molecular Diagnostics Approach.
Bastepe M; Xin W
Curr Protoc Hum Genet; 2015 Oct; 87():9.26.1-9.26.23. PubMed ID: 26439718
[TBL] [Abstract][Full Text] [Related]
6. Enhanced Detection and Sizing of the HTT CAG Repeat Expansion in Huntington Disease Using an Improved Triplet-Primed PCR Assay.
Zhao M; Lee CG; Law HY; Chong SS
Neurodegener Dis; 2016; 16(5-6):348-51. PubMed ID: 27207688
[TBL] [Abstract][Full Text] [Related]
7. Results on single cell PCR for Huntington's gene and WAVE product analysis for preimplantation genetic diagnosis.
Drury KC; Liu MC; Lilleberg S; Kipersztok S; Williams RS
Mol Cell Endocrinol; 2001 Oct; 183 Suppl 1():S1-4. PubMed ID: 11576724
[TBL] [Abstract][Full Text] [Related]
8. Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: use of internal standards.
Williams LC; Hegde MR; Herrera G; Stapleton PM; Love DR
Mol Cell Probes; 1999 Aug; 13(4):283-9. PubMed ID: 10441201
[TBL] [Abstract][Full Text] [Related]
9. Characterization of large CTG repeat expansions in myotonic dystrophy alleles using PCR.
Cheng S; Barceló JM; Korneluk RG
Hum Mutat; 1996; 7(4):304-10. PubMed ID: 8723679
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Single-step scalable-throughput molecular screening for Huntington disease.
Teo CR; Wang W; Yang Law H; Lee CG; Chong SS
Clin Chem; 2008 Jun; 54(6):964-72. PubMed ID: 18403567
[TBL] [Abstract][Full Text] [Related]
13. Single-cell analysis of unstable genes.
Daniels R; Holding C; Kontogianni E; Monk M
J Assist Reprod Genet; 1996 Feb; 13(2):163-9. PubMed ID: 8688590
[TBL] [Abstract][Full Text] [Related]
14. Novel heat pulse extension-PCR-based method for detection of large CTG-repeat expansions in myotonic dystrophy type 1.
Orpana AK; Ho TH; Alagrund K; Ridanpää M; Aittomäki K; Stenman J
J Mol Diagn; 2013 Jan; 15(1):110-5. PubMed ID: 23159592
[TBL] [Abstract][Full Text] [Related]
15. Improved high sensitivity screen for Huntington disease using a one-step triplet-primed PCR and melting curve assay.
Zhao M; Cheah FSH; Chen M; Lee CG; Law HY; Chong SS
PLoS One; 2017; 12(7):e0180984. PubMed ID: 28700716
[TBL] [Abstract][Full Text] [Related]
16. A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms.
Chheda P; Chanekar M; Salunkhe Y; Dama T; Pais A; Pande S; Bendre R; Shah N
Mol Diagn Ther; 2018 Jun; 22(3):353-359. PubMed ID: 29619771
[TBL] [Abstract][Full Text] [Related]
17. Null alleles at the Huntington disease locus: implications for diagnostics and CAG repeat instability.
Williams LC; Hegde MR; Nagappan R; Faull RL; Giles J; Winship I; Snow K; Love DR
Genet Test; 2000; 4(1):55-60. PubMed ID: 10794362
[TBL] [Abstract][Full Text] [Related]
18. Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.
Redman JB; Fenwick RG; Fu YH; Pizzuti A; Caskey CT
JAMA; 1993 Apr; 269(15):1960-5. PubMed ID: 8464127
[TBL] [Abstract][Full Text] [Related]
19. Fast Assays to Detect Interruptions in CTG.CAG Repeat Expansions.
Tomé S; Gourdon G
Methods Mol Biol; 2020; 2056():11-23. PubMed ID: 31586339
[TBL] [Abstract][Full Text] [Related]
20. A general method for the detection of large CAG repeat expansions by fluorescent PCR.
Warner JP; Barron LH; Goudie D; Kelly K; Dow D; Fitzpatrick DR; Brock DJ
J Med Genet; 1996 Dec; 33(12):1022-6. PubMed ID: 9004136
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
