Polymorphism, Restriction Fragment Length
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Subject Areas on Research
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A Bgl II polymorphism detected by LDR152 [D19S19].
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A PCR-RFLP typing method for adhesion molecule gene polymorphisms and allele frequencies in a normal UK population.
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A deletion unit on chromosome 17q in epithelial ovarian tumors distal to the familial breast/ovarian cancer locus.
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A frequent human CD20 (B1) differentiation antigen DNA polymorphism detected with MspI is located near 11q12-13.
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A highly polymorphic cDNA probe in the NF1 gene.
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A lack of genetic linkage of renin gene restriction fragment length polymorphisms with human hypertension.
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A multi-locus assessment of connectivity and historical demography in the bluehead wrasse (Thalassoma bifasciatum).
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A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11.
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A polymorphic cDNA probe on chromosome 17q11.2 located within the NF1 gene [D17S376].
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A promoter polymorphism (-77T>C) of DNA repair gene XRCC1 is associated with risk of lung cancer in relation to tobacco smoking.
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A single-base deletion in the 3'-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type IIIA in a population of North African Jewish patients.
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A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations.
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A three allele TaqI polymorphism at TOP1 gene.
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A universal molecular method for identifying underground plant parts to species.
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Abundance and diversity of Schizophyllum commune spore clouds in the Caribbean detected by selective sampling.
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Alterations in HLA-DP and HLA-DQ antigen frequency in patients with dermatitis herpetiformis.
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Alterations of the P53 gene are associated with the progression of a human prostate carcinoma.
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An EcoRI RFLP in the 5' region of the human NF1 gene.
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An HLA class II region restriction fragment length polymorphism (RFLP) in patients with dermatitis herpetiformis: association with HLA-DP phenotype.
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Analysis of Huntington disease linkage and age-of-onset distributions.
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Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphisms.
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Association between ICAM-1 Gly-Arg polymorphism and renal parenchymal scarring following childhood urinary tract infection.
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Association between genetic variation at the porphobilinogen deaminase gene and schizophrenia.
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Association between the V109G polymorphism of the p27 gene and the risk and progression of oral squamous cell carcinoma.
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Association of estrogen receptor β polymorphisms with posterior tibial tendon dysfunction.
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Association of hypertension with beta2- and alpha2c10-adrenergic receptor genotype.
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Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase.
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Bartonella vinsonii subsp. berkhoffii subsp. nov., isolated from dogs; Bartonella vinsonii subsp. vinsonii; and emended description of Bartonella vinsonii.
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Biology of small cell lung cancer.
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Chromosomal localization of seven members of the murine TGF-beta superfamily suggests close linkage to several morphogenetic mutant loci.
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Circadian clock-controlled genes isolated from Neurospora crassa are late night- to early morning-specific.
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Clonality of combined tumors.
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Comparison of 5.8S ribosomal DNA sequences among the basidiomycetous yeast genera Cystofilobasidium, Filobasidium and Filobasidiella.
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Comparison of direct and indirect methods of carrier detection in an X-linked disease.
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D21S194, a jump clone from D21S16.
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DNA sequence analysis and restriction fragment length polymorphism (RFLP) typing of the HLA-DQw2 alleles associated with dermatitis herpetiformis.
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Detection of the JAK2 V617F mutation by LightCycler PCR and probe dissociation analysis.
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Determination of human platelet antigen typing by molecular methods: Importance in diagnosis and early treatment of neonatal alloimmune thrombocytopenia.
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Determinations of restriction fragment length polymorphism in bacteria using ribosomal RNA genes.
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Differentiation of strains in Mycobacterium tuberculosis complex by DNA sequence polymorphisms, including rapid identification of M. bovis BCG.
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Direct carrier testing in 14 families with haemophilia B.
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Dr(a-) polymorphism of decay accelerating factor. Biochemical, functional, and molecular characterization and production of allele-specific transfectants.
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Effects of MDM2 promoter polymorphisms and p53 codon 72 polymorphism on risk and age at onset of squamous cell carcinoma of the head and neck.
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Epidemiological investigation of vaginal Saccharomyces cerevisiae isolates by a genotypic method.
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Evidence for sexuality in the opportunistic fungal pathogen Aspergillus fumigatus.
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Evidence of sexual recombination among Cryptococcus neoformans serotype A isolates in sub-Saharan Africa.
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Expression and amplification of the HER-2/neu (c-erbB-2) protooncogene in epithelial ovarian tumors and cell lines.
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Familial erythrocytosis associated with a short deletion in the erythropoietin receptor gene.
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Familial inheritance of a DXS164 deletion mutation from a heterozygous female.
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Fas A670G polymorphism, apoptotic capacity in lymphocyte cultures, and risk of lung cancer.
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Fine mapping of a putative rd cDNA and its co-segregation with rd expression.
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Functional polymorphisms of matrix metalloproteinase-9 are associated with risk of occurrence and metastasis of lung cancer.
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Gastrostomy in oropharyngeal cancer patients with ERCC4 (XPF) germline variants.
