Search Results - "ALDRED, MICHEALA A"
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Genetics and genomics of pulmonary arterial hypertension
Published in The European respiratory journal (01-01-2019)“…Since 2000 there have been major advances in our understanding of the genetic and genomics of pulmonary arterial hypertension (PAH), although there remains…”
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Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects
Published in Human mutation (01-12-2015)“…ABSTRACT Pulmonary arterial hypertension (PAH) is an often fatal disorder resulting from several causes including heterogeneous genetic defects. While…”
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Low-Dose FK506 (Tacrolimus) in End-Stage Pulmonary Arterial Hypertension
Published in American journal of respiratory and critical care medicine (15-07-2015)Get full text
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Correction of nonsense BMPR2 and SMAD9 mutations by ataluren in pulmonary arterial hypertension
Published in American journal of respiratory cell and molecular biology (01-09-2013)“…Heritable pulmonary arterial hypertension (HPAH) is a serious lung vascular disease caused by heterozygous mutations in the bone morphogenetic protein (BMP)…”
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Human Lungs Airway Epithelium Upregulate MicroRNA-17 and MicroRNA-548b in Response to Cold Ischemia and Ex Vivo Reperfusion
Published in Transplantation (01-09-2020)“…BACKGROUND.Lung ischemia-reperfusion injury after transplantation is associated with worse clinical outcomes. MicroRNA (miR) are critical regulators of gene…”
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Identification and validation of a novel pathogenic variant in GDF2 (BMP9) responsible for hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations
Published in American journal of medical genetics. Part A (01-03-2022)“…Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant multisystemic vascular dysplasia, characterized by arteriovenous malformations (AVMs),…”
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Mitochondrial Haplogroups and Risk of Pulmonary Arterial Hypertension
Published in PloS one (25-05-2016)“…Pulmonary arterial hypertension (PAH) is a serious and often fatal disease. It is a panvasculopathy of the pulmonary microcirculation characterized by…”
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Circulating Angiogenic Precursors in Idiopathic Pulmonary Arterial Hypertension
Published in The American journal of pathology (01-03-2008)“…Vascular remodeling in idiopathic pulmonary arterial hypertension (IPAH) involves hyperproliferative and apoptosis-resistant pulmonary artery endothelial…”
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Food for Thought: The Emerging Role of Intestinal Microbiota in Pulmonary Arterial Hypertension
Published in American journal of respiratory cell and molecular biology (01-04-2022)“…Aldred discusses the paper by Huang et al which examines the emerging role of intestinal microbiota in pulmonary arterial hypertension. To elucidate the…”
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BMPR2 gene rearrangements account for a significant proportion of mutations in familial and idiopathic pulmonary arterial hypertension
Published in Human mutation (01-02-2006)“…Mutations of the BMPR2 gene predispose to pulmonary arterial hypertension (PAH), a serious, progressive disease of the pulmonary vascular system. However,…”
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Regulating the Regulators: Epigenetic Modulation of Regulatory T Cells in Pulmonary Hypertension
Published in American journal of respiratory and critical care medicine (15-10-2023)“…Farha and Aldred discuss the study by Chen and colleagues on the role of histone acetylation in regulating FOXP3 Tregs in human and experimental pulmonary…”
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PHorecasting Heritable Pulmonary Arterial Hypertension: Are We Nearly There Yet?
Published in American journal of respiratory and critical care medicine (01-12-2020)“…Aldred discusses two case studies by Amin and colleagues that gives a snapshot of clinical "conversion" from healthy to a diagnosis of PAH in two teenagers who…”
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Loss of Heterozygosity at 2q37 in Sporadic Wilms' Tumor: Putative Role for miR-562
Published in Clinical cancer research (01-10-2009)“…Purpose: Wilms' tumor is a childhood cancer of the kidney with an incidence of ∼1 in 10,000. Cooccurrence of Wilms' tumor with 2q37 deletion syndrome, an…”
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Genetic Classification of Benign and Malignant Thyroid Follicular Neoplasia Based on a Three-Gene Combination
Published in The journal of clinical endocrinology and metabolism (01-05-2005)“…Thyroid carcinoma is a common endocrine cancer with a favorable prognosis if subjected to timely treatment. However, the clinical identification of follicular…”
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RASA3 is a candidate gene in sickle cell disease‐associated pulmonary hypertension and pulmonary arterial hypertension
Published in Pulmonary circulation (01-04-2023)“…Pulmonary hypertension (PH) is associated with significant morbidity and mortality. RASA3 is a GTPase activating protein integral to angiogenesis and…”
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New Mutations and Pathogenesis of Pulmonary Hypertension: Progress and Puzzles in Disease Pathogenesis
Published in Circulation research (29-04-2022)“…Pulmonary arterial hypertension (PAH) is a complex multifactorial disease with poor prognosis characterized by functional and structural alterations of the…”
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Papillary and Follicular Thyroid Carcinomas Show Distinctly Different Microarray Expression Profiles and Can Be Distinguished by a Minimum of Five Genes
Published in Journal of clinical oncology (01-09-2004)“…We have previously conducted independent microarray expression analyses of the two most common types of nonmedullary thyroid carcinoma, namely papillary…”
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Human Primary Lung Endothelial Cells in Culture
Published in American journal of respiratory cell and molecular biology (01-06-2012)Get full text
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DNA Damage and Repair in Pulmonary Arterial Hypertension
Published in Genes (19-10-2020)“…Pulmonary arterial hypertension (PAH) is a complex multifactorial disease with both genetic and environmental dynamics contributing to disease progression…”
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Selective enhancement of endothelial BMPR-II with BMP9 reverses pulmonary arterial hypertension
Published in Nature medicine (01-07-2015)“…BMP9 activates signaling through the BMPR-II receptor in endothelial cells and reverses established disease in three animal models of pulmonary hypertension,…”
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