About: Nicholas W Morrell

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher ORCID ID = 0000-0001-5700-9792

Attributes	Values
rdf:type	Item
description	연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) researcher ORCID ID = 0000-0001-5700-9792 (en)
rdfs:label	Nicholas W Morrell (en) Nicholas W Morrell (nl) Nicholas W Morrell (ast) Nicholas W. Morrell (tr)
skos:prefLabel	Nicholas W Morrell (en) Nicholas W Morrell (nl) Nicholas W Morrell (ast) Nicholas W. Morrell (tr)
name	Nicholas W Morrell (en) Nicholas W Morrell (nl) Nicholas W Morrell (ast) Nicholas W. Morrell (tr)
given name	wds:Q60960702-67430099-79B4-4B4D-81FE-DCBC5750C868
given name	Nicholas
instance of	wds:Q60960702-42C50FA8-806C-498E-9F85-4C29155D1A34
instance of	Homo sapiens
skos:altLabel	Nicholas Morrell (en)
occupation	wds:Q60960702-67173625-4cfe-0df1-6370-d0355db47490
employer	wds:Q60960702-07193F0B-FF89-417D-8A64-E8F39A922428 wds:Q60960702-EEE093F2-60FB-4E08-97BF-E7836A79BAF4
sex or gender	wds:Q60960702-11648644-476c-3f74-c4da-02c2f141dbed
VIAF ID	wds:Q60960702-2716A2DB-4BBD-4DBA-AA7C-71492ADEB5EE
educated at	wds:Q60960702-63CD91A3-3883-48D3-8497-CEB1DCE25249 wds:Q60960702-7AACB864-41DD-4CFD-BDBB-E2C56A1A8C55 wds:Q60960702-CBCFB838-D8F8-47EF-B0C9-121A51C5BE3F
family name	wds:Q60960702-35E6C58E-A87D-4428-804E-A83D06C04BC6
WorldCat Identities ID (superseded)	wds:Q60960702-99E3848A-4DC1-4FE1-99CB-20EB89251A4D
National Library of Israel J9U ID	wds:Q60960702-14BBDC64-3128-43D9-9E2E-2449B28D1232
VIAF ID	http://viaf.org/viaf/270463185
occupation	researcher
employer	John Ffowcs Williams University of Cambridge Medicine
sex or gender	male
VIAF ID	270463185
educated at	John Ffowcs Williams University of London
family name	Morrell
WorldCat Identities ID (superseded)	lccn-nb2002022806
National Library of Israel J9U ID	987007375900405171
ORCID iD	wds:Q60960702-F7A47F39-285A-4E61-8C8A-0AF51230702E
ORCID iD	https://orcid.org/0000-0001-5700-9792
ORCID iD	0000-0001-5700-9792
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q60960702
is author of	A novel RASA1 mutation causing capillary malformation-arteriovenous malformation (CM-AVM) presenting during pregnancy Inflammation, growth factors, and pulmonary vascular remodeling Tenascin-C is induced by mutated BMP type II receptors in familial forms of pulmonary arterial hypertension. Selective enhancement of endothelial BMPR-II with BMP9 reverses pulmonary arterial hypertension. Pulmonary vascular remodeling correlates with lung eggs and cytokines in murine schistosomiasis. Gremlin plays a key role in the pathogenesis of pulmonary hypertension Collateral ventilation and gas exchange in emphysema. MicroRNA-124 controls the proliferative, migratory, and inflammatory phenotype of pulmonary vascular fibroblasts Genetics and the molecular pathogenesis of pulmonary arterial hypertension Myocardin regulates vascular smooth muscle cell inflammatory activation and disease ET(A) and ET(B) receptors modulate the proliferation of human pulmonary artery smooth muscle cells Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertension Receptor for Activated C-Kinase 1, a Novel Interaction Partner of Type II Bone Morphogenetic Protein Receptor, Regulates Smooth Muscle Cell Proliferation in Pulmonary Arterial Hypertension A Role for miR-145 in Pulmonary Arterial Hypertension Vascular remodeling and ET-1 expression in rat strains with different responses to chronic hypoxia Altered growth responses of pulmonary artery smooth muscle cells from patients with primary pulmonary hypertension to transforming growth factor-beta(1) and bone morphogenetic proteins Cellular and molecular pathobiology of pulmonary arterial hypertension Cellular and molecular basis of pulmonary arterial hypertension Primary pulmonary hypertension is associated with reduced pulmonary vascular expression of type II bone morphogenetic protein receptor Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood Investigation of Second Genetic Hits at the BMPR2 Locus as a Modulator of Disease Progression in Familial Pulmonary Arterial Hypertension Relevant issues in the pathology and pathobiology of pulmonary hypertension cAMP phosphodiesterase inhibitors potentiate effects of prostacyclin analogs in hypoxic pulmonary vascular remodeling Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia. Pulmonary hypertension due to BMPR2 mutation: a new paradigm for tissue remodeling? Tumour necrosis factor-α gene promoter polymorphism in chronic obstructive pulmonary disease Anticipated classes of new medications and molecular targets for pulmonary arterial hypertension Altered bone morphogenetic protein and transforming growth factor-beta signaling in rat models of pulmonary hypertension: potential for activin receptor-like kinase-5 inhibition in prevention and progression of disease Sildenafil potentiates bone morphogenetic protein signaling in pulmonary arterial smooth muscle cells and in experimental pulmonary hypertension Dynamic changes in lung microRNA profiles during the development of pulmonary hypertension due to chronic hypoxia and monocrotaline Mechanism of cicaprost-induced desensitization in rat pulmonary artery smooth muscle cells involves a PKA-mediated inhibition of adenylyl cyclase Functional analysis of bone morphogenetic protein type II receptor mutations underlying primary pulmonary hypertension Caveolae protect endothelial cells from membrane rupture during increased cardiac output MicroRNA-143 Activation Regulates Smooth Muscle and Endothelial Cell Crosstalk in Pulmonary Arterial Hypertension Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects Molecular mechanisms of pulmonary arterial hypertension: role of mutations in the bone morphogenetic protein type II receptor The transforming growth factor-β-bone morphogenetic protein type signalling pathway in pulmonary vascular homeostasis and disease Bone morphogenetic protein (BMP) and activin type II receptors balance BMP9 signals mediated by activin receptor-like kinase-1 in human pulmonary artery endothelial cells Pilot study of losartan for pulmonary hypertension in chronic obstructive pulmonary disease Angiotensin converting enzyme expression is increased in small pulmonary arteries of rats with hypoxia-induced pulmonary hypertension. Utility of echocardiography in assessment of pulmonary hypertension secondary to COPD Angiotensin II activates MAPK and stimulates growth of human pulmonary artery smooth muscle via AT1 receptors Role of angiotensin-converting enzyme and angiotensin II in development of hypoxic pulmonary hypertension Expression of pulmonary vascular angiotensin-converting enzyme in primary and secondary plexiform pulmonary hypertension Treatment with anti-gremlin 1 antibody ameliorates chronic hypoxia/SU5416-induced pulmonary arterial hypertension in mice Characterization of the BMPR2 5'-untranslated region and a novel mutation in pulmonary hypertension

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