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Genetic changes in human adrenocortical carcinomas.
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Genetic diversity in the Mycobacterium tuberculosis complex based on variable numbers of tandem DNA repeats.
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Genetic isolation by distance in Arabidopsis thaliana: biogeography and postglacial colonization of Europe.
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Genetic linkage analysis of nerve growth factor (beta) in familial Alzheimer's disease.
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Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene.
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Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.
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Genetic polymorphism at the glutathione S-transferase (GST) P1 locus is a breast cancer risk modifier.
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Genetic structure and DNA sequences at junctions involved in the rearrangements of Bacillus subtilis strains carrying the trpE26 mutation.
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Genetic structure of typical and atypical populations of Candida albicans from Africa.
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Genetic variation in the spread of Drosophila subobscura from a nonequilibrium population.
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Genomic organization and polymorphism of human angiotensin II type 2 receptor: no evidence for its gene mutation in two families of human premature ovarian failure syndrome.
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Genomic organization of adrenergic and serotonin receptors in the mouse: linkage mapping of sequence-related genes provides a method for examining mammalian chromosome evolution.
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Glutathione S-transferase polymorphisms and survival in primary malignant glioma.
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HLA-DM polymorphism and risk of trichloroethylene induced medicamentosa-like dermatitis.
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HLA-DR and -DQ genotyping in anti-GBM disease.
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Ha-ras polymorphisms in epithelial ovarian cancer.
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Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.
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Human factor IXLincoln Park: a molecular characterization.
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Identification and functional characterization of JWA polymorphisms and their association with risk of gastric cancer and esophageal squamous cell carcinoma in a Chinese population.
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Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms.
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Identification of quantitative trait loci influencing wood specific gravity in an outbred pedigree of loblolly pine.
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Interaction of the cytochrome P4501A2, SULT1A1 and NAT gene polymorphisms with smoking and dietary mutagen intake in modification of the risk of pancreatic cancer.
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Interactions between life stress factors and carrying the APOE4 allele adversely impact self-reported health in old adults.
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Investigation of the basis of virulence in serotype A strains of Cryptococcus neoformans from apparently immunocompetent individuals.
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Isolation of Cryptococcus gattii and Cryptococcus neoformans var. grubii from the flowers and bark of Eucalyptus trees in India.
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Lack of genetic differentiation between two geographically diverse samples of Candida albicans isolated from patients infected with human immunodeficiency virus.
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Large scale isolation of genes as DNA fragment lengths by continuous elution electrophoresis through an agarose matrix.
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Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease.
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Linkage of kdr-type resistance and the para-homologous sodium channel gene in German cockroaches (Blattella germanica).
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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.
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Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.
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Localization of the mouse gene for secreted phosphoprotein 1 (Spp-1) (2ar, osteopontin, bone sialoprotein 1, 44-kDa bone phosphoprotein, tumor-secreted phosphoprotein) to chromosome 5, closely linked to Ric (Rickettsia resistance).
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Loss of heterozygosity for 10q loci in human gliomas.
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MHC-restricted recognition of autologous melanoma by tumor-specific cytotoxic T cells. Evidence for restriction by a dominant HLA-A allele.
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MTL genotypes, phenotypic switching, and susceptibility profiles of Candida parapsilosis species group compared to Lodderomyces elongisporus.
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Mapping of the mouse Rxr loci encoding nuclear retinoid X receptors RXR alpha, RXR beta, and RXR gamma.
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Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: the prevalent mutation G985 (K304E) is subject to a strong founder effect from northwestern Europe.
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Microphthalmia-associated transcription factor (MITF) locus lacks linkage to human vitiligo or osteopetrosis: an evaluation.
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Mitotic recombination in the rDNA of S. cerevisiae is suppressed by the combined action of DNA topoisomerases I and II.
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Molecular biology of renal injury: emphasis on the role of the renin-angiotensin system.
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Molecular characteristics of mantle cell lymphoma presenting with clonal plasma cell component.
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MspI RFLP for microtubule associated protein-2 (MAP2).
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Multilocus mapping of the X-linked hypophosphatemic rickets gene.
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Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly.
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Mutations at arginine residues in two Asian hemophilia B patients.
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Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene.
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North Carolina macular dystrophy: exclusion map using RFLPs and microsatellites.
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Occurrence of amino acid mutation (Ala98Val) of HNF1α in association with type II diabetes.
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PCR-restriction fragment length polymorphism (RFLP) analyses reveal both extensive clonality and local genetic differences in Candida albicans.
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Paradoxical expression of adenosine deaminase in T cells cultured from a patient with adenosine deaminase deficiency and combine immunodeficiency.
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Persistent bacteremia due to methicillin-resistant Staphylococcus aureus infection is associated with agr dysfunction and low-level in vitro resistance to thrombin-induced platelet microbicidal protein.
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Phenol sulfotransferases: hormonal regulation, polymorphism, and age of onset of breast cancer.
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Polymorphism and altered methylation of the lactoferrin gene in normal leukocytes, leukemic cells, and breast cancer.
