Zobrazeno 1 - 10
of 22
pro vyhledávání: '"John Brewin"'
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Externí odkaz:
https://doaj.org/article/3fe6f65ae4ea4f5abd0b7db3950e4155
Autor:
Margherita DI Mauro, Amina Nardo‐marino, Sara Stuart-Smith, Sara El Hoss, John Strouboulis, Stephan Menzel, John Gibson, David Rees, John Brewin
Publikováno v:
HemaSphere, Vol 7, p e81245b4 (2023)
Externí odkaz:
https://doaj.org/article/7c568c2654dc4b93a20c5e5d9faf54c2
Autor:
Daniel Hayes, Claire Henderson, Ioannis Bakolis, Vanessa Lawrence, Rachel A. Elliott, Amy Ronaldson, Gabrielle Richards, Julie Repper, Peter Bates, John Brewin, Sara Meddings, Gary Winship, Simon Bishop, Richard Emsley, Daniel Elton, Rebecca McNaughton, Rob Whitley, David Smelson, Katy Stepanian, Merly McPhilbin, Danielle Dunnett, Holly Hunter-Brown, Caroline Yeo, Tesnime Jebara, Mike Slade
Publikováno v:
BMC Psychiatry, Vol 22, Iss 1, Pp 1-14 (2022)
Abstract Background Recovery Colleges are a relatively recent initiative within mental health services. The first opened in 2009 in London and since then numbers have grown. They are based on principles of personal recovery in mental health, co-produ
Externí odkaz:
https://doaj.org/article/e17b4447789c4632b8b9a02c3854c985
Autor:
Huan Cao, Aristotelis Antonopoulos, Sadie Henderson, Heather Wassall, John Brewin, Alanna Masson, Jenna Shepherd, Gabriela Konieczny, Bhinal Patel, Maria-Louise Williams, Adam Davie, Megan A. Forrester, Lindsay Hall, Beverley Minter, Dimitris Tampakis, Michael Moss, Charlotte Lennon, Wendy Pickford, Lars Erwig, Beverley Robertson, Anne Dell, Gordon D. Brown, Heather M. Wilson, David C. Rees, Stuart M. Haslam, J. Alexandra Rowe, Robert N. Barker, Mark A. Vickers
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-13 (2021)
Red blood cells (RBCs) are phagocytosed in the spleen in sickle cell disease and malaria. Here, Cao et al. show that high mannose N-glycans, exposed on diseased or oxidized RBC surfaces, bind mannose receptor CD206 on host cells, mediating phagocytos
Externí odkaz:
https://doaj.org/article/73b50900a7f8419f8344f99ed38257e2
Publikováno v:
Haematologica, Vol 107, Iss 1 (2021)
Externí odkaz:
https://doaj.org/article/1a9fa213caae42888bd3787f9cdf607c
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Oxidative damage to red blood cells (RBCs) may contribute to pathogenesis of sickle cell anemia. Reducing the deleterious effects of oxidants by exposing RBCs to a number of antioxidants has been shown to have protective effects against lipid and pro
Externí odkaz:
https://doaj.org/article/4dbec1d684f04d5b9bcb2eb209b2b8e0
Autor:
Helen Rooks, John Brewin, Kate Gardner, Subarna Chakravorty, Stephan Menzel, Anke Hannemann, John Gibson, David C. Rees
Publikováno v:
Haematologica, Vol 104, Iss 3 (2019)
Externí odkaz:
https://doaj.org/article/0ea68c5a2e7949b2a6be8eb916ebb8a1
Autor:
Sanjay Tewari, George Renney, John Brewin, Kate Gardner, Fenella Kirkham, Baba Inusa, James E Barrett, Stephan Menzel, Swee Lay Thein, Malcolm Ward, David C. Rees
Publikováno v:
Haematologica, Vol 103, Iss 7 (2018)
Silent cerebral infarction is the most common neurological abnormality in children with sickle cell anemia, affecting 30-40% of 14 year olds. There are no known biomarkers to identify children with silent cerebral infarcts, and the pathological basis
Externí odkaz:
https://doaj.org/article/8ac1ae17c8304c48871e56dbe00de8dc
Autor:
John Brewin, Sanjay Tewari, Anke Hannemann, Halima Al Balushi, Claire Sharpe, John S. Gibson, David C. Rees
Publikováno v:
HemaSphere, Vol 1, Iss 1 (2017)
Abstract. The early stages of sickle cell nephropathy (SCN) manifest in children with sickle cell anemia (SCA) as hyperfiltration and proteinuria. The physiological conditions of the renovascular system are among the most conducive to hemoglobin S po
Externí odkaz:
https://doaj.org/article/80c56d0d1dd34c8780da8601f9514181
Autor:
Oyesola O. Ojewunmi, Titilope A. Adeyemo, Ajoke I. Oyetunji, Bassey Inyang, Afolashade Akinrindoye, Baraka S. Mkumbe, Kate Gardner, Helen Rooks, John Brewin, Hamel Patel, Sang-Hyuck Lee, Raymond Chung, Sara Rashkin, Guolian Kang, Reuben Chianumba, Raphael Sangeda, Liberata Mwita, Hezekiah Isa, Uche-Nnebe Agumadu, Rosemary Ekong, Jamilu A. Faruk, Bello Y. Jamoh, Niyi M. Adebiyi, Ismail A. Umar, Abdulaziz Hassan, Christopher Grace, Anuj Goel, Baba P.D. Inusa, Mario Falchi, Siana Nkya, Julie Makani, Hafsat R. Ahmad, Obiageli Nnodu, John Strouboulis, Stephan Menzel
BackgroundThe clinical severity of sickle cell disease (SCD) is strongly influenced by the level of fetal haemoglobin (HbF) persistent in each patient. Three major HbF loci (BCL11A,HBS1L-MYB, andXmn1-HBG2) have been reported, but a considerable hidde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eec5aa8af3810e908446c6f3dd1ab4d2
https://doi.org/10.1101/2023.05.16.23289851
https://doi.org/10.1101/2023.05.16.23289851