173 related articles for article (PubMed ID: 15140060)
1. Tumour necrosis factor receptor superfamily member 6 gene mutation detection by denaturing high-performance liquid chromatography.
Etokebe GE; Abrahamsen TG; Bogen B; Spurkland A
Scand J Immunol; 2004 May; 59(5):496-503. PubMed ID: 15140060
[TBL] [Abstract][Full Text] [Related]
2. Evaluation of denaturing high-performance liquid chromatography as a rapid detection method for identification of epidermal growth factor receptor mutations in nonsmall-cell lung cancer.
Cohen V; Agulnik JS; Jarry J; Batist G; Small D; Kreisman H; Tejada NA; Miller WH; Chong G
Cancer; 2006 Dec; 107(12):2858-65. PubMed ID: 17096434
[TBL] [Abstract][Full Text] [Related]
3. Detection of alpha-galactosidase a mutations causing Fabry disease by denaturing high performance liquid chromatography.
Shabbeer J; Robinson M; Desnick RJ
Hum Mutat; 2005 Mar; 25(3):299-305. PubMed ID: 15712228
[TBL] [Abstract][Full Text] [Related]
4. Evaluation of denaturing high performance liquid chromatography for the mutational analysis of the MEN1 gene.
Crépin M; Pigny P; Escande F; Bauters CC; Calender A; Lefevre S; Buisine MP; Porchet N; Odou MF
J Mol Endocrinol; 2006 Apr; 36(2):369-76. PubMed ID: 16595707
[TBL] [Abstract][Full Text] [Related]
5. Evaluation of denaturing high performance liquid chromatography (DHPLC) for the mutational analysis of the neurofibromatosis type 1 ( NF1) gene.
Han SS; Cooper DN; Upadhyaya MN
Hum Genet; 2001 Nov; 109(5):487-97. PubMed ID: 11735023
[TBL] [Abstract][Full Text] [Related]
6. A high-throughput denaturing high-performance liquid chromatography method for the identification of variant alleles associated with dihydropyrimidine dehydrogenase deficiency.
Ezzeldin H; Okamoto Y; Johnson MR; Diasio RB
Anal Biochem; 2002 Jul; 306(1):63-73. PubMed ID: 12069415
[TBL] [Abstract][Full Text] [Related]
7. [Denaturing high-performance liquid chromatography for screening antithrombin III gene mutation and polymorphisms in patients with cerebral venous thrombosis].
Wang LP; Qiu YW; Yin AL; Ma YY; Liu KL; Xiong L; Yu YH; Zhong M; Wang C
Nan Fang Yi Ke Da Xue Xue Bao; 2009 Oct; 29(10):1982-6. PubMed ID: 19861246
[TBL] [Abstract][Full Text] [Related]
8. A comparison of high-resolution melting analysis with denaturing high-performance liquid chromatography for mutation scanning: cystic fibrosis transmembrane conductance regulator gene as a model.
Chou LS; Lyon E; Wittwer CT
Am J Clin Pathol; 2005 Sep; 124(3):330-8. PubMed ID: 16191501
[TBL] [Abstract][Full Text] [Related]
9. Use of the denaturing gradient gel electrophoresis (DGGE) method for mutational screening of patients with familial hypercholesterolaemia (FH) and Familial defective apolipoprotein B100 (FDB).
Azian M; Hapizah MN; Khalid BA; Khalid Y; Rosli A; Jamal R
Malays J Pathol; 2006 Jun; 28(1):7-15. PubMed ID: 17694954
[TBL] [Abstract][Full Text] [Related]
10. Rapid detection of beta-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC.
Su YN; Lee CN; Hung CC; Chen CA; Cheng WF; Tsao PN; Yu CL; Hsieh FJ
Hum Mutat; 2003 Oct; 22(4):326-36. PubMed ID: 12955718
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography.
Biggin A; Henke R; Bennetts B; Thorburn DR; Christodoulou J
Mol Genet Metab; 2005 Jan; 84(1):61-74. PubMed ID: 15639196
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Blind analysis of denaturing high-performance liquid chromatography as a tool for mutation detection.
O'Donovan MC; Oefner PJ; Roberts SC; Austin J; Hoogendoorn B; Guy C; Speight G; Upadhyaya M; Sommer SS; McGuffin P
Genomics; 1998 Aug; 52(1):44-9. PubMed ID: 9740670
[TBL] [Abstract][Full Text] [Related]
15. Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone disease.
Yu B; Sawyer NA; Caramins M; Yuan ZG; Saunderson RB; Pamphlett R; Richmond DR; Jeremy RW; Trent RJ
J Clin Pathol; 2005 May; 58(5):479-85. PubMed ID: 15858117
[TBL] [Abstract][Full Text] [Related]
16. Evaluation of dHPLC in mutation screening of the APC gene in a Greek FAP cohort.
Mihalatos M; Apessos A; Triantafillidis JK; Kosmidis PA; Fountzilas G; Agnantis NJ; Yannoukakos D; Nasioulas G
Anticancer Res; 2003; 23(3B):2691-5. PubMed ID: 12894559
[TBL] [Abstract][Full Text] [Related]
17. Rapid and accurate detection of atypical and Kalow variants in the butyrylcholinesterase gene using denaturing high performance liquid chromatography.
Levano S; Keller D; Schobinger E; Urwyler A; Girard T
Anesth Analg; 2008 Jan; 106(1):147-51, table of contents. PubMed ID: 18165570
[TBL] [Abstract][Full Text] [Related]
18. Mutation detection in congenital long QT syndrome: cardiac channel gene screen using PCR, dHPLC, and direct DNA sequencing.
Tester DJ; Will ML; Ackerman MJ
Methods Mol Med; 2006; 128():181-207. PubMed ID: 17071997
[TBL] [Abstract][Full Text] [Related]
19. Comparative analysis of the HV1 and HV2 regions of human mitochondrial DNA by denaturing high-performance liquid chromatography.
Kristinsson R; Lewis SE; Danielson PB
J Forensic Sci; 2009 Jan; 54(1):28-36. PubMed ID: 19120825
[TBL] [Abstract][Full Text] [Related]
20. Detection of C677T mutation in methylenetetrahydrofolate reductase gene by denaturing high performance liquid chromatography.
Fang N; Lin L; Ren J; Wu D
Biomed Chromatogr; 2004 Nov; 18(9):625-9. PubMed ID: 15386507
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]