Zobrazeno 1 - 10
of 144
pro vyhledávání: '"Mark E, Roberts"'
Autor:
Chengjun Wu, Junhuan Ding, Graham W. Tindall, Zachariah A. Pittman, Mark C. Thies, Mark E. Roberts
Publikováno v:
Molecules, Vol 29, Iss 16, p 3879 (2024)
Over the past decade, the production of biofuels from lignocellulosic biomass has steadily increased to offset the use of fuels from petroleum. To make biofuels cost-competitive, however, it is necessary to add value to the “ligno-” components (u
Externí odkaz:
https://doaj.org/article/99ee2d12e8cc4dafb8f1882a6bf75203
Publikováno v:
Advanced Energy & Sustainability Research, Vol 3, Iss 1, Pp n/a-n/a (2022)
The power density of redox flow batteries (RFBs) utilized on iron‐containing electrolytes is improved by incorporating iron particle redox mediators into the electrodes. Nonpurified carbon nanotube (CNT) electrodes containing iron nanoparticles, fo
Externí odkaz:
https://doaj.org/article/0f11baa4368648389930a6b673272391
Publikováno v:
ERJ Open Research, Vol 7, Iss 3 (2021)
Type 1 myotonic dystrophy (DM1) causes sleep disordered breathing and respiratory failure due to a combination of obstructive sleep apnoea, reduced central drive and respiratory muscle weakness. Noninvasive ventilation (NIV) is commonly used for trea
Externí odkaz:
https://doaj.org/article/57d8f625ad34486195973159a3ff325e
Autor:
Yi Shiau Ng, Kyle Thompson, Daniela Loher, Sila Hopton, Gavin Falkous, Steven A. Hardy, Andrew M. Schaefer, Sandip Shaunak, Mark E. Roberts, James B. Lilleker, Robert W. Taylor
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Mitochondrial complex I deficiency is associated with a diverse range of clinical phenotypes and can arise due to either mitochondrial DNA (mtDNA) or nuclear gene defects. We investigated two adult patients who exhibited non-syndromic neurological fe
Externí odkaz:
https://doaj.org/article/8915da29156e45bda3e021d246a36389
Autor:
James B. Lilleker, Patrick Gordon, Janine A. Lamb, Heidi Lempp, Robert G. Cooper, Mark E. Roberts, Paula Jordan, Hector Chinoy, On behalf of the UK Myositis Network (UKMYONET), Myositis UK
Publikováno v:
BMC Rheumatology, Vol 1, Iss 1, Pp 1-6 (2017)
Abstract Background The idiopathic inflammatory myopathies (IIM, myositis) are a heterogeneous group of chronic autoimmune disorders causing considerable physical and mental health impact. There is a lack of formalised guidance defining best practice
Externí odkaz:
https://doaj.org/article/6bc5cb68bc6642bb8c5eea76cae7d087
Autor:
Neil O. Carragher, Mark E. Roberts, Rob Eagle, Tom Houslay, Sandeep Daya, Alexandra Ingleston-Orme, Rebecca E. Walls, Peter D. Caie
Supplementary Data from High-Content Phenotypic Profiling of Drug Response Signatures across Distinct Cancer Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::017dbfe177e178287bcfa61016733c74
https://doi.org/10.1158/1535-7163.22486082
https://doi.org/10.1158/1535-7163.22486082
Autor:
Joery P. Molenaar, Gaetano Vattemi, E. Kamsteeg, Benno Küsters, Damien Sternberg, Valeria Guglielmi, Amaia Martínez-Arroyo, K. Suetterlin, Corrie E. Erasmus, Barbara W. Brandom, Juergen Seeger, Susan Treves, Nicol C. Voermans, Thierry Kuntzer, Jérôme Franques, Mark E. Roberts, Roberto Fernández-Torrón, Frédéric Chevessier, Jamie I Verhoeven, Guillaume Bassez, Baziel G.M. van Engelen, Anthony Behin, Lucie Guyant-Maréchal, Richard J. Rodenburg, Savine Vicart, Jean Mathieu, Bruno Eymard, Armelle Magot, Michael G. Hanna, Yann Péréon, M.M.J. Snoeck
Publikováno v:
Brain
Brain, 143, 2, pp. 452-466
Brain, 143, 452-466
Brain, vol. 143, no. 2, pp. 452-466
Brain, 143, 2, pp. 452-466
Brain, 143, 452-466
Brain, vol. 143, no. 2, pp. 452-466
Brody disease is a rare myopathy characterized by exercise-induced muscle stiffness caused by mutations in the ATP2A1 gene. In the largest cohort of Brody patients to date, Molenaar et al. clarify the phenotype and diagnostic possibilities to help im
Publikováno v:
Molecular Genetics and Metabolism. 138:107245