Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Keira L. Watts"'
Autor:
Gourab Misra, Julius Sim, Shaughn O’Brien, Suzanne Jerreat, Thomas Coia, Zeiad El-Gizawy, Keira L. Watts, Joanne Ritchie
Objective To compare electrodiathermy with helium thermal coagulation in laparoscopic treatment of mild-to-moderate endometriosis. Design Parallel-group randomised controlled trial. Setting A UK endometriosis centre. Population Non-pregnant women age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afcc24e2b9bee6eb0a93289d547f8319
Autor:
Keira L. Watts, Michael Murray, Thomas A. Shepherd, Simon J. Ellis, Laura Longshaw, Andrew R. Mayes, Julius Sim, Nicola M.J. Edelstyn
Publikováno v:
Pilot and Feasibility Studies, Vol 4, Iss 1, Pp 1-12 (2017)
Pilot and Feasibility Studies
Shepherd, T A, Edelstyn, N M J, Longshaw, L, Sim, J, Watts, K, Mayes, A R, Murray, M & Ellis, S J 2018, ' Feasibility of a randomized single-blind crossover trial to assess the effects of the second-generation slow-release dopamine agonists pramipexole and ropinirole on cued recall memory in idiopathic mild or moderate Parkinson's disease without cognitive impairment ', Pilot and Feasibility Studies, vol. 4, no. 1, 11 . https://doi.org/10.1186/s40814-017-0154-7
Pilot and Feasibility Studies
Shepherd, T A, Edelstyn, N M J, Longshaw, L, Sim, J, Watts, K, Mayes, A R, Murray, M & Ellis, S J 2018, ' Feasibility of a randomized single-blind crossover trial to assess the effects of the second-generation slow-release dopamine agonists pramipexole and ropinirole on cued recall memory in idiopathic mild or moderate Parkinson's disease without cognitive impairment ', Pilot and Feasibility Studies, vol. 4, no. 1, 11 . https://doi.org/10.1186/s40814-017-0154-7
Background The aim was to assess the feasibility of a single-centre, single-blind, randomized, crossover design to explore the effects of two slow-release dopamine agonists, ropinirole and pramipexole, on cued recall in Parkinson’s disease. As the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8c34bd19632db6eded73c31becc422d
Publikováno v:
American Journal of Respiratory Cell and Molecular Biology. 32:290-300
Simvastatin is best known for its antilipidemic action and use in cardiovascular disease due to its inhibition of 3-hydroxy-3-methylglutaryl CoenzymeA (HMG CoA) reductase, a key enzyme in the cholesterol synthesis pathway. Inhibition of biological pr
Autor:
Monica A. Spiteri, Keira L. Watts
Publikováno v:
American Journal of Physiology-Lung Cellular and Molecular Physiology. 287:L1323-L1332
Connective tissue growth factor (CTGF), a potent profibrotic mediator, acts downstream and in concert with transforming growth factor (TGF)-β to drive fibrogenesis. Significant upregulation of CTGF has been reported in fibrogenic diseases, including
Publikováno v:
A97. EPIGENETIC MECHANISMS IN LUNG FIBROSIS.
Publikováno v:
Molecular and cellular biology. 30(12)
Targeted repression of a subset of key genes involved in tissue remodeling is a cardinal feature of idiopathic pulmonary fibrosis (IPF). The mechanism is unclear but is potentially important in disease pathogenesis and therapeutic targeting. We have
Publikováno v:
Molecular and cellular biology. 29(15)
Diminished cyclooxygenase 2 (COX-2) expression in fibroblasts, with a resultant defect in the production of the antifibrotic mediator prostaglandin E(2), plays a key role in the pathogenesis of idiopathic pulmonary fibrosis (IPF). Here, we have chara
Publikováno v:
C19. BEYOND THE CODE: EPIGENETICS IN DIFFERENTIATION AND DISEASE.
Diminished cyclooxygenase 2 (COX-2) expression in fibroblasts, with a resultant defect in the production of the antifibrotic mediator prostaglandin E(2), plays a key role in the pathogenesis of idiopathic pulmonary fibrosis (IPF). Here, we have chara
Publikováno v:
Respiratory Research
Respiratory Research, Vol 7, Iss 1, p 88 (2006)
Respiratory Research, Vol 7, Iss 1, p 88 (2006)
Background Idiopathic Pulmonary Fibrosis (IPF) is a debilitating disease characterized by exaggerated extracellular matrix deposition and aggressive lung structural remodeling. Disease pathogenesis is driven by fibroblastic foci formation, consequent