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Mark Woodward

Researcher at Bristol Royal Hospital for Children

Publications -  35
Citations -  2023

Mark Woodward is an academic researcher from Bristol Royal Hospital for Children. The author has contributed to research in topics: Neural crest & Embryonic stem cell. The author has an hindex of 13, co-authored 34 publications receiving 1699 citations. Previous affiliations of Mark Woodward include University of Bristol & University Hospitals Bristol NHS Foundation Trust.

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Metabolic mediators of the effects of body-mass index, overweight, and obesity on coronary heart disease and stroke: A pooled analysis of 97 prospective cohorts with 1·8 million participants

TL;DR: How much of the effects of BMI on coronary heart disease and stroke are mediated through blood pressure, cholesterol, and glucose, and how much is independent of these factors is quantified.
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Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies

Nadeem Sarwar, +96 more
TL;DR: In this article, a functional genetic variant known to affect IL6R signalling was studied to assess whether this pathway is causally relevant to coronary heart disease, and Asp358Ala was not associated with lipid concentrations, blood pressure, adiposity, dysglycaemia, or smoking.
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Expression of endothelin 3 by mesenchymal cells of embryonic mouse caecum

TL;DR: Mesenchymal cells of the caecum express high levels of EDN3 mRNA during embryogenesis and hence the production ofEDN3 at the caecaum is likely to act on neural crest cells as a paracrine factor necessary for subsequent innervation of the terminal gut.
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Clinical and genetic analysis of patients with cystinuria in the United Kingdom.

TL;DR: Patients with cystinuria in the United Kingdom often present atypically with staghorn calculi at ≥40 years old and commonly develop significant renal impairment, and treatments directed toward reducing stone burden need to be rationalized and developed to optimize patient care.
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Time-dependent effects of endothelin-3 on enteric nervous system development in an organ culture model of Hirschsprung's disease

TL;DR: An organ culture model has been developed in which NCC colonisation of embryonic gut mirrors that described in vivo, and blockade of the EDN3/EDNRB receptor pathway shows that the interaction of endothelin-3 with its receptor is only necessary for NCC Colonisation at early time-points, despite the continued expression of endethelin- 3 mRNA in the gut.