Global ETD Search

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Showing 1 to 7 of 7 for “"Autosomal chromosomes"”.

  1. Meiotic defects in infertile men

    … to observe the synapsis and recombination of chromosomes during meiosis, and fluorescent in-situ hybridization (FISH) to assess sperm aneuploidy. We analyzed testicular tissue from thirty-one men (10 fertile and 21 infertile men). We observed that ~36% (5/14) of men with impaired …

    ubc Repository record for Meiotic defects in infertile men (opens in a new tab)

  2. Super-resolution Imaging of Chromatin and Functional Nuclear Architecture

    … the use of transcription inhibition, and on the autosomal chromosomes through mutant fly lines, using empty-space statistics to quantify their organisation. This indicated that the Y loop chains of clusters structure was unlikely to be determined by transcription. Active and inactive histone …

    cambridge Repository record for Super-resolution Imaging of Chromatin and Functional Nuclear Architecture (opens in a new tab)

  3. Sex Chromosome Evolution in Blow Flies

    … in blow flies is highly conserved (five pairs of autosomal chromosomes and one pair sex chromosome), there is variation in sex determining mechanisms and sex chromosome structure within closely related species in blow flies. The evolutionary history of sex chromosomes in blow fly species have not …

    iupui Repository record for Sex Chromosome Evolution in Blow Flies (opens in a new tab)

  4. Single Nucleotide Polymorphisms:Characterisation and Application to Profiling of Degraded DNA

    … from the non-coding region of the 22 pairs of autosomal chromosomes were identified and SNP assays developed. Instead of selecting the SNPs from the available GenBank® sites, SNPs were typed from Arab individuals from Kuwait and United Arab Emirates (UAE) to identify polymorphic SNPs. In order …

    cent-lancashire Repository record for Single Nucleotide Polymorphisms:Characterisation and Application to Profiling of Degraded DNA (opens in a new tab)

  5. Exploring the Grey Zone between Type 1 and Type 2 Diabetes

    … is a monogenic form of diabetes inherited in an autosomal dominant fashion (individual has one copy of a mutant gene and one normal gene on a pair of autosomal chromosomes) characterized by nonketotic diabetes, age at onset before 25 years and primarily defect in beta-cell function. Until now, …

    lund Repository record for Exploring the Grey Zone between Type 1 and Type 2 Diabetes (opens in a new tab)

  6. Análisis molecular de variación de polimorfismos str autosómicos y de cromosoma "y" en grupos étnicos de ecuador con aplicación médico - forense.

    En este trabajo se analizó un total de 1438 muestras de 4 gupos étnicos de Ecuador, entre ellos mestizos, amerindios hollaras, amerindios waorani y negros afroamericanos; se analizó por técnicas manuales y electroforesis capilar 20 microsatelites autonómicos D3S1358, HumFGA, D21S11, Penta E, Penta …

    dialnet Repository record for Análisis molecular de variación de polimorfismos str autosómicos y de cromosoma "y" en grupos étnicos de ecuador con aplicación médico - forense. (opens in a new tab)

  7. Functional Genome-wide Association Studies (fGWAS) and genomics landscape of signatures of polygenic adaptation in Botswana populations with HIV-1 C infection

    … (WGS) of Batswana exposed to HIV-1C. Although autosomal SNPs are widely utilized for functional-GWAS research, recent studies have also linked mitochondria DNA (mtDNA) haplotypes to various HIV outcomes. We explored the possibility of using both autosomal and mtDNA SNPs to enrich fGWAS …

    cape-town Repository record for Functional Genome-wide Association Studies (fGWAS) and genomics landscape of signatures of polygenic adaptation in Botswana populations with HIV-1 C infection (opens in a new tab)