Search Results - Additive genetic variable

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  1. Microsatellite marker development and parentage assignment in Haliotis midae by Van den Berg, Nicol-Candice

    Published 2012
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  2. Molecular and evolutionary analysis of a gene conserved in most Orthopoxviruses by Douglass, Nicola Jennifer

    Published 2017
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  3. Characterisation of the population genetics of farm-bred Haliotis midae using microsatellite DNA markers by Naidoo, René Kathleen

    Published 2014
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  4. Characterisation of the genetic diversity of the southern cattle tick, Rhipicephalus microplus, populations from South Africa

    Published 2015
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  5. Genetic diversity and candidate gene association analysis for growth in the South African Yellowtail (Seriola lalandi) by Jansen van Rensburg, Mieke

    Published 2026
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  6. Occurrence and genetic diversity of Anaplasma marginale in cattle from two diptanks in Zambezia Province Mozambique

    Published 2017
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  7. Population genetics of South African Protea L. (Proteaceae) species associated with various pollinator guilds by Smith, Megan

    Published 2020
    “…However, it is often uncertain how these pollination systems affect gene flow between plant populations, mating system outcome, and subsequent genetic health of plant species. Genetic variability is an important aspect in understanding the long-term survival of a species because excessive homozygosity, as a result of high amounts of inbreeding, may restrict a species’ long-term local adaptive potential. …”
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  8. Human Immunodeficiency Virus/Human Papillomavirus co-infection and host molecular genetics of cervical carcinoma by Chambuso, Ramadhani Salum

    Published 2020
    “…This study suggests that the dual pro-oncogenic effects of HPV oncoproteins E6/E7 and the HIV-1 oncoprotein Tat, may exacerbate and accelerate the rate of cervical disease progression in a subgroup of HIV-1-positive women. Additionally, HIV-1-positive cervical cancer has three important carcinogenesis steps: firstly, HPV integration into the host genome, secondly, dual pro-oncogenic effects of HPV oncoproteins E6/E7, and the HIV-1 Tat oncoprotein in the host genome and, thirdly, the accumulation of repeated, unrepaired genetic mutations and genetic alterations within the host chromosomal DNA. …”
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  9. Congenital and genetic disruptions of human ocular motility and alignment – phenotypic / genotypic bi-directional algorithm by Oystreck, Darren T

    Published 2019
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  10. The role of non-structural protein NS3 in the African horse sickness virus infection cycle in mammalian and insect cells

    Published 2020
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  11. Genetic Contributors to Parkinson’s Disease and Vascular Parkinsonism in the Egyptian Population: Validation and Discovery Across the Parkinsonian Spectrum by ElShafie, Salma

    Published 2026
    “…Despite major advances in genomics of parkinsonism, individuals of Middle Eastern and North African ancestry -including Egyptians- remain markedly underrepresented in genetic studies. This gap limits our understanding of disease risk, phenotypic variability, and ancestry-specific genetic mechanisms. …”
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  12. Leveraging the microbiome in host genome wide association studies by Awany, Denis

    Published 2021
    “…Genome-wide association study (GWAS) has emerged as an effective method for detecting genetic polymorphisms associated with expressed phenotypes. …”
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  13. Pharmacogenomics of sickle cell disease therapeutics: pain and drug metabolism associated gene variants and hydroxyurea-induced post-transcriptional expression of miRNAs by Mnika,Khuthala

    Published 2022
    “…Moreover, association studies were carried out on pharmacogenes variants with SCD clinical variability. Additionally, protein-protein interaction (PPI) network and enriched biological processes and pathways were investigated. …”
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  14. Identifying Genes and Novel Variants Involved in Nonsyndromic Hearing Impairment, and Assessment of the Psychosocial Burden of Hearing Impairment in Cameroon by Wonkam, Tingang Edmond

    Published 2022
    “…Hereditary HI can be syndromic or non-syndromic, depending on whether it is associated with additional abnormalities in other organs or not. Non-syndromic HI (NSHI) accounts for 70% of hereditary hearing loss, and is genetically highly heterogeneous, with approximately 170 loci and 121 genes identified to date. …”
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  15. Functional Genome-wide Association Studies (fGWAS) and genomics landscape of signatures of polygenic adaptation in Botswana populations with HIV-1 C infection by Choga, Wonderful Tatenda

    Published 2023
    “…We demonstrated that research on host genetic variables that affect HIV-1C clinical outcomes among Batswana are still understudied. …”
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  16. Characterization of the mitochondrial genomes of Diuraphis noxia biotypes by De Jager, Laura-Ellen

    Published 2015
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