Search Results - "TOSHNER, Mark R"

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    The pulmonary endothelium in acute respiratory distress syndrome: insights and therapeutic opportunities by Millar, Fraser R, Summers, Charlotte, Griffiths, Mark J, Toshner, Mark R, Proudfoot, Alastair G

    Published in Thorax (01-05-2016)
    “…The pulmonary endothelium is a dynamic, metabolically active layer of squamous endothelial cells ideally placed to mediate key processes involved in lung…”
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    Journal Article
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    Long-term use of sildenafil in inoperable chronic thromboembolic pulmonary hypertension by Suntharalingam, Jay, Treacy, Carmen M, Doughty, Natalie J, Goldsmith, Kimberley, Soon, Elaine, Toshner, Mark R, Sheares, Karen K, Hughes, Rodney, Morrell, Nicholas W, Pepke-Zaba, Joanna

    Published in Chest (01-08-2008)
    “…There are currently no licensed medical therapies for inoperable chronic thromboembolic pulmonary hypertension (CTEPH). In this double-blind,…”
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    Decreased time constant of the pulmonary circulation in chronic thromboembolic pulmonary hypertension by MacKenzie Ross, Robert V, Toshner, Mark R, Soon, Elaine, Naeije, Robert, Pepke-Zaba, Joanna

    “…This study analyzed the relationship between pulmonary vascular resistance (PVR) and pulmonary arterial compliance (Ca) in patients with idiopathic pulmonary…”
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    Approaches to treat pulmonary arterial hypertension by targeting BMPR2: from cell membrane to nucleus by Dunmore, Benjamin J, Jones, Rowena J, Toshner, Mark R, Upton, Paul D, Morrell, Nicholas W

    Published in Cardiovascular research (28-09-2021)
    “…Abstract Pulmonary arterial hypertension (PAH) is estimated to affect between 10 and 50 people per million worldwide. The lack of cure and devastating nature…”
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    Prevalence and clinical significance of conduction disease in patients with idiopathic pulmonary arterial hypertension by Reddy, Sathineni Ashwin, Nethercott, Sarah L., Teh, Wen, De Bie, Eckart MDD, Pepke-Zaba, Joanna, Toshner, Mark R., Martin, Claire A.

    “…Anatomical and physiological changes in the right heart as a direct consequence of the upstream pressure overload characteristic of idiopathic pulmonary…”
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    The lysosomal inhibitor, chloroquine, increases cell surface BMPR-II levels and restores BMP9 signalling in endothelial cells harbouring BMPR-II mutations by Dunmore, Benjamin J, Drake, Kylie M, Upton, Paul D, Toshner, Mark R, Aldred, Micheala A, Morrell, Nicholas W

    Published in Human molecular genetics (15-09-2013)
    “…Pulmonary arterial hypertension (PAH) is characterized by dysregulated pulmonary artery endothelial cell (PAEC) proliferation, apoptosis and permeability…”
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    Deprivation and prognosis in patients with pulmonary arterial hypertension: missing the effect of deprivation on a rare disease? by Sofianopoulou, Eleni, Church, Colin, Coghlan, Gerry, Howard, Luke, Johnson, Martin, Kiely, David G, Lawrie, Allan, Lordan, James, Wilkins, Martin R, Wort, Stephen J, Morrell, Nicholas W, Toshner, Mark R

    Published in The European respiratory journal (01-08-2020)
    “…In this journal, P ellino et al. [1] presented a survival analysis to assess how deprivation affects prognosis in patients with pulmonary arterial hypertension…”
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    Generation and Culture of Blood Outgrowth Endothelial Cells from Human Peripheral Blood by Ormiston, Mark L, Toshner, Mark R, Kiskin, Fedir N, Huang, Christopher J Z, Groves, Emily, Morrell, Nicholas W, Rana, Amer A

    Published in Journal of visualized experiments (23-12-2015)
    “…Historically, the limited availability of primary endothelial cells from patients with vascular disorders has hindered the study of the molecular mechanisms…”
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    Unexplained iron deficiency in idiopathic and heritable pulmonary arterial hypertension by Soon, Elaine, Treacy, Carmen M, Toshner, Mark R, MacKenzie-Ross, Robert, Manglam, Vijay, Busbridge, Mark, Sinclair-McGarvie, Mark, Arnold, Jayantha, Sheares, Karen K, Morrell, Nicholas W, Pepke-Zaba, Joanna

    Published in Thorax (01-04-2011)
    “…Anaemia is common in left heart failure and is associated with a poorer outcome. Many patients with pulmonary arterial hypertension (PAH) are anaemic or…”
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