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Polymorphism of DNA ligase I and risk of lung cancer--a case-control analysis.
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Polymorphisms of DNA repair gene XRCC3 Thr241Met and risk of gastric cancer in a Chinese population.
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Polymorphisms of DNA repair genes and risk of glioma.
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Polymorphisms of the DNA repair gene XPD and risk of lung cancer in a Chinese population.
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Polymorphisms of the DNA repair gene XRCC1 and risk of gastric cancer in a Chinese population.
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Polymorphisms of vitamin D receptor gene protect against the risk of head and neck cancer.
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Preliminary evidence of linkage of salt sensitivity in black Americans at the beta 2-adrenergic receptor locus.
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Prenatal diagnosis and carrier detection for glycogen storage disease type III using polymorphic DNA markers.
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Prevalence of clinical isolates of Cryptococcus gattii serotype C among patients with AIDS in Sub-Saharan Africa.
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Production and characterization of two ependymoma xenografts.
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Putative functional polymorphisms of MMP9 predict survival of NSCLC in a Chinese population.
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Quantitation of hepatitis B viremia and emergence of YMDD variants in patients with chronic hepatitis B treated with lamivudine.
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RFLPs for linkage analysis in families with glycogen storage disease type III.
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RNASEL mutations in hereditary prostate cancer.
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Rapid communication: BamHI restriction fragment length polymorphism detected with a pig gastric mucin (MUC5AC) probe.
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Recombination of 4p16 DNA markers in an unusual family with Huntington disease.
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Recurrent nonsense mutations at arginine residues cause severe hemophilia B in unrelated hemophiliacs.
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Reduced DNA repair of benzo[a]pyrene diol epoxide-induced adducts and common XPD polymorphisms in breast cancer patients.
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Report of the committee on the genetic constitution of chromosome 19.
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Restriction fragment length polymorphism of the apoprotein A-I-C-III gene cluster in control and stroke-prone white and black subjects: racial differences.
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Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase.
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Reverse genetics with a full-length infectious cDNA of the Middle East respiratory syndrome coronavirus.
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Rhizobium gone native: unexpected plasmid stability of indigenous Rhizobium leguminosarum.
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Role of TGF-beta1 in renal parenchymal scarring following childhood urinary tract infection.
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Role of the angiotensin type 2 receptor gene in congenital anomalies of the kidney and urinary tract, CAKUT, of mice and men.
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RsaI RFLP for electron transport flavoprotein-beta(ETFB).
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S-allele diversity in a natural population of Physalis crassifolia (Solanaceae) (ground cherry) assessed by RT-PCR.
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S-allele sequence diversity in natural populations of Solanum carolinense (Horsenettle).
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SP75 is encoded by the DP87 gene and belongs to a family of modular Dictyostelium discoideum outer layer spore coat proteins.
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Single nucleotide polymorphism at rs1982073:T869C of the TGFbeta 1 gene is associated with the risk of radiation pneumonitis in patients with non-small-cell lung cancer treated with definitive radiotherapy.
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Somatic mutations in the neurofibromatosis 1 gene in gliomas and primitive neuroectodermal tumours.
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Species identification and virulence attributes of Saccharomyces boulardii (nom. inval.).
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Suppression of tumorigenicity of A549 lung adenocarcinoma cells by human chromosomes 3 and 11 introduced via microcell-mediated chromosome transfer.
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Systematic gene mapping in man: data management considerations.
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TP53 and RAS mutations in metachronous tumors from patients with cancer of the upper aerodigestive tract.
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The 8.5-kb PstI allele of the stress protein gene, Hsp70-2: an independent risk factor for systemic lupus erythematosus in African Americans?
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The HOX-5 and surfeit gene clusters are linked in the proximal portion of mouse chromosome 2.
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The association of polymorphisms of CDT1 and GMNN gene with the risk of breast cancer in Chinese women: a case-control analysis.
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The diversity and biogeography of soil bacterial communities.
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The gene for a novel epidermal antigen maps near the neurofibromatosis 1 gene.
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The genetics of reproductive isolation and the potential for gene exchange between Drosophila pseudoobscura and D. persimilis via backcross hybrid males.
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The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain.
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The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14.
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The segment polarity gene porcupine encodes a putative multitransmembrane protein involved in Wingless processing.
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Tumour necrosis factor receptor II polymorphism and juvenile idiopathic arthritis.
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Two sensitive PCR-based methods for detection of hepatitis B virus variants associated with reduced susceptibility to lamivudine.
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Uniparental mitochondrial transmission in sexual crosses in Cryptococcus neoformans.
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Unisexual and heterosexual meiotic reproduction generate aneuploidy and phenotypic diversity de novo in the yeast Cryptococcus neoformans.
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Variability of the SIRT3 gene, human silent information regulator Sir2 homologue, and survivorship in the elderly.
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Vitamin D receptor polymorphisms and prostate cancer.
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Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma.
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Watershed urbanization alters the composition and function of stream bacterial communities.
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Keywords of People