Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Nigel B. Rendell"'
Autor:
Janev Fehmi, Alexander J. Davies, Marilina Antonelou, Stephen Keddie, Sonja Pikkupeura, Luis Querol, Emilien Delmont, Andrea Cortese, Diego Franciotta, Staffan Persson, Jonathan Barratt, Ruth Pepper, Filipa Farinha, Anisur Rahman, Diana Canetti, Janet A. Gilbertson, Nigel B. Rendell, Aleksandar Radunovic, Thomas Minton, Geraint Fuller, Sinead M. Murphy, Aisling S. Carr, Mary R. Reilly, Filip Eftimov, Luuk Wieske, Charlotte E. Teunissen, Ian S. D. Roberts, Neil Ashman, Alan D. Salama, Simon Rinaldi
Publikováno v:
PLoS ONE, Vol 18, Iss 3 (2023)
Membranous glomerulonephritis (MGN) is a common cause of nephrotic syndrome in adults, mediated by glomerular antibody deposition to an increasing number of newly recognised antigens. Previous case reports have suggested an association between patien
Externí odkaz:
https://doaj.org/article/dff9589eb34c4a748b786c06b1069e74
Autor:
Carina C. Kern, StJohn Townsend, Antoine Salzmann, Nigel B. Rendell, Graham W. Taylor, Ruxandra M. Comisel, Lazaros C. Foukas, Jürg Bähler, David Gems
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
It is unclear why C. elegans continues to produce large quantities of yolk after reproduction. Here the authors show that post-reproductive C. elegans mothers vent yolk which supports their offspring’s growth, serving as a form of primitive lactati
Externí odkaz:
https://doaj.org/article/055664668cb24b469c3a15be409762ad
Autor:
Graham W. Taylor, Janet A. Gilbertson, Rabya Sayed, Angel Blanco, Nigel B. Rendell, Dorota Rowczenio, Tamer Rezk, P. Patrizia Mangione, Diana Canetti, Paul Bass, Philip N. Hawkins, Julian D. Gillmore
Publikováno v:
Kidney International Reports, Vol 4, Iss 7, Pp 977-986 (2019)
Introduction: Hereditary fibrinogen Aα-chain (AFib) amyloidosis is a relatively uncommon renal disease associated with a small number of pathogenic fibrinogen Aα (FibA) variants; wild-type FibA normally does not result in amyloid deposition. Proteo
Externí odkaz:
https://doaj.org/article/034578518fe347d4a2ac583d09552583
Autor:
Diana Canetti, Francesca Brambilla, Nigel B. Rendell, Paola Nocerino, Janet A. Gilbertson, Dario Di Silvestre, Andrea Bergamaschi, Francesca Lavatelli, Giampaolo Merlini, Julian D. Gillmore, Vittorio Bellotti, Pierluigi Mauri, Graham W. Taylor
Publikováno v:
Molecules, Vol 26, Iss 7, p 1913 (2021)
Amyloidosis is a relatively rare human disease caused by the deposition of abnormal protein fibres in the extracellular space of various tissues, impairing their normal function. Proteomic analysis of patients’ biopsies, developed by Dogan and coll
Externí odkaz:
https://doaj.org/article/c017e28d85fb481d96668e37ce4a88b4
Autor:
Tamer Rezk, Janet A Gilbertson, P Patrizia Mangione, Dorota Rowczenio, Nigel B Rendell, Diana Canetti, Helen J Lachmann, Ashutosh D Wechalekar, Paul Bass, Philip N Hawkins, Vittorio Bellotti, Graham W Taylor, Julian D Gillmore
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 5, Iss 3, Pp 145-153 (2019)
Abstract The tissue diagnosis of amyloidosis and confirmation of fibril protein type, which are crucial for clinical management, have traditionally relied on Congo red (CR) staining followed by immunohistochemistry (IHC) using fibril protein specific
Externí odkaz:
https://doaj.org/article/9387814b13b64cdd87bd2fdab0cb78d9
Autor:
Dorota Rowczenio, Nicola A. Botcher, Guglielmo Verona, Paola Nocerino, Graham W. Taylor, Palma Mangione, Philip N. Hawkins, Diana Canetti, Angel Blanco, Janet A. Gilbertson, Vittorio Bellotti, Julian D. Gillmore, Lucia Di Vagno, Nigel B. Rendell
