Amplification-refractory mutation system (ARMS) analysis of point mutations.

scientific article

Amplification-refractory mutation system (ARMS) analysis of point mutations. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/0471142905.HG0908S07
P698PubMed publication ID18428319

P2093author name stringS Little
P304page(s)Unit 9.8
P577publication date2001-05-01
P1433published inCurrent protocols in human genetics / editorial board, Nicholas C, Dracapoli ... [et al.]Q26842512
P1476titleAmplification-refractory mutation system (ARMS) analysis of point mutations.
P478volumeChapter 9

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cites work (P2860)
Q36256816A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells
Q92893131A multiplex PCR strategy to screen for known mutations in families with sudden cardiac death burden
Q52608177A novel compound-primed multiplex ARMS-PCR (CPMAP) for simultaneous detection of common PAH gene mutations.
Q45893225Allele specific LAMP- gold nanoparticle for characterization of single nucleotide polymorphisms.
Q37061245Allele-Specific Quantitative PCR for Accurate, Rapid, and Cost-Effective Genotyping.
Q89915713An Overview of Molecular Genetic Diagnosis Techniques
Q37239169An asthma-associated IL4R variant exacerbates airway inflammation by promoting conversion of regulatory T cells to TH17-like cells
Q36391841An improved allele-specific PCR primer design method for SNP marker analysis and its application
Q37403244Apolipoprotein E genotyping using PCR-GoldMag lateral flow assay and its clinical applications
Q35124793BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.
Q90600972Beneficial mutations for carotenoid production identified from laboratory-evolved Saccharomyces cerevisiae
Q37457413Careful neuropsychological testing reveals a novel genetic marker, GSTO1*C, linked to the pre-stage of Alzheimer's disease
Q64263552Considerations and quality controls when analyzing cell-free tumor DNA
Q38726143Current Role of Genetics in Hematologic Malignancies
Q37706384Design and implementation of a mobile system for lung cancer patient follow-up in China and initial report of the ongoing patient registry
Q34879539Designing, optimization and validation of tetra-primer ARMS PCR protocol for genotyping mutations in caprine Fec genes.
Q93063128Detecting Graft-Derived Cell-Free DNA Through Amplification Refractory Mutation System Polymerase Chain Reaction in Living-Donor Liver Transplantation: Report of 2 Cases
Q36521356Detection of Rare Drug Resistance Mutations by Digital PCR in a Human Influenza A Virus Model System and Clinical Samples.
Q34049474Detection of rare point mutation via allele-specific amplification in emulsion PCR.
Q92980430Development and validation of a PCR-based functional marker system for identifying the low amylose content-associated gene Wx hp in rice
Q41986044Development of allele-specific multiplex PCR to determine the length of poly-T in intron 8 of CFTR.
Q64240900Diagnostic methods for Lysosomal Storage Disease
Q35157950Exonic single nucleotide polymorphisms within TLR3 associated with infant responses to serogroup C meningococcal conjugate vaccine
Q34610322Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype
Q38570314Gold nanoprobe-based non-crosslinking hybridization for molecular diagnostics.
Q87275546Guidelines for the tetra-primer ARMS-PCR technique development
Q36110377HapMap-based study of CIP2A gene polymorphisms and HCC susceptibility
Q39743537High-throughput quantitative real-time RT-PCR assay for determining expression profiles of types I and III interferon subtypes
Q36225340High-throughput quantitative real-time polymerase chain reaction array for absolute and relative quantification of rhesus macaque types I, II, and III interferon and their subtypes
Q34702170Homozygosity mapping in patients with cone-rod dystrophy: novel mutations and clinical characterizations
Q33666264Malassezia Yeast and Cytokine Gene Polymorphism in Atopic Dermatitis.
Q57472222MutLγ promotes repeat expansion in a Fragile X mouse model while EXO1 is protective
Q57023127Novel multiplex PCR-SSP method for centromeric KIR allele discrimination
Q34515855Optimised Pre-Analytical Methods Improve KRAS Mutation Detection in Circulating Tumour DNA (ctDNA) from Patients with Non-Small Cell Lung Cancer (NSCLC)
Q36134534Optimized Multiplex Detection of 7 KRAS Mutations by Taqman Allele-Specific qPCR.
Q36055938Polymorphism on Chromosome 9p21.3 Is Associated with Severity and Early-Onset CAD in Type 2 Diabetic Tunisian Population
Q30951240RExPrimer: an integrated primer designing tool increases PCR effectiveness by avoiding 3' SNP-in-primer and mis-priming from structural variation
Q93083355Rapid, low cost and sensitive detection of Calreticulin mutations by a PCR based amplicon length differentiation assay for diagnosis of myeloproliferative neoplasms
Q50219695Scarless Cas9 Assisted Recombineering (no-SCAR) in Escherichia coli, an Easy-to-Use System for Genome Editing
Q47254650Sexual recombination and increased mutation rate expedite evolution of Escherichia coli in varied fitness landscapes
Q37111992Simple allele-discriminating PCR for cost-effective and rapid genotyping and mapping
Q35667841Single nucleotide polymorphisms of the GJB2 and GJB6 genes are associated with autosomal recessive nonsyndromic hearing loss
Q58578019Techniques of using circulating tumor DNA as a liquid biopsy component in cancer management
Q35813169The BDNF Val66Met polymorphism moderates the relationship between cognitive reserve and executive function
Q89860151The Co-Expression of Programmed Death-Ligand 1 (PD-L1) in Untreated EGFR-Mutated Metastatic Lung Adenocarcinoma
Q90733060The Non-synonymous rs763780 Single-Nucleotide Polymorphism in IL17F Gene Is Associated With Susceptibility to Tuberculosis and Advanced Disease Severity in Argentina
Q28508280The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors
Q42224550Transforming growth factor beta and excess burden of renal disease.
Q34465859Transgene detection by digital droplet PCR
Q35905048Validation of a Multiplex Allele-Specific Polymerase Chain Reaction Assay for Detection of KRAS Gene Mutations in Formalin-Fixed, Paraffin-Embedded Tissues from Colorectal Cancer Patients

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