HFE gene mutations in a population of Italian Parkinson's disease patients
Keywords: Parkinson's disease; Iron; HFE gene; DNA mutations; DHPLC
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Denaturing High-performance Liquid Chromatography mutation analysis in patients with reduced Protein S levels
Keywords: DHPLC; Mutation detection; Protein S
A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL)
Keywords: CDKN2A; Melanoma; Mutation detection; Sequencing; Polymorphism; Audit; DHPLC; False negative;
Microbial diversity in Natural Whey Cultures used for the production of Caciocavallo Silano PDO cheese
Keywords: Caciocavallo Silano PDO cheese; Natural Whey Cultures; DGGE; DHPLC; Geographical origin
Myofilament Protein Gene Mutation Screening and Outcome of Patients With Hypertrophic Cardiomyopathy
Keywords: CI; confidence interval; DHPLC; denaturing high-performance liquid chromatography; HCM; hypertrophic cardiomyopathy; HR; hazard ratio; LV; left ventricular; NYHA; New York Heart Association;
RAS Signaling in Colorectal Carcinomas through Alteration of RAS, RAF, NF1, and/or RASSF1A
Keywords: CRC; colorectal cancer; MAPK; mitogen-activated protein kinase; MSI; microsatellite instability; MSS; microsatellite stable; dHPLC; denaturing high-performance liquid chromatography; MSP; methylation-specific PCR; MLPA; multiple ligation-dependent probe a
Expression status of ataxia-telangiectasia-mutated gene correlated with prognosis in advanced gastric cancer
Keywords: ATM; Gastric cancer; Prognosis; DHPLC;
Diagnosis of BSEP/ABCB11 Mutations in Asian Patients with Cholestasis Using Denaturing High Performance Liquid Chromatography
Keywords: BRIC; Benign recurrent intrahepatic cholestasis; BSEP; Bile salt export pump; DHPLC; Denaturing high performance liquid chromatography; PFIC; Progressive familial intrahepatic cholestasis;
Detection of BCR-ABL gene mutations in Philadelphia chromosome positive leukemia patients resistant to STI-571 cancer therapy
Keywords: ALL; CML; MRD; dHPLC; STI571; Imatinib; Gene mutation
Resolving mtDNA mixtures by denaturing high-performance liquid chromatography and linkage phase determination
Keywords: DHPLC; Mitochondrial DNA; Forensics; DNA mixture; Fractionation; Linkage phase
Mutational spectrum of dihydropyrimidine dehydrogenase gene (DPYD) in the Tunisian population
Keywords: 5-Fluorouracile; Tunisian population; Dihydropyrimidine dehydrogenase gene; DHPLC5-Fluorouracile; Population tunisienne; Gène de la dihydropyrimidine déhydrogenase; DHPLC
Detection of streptomycin resistance in Mycobacterium tuberculosis clinical isolates from China as determined by denaturing HPLC analysis and DNA sequencing
Keywords: Mycobacterium tuberculosis; Streptomycin resistance; DHPLC; rpsL; rrs; MICMDR, multidrug-resistant; MIC, minimal inhibitory concentration; M. tuberculosis, Mycobacterium tuberculosis; TB, tuberculosis; Denaturing HPLC, denaturing high-performance liquid c
Analysis of Keratin Polypeptides 8 and 19 Variants in Inflammatory Bowel Disease
Keywords: Ab; antibody; CD; crohn's disease; CI; confidence interval; DHPLC; denaturing high-performance liquid chromatography; IBD; inflammatory bowel disease; IF; intermediate filaments; K; proteins; KRT8; keratin-8; OR; odds ratio; PCR; polymerase chain reacti
Molecular monitoring of the intestinal flora by denaturing high performance liquid chromatography
Keywords: 16S rRNA; Gut flora; DHPLC
Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia
Keywords: Hereditary spastic paraplegia; Spastin; SPG4; DHPLC
Identification of a novel VNTR polymorphism in C6orf37 and its association with colorectal cancer risk in Chinese population
Keywords: VNTR, variable number tandem repeat; DHPLC, denaturing high-performance liquid chromatography; RT-PCR, reverse transcription-polymerase chain reaction; TEAA, triethylammonium acetateVNTR polymorphism; C6orf37; Colorectal cancer; DHPLC; Chinese population
Calpain 10 and development of diabetes mellitus in cystic fibrosis
Keywords: Calpain 10; Cystic fibrosis; dHPLC; Diabetes mellitus
Detection of 12 new mutations in Gaucher disease Brazilian patients
Keywords: Gaucher disease; dHPLC; GBA gene
Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference
Keywords: ACE; Angiotensin converting enzyme; ADPKD; Autosomal dominant polycystic kidney disease; ARB; Angiotensin II receptor blocker; ARPKD/CHF; Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis; cAMP; Cyclic adenosine monophosphate;
Mutation and expression analysis of LZTS1 in ovarian cancer
Keywords: Ovarian adenocarcinoma; LZTS1; DHPLC; RT-PCR; Loss of heterozygosity
Identification of BRCA1 and BRCA2 mutations from Korean breast cancer patients using denaturing HPLC
Keywords: Breast cancer; Germline mutations; BRCA1; BRCA2; Hereditary; DHPLC;
A novel mutation detection approach of hMLH1 and hMSH2 genes for screening of colorectal cancer
