194 related articles for article (PubMed ID: 16924651)
1. 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]
2. Reliability of DHPLC in mutational screening of beta-globin (HBB) alleles.
Colosimo A; Guida V; De Luca A; Cappabianca MP; Bianco I; Palka G; Dallapiccola B
Hum Mutat; 2002 Mar; 19(3):287-95. PubMed ID: 11857746
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. [Accurate and rapid prenatal diagnosis of beta-thalassemia by a multiplex primer extension and denaturing high-performance liquid chromatography technique].
Hua L; Zhu H; Li XR; Li J; Mo QH; Liao C; Hou YX; Zhong M; Xu XM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):600-3. PubMed ID: 15583991
[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. Agamma-haplotypes: a new group of genetic markers for thalassemic mutations inside the 5' regulatory region of the human Agamma-globin gene.
Patrinos GP; Kollia P; Papapanagiotou E; Loutradi-Anagnostou A; Loukopoulos D; Papadakis MN
Am J Hematol; 2001 Feb; 66(2):99-104. PubMed ID: 11421306
[TBL] [Abstract][Full Text] [Related]
8. A comprehensive scanning method for rapid detection of beta-globin gene mutations and polymorphisms.
Ghanem N; Girodon E; Vidaud M; Martin J; Fanen P; Plassa F; Goossens M
Hum Mutat; 1992; 1(3):229-39. PubMed ID: 1301930
[TBL] [Abstract][Full Text] [Related]
9. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
Garewal G; Das R; Awasthi A; Ahluwalia J; Marwaha RK
Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
[TBL] [Abstract][Full Text] [Related]
10. Accurate and rapid prenatal diagnosis of the most frequent East Mediterranean beta-thalassemia mutations.
Naja RP; Kaspar H; Shbaklo H; Chakar N; Makhoul NJ; Zalloua PA
Am J Hematol; 2004 Apr; 75(4):220-4. PubMed ID: 15054814
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Denaturing HPLC for mutation screening.
Mitchell M; Cutler J
Methods Mol Biol; 2011; 688():17-33. PubMed ID: 20938830
[TBL] [Abstract][Full Text] [Related]
14. [A rare transcription mutation (-90 C-->T) in a Chinese family with beta-thalassemia].
Li WJ; Lao XW; Jai SQ; Liang FA; Mo QH; Ma JY; Xu XM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec; 20(6):468-70. PubMed ID: 14669211
[TBL] [Abstract][Full Text] [Related]
15. Rapid detection of beta-Thalassemia alleles in Egypt using naturally or amplified created restriction sites and direct sequencing: a step in disease control.
Hussein G; Fawzy M; Serafi TE; Ismail EF; Metwally DE; Saber MA; Giansily M; Schved JF; Pissard S; Martinez PA
Hemoglobin; 2007; 31(1):49-62. PubMed ID: 17365005
[TBL] [Abstract][Full Text] [Related]
16. Enhanced detection of TP53 mutations using a GC-clamp in denaturing high performance liquid chromatography.
Greiner TC
Diagn Mol Pathol; 2007 Mar; 16(1):32-7. PubMed ID: 17471156
[TBL] [Abstract][Full Text] [Related]
17. The molecular heterogeneity of beta-thalassemia in Greece.
Boussiou M; Karababa P; Sinopoulou K; Tsaftaridis P; Plata E; Loutradi-Anagnostou A
Blood Cells Mol Dis; 2008; 40(3):317-9. PubMed ID: 18096416
[TBL] [Abstract][Full Text] [Related]
18. Denaturing HPLC-based approach for detection of COL7A1 gene mutations causing dystrophic epidermolysis bullosa.
Posteraro P; Pascucci M; Colombi M; Barlati S; Giannetti A; Paradisi M; Mustonen A; Zambruno G; Castiglia D
Biochem Biophys Res Commun; 2005 Dec; 338(3):1391-401. PubMed ID: 16271705
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
El-Gawhary S; El-Shafie S; Niazi M; Aziz M; El-Beshlawy A
Hemoglobin; 2007; 31(1):63-9. PubMed ID: 17365006
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
