Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection.
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The molecular basis of malonyl-CoA decarboxylase deficiency.Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene.Haplotype and functional analysis of four flavin-containing monooxygenase isoform 2 (FMO2) polymorphisms in Hispanics.Identification of colorectal cancer patients with tumors carrying the TP53 mutation on the codon 72 proline allele that benefited most from 5-fluorouracil (5-FU) based postoperative chemotherapy.Rapid detection of 3500Q and 3531 mutations and MspI polymorphism in exon 26 at the apolipoprotein B gene.Mapping a candidate gene (MdMYB10) for red flesh and foliage colour in apple.Functional promoter haplotypes of the human FAS gene are associated with the phenotype of SLE characterized by thrombocytopenia.Alpha-adducin Gly460Trp polymorphism and essential hypertension in KoreaThe tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years.Progression from mild cognitive impairment to Alzheimer's disease: effects of sex, butyrylcholinesterase genotype, and rivastigmine treatment.Mutagenically separated PCR assay for rapid detection of M41L and K70R zidovudine resistance mutations in CRF01_AE (subtype E) human immunodeficiency virus type 1.Survey and summary: The applications of universal DNA base analoguesMitochondrial genetic analyses suggest selection against maternal lineages in bipolar affective disorder.Use of chromatin immunoprecipitation (ChIP) to detect transcription factor binding to highly homologous promoters in chromatin isolated from unstimulated and activated primary human B cells.Improving the fidelity of Thermus thermophilus DNA ligase.Interleukin-6 c.-174G>C Polymorphism and Periodontitis in a Brazilian PopulationAssociation of the T+294C polymorphism in PPAR delta with low HDL cholesterol and coronary heart disease risk in women.Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome.Haplotypes of angiotensinogen in essential hypertensionGenotyping of PCR-based polymorphisms and linkage-disequilibrium analysis at the NF1 locus.Helios marks strongly autoreactive CD4+ T cells in two major waves of thymic deletion distinguished by induction of PD-1 or NF-κB.New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a geneAnalysis of renin-angiotensin aldosterone system gene polymorphisms in Malaysian essential hypertensive and type 2 diabetic subjects.Long noncoding RNA ZNFX1-AS1 suppresses growth of hepatocellular carcinoma cells by regulating the methylation of miR-9.A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro.Angiotensinogen T235 expression is elevated in decidual spiral arteries.Rasgrp1 mutation increases naive T-cell CD44 expression and drives mTOR-dependent accumulation of Helios⁺ T cells and autoantibodies.RPGRIP1 is essential for normal rod photoreceptor outer segment elaboration and morphogenesis.Molecular diagnostics of α1-antitrypsin deficiency.Multiplex PCR/LDR for detection of K-ras mutations in primary colon tumors.Genetic polymorphisms of interleukin 6 and interleukin 10 in Egyptian patients with systemic lupus eythematosus.CD38 and interleukin 6 gene polymorphism in egyptians with diffuse large B-cell lymphoma (DLBCL).Detection of all single-base mismatches in solution by chemiluminescence.Colorimetric detection of immobilised PCR products generated on a solid support.A microarray-based high throughput molecular marker genotyping method: the tagged microarray marker (TAM) approach.Diagnosis of mutations by the PCR double RFLP method (PCR-dRFLP).Genotyping of single nucleotide substitutions.Gene-based sequence diversity analysis of field pea (Pisum).Selectivity of Enzymatic Conversion of Oligonucleotide Probes during Nucleotide Polymorphism Analysis of DNA.Multiplex mutagenically separated polymerase chain reaction assay for rapid detection of human mitochondrial DNA variations in coding area.
P2860
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P2860
Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Mutagenically separated PCR (M ...... e for easy mutation detection.
@en
type
label
Mutagenically separated PCR (M ...... e for easy mutation detection.
@en
prefLabel
Mutagenically separated PCR (M ...... e for easy mutation detection.
@en
P2093
P2860
P356
P1476
Mutagenically separated PCR (M ...... e for easy mutation detection.
@en
P2093
P2860
P304
P356
10.1093/NAR/21.16.3623
P577
1993-08-01T00:00:00Z