Search results for "genetic analysis"

showing 10 items of 145 documents

Molecular typing of clinical Candida strains using random amplified polymorphic DNA and contour-clamped homogenous electric fields electrophoresis.

2009

Aims:  This report describes an investigation into the genetic profiles of 38 Candida albicans and 19 Candida glabrata strains collected from a dental hospital of Monastir (Tunisia) and the Laboratory of Parasitology, Farhat Hached Hospital of Sousse (Tunisia), using two typing methods: random amplified polymorphic DNA (RAPD) and contour-clamped homogenous electric fields (CHEF). Methods and Results:  The two methods (RAPD and CHEF electrophoresis) were able to identify clonal-related isolates from different patients. RAPD method using two primers (CA1 and CA2) exhibited the highest discriminatory power by discriminating 22 genotypes for C. albicans with CA1 oligonucleotides and 19 genotype…

GeneticsElectrophoresisPolymorphism GeneticTunisiaCandida glabratabiologyCandidiasisCandida glabrataGeneral Medicinebacterial infections and mycosesbiology.organism_classificationApplied Microbiology and BiotechnologyGenetic analysisRAPDRandom Amplified Polymorphic DNA TechniqueDNA profilingParasitologyGenotypeCandida albicansHumansTypingCandida albicansBiotechnologyDNA PrimersJournal of applied microbiology
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A Novel Homozygous Mutation in the Solute Carrier Family 26 Member 7 Gene Causes Thyroid Dyshormonogenesis in a Girl with Congenital Hypothyroidism

2020

We investigated the genetic cause of thyroid dyshormonogenesis in a girl with congenital hypothyroidism. Genetic analysis showed that she was homozygous for a hitherto not described mutation (c.1432_1433delGT, p.V478KfsX11) in the solute carrier family 26 member 7 (SLC26A7) gene. SLC26A7 is proposed to be an anion transporter in the thyroid gland. The mutation leads to a frameshift and a premature stop codon. The predicted protein is truncated and very likely to be nonfunctional if it was expressed at all. In addition, in silico studies predict the mutation to be pathogenic.

GeneticsEndocrinology Diabetes and MetabolismThyroid030209 endocrinology & metabolismBiologymedicine.diseaseGenetic analysisCongenital hypothyroidismFrameshift mutationSolute carrier family03 medical and health sciences0302 clinical medicineEndocrinologymedicine.anatomical_structureThyroid dyshormonogenesis030220 oncology & carcinogenesisMutation (genetic algorithm)medicineGeneThyroid
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Genetic analysis of Citrus aurantium L. (Rutaceae) cultivars by ISSR molecular markers

2011

Eight cultivars of Citrus aurantium L., showing peculiar morphological traits of the fruits and leaves, were analyzed genetically. Inter simple sequence repeat (ISSR) was chosen as molecular markers because they represent a highly efficient system for investigating variability at intraspecific level. The particular morphological traits were discussed, the genetic identity and distance matrix based on Nei index was calculated, and the unweighted pair group method with arithmetic mean (UPGMA) dendrogram was generated. A total of 53 clearly distinguished DNA bands were considered for the ISSR analysis of which 24 were polymorphic. A basic C. aurantium fingerprinting pattern was obtained. The I…

GeneticsSettore BIO/02 - Botanica SistematicaDendrogramUPGMAPlant ScienceBiologyGenetic analysisDNA profilingGenetic markerGenetic variationBotanyGenotypeMicrosatelliteCitrus genetic resources genetic analysis ISSR sour orange cultivarsEcology Evolution Behavior and Systematics
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Restriction fragment polymorphisms of the HLA-DR, HLA-DQ, and insulin gene regions in IDDM: The GAW5 data

1989

The primary aim of the insulin-dependent diabetes mellitus (IDDM) component of Genetic Analysis Workshop 5 (GAW5) was to collect and analyze new data on DNA polymorphisms closely linked to the HLA-D region and the insulin gene. The probes and restriction enzymes described here were used by all ten participating labs, and the data from Southern blotting were interpreted and reported according to conventions developed for the Workshop. These DNA data on members of 94 families with two or more IDDM sibs constitute the largest such sample available. The data were used in most of the analyses presented at the Workshop meeting, and are available on request.

GeneticsbiologyEpidemiologyHuman leukocyte antigenmedicine.diseaseGenetic analysisRestriction fragmentRestriction enzymeDiabetes mellitusHLA-DQmedicinebiology.proteinHLA-DRGenetics (clinical)Southern blotGenetic Epidemiology
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Multiple methods for the identification of polymorphic simple sequence repeats (SSRs) in sorghum [Sorghum bicolor (L.) Moench]

1995

Simple sequence repeats (SSRs), also known as microsatellites, are highly variable DNA sequences that can be used as markers for the genetic analysis of plants. Three approaches were followed for the development of PCR primers for the amplification of DNA fragments containing SSRs from sorghum [Sorghum bicolor (L.) Moench]: a search for sorghum SSRs in public DNA databases; the use of SSR-specific primers developed in the Poaceae species maize (Zea mays L.) and seashore paspalum grass (Paspalum vaginatum Swartz); and the screening of sorghum genomic libraries by hybridization with SSR oligonucleotides. A total of 49 sorghum SSR-specific PCR primer pairs (two designed from GenBank SSR-contai…

