Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid
Reexamination Certificate
2007-03-13
2007-03-13
Horlick, Kenneth R. (Department: 1637)
Chemistry: molecular biology and microbiology
Measuring or testing process involving enzymes or...
Involving nucleic acid
C435S091200, C435S091510
Reexamination Certificate
active
10370884
ABSTRACT:
The present invention relates to methods for identifying variations that occur in the genome of an organism. In particular, the present invention relates to identifying variations without the need for specialized oligonucleotides complementary to each SNP and without a priori knowledge of the sequence or position of the variants.
REFERENCES:
patent: 5270184 (1993-12-01), Walker et al.
patent: 5556750 (1996-09-01), Modrich et al.
patent: 5571676 (1996-11-01), Shuber
patent: 5707806 (1998-01-01), Shuber
patent: 6008031 (1999-12-01), Modrich et al.
patent: 6048696 (2000-04-01), Hoffman et al.
patent: 6110684 (2000-08-01), Kemper et al.
patent: 6277578 (2001-08-01), Shultz et al.
patent: 6322988 (2001-11-01), Dawson et al.
patent: 6548247 (2003-04-01), Chirikjian et al.
Nicholl I.D. et al., “Reconstitution of human base excision repair with purified proteins”,Biochemistry, Jun. 17, 1997, vol. 36, No. 24. pp. 7557-7566.
Dianov G. et al., “Reconstitution of the DNA base excision-repair pathway”,Current Biology, CB. Dec. 1, 1994, vol. 4, No. 122, pp. 1069-1076.
Dianov G. et al., “Generation of single-nucleotide repair patches following excision of uracil residues from DNA”,Molecular And Cellular Biology, Apr. 1992, vol. 12, No. 4, pp. 1605-1612.
Zhang, Y. et al, “An amplification and ligation-based method to scan for unknown mutations in DNA”,Human MutationAug. 2002, vol. 20, No. 2, pp. 139-147.
McCullough A.K. et al., Initiation of base excision repair: glycosylase mechanisms and structures,Annual Review of Biochemistry, 1999, vol. 68, pp. 255-285.
Bioteux S. et al., “The human OGG1 gene: Structure, functions, and its implication in the process of carcinogenesis ”,Archives of Biochemistry And Biophysics, New York, US, vol. 377, No. 1, pp. 1-8.
PCT Search Report, Aug. 6, 2004.
Evans et al., “Going APE over ref-1”,Elsevier, 461:83-108 (2000).
Hall et al., “Sensitive detection of DNA polymorphisms by the serial invasive signal amplification reaction”,PNAS, 97:8272-8277 (2000).
Schweitzer and Kingsmore, “Combining nucleic acid amplification and detection”,Current Opinion in Biology, 12:21-27 (2001).
Kota et al., “Application of denaturing high-performance liquid chromatography for mapping of single nucleotide polymorphisms in barley (Hordeum vulgareL.)”,Genome, 44:523-528 (2001).
Arnold et al., “One-Step Fluorescent Probe Product-Enhanced Reverse Transcriptase Assay”,BioTechniques, 25:98-106 (1998).
McCullough et al., “Initiation of Base Excision Repair: Glycosylase Mechanisms And Structures”,Annu. Rev. Biochem, 68:255-285 (1999).
Williams and David, Evidence that MutY is a monofuctional glycosylase capable of forming a covalent Schiff base intermediate with substrate DNA, Nucleic Acids Research.
Sancar, “DNA Excision Repair”,Annu. Rev. Biochem., 65:43-81 (1996).
Hessner et al., “Genotyping of Factor VG1691A (Leiden) without the Use of PCR by Invasive Cleavage of Oligonucleotide Probes”,Clinical Chemistry, 46:1051-1056 (2000).
Shapero et al., “SNP Genotyping by Multiplexed Solid-Phase Amplification and Fluorescent Minisequencing”,Genome Research, 11:1926-1934 (2001).
Porat Boaz
Porat Noga
Friedman Mark M.
Horlick Kenneth R.
Porat Noga
Tung Joyce
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