review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Mike Makrigiorgos G | |
P2860 | cites work | Laser capture microdissection | Q28293867 |
Linkage disequilibrium in the human genome | Q29616097 | ||
Detection of simple mutations and polymorphisms in large genomic regions | Q30715152 | ||
Tech.Sight. Understanding disease cell by cell. | Q31057519 | ||
The mutY gene: a mutator locus in Escherichia coli that generates G.C----T.A transversions | Q33567384 | ||
Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations | Q33582011 | ||
A sensitive scanning technology for low frequency nuclear point mutations in human genomic DNA. | Q33631409 | ||
Enzymatic and chemical cleavage methods | Q33669200 | ||
Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER) | Q33948446 | ||
Haplotype variation and linkage disequilibrium in 313 human genes | Q33953585 | ||
Fidelity of DNA polymerases in DNA amplification | Q34322626 | ||
A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies | Q34385302 | ||
Prospects for applying genotypic selection of somatic oncomutation to chemical risk assessment | Q34416553 | ||
Genomic sequencing and methylation analysis by ligation mediated PCR. | Q34550393 | ||
Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII. | Q34804051 | ||
Association mapping of disease loci, by use of a pooled DNA genomic screen | Q35249321 | ||
Effects of different DNA polymerases in ligation-mediated PCR: enhanced genomic sequencing and in vivo footprinting | Q36815765 | ||
Ligation of a primer at a mutation: a method to detect low level mutations in DNA. | Q38363467 | ||
An amplification and ligation-based method to scan for unknown mutations in DNA. | Q38364134 | ||
Detecting colorectal cancer in stool with the use of multiple genetic targets | Q39569642 | ||
Rapid detection of the factor V Leiden (1691 G > A) and haemochromatosis (845 G > A) mutation by fluorescence resonance energy transfer (FRET) and real time PCR. | Q39621691 | ||
Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations | Q39723322 | ||
Mutation detection using a novel plant endonuclease | Q39725311 | ||
Novel amplification of DNA in a hairpin structure: towards a radical elimination of PCR errors from amplified DNA. | Q39744781 | ||
Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers | Q40538213 | ||
Mutational spectrometry: means and ends. | Q40597365 | ||
A versatile mismatch recognition agent: specific cleavage of a plasmid DNA at a single base mispair | Q41645389 | ||
Genotypic selection methods for the direct analysis of point mutations | Q41645720 | ||
A simple and accurate method for determination of microsatellite total allele content differences between DNA pools | Q41727943 | ||
Mapping of copper/hydrogen peroxide-induced DNA damage at nucleotide resolution in human genomic DNA by ligation-mediated polymerase chain reaction | Q43769111 | ||
Sensitive and quantitative detection of mutations associated with clinical resistance to STI-571. | Q44512456 | ||
Truncated amplification: a method for high-fidelity template-driven nucleic acid amplification | Q47569168 | ||
Detection of hotspot mutations and polymorphisms using an enhanced PCR-RFLP approach | Q47995789 | ||
Needle-in-a-haystack detection and identification of base substitution mutations in human tissues. | Q53419192 | ||
Substrate specificity of Escherichia coli MutY protein. | Q54579279 | ||
Detection of single base substitutions in total genomic DNA | Q59092301 | ||
Large-scale genotyping of single nucleotide polymorphisms by Pyrosequencing? and validation against the 5?nuclease (Taqman�) assay | Q63502685 | ||
MutY DNA glycosylase: base release and intermediate complex formation | Q64389057 | ||
Ligation of single-stranded oligodeoxyribonucleotides by T4 RNA ligase | Q69711519 | ||
Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders | Q73911223 | ||
Assessing allele frequencies of single nucleotide polymorphisms in DNA pools by pyrosequencing technology | Q74133504 | ||
Mutation detection using fluorescent enzyme mismatch cleavage with T4 endonuclease VII | Q77918358 | ||
P433 | issue | 5 | |
P304 | page(s) | 406-412 | |
P577 | publication date | 2004-05-01 | |
P1433 | published in | Human Mutation | Q5937269 |
P1476 | title | PCR-based detection of minority point mutations | |
P478 | volume | 23 |