Keywords: Condition-oriented-PCR primer-embedded-reactor plate; hMLH1 and hMSH2; Colorectal cancer (CRC); Hereditary nonpolyposis colorectal cancer; DHPLC; Denaturing High-Performance Liquid Chromatography; Germline mutations; Mismatch repair; High-throughput techn
ATM sequence variants and risk of radiation-induced subcutaneous fibrosis after postmastectomy radiotherapy
Keywords: ATM; Breast cancer; DHPLC; Fibrosis; Radiation sensitivity;
Genetic mutations in von Willebrand disease identified by DHPLC and DNA sequence analysis
Keywords: von Willebrand disease; DHPLC; Mutation detection
Cancer Risks For Mismatch Repair Gene Mutation Carriers: A Population-Based Early Onset Case-Family Study
Keywords: CI; confidence interval; DHPLC; denaturing high-performance liquid chromatography; HNPCC; hereditary nonpolyposis colorectal cancer; MMR; mismatch repair; MSI; microsatellite instability;
Optimized PCR fragments for heteroduplex analysis of the whole human mitochondrial genome with denaturing HPLC
Keywords: dHPLC, denaturing high pressure liquid chromatography; TEAA, triethylammoniumacetate; Tann, annealing temperature in PCRMitochondrial disease; Mitochondrial DNA; Mutation discovery; Heteroplasmy; Heteroduplex analysis; Denaturing HPLC; dHPLC
Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients
Keywords: Dyslexia; FOXP2; DHPLC; 7q;
Idiopathic achalasia is not allelic to alacrima achalasia adrenal insufficiency syndrome at the ALADIN locus
Keywords: AAAS; alacrima, achalasia and adrenocorticotropin-resistant adrenal insufficiency syndrome; ALADIN; alacrima-achalasia-adrenal insufficiency with neurological disorders; DHPLC; denaturing high-performance liquid chromatography; LES; lower oesophageal
Single nucleotide polymorphism detection in promoter I of the acetyl-CoA carboxylase-α gene in sheep
Keywords: Sheep; Acetyl-CoA carboxylase gene; SNPs; DHPLC;
DNA sequence variations in the prolyl isomerase Pin1 gene and Alzheimer's disease
Keywords: Alzheimer's disease; Pin1; Tau; SNP; DHPLC;
Yield of Genetic Testing in Hypertrophic Cardiomyopathy
Keywords: DHPLC; denaturing high-performance liquid chromatography; HCM; hypertrophic cardiomyopathy; ICD; implantable cardioverter-defibrillator; LVWT; left ventricular wall thickness; MYBPC3; myosin binding protein C; MYH7; myosin heavy chain; SCD; sudden cardiac
DHPLC analysis of the matrix metalloproteinase-1 promoter 1G/2G polymorphism that can be easily used to screen large population
Keywords: DHPLC; Matrix metalloproteinase-1; Single nucleotide polymorphism;
ATM sequence variants are predictive of adverse radiotherapy response among patients treated for prostate cancer
Keywords: ATM gene; Radiation sensitivity; DHPLC; Prostate cancer; Brachytherapy;
DHPLC in clinical molecular diagnostic services
Keywords: Mutation analysis; Multiple malformation syndrome; DHPLC; Heteroduplex analysis; Molecular diagnosis;
Impact of polymorphisms in the genes encoding xylosyltransferase I and a homologue in type 1 diabetic patients with and without nephropathy
Keywords: type 1 diabetes; diabetic nephropathy; heparan sulfate proteoglycans; xylosyltransferase; genetic variations; polymorphisms; SNPs; DHPLC;
The possible role of TP53 mutation status in the treatment of squamous cell carcinomas of the head and neck (HNSCC) with radiotherapy with different overall treatment times
Keywords: Radiotherapy; Head and neck; Squamous cell carcinoma; TP53; Mutation; DHPLC;
A functional SNP in the promoter region of TCOF1 is associated with reduced gene expression and YY1 DNA-protein interaction
Keywords: TCOF1; Treacher Collins-Franceschetti syndrome gene; YY1; Ying Yang 1 transcription factor; EMSA; Eletrophoretic Mobility Shift Assay; SNP; Single Nucleotide Polymorphisms; SSCP; Single Strand Conformation Polymorphism; dHPLC; Denaturing High-Performanc
Linkage disequilibrium analysis identifies an FGFR1 haplotype-tag SNP associated with normal variation in craniofacial shape
Keywords: FGFR1; TWIST1; Cranial vault; Calvarial suture; LD; htSNP; dHPLC; Population;
Denaturing HPLC-based approach for detection of COL7A1 gene mutations causing dystrophic epidermolysis bullosa
Keywords: Denaturing high performance liquid chromatography; DHPLC; Dystrophic epidermolysis bullosa; Type VII collagen; COL7A1; Mutation detection;
Niemann-Pick C disease: Use of denaturing high performance liquid chromatography for the detection of NPC1 and NPC2 genetic variations and impact on management of patients and families
Keywords: Niemann-Pick disease; NPC2; NPC1; Denaturing high-performance liquid chromatography; DHPLC; Mutation detection;
Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography
Keywords: Mutation detection; Mitochondrial genome; DHPLC; Pyrosequencing; Heteroplasmy; DNA;
Profiling and monitoring of microbial populations by denaturing high-performance liquid chromatography
Keywords: DHPLC; Profiling; Monitoring; Bacteria identification; 16S rDNA;