Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing compound containing saccharide radical
Patent
1995-08-01
1998-01-27
Jones, W. Gary
Chemistry: molecular biology and microbiology
Micro-organism, tissue cell culture or enzyme using process...
Preparing compound containing saccharide radical
435 6, 435 911, 435 915, 435 9151, 435 9152, C12P 1934, C12Q 168
Patent
active
057121265
ABSTRACT:
The present invention provides methods to analyze gene expression by selective PCR amplification and display of 3'-end restriction fragments of double stranded cDNAs.
REFERENCES:
patent: 5459037 (1995-10-01), Sutcliffe et al.
Fischer et al., "Restriction fragment length polymorphism-coupled domain-directed differential display: A highly efficient technique for expression analysis of multigene families," Proc. Natl. Acad. Sci. USA 92:5331-5335, 1995.
Frohman et al., "Rapid production of full-length cDNAs from rare transcripts: Amplification using a single gene-specific oligonucleotide primer," Proc. Natl. Acad. Sci. USA 85:8998-9002, 1988.
Ko et al., "Unbiased amplification of a highly complex mixture of DNA fragments by `lone linker` -tagged PCR,"Nucleic Acids Research 18(14):4293-4294, 1990.
Liang and Pardee, "Differential Display of Eukaryotic Messenger RNA by Means of the Polymerase Chain Reaction," Science 257: 967-971, 1992.
Loh et al., "Polymerase Chain Reaction with Single-Sided Specificity: Analysis of T Cell Receptor .delta. Chain," Science 243:217-220, 1989.
Prashar and Weissman, "Analysis of differential gene expression by display of 3' end restriction fragments of cDNAs," Proc. Natl. Acad. Sci. USA 93:659-663, 1996.
Roux and Dhanarajan, "A Strategy for Single Site PCR Amplification of dsDNA: Priming Digested Cloned or Genomic DNA from an Anchor-Modified Restriction Site and a Short Internal Sequence," BioTechniques 8(1):48, 1990.
Averboukh et al., "Better Gel Resolution and Longer cDNAs Increase the Precision of Differential Display," BioTechniques 20(5):918-921, 1996.
Zhao et al., "New Primer Strategy Improves Precision of Differential Display," BioTechniques 18(5):842-850, 1995.
Liang et al., "Differential Display and Cloning of Messenger RNAs from Human Breast Cancer versus Mammary Epithelial Cells," Cancer Research 52:6966-6968, 1992.
Liang et al., "Distribution and cloning of eukaryotic mRNAs by means of differential display: refinements and optimization," Nucleic Acids Research 21(14):3269-3275, 1993.
Reeves et al., "General Method for PCR Amplification and Direct Sequencing of mRNA Differential Display Products," Biothechniques 18(1):18-20, 1995.
Liang et al. (1994) Nucleic Acids Research 22:5763-4.
Zeng et al. (1994) Nucleic Acids Research 22:4381-5.
Cecchini et al. (1993) Nucleic Acids Research 21:5742-7.
Duguid and Dinauer (1990) Nucleic Acids Research 9:2789-92.
Liang et al. (1993) Nucleic aCids Research 21:3269-75.
Wang and Brown (1991) Proc. Natl. Acad. Sci. USA 88:11505-9.
Lisistyn et al. (1993) Science 259:946-51.
Navarro et al. (1996) J. Virol. Methods 56:59-66.
Diachenko et al. (1996) Biochemical and Biophysical Research Communications 219:824-8.
Kato (1995) Nucleic Acids Research 23:3685-90.
Kato (1996) Nucleic Acids Research 24:394-5.
Chenchik et al. (1996) BioTechniques 21:526-34.
Vectors from nucleic acid databases.
Prashar Yatindra
Weissman Sherman M.
Atzel Amy
Jones W. Gary
Yale University
LandOfFree
Analysis of gene expression by display of 3-end restriction frag does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Analysis of gene expression by display of 3-end restriction frag, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Analysis of gene expression by display of 3-end restriction frag will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-341034