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Showing 1 to 8 of 8 for “"TAAD"”.

  1. Molecular Mechanisms of Vascular Disease In Patients With Rare Variants In Myh11

    <p>Thoracic aortic aneurysms and dissections (TAAD) are the primary disease affecting the thoracic ascending aorta, with an incidence rate of 10.4/100,000. Although about 20% of patients carry a mutation in a single gene that causes their disease, the remaining 80% of patients may also have genetic …

    uthsc Repository record for Molecular Mechanisms of Vascular Disease In Patients With Rare Variants In Myh11 (opens in a new tab)

  2. Pharmacologic and Genetic Manipulations of Angiotensin Signaling In Thoracic Aortic Disease Models

    <p>Thoracic aortic aneurysms and dissections (TAAD) are a major cause of morbidity and mortality in patients. Many different risk factors have been associated TAAD, but hypertension is the largest risk factor. Subsets of TAAD patients have identifiable syndromic genetic diseases, yet a number of …

    uthsc Repository record for Pharmacologic and Genetic Manipulations of Angiotensin Signaling In Thoracic Aortic Disease Models (opens in a new tab)

  3. Effects of The Acta2 R258C Mutation On Vascular Smooth Muscle Cell Phenotype and Properties

    <p>Thoracic Aortic Aneurysms and Dissections (TAAD) are the fifteenth leading cause of death in the United States. About 15% of TAAD patients have family history of the disease. The most commonly mutated gene in these families is <em>ACTA2</em>, encoding smooth muscle-specific α-actin. …

    uthsc Repository record for Effects of The Acta2 R258C Mutation On Vascular Smooth Muscle Cell Phenotype and Properties (opens in a new tab)

  4. Mechanism of Rare Variant In Acta2, P.Arg149Cys, Driving Diverse Vascular Disease

    … to thoracic aortic aneurysms and dissections (TAAD) and early-onset coronary artery disease (CAD). The most common <em>ACTA2</em> mutation is a genetic alteration of arginine 149 to a cysteine, <em>ACTA2</em> p.Arg149Cys, which accounts for disease in 24% of all <em>ACTA2</em> mutation …

    uthsc Repository record for Mechanism of Rare Variant In Acta2, P.Arg149Cys, Driving Diverse Vascular Disease (opens in a new tab)

  5. Characterization of The Vascular Pathology In The Acta2 R258C Mouse Model and Cerebrovascular Characterization of The Acta2 Null Mouse

    … associated with thoracic aortic aneurysms (TAAD) and dissections (TAAD) and strokes. TAAD in patients is characterized by aortic media degeneration and loss in contractile force generation followed by aortic enlargement and subsequent rupture. Most stroke cases associated with <em>ACTA2</em> …

    uthsc Repository record for Characterization of The Vascular Pathology In The Acta2 R258C Mouse Model and Cerebrovascular Characterization of The Acta2 Null Mouse (opens in a new tab)

  6. Strategies to maximize feed quality and poultry performance

    … and subsequent true amino acid digestibility (TAAD) of practical turkey diets. Experiment 1 was a 3 Binder (Binder 1, Binder 2, or No Binder) x 2 MTECH (1% MAF + 38.1 mm die or 3% MAF + 44.96 mm die) factorial design that utilized practical turkey starter diets manufactured at West Virginia …

    wvu Repository record for Strategies to maximize feed quality and poultry performance (opens in a new tab)

  7. Smooth Muscle Hyperplasia Due to Acta2/Myh11 Mutations: Identification of Novel Pathology and Pathways Leading to Aneurysms and Diverse Vascular Occlusive Diseases

    … thoracic aortic aneurysms and dissections (TAAD) and early onset coronary artery disease and stroke. The mechanism by which these mutations lead to dilatation of some arteries but occlusion of others is unknown. We hypothesized that the mutations act through two distinct mechanisms to cause …

    uthsc Repository record for Smooth Muscle Hyperplasia Due to Acta2/Myh11 Mutations: Identification of Novel Pathology and Pathways Leading to Aneurysms and Diverse Vascular Occlusive Diseases (opens in a new tab)

  8. Characterizing A Novel Genetic Locus Associated With Familial Co-Occurrence of Thoracic Aortic Aneurysms and Intracranial Aneurysms

    The Mendelian inheritance of genetic mutations can lead to adult-onset cardiovascular disease. Several genetic loci have been mapped for the familial form of Thoracic Aortic Aneurysms (TAA), and many causal mutations have been identified for this disease. Intracranial Aneurysms (ICA) also show …

    uthsc Repository record for Characterizing A Novel Genetic Locus Associated With Familial Co-Occurrence of Thoracic Aortic Aneurysms and Intracranial Aneurysms (opens in a new tab)