Polymerase chain reaction amplification of specific alleles: a general method of detection of mutations, polymorphisms, and haplotypes

Study on the quality and stability of compost through a Demo Compost Plant.

Waste management (New York, N.Y.)·2012

Ha-ras codon 12 mutation in papillary tumors of the urinary-bladder - a retrospective study.

International journal of oncology·2011

Risk factors for inhibitor formation in haemophilia: a prevalent case-control study.

Haemophilia : the official journal of the World Federation of Hemophilia·2009

High frequency of de novo mutations in Li-Fraumeni syndrome.

Journal of medical genetics·2009

Detection of mutations by single-strand conformation polymorphism (SSCP) analysis and SSCP-hybrid methods.

Current protocols in human genetics·2008

EGFR somatic doublets in lung cancer are frequent and generally arise from a pair of driver mutations uncommonly seen as singlet mutations: one-third of doublets occur at five pairs of amino acids.

Oncogene·2008

Comparative methods for recombinant production and characterization of 1-deoxy-D-xylulose-5-phosphate synthase from bacterial and apicomplexan sources.

Methods in enzymology·2026

Current methods and applications in the study of 1-Deoxy-D-xylulose 5-phosphate synthase (DXPS).

Methods in enzymology·2026

Thiamine pyrophosphate-dependent enzymes in Toxoplasma gondii and functional significance of an apicoplast-localized pyruvate dehydrogenase.

Methods in enzymology·2026

Biochemical and cryo-EM studies of the pyruvate dehydrogenase complex from native cell extracts.

Methods in enzymology·2026

Synthesis of phosphonate and phosphinate analogs of 2-oxo acids for site-specific inhibition of thiamine-diphosphate-dependent dehydrogenases of 2-oxo acids in vivo.

Methods in enzymology·2026

Use of dihydroxyacetone synthase for the assimilation of methanol in E. coli.

Methods in enzymology·2026

A Biallelic ITGA10 Variant as a Candidate for Inherited Thrombocytopenia: Insights From a Whole-Exome Sequencing Cohort.

Pediatric blood & cancer·2026

The grammar of the pangenome: terms, concepts, methods, and emerging patterns-a general framework for comparative genomics and genome biology.

Microbiology and molecular biology reviews : MMBR·2026

Related Experiment Videos

Polymerase chain reaction amplification of specific alleles: a general method of detection of mutations,

Related Concept Videos

Study on the quality and stability of compost through a Demo Compost Plant.

Ha-ras codon 12 mutation in papillary tumors of the urinary-bladder - a retrospective study.

Risk factors for inhibitor formation in haemophilia: a prevalent case-control study.

High frequency of de novo mutations in Li-Fraumeni syndrome.

Detection of mutations by single-strand conformation polymorphism (SSCP) analysis and SSCP-hybrid methods.

EGFR somatic doublets in lung cancer are frequent and generally arise from a pair of driver mutations uncommonly seen as singlet mutations: one-third of doublets occur at five pairs of amino acids.

Comparative methods for recombinant production and characterization of 1-deoxy-D-xylulose-5-phosphate synthase from bacterial and apicomplexan sources.

Current methods and applications in the study of 1-Deoxy-D-xylulose 5-phosphate synthase (DXPS).

Thiamine pyrophosphate-dependent enzymes in Toxoplasma gondii and functional significance of an apicoplast-localized pyruvate dehydrogenase.

Biochemical and cryo-EM studies of the pyruvate dehydrogenase complex from native cell extracts.

Synthesis of phosphonate and phosphinate analogs of 2-oxo acids for site-specific inhibition of thiamine-diphosphate-dependent dehydrogenases of 2-oxo acids in vivo.

Use of dihydroxyacetone synthase for the assimilation of methanol in E. coli.

A Biallelic ITGA10 Variant as a Candidate for Inherited Thrombocytopenia: Insights From a Whole-Exome Sequencing Cohort.

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Polymerase chain reaction amplification of specific alleles: a general method of detection of mutations,...

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Polymerase chain reaction amplification of specific alleles: a general method of detection of mutations,