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Showing 1 to 7 of 7 for “"primary ciliary dyskinesia (PCD)"”.

  1. Primary Ciliary Dyskinesia: An Epidemiological Exploration. Furthering our understanding of the burden of disease in PCD

    Primary ciliary dyskinesia (PCD) is an underrecognized multisystem genetic disorder that is characterized by dysfunctional motile cilia and abnormal mucociliary clearance. In recent years, there have been significant advancements in the understanding of PCD including, but are not limited to, …

    toronto-retro Repository record for Primary Ciliary Dyskinesia: An Epidemiological Exploration. Furthering our understanding of the burden of disease in PCD (opens in a new tab)

  2. Genetic Approach to Discover ARMC4 as a Novel NF-κB Negative Regulator and Tumor Suppressor in Colorectal Cancer

    … protein only known to date for its role in primary ciliary dyskinesia (PCD) and mouse spermatogenesis. Thus, my work reveals a completely new facet of ARMC4 function that has never been reported before. We showed that ARMC4 overexpression downregulated the expression of NF-κB-dependent …

    iupui Repository record for Genetic Approach to Discover ARMC4 as a Novel NF-κB Negative Regulator and Tumor Suppressor in Colorectal Cancer (opens in a new tab)

  3. Building capacity for diagnosis of Primary Ciliary Dyskinesia in South Africa: a descriptive study

    Background: Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterized by abnormal cilia motility. Diagnostic capacity for PCD in sub-Saharan Africa (sSA) is limited; and incidence of PCD and genotype in sSA is unknown. Objectives: To determine the prevalence of PCD in children and …

    cape-town Repository record for Building capacity for diagnosis of Primary Ciliary Dyskinesia in South Africa: a descriptive study (opens in a new tab)

  4. Primary ciliary dyskinesia: a biopsychosocial approach

    Background: Primary ciliary dyskinesia (PCD) is a rare heterogeneous genetic disorder associated with abnormal ciliary structure and function and characterised by progressive sinopulmonary disease. There is no ‘gold standard’ for diagnosing PCD. This thesis aimed: to provide an overview of the PCD

    cork Repository record for Primary ciliary dyskinesia: a biopsychosocial approach (opens in a new tab)

  5. The role of hydrodynamic forces in synchronisation and alignment of mammalian motile cilia

    … conditions such as cystic fibrosis (CF), primary ciliary dyskinesia (PCD) or asthma. In the brain, the multiciliated ependymal cells cover all the ventricles. Their cilia beat in a coordinated fashion to ensure the cerebrospinal fluid circulation necessary for brain homoeostasis, toxin …

    cambridge Repository record for The role of hydrodynamic forces in synchronisation and alignment of mammalian motile cilia (opens in a new tab)

  6. Mutationen in DNAH5 verursachen Primäre Ziliäre Dyskinesie

    … vererbte Primäre Ziliäre Dyskinesie (PCD) ist durch rezidivierende Infektionen der oberen und unteren Atemwege aufgrund einer eingeschränkten mukoziliären Reinigung charakterisiert. Einige Patienten leiden unter reduzierter Fertilität durch Dysmotilität der Spermien oder der Zilien des …

    freiburg-diss Repository record for Mutationen in DNAH5 verursachen Primäre Ziliäre Dyskinesie (opens in a new tab)

  7. Investigating the role of R2TP-like co-chaperone complexes during axonemal dynein assembly

    … is defective, it can lead to a disorder called Primary Ciliary Dyskinesia, or PCD. This is a heterogeneous, autosomal recessive disorder – symptoms of which include abnormally positioned organs, chronic respiratory infections and infertility. Therefore, the development and structure of the …

    edinburgh Repository record for Investigating the role of R2TP-like co-chaperone complexes during axonemal dynein assembly (opens in a new tab)