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Volumn 50, Issue 8, 2004, Pages 1417-1420

Convenient single-nucleotide polymorphism typing from whole blood by probe extension and bioluminescence detection

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); GENOMIC DNA; LUCIFERASE; LUCIFERIN; STREPTAVIDIN; TAQ POLYMERASE;

EID: 3242785669     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1373/clinchem.2004.031500     Document Type: Article
Times cited : (2)

References (10)
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    • The International SNP Map Working Group. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 2001;409:928-33.
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  • 2
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    • Thorisson GA, Stein LD. The SNP Consortium website: past, present and future. Nucleic Acids Res 2003;31:124-7.
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    • Thorisson, G.A.1    Stein, L.D.2
  • 3
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    • Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER)
    • Zhou GH, Kamahori M, Okano K, Chuan G, Harada K, Kambara H. Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER). Nucleic Acids Res 2001;29:E93.
    • (2001) Nucleic Acids Res , vol.29
    • Zhou, G.H.1    Kamahori, M.2    Okano, K.3    Chuan, G.4    Harada, K.5    Kambara, H.6
  • 4
    • 3242751533 scopus 로고    scopus 로고
    • BAMPER (Bioluminometric Assay coupled with Modified Primer Extension Reactions): A new multiplex SNP genotyping method being operated in one tube with double-stranded DNAs as templates
    • HGM2002. April Shanghai, China
    • Zhou GH, Shirakura H, Kamahori M, Okano K, Nagai K, Kambara H. BAMPER (Bioluminometric Assay coupled with Modified Primer Extension Reactions): a new multiplex SNP genotyping method being operated in one tube with double-stranded DNAs as templates [Abstract]. HUGO'S 7th Human Genome Meeting, HGM2002. April 2002, Shanghai, China. http://hgm2002.hgu. mrc.ac.uk/Abstracts/Publish/ WorkshopPosters/WorkshopPoster12/hgm0654. htm (accessed June 2004).
    • (2002) HUGO'S 7th Human Genome Meeting
    • Zhou, G.H.1    Shirakura, H.2    Kamahori, M.3    Okano, K.4    Nagai, K.5    Kambara, H.6
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    • Characteristics of selective polymerase chain reaction (PCR) using two-base anchored primers and improvement of its specificity
    • Okano K, Uematsu C, Matsunaga H, Kambara H. Characteristics of selective polymerase chain reaction (PCR) using two-base anchored primers and improvement of its specificity. Electrophoresis 1998;19:3071-8.
    • (1998) Electrophoresis , vol.19 , pp. 3071-3078
    • Okano, K.1    Uematsu, C.2    Matsunaga, H.3    Kambara, H.4
  • 8
    • 0033105975 scopus 로고    scopus 로고
    • An enzymatic cycling method using pyruvate orthophosphate dikinase and firefly luciferase for the simultaneous determination of ATP and AMP (RNA)
    • Sakakibara T, Murakami S, Eisaki N, Nakajima M, Imai K. An enzymatic cycling method using pyruvate orthophosphate dikinase and firefly luciferase for the simultaneous determination of ATP and AMP (RNA). Anal Biochem 1999;268:94-101.
    • (1999) Anal Biochem , vol.268 , pp. 94-101
    • Sakakibara, T.1    Murakami, S.2    Eisaki, N.3    Nakajima, M.4    Imai, K.5
  • 9
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    • High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
    • Buetow KH, Edmonson M, MacDonald R, Clifford R, Yip P, Kelley J, et al. High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Proc Natl Acad Sci U S A 2001;98:581-4.
    • (2001) Proc Natl Acad Sci U S A , vol.98 , pp. 581-584
    • Buetow, K.H.1    Edmonson, M.2    MacDonald, R.3    Clifford, R.4    Yip, P.5    Kelley, J.6
  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.