Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers.
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SNP Cutter: a comprehensive tool for SNP PCR-RFLP assay designPCR-based methods for the enrichment of minority alleles and mutationsDigital PCRSpread of Botrytis cinerea Strains with Multiple Fungicide Resistance in German HorticultureDevelopment of single-nucleotide polymorphism-based phylum-specific PCR amplification technique: application to the community analysis using ciliates as a reference organism.Efficient SNP Discovery by Combining Microarray and Lab-on-a-Chip Data for Animal Breeding and Selection.Fine mapping and DNA fiber FISH analysis locates the tobamovirus resistance gene L3 of Capsicum chinense in a 400-kb region of R-like genes cluster embedded in highly repetitive sequences.PCR assay confirms diagnosis in syndrome with variably expressed phenotype: mutation detection in Stickler syndrome.Identification of five novel germline mutations of the MEN1 gene in Japanese multiple endocrine neoplasia type 1 (MEN1) families.A rapid PCR ELISA for the detection of activated K-ras in colorectal cancer.ras and p53 in the prediction of survival in Dukes' stage B colorectal carcinoma.Heterogeneous proliferative potential of occult metastatic cells in bone marrow of patients with solid epithelial tumorsCysteine substitutions in epidermal growth factor-like domains of fibrillin-1: distinct effects on biochemical and clinical phenotypes.Tools for molecular genetic epidemiology: a comparison of MADGE methodology with other systems.X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome.Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype.Detection of c-Ki-ras gene codon 12 mutations from pancreatic duct brushings in the diagnosis of pancreatic tumours.Intronic polymorphisms affecting alternative splicing of human dopamine D2 receptor are associated with cocaine abuse.Estimation of the proportions of mutant and normal N-ras alleles by allele specific restriction analysis.The polymerase chain reaction: its use in the molecular characterization and diagnosis of cancers.Pancreatic carcinomas of acinar and mixed acinar/ductal phenotypes in Ela-1-myc transgenic mice do not contain c-K-ras mutations.Elimination of unaltered DNA in mixed clinical samples via nuclease-assisted minor-allele enrichmentSelective 'stencil'-aided pre-PCR cleavage of wild-type sequences as a novel approach to detection of mutant K-RAS.Multiplex PCR/LDR for detection of K-ras mutations in primary colon tumors.Characterization of an extremely thermostable restriction enzyme, PspGI, from a Pyrococcus strain and cloning of the PspGI restriction-modification system in Escherichia coli.Simple and sensitive detection of mutations in the ras proto-oncogenes using PNA-mediated PCR clamping.Diagnosis of mutations by the PCR double RFLP method (PCR-dRFLP).A novel blocker-PCR method for detection of rare mutant alleles in the presence of an excess amount of normal DNA.Multiplexed Elimination of Wild-Type DNA and High-Resolution Melting Prior to Targeted Resequencing of Liquid Biopsies.An abasic site analogue activates a c-Ha-ras gene by a point mutation at modified and adjacent positions.A specific test for transthyretin 122 (Val----Ile), based on PCR-primer-introduced restriction analysis (PCR-PIRA): confirmation of the gene frequency in blacks.DNA enrichment by allele-specific hybridization (DEASH): a novel method for haplotyping and for detecting low-frequency base substitutional variants and recombinant DNA molecules.Cytotoxicity of simvastatin to pancreatic adenocarcinoma cells containing mutant ras gene.A new detection method for the K variant of butyrylcholinesterase based on PCR primer introduced restriction analysis (PCR-PIRA).Transforming activity of a synthetic c-Ha-ras gene containing O6-methylguanine in codon 12.Clinical applications of the polymerase chain reaction.RNA editing produces glycine receptor alpha3(P185L), resulting in high agonist potency.Polymorphisms within ovine CSN3 identified by DNA- and mRNA-sequence analysis.Analyses of the APC and TGF-beta type II receptor genes, and microsatellite instability in mucosal colorectal carcinomas.Polymorphism of the APEX nuclease 1 gene in keratoconus and Fuchs endothelial corneal dystrophy.
P2860
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P2860
Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
Detection of minority point mu ...... of tumor-progression markers.
@en
type
label
Detection of minority point mu ...... of tumor-progression markers.
@en
prefLabel
Detection of minority point mu ...... of tumor-progression markers.
@en
P2093
P2860
P356
P1476
Detection of minority point mu ...... of tumor-progression markers.
@en
P2093
P2860
P304
P356
10.1093/NAR/17.20.8093
P577
1989-10-01T00:00:00Z