Search Results - "West, James D"
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Longitudinal Analysis Casts Doubt on the Presence of Genetic Anticipation in Heritable Pulmonary Arterial Hypertension
Published in American journal of respiratory and critical care medicine (01-11-2012)“…Analysis of the age of onset in heritable pulmonary arterial hypertension (HPAH) has led to the hypothesis that genetic anticipation causes younger age of…”
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Serotonin 2B Receptor Antagonism Prevents Heritable Pulmonary Arterial Hypertension
Published in PloS one (10-02-2016)“…Serotonergic anorexigens are the primary pharmacologic risk factor associated with pulmonary arterial hypertension (PAH), and the resulting PAH is clinically…”
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Thromboxane-Prostanoid Receptor Signaling Drives Persistent Fibroblast Activation in Pulmonary Fibrosis
Published in American journal of respiratory and critical care medicine (01-09-2022)“…Although persistent fibroblast activation is a hallmark of idiopathic pulmonary fibrosis (IPF), mechanisms regulating persistent fibroblast activation in the…”
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Small Molecule Activators of the Heat Shock Response: Chemical Properties, Molecular Targets, and Therapeutic Promise
Published in Chemical research in toxicology (15-10-2012)“…All cells have developed various mechanisms to respond and adapt to a variety of environmental challenges, including stresses that damage cellular proteins…”
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Activation of heat shock and antioxidant responses by the natural product celastrol: transcriptional signatures of a thiol-targeted molecule
Published in Molecular biology of the cell (01-03-2008)“…Stress response pathways allow cells to sense and respond to environmental changes and adverse pathophysiological states. Pharmacological modulation of…”
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The yeast Hsp70 Ssa1 is a sensor for activation of the heat shock response by thiol-reactive compounds
Published in Molecular biology of the cell (01-09-2012)“…The heat shock transcription factor HSF1 governs the response to heat shock, oxidative stresses, and xenobiotics through unknown mechanisms. We demonstrate…”
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Disruption of lineage specification in adult pulmonary mesenchymal progenitor cells promotes microvascular dysfunction
Published in The Journal of clinical investigation (01-06-2017)“…Pulmonary vascular disease is characterized by remodeling and loss of microvessels and is typically attributed to pathological responses in vascular…”
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Bone Marrow–Derived Proangiogenic Cells Mediate Pulmonary Arteriole Stiffening via Serotonin 2B Receptor Dependent Mechanism
Published in Circulation research (07-12-2018)“…RATIONALE:Pulmonary arterial hypertension is a deadly disease of the pulmonary vasculature for which no disease-modifying therapies exist. Small-vessel…”
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KCNK3 Mutation Causes Altered Immune Function in Pulmonary Arterial Hypertension Patients and Mouse Models
Published in International journal of molecular sciences (09-05-2021)“…Loss of function KCNK3 mutation is one of the gene variants driving hereditary pulmonary arterial hypertension (PAH). KCNK3 is expressed in several cell and…”
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Redox requirements for ubiquitin-like urmylation of Ahp1, a 2-Cys peroxiredoxin from yeast
Published in Redox biology (01-02-2020)“…The yeast peroxiredoxin Ahp1, like related anti-oxidant enzymes in other species, undergoes urmylation, a lysine-directed conjugation to ubiquitin-like…”
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Systems-level regulation of microRNA networks by miR-130/301 promotes pulmonary hypertension
Published in The Journal of clinical investigation (16-05-2022)Get full text
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Endothelial HIF signaling regulates pulmonary fibrosis-associated pulmonary hypertension
Published in American journal of physiology. Lung cellular and molecular physiology (01-02-2016)“…Pulmonary hypertension (PH) complicating chronic parenchymal lung disease, such as idiopathic pulmonary fibrosis, results in significant morbidity and…”
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rhACE2 Therapy Modifies Bleomycin-Induced Pulmonary Hypertension via Rescue of Vascular Remodeling
Published in Frontiers in physiology (09-04-2018)“…Pulmonary hypertension (PH) is a progressive cardiovascular disease, characterized by endothelial and smooth muscle dysfunction and vascular remodeling,…”
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Experimental Approaches for Investigating Disulfide-Based Redox Relays in Cells
Published in Chemical research in toxicology (17-10-2022)“…Reversible oxidation of cysteine residues within proteins occurs naturally during normal cellular homeostasis and can increase during oxidative stress…”
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Identification of a common Wnt-associated genetic signature across multiple cell types in pulmonary arterial hypertension
Published in American Journal of Physiology: Cell Physiology (01-09-2014)“…Understanding differences in gene expression that increase risk for pulmonary arterial hypertension (PAH) is essential to understanding the molecular basis for…”
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Myeloid-Derived Suppressor Cells and Pulmonary Hypertension
Published in International journal of molecular sciences (03-08-2018)“…Myeloid⁻derived suppressor cells (MDSCs) comprised a heterogeneous subset of bone marrow⁻derived myeloid cells, best studied in cancer research, that are…”
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Pulmonary Vascular Platform Models the Effects of Flow and Pressure on Endothelial Dysfunction in BMPR2 Associated Pulmonary Arterial Hypertension
Published in International journal of molecular sciences (29-08-2018)“…Endothelial dysfunction is a known consequence of bone morphogenetic protein type II receptor ( ) mutations seen in pulmonary arterial hypertension (PAH)…”
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l‐Carnitine therapy improves right heart dysfunction through Cpt1‐dependent fatty acid oxidation
Published in Pulmonary circulation (01-07-2022)“…Pulmonary arterial hypertension (PAH) is a fatal vasculopathy that ultimately leads to elevated pulmonary pressure and death by right ventricular (RV) failure,…”
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Monitoring uterine contractility in mice using a transcervical intrauterine pressure catheter
Published in Reproduction (Cambridge, England) (01-05-2018)“…In mouse models used to study parturition or pre-clinical therapeutic testing, measurement of uterine contractions is limited to either ex vivo isometric…”
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Urm1, not quite a ubiquitin-like modifier?
Published in Microbial cell (01-11-2021)“…Ubiquitin related modifier 1 (Urm1) is a unique eukaryotic member of the ubiquitin-fold (UbF) protein family and conserved from yeast to humans. Urm1 is…”
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