108 related articles for article (PubMed ID: 16550498)
21. Rapid genotyping of known mutations and polymorphisms in beta-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes.
Li Q; Li LY; Huang SW; Li L; Chen XW; Zhou WJ; Xu XM
Clin Biochem; 2008 Jun; 41(9):681-7. PubMed ID: 18339318
[TBL] [Abstract][Full Text] [Related]
22. Novel mutations of dystrophin gene in DMD patients detected by rapid scanning in biplex exons DHPLC analysis.
Muscarella LA; Piemontese MR; Barbano R; Fazio A; Guarnieri V; Quattrone A; Zelante L
Biomol Eng; 2007 Jun; 24(2):231-6. PubMed ID: 17145200
[TBL] [Abstract][Full Text] [Related]
23. Multiplex capillary denaturing high-performance liquid chromatography with laser-induced fluorescence detection.
Xiao W; Stern D; Jain M; Huber CG; Oefner PJ
Biotechniques; 2001 Jun; 30(6):1332-8. PubMed ID: 11414227
[TBL] [Abstract][Full Text] [Related]
24. Use of denaturing HPLC to provide efficient detection of mutations causing guanidinoacetate methyltransferase deficiency.
Item CB; Stöckler-Ipsiroglu S; Willheim C; Mühl A; Bodamer OA
Mol Genet Metab; 2005; 86(1-2):328-34. PubMed ID: 16054853
[TBL] [Abstract][Full Text] [Related]
25. A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
van der Hout AH; van den Ouweland AM; van der Luijt RB; Gille HJ; Bodmer D; Brüggenwirth H; Mulder IM; van der Vlies P; Elfferich P; Huisman MT; ten Berge AM; Kromosoeto J; Jansen RP; van Zon PH; Vriesman T; Arts N; Lange MB; Oosterwijk JC; Meijers-Heijboer H; Ausems MG; Hoogerbrugge N; Verhoef S; Halley DJ; Vos YJ; Hogervorst F; Ligtenberg M; Hofstra RM
Hum Mutat; 2006 Jul; 27(7):654-66. PubMed ID: 16683254
[TBL] [Abstract][Full Text] [Related]
26. A single, multiplex analysis for all relevant activating NRAS gene mutations using heteroduplex generators.
Belli C; Bowen DJ; De Brasi C; Larripa I
Br J Haematol; 2004 Aug; 126(4):602-5. PubMed ID: 15287955
[TBL] [Abstract][Full Text] [Related]
27. Denaturing high-performance liquid chromatography for mutation detection and genotyping.
Fackenthal DL; Chen PX; Das S
Methods Mol Biol; 2005; 311():73-96. PubMed ID: 16100401
[TBL] [Abstract][Full Text] [Related]
28. SNP genotyping by heteroduplex analysis.
Paniego N; Fusari C; Lia V; Puebla A
Methods Mol Biol; 2015; 1245():141-50. PubMed ID: 25373754
[TBL] [Abstract][Full Text] [Related]
29. Technology to accelerate pangenomic scanning for unknown point mutations in exonic sequences: cycling temperature capillary electrophoresis (CTCE).
Ekstrøm PO; Bjørheim J; Thilly WG
BMC Genet; 2007 Aug; 8():54. PubMed ID: 17697348
[TBL] [Abstract][Full Text] [Related]
30. A versatile denaturing HPLC approach for human beta-globin gene mutation screening.
Bournazos SN; Tserga A; Patrinos GP; Papadakis MN
Am J Hematol; 2007 Feb; 82(2):168-70. PubMed ID: 16924651
[TBL] [Abstract][Full Text] [Related]
31. A rapid high-throughput method for the detection and quantification of RNA editing based on high-resolution melting of amplicons.
Chateigner-Boutin AL; Small I
Nucleic Acids Res; 2007; 35(17):e114. PubMed ID: 17726051
[TBL] [Abstract][Full Text] [Related]
32. Advantages of the high resolution melting in the detection of BRCA1 or BRCA2 mutation carriers.
Jiménez Ide J; Esteban Cardeñosa E; Palanca Suela S; González EB; Bolufer Gilabert P;
Clin Biochem; 2009 Oct; 42(15):1572-6. PubMed ID: 19616529
[TBL] [Abstract][Full Text] [Related]
33. Development of a denaturing high-performance liquid chromatography screening method for SMAD4 in juvenile polyposis syndrome.
Hatch SL; Trewick AL; Payne SJ
Ann Clin Biochem; 2007 Mar; 44(Pt 2):159-63. PubMed ID: 17362581
[TBL] [Abstract][Full Text] [Related]
34. Rapid genetic analysis of oculocutaneous albinism (OCA1) using denaturing high performance liquid chromatography (DHPLC) system.
Lin SY; Chien SC; Su YN; Lee CN; Chen CP
Prenat Diagn; 2006 May; 26(5):466-70. PubMed ID: 16570240
[TBL] [Abstract][Full Text] [Related]
35. Large genomic BRCA2 rearrangements and male breast cancer.
Karhu R; Laurila E; Kallioniemi A; Syrjäkoski K
Cancer Detect Prev; 2006; 30(6):530-4. PubMed ID: 17113724
[TBL] [Abstract][Full Text] [Related]
36. [Analysis of BRCA2 gene mutations among familial and/or early-onset breast cancer patients in eastern Shandong of China].
Ma ZL; Cao MZ; Li WF
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr; 25(2):195-8. PubMed ID: 18393245
[TBL] [Abstract][Full Text] [Related]
37. Efficient SNP analysis enabled by joint application of the muTGGE and heteroduplex methods.
Salimullah M; Hamano K; Tachibana M; Inoue K; Nishigaki K
Cell Mol Biol Lett; 2005; 10(2):237-45. PubMed ID: 16010289
[TBL] [Abstract][Full Text] [Related]
38. Mutation analysis of BRCA1 and BRCA2 from 793 Korean patients with sporadic breast cancer.
Han SH; Lee KR; Lee DG; Kim BY; Lee KE; Chung WS
Clin Genet; 2006 Dec; 70(6):496-501. PubMed ID: 17100994
[TBL] [Abstract][Full Text] [Related]
39. Validation of high-resolution DNA melting analysis for mutation scanning of the LMNA gene.
Millat G; Chanavat V; Julia S; Crehalet H; Bouvagnet P; Rousson R
Clin Biochem; 2009 Jun; 42(9):892-8. PubMed ID: 19318026
[TBL] [Abstract][Full Text] [Related]
40. Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis.
Hung CC; Lee CN; Chang CH; Jong YJ; Chen CP; Hsieh WS; Su YN; Lin WL
Clin Biochem; 2008 Feb; 41(3):162-6. PubMed ID: 18199430
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
