Resultados da busca - Nicola Roberts
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Health literacy in COPD por Nicola Roberts, Ramesh Ghiassi, Martyn R Partridge
Publicado em 2008Revisão -
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NBS1 is involved in DNA repair and plays a synergistic role with ATM in mediating meiotic homologous recombination in plants por Wanda M. Waterworth, Cagla Altun, Susan J. Armstrong, Nicola Roberts, P. Dean, Kim Young, Clifford F. Weil, Clifford M. Bray, Christopher E. West
Publicado em 2007Artigo -
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Effects of Regular Physical Activity on the Immune System, Vaccination and Risk of Community-Acquired Infectious Disease in the General Population: Systematic Review and Meta-Analy... por Sébastien Chastin, Ukachukwu Okoroafor Abaraogu, Jan Bourgois, Philippa Dall, J. Darnborough, Elaine Duncan, Jasmien Dumortier, David Jiménez Pavón, Joanna McParland, Nicola Roberts, Mark Hamer
Publicado em 2021Revisão -
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British Thoracic Society Clinical Statement on pulmonary rehabilitation por William D‐C Man, Emma Chaplin, Enya Daynes, Alistair Drummond, Rachael A. Evans, Neil Greening, Claire M. Nolan, Matthew Pavitt, Nicola Roberts, Ioannis Vogiatzis, Sally Singh
Publicado em 2023Artigo -
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Melatonin and health: an umbrella review of health outcomes and biological mechanisms of action por Paul Posadzki, Ram Bajpai, Bhone Myint Kyaw, Nicola Roberts, Amnon Brzezinski, George I. Christopoulos, Ushashree Divakar, Shweta Bajpai, Michael Soljak, Gerard Dunleavy, Krister Järbrink, Nang Ei Ei Khaing, Chee Kiong Soh, Josip Car
Publicado em 2018Revisão -
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Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling por Kate Baker, Sarah L. Gordon, Detelina Grozeva, Margriet van Kogelenberg, Nicola Roberts, Michael Pike, Edward Blair, Matthew E. Hurles, W.K. Chong, Torsten Baldeweg, Manju A. Kurian, Stewart Boyd, Michael A. Cousin, F. Lucy Raymond
Publicado em 2015Artigo -
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Pathogenic Variants in PIGG Cause Intellectual Disability with Seizures and Hypotonia por Periklis Makrythanasis, Mitsuhiro Kato, Maha S. Zaki, Hirotomo Saitsu, Kazuyuki Nakamura, Federico Santoni, Satoko Miyatake, Mitsuko Nakashima, Mahmoud Y. Issa, Michel Guipponi, Audrey Letourneau, Clare V. Logan, Nicola Roberts, David Parry, Colin A. Johnson, Naomichi Matsumoto, Hanan Hamamy, Eamonn Sheridan, Taroh Kinoshita, Stylianos E. Antonarakis, Yoshiko Murakami
Publicado em 2016Artigo -
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De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome por Ghayda Mirzaa, David Parry, Andrew E. Fry, Kristin A. Giamanco, Jeremy Schwartzentruber, Megan R. Vanstone, Clare V. Logan, Nicola Roberts, Colin A. Johnson, Shawn Singh, Stanislav S. Kholmanskikh, Carissa Adams, Rebecca D. Hodge, Robert F. Hevner, David T. Bonthron, Kees P. J. Braun, Laurence Faivre, Jean‐Baptiste Rivière, Judith St‐Onge, Karen W. Gripp, Grazia M.S. Mancini, Ki Pang, Elizabeth Sweeney, Hilde Van Esch, Nienke E. Verbeek, Dagmar Wieczorek, Michelle Steinraths, Jacek Majewski, Kym M. Boycott, Daniela T. Pilz, M. Elizabeth Ross, William B. Dobyns, Eamonn Sheridan
Publicado em 2014Artigo -
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Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling por Clare V. Logan, György Szabadkai, Jenny A. Sharpe, David Parry, Silvia Torelli, Anne‐Marie Childs, Marjolein Kriek, Rahul Phadke, Colin A. Johnson, Nicola Roberts, David T. Bonthron, Karen Pysden, Tamieka Whyte, Iulia Munteanu, A. Reghan Foley, Gabrielle Wheway, Katarzyna Szymańska, Subaashini Natarajan, Zakia A. Abdelhamed, Joanne Morgan, H. Roper, Gijs W.E. Santen, Erik H. Niks, W. Ludo van der Pol, Dick Lindhout, Anna Raffaello, Diego De Stefani, Johan T. den Dunnen, Yu Sun, Ieke B. Ginjaar, Caroline A. Sewry, Matthew E. Hurles, Rosario Rizzuto, Michael R. Duchen, Francesco Muntoni, Eamonn Sheridan
Publicado em 2013Artigo
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Medicine
Internal medicine
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COPD
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Psychological intervention
Cell biology
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