Geneticsbiologyfood and beveragesGeneral MedicineSorghumbiology.organism_classificationGenetic analysisGenetic markerGenBankBotanyGeneticsMicrosatelliteGenomic libraryPrimer (molecular biology)Agronomy and Crop SciencePaspalumBiotechnologyTheoretical and Applied Genetics
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Development of a quadruplex PCR system for the genetic analysis of X-chromosomal STR loci

2003

Short tandem repeat systems on the X chromosome are the natural counterpart to the well-established Y-chromosomal STR loci. The X-linked systems are inherited as a single haplotype only in males, whereas in females, the X chromosomes recombine and exhibit the same characteristics as the autosomes. Nevertheless, X-linked systems may provide a useful tool in paternity cases with female offspring, in particular when the alleged father is not available for testing, or in forensic identification cases based on the comparison with firstor second-degree relatives. Only a small number of STR loci have been described on the X chromosome, and a number of these are not highly informative. Therefore, w…

Geneticseducation.field_of_studyAutosomeSTR multiplex systemPopulationHaplotypeMicrosatelliteLocus (genetics)General MedicineBiologyeducationGenetic analysisX chromosomeInternational Congress Series
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PrP Gene Polymorphism in Medieval Remains of Sicilian Sheep

2015

Encephalopathy in sheep was at first described in Ireland in 1732 and was called scrapie. Ancient DNA in archaeogenetics represents an effective method to evaluate the ancestral pedigree of living animals and track evolutionary changes occurred between the past and the present day. Since several point mutations are today widely described in modern scrapie, no data about both sequence and frequency are still available for the prion protein (PrP) gene in ancient breeds. In order to evaluate whether the haplotypes distribution in ancient sheep differed from those of the modern population we evaluated polymorphism at four well know codons of the Prp Open Reading Frame. In the present work, we c…

Geneticseducation.field_of_studyPopulationHaplotypeSingle-nucleotide polymorphismScrapieBiologySettore BIO/08 - AntropologiaGenetic analysisAncient DNAScrapie Prion Protein SNPs Ancient GenotypeGenotypeeducationGene
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Genetic analysis of IDDM: The GAW5 multiplex family dataset

1989

In a collaborative effort by 12 centers from Europe and North America, data were assembled from 94 multiplex families with insulin-dependent diabetes mellitus (IDDM) for analysis of genetic and other factors of possible etiological importance. The dataset contains information on the following genetic markers: HLA-DR beta and -DQ beta restriction fragment length polymorphisms (RFLPs), three RFLPs detected with two probes that map 5' to the insulin gene, the serologically defined HLA loci, and the immunoglobulin allotypes. Data also were included for auto-antibodies to insulin and pancreatic islet cells as possible indicators of pathogenesis and for antibodies to certain viruses that have bee…

Geneticsendocrine system diseasesEpidemiologyImmunoglobulin AllotypesHuman leukocyte antigenBiologymedicine.diseaseGenetic analysisGenetic markerDiabetes mellitusmedicinebiology.proteinMultiplexRestriction fragment length polymorphismAntibodyGenetics (clinical)Genetic Epidemiology
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A Major Effect Gene Controlling Development and Pathogenicity in Botrytis cinerea Identified Through Genetic Analysis of Natural Mycelial Non-pathoge…

2021

Botrytis cinerea is a necrotrophic plant pathogenic fungus with a wide host range. Its natural populations are phenotypically and genetically very diverse. A survey of B. cinerea isolates causing gray mold in the vineyards of Castilla y León, Spain, was carried out and as a result eight non-pathogenic natural variants were identified. Phenotypically these isolates belong to two groups. The first group consists of seven isolates displaying a characteristic mycelial morphotype, which do not sporulate and is unable to produce sclerotia. The second group includes one isolate, which sporulates profusely and does not produce sclerotia. All of them are unresponsive to light. Crosses between a repr…

Geneticsgray moldBulked segregant analysisLocus (genetics)bulked segregant analysiPlant SciencePathogenic fungusBiologylcsh:Plant cultureacetyl transferasebiology.organism_classificationGenetic analysisLaboratorium voor PhytopathologieDNA binding domainComplementationbulked segregant analysisLaboratory of Phytopathologygenetic complementationlcsh:SB1-1110AlleleEPSGeneBotrytis cinereaOriginal ResearchFrontiers in Plant Science
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Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments

2004

The most common mutation in the USH2A gene (Usherin), 2299delG, causes both typical Usher (USH) syndrome type II and atypical USH syndrome, two autosomal recessive disorders, characterised by moderate to severe sensorineural hearing loss and retinitis pigmentosa (RP). Furthermore, the C759F mutation in the USH2A gene has been described in 4.5% of patients with nonsyndromic recessive RP. We have investigated the presence of the 2299delG and/or the C759F mutations in 191 unrelated Spanish patients with different syndromic and nonsyndromic retinal diseases, or with nonsyndromic hearing impairment. The 2299delG mutation was observed in patients with clinical signs of USHII or of atypical USH sy…

GenotypeHearing Loss SensorineuralEye diseaseDNA Mutational AnalysisMutation MissenseGenetic analysisGene FrequencyGenotypeRetinitis pigmentosaotorhinolaryngologic diseasesGeneticsmedicineHumansAlleleAllelesPolymorphism Single-Stranded ConformationalGenetics (clinical)Sequence DeletionGeneticsExtracellular Matrix Proteinsbusiness.industryDNAmedicine.diseasePhenotypePhenotypeSpainMutation (genetic algorithm)Sensorineural hearing lossbusinessRetinitis PigmentosaEuropean Journal of Human Genetics
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