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 58:948-957
Systemic amyloidosis is a serious disease which is caused when normal circulating proteins misfold and aggregate extracellularly as insoluble fibrillary deposits throughout the body. This commonly results in cardiac, renal and neurological damage. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1809443c2193bd184f8c28f4bd040d4
https://doi.org/10.1515/cclm-2019-1007
https://doi.org/10.1515/cclm-2019-1007
Autor:
Guglielmo Verona, Paola Nocerino, Angel Blanco, Vittorio Bellotti, Loredana Marchese, Julian D. Gillmore, Dorota Rowczenio, Philip N. Hawkins, Nicola A. Botcher, Per Westermark, Alessandra Morelli, Janet A. Gilbertson, Palma Mangione, Alessandra Corazza, Graham W. Taylor, Diana Canetti, Sofia Giorgetti, Nigel B. Rendell
Publikováno v:
The Journal of pathology. 255(3)
Apolipoprotein A-IV amyloidosis is an uncommon form of the disease normally resulting in renal and cardiac dysfunction. ApoA-IV amyloidosis was identified in 16 patients attending the National Amyloidosis Centre and in eight clinical samples received
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d53fe8148f5aa0c299b0235c647dc2d6
https://pubmed.ncbi.nlm.nih.gov/34331462
https://pubmed.ncbi.nlm.nih.gov/34331462
Autor:
Tamer Rezk, Rabya Sayed, Nigel B. Rendell, Janet A. Gilbertson, Philip N. Hawkins, Diana Canetti, Angel Blanco, Julian D. Gillmore, Palma Mangione, Paul Bass, Graham W. Taylor, Dorota Rowczenio
Publikováno v:
Kidney International Reports, Vol 4, Iss 7, Pp 977-986 (2019)
Kidney International Reports
Kidney International Reports
Introduction: Hereditary fibrinogen Aα-chain (AFib) amyloidosis is a relatively uncommon renal disease associated with a small number of pathogenic fibrinogen Aα (FibA) variants; wild-type FibA normally does not result in amyloid deposition. Proteo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36377956339192dfffb7a67f465968d8
http://www.sciencedirect.com/science/article/pii/S2468024919301548
http://www.sciencedirect.com/science/article/pii/S2468024919301548
Autor:
Janet A. Gilbertson, Vittorio Bellotti, Julian D. Gillmore, Francesca Lavatelli, Diana Canetti, Graham W. Taylor, Paola Nocerino, Dario Di Silvestre, Giampaolo Merlini, Andrea Bergamaschi, Pierluigi Mauri, Francesca Brambilla, Nigel B. Rendell
Publikováno v:
Molecules
Molecules, Vol 26, Iss 1913, p 1913 (2021)
Volume 26
Issue 7
Molecules, Vol 26, Iss 1913, p 1913 (2021)
Volume 26
Issue 7
Amyloidosis is a relatively rare human disease caused by the deposition of abnormal protein fibres in the extracellular space of various tissues, impairing their normal function. Proteomic analysis of patients’ biopsies, developed by Dogan and coll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c494aa20dc6d7e83e5dcaf53cf6ff170
http://europepmc.org/articles/PMC8037974
http://europepmc.org/articles/PMC8037974
Autor:
Jürg Bähler, Graham W. Taylor, StJohn Townsend, Lazaros C. Foukas, Ruxandra M. Comisel, Nigel B. Rendell, Antoine Salzmann, Carina C. Kern, David Gems
Publikováno v:
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
The nematode Caenorhabditis elegans exhibits rapid senescence that is promoted by the insulin/IGF-1 signalling (IIS) pathway via regulated processes that are poorly understood. IIS also promotes production of yolk for egg provisioning, which in post-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d7823c7ce4a238cab80caf945e19499
https://pubmed.ncbi.nlm.nih.gov/34611154
https://pubmed.ncbi.nlm.nih.gov/34611154