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pro vyhledávání: '"S. Tarr"'
Akademický článek
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Publikováno v:
International journal of inflammation. 2022
Background. The loss of muscle mass in rheumatoid arthritis (RA), termed rheumatoid cachexia, is predicted to result from the complex interactions between different cell types involved in the maintenance of skeletal muscle mass, namely, myoblasts, fi
Publikováno v:
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde. 112(2)
Biological disease-modifying antirheumatic drugs (bDMARDs) have been shown to be highly effective in the treatment of rheumatic conditions, but may increase the risk of infections. Development of tuberculosis (TB) while on bDMARD therapy is of partic
Autor:
K. Junday, Diane Fatkin, S. Hesselson, Siiri E. Iismaa, Jason C. Kovacic, Lucy McGrath-Cadell, Eleni Giannoulatou, Ingrid S. Tarr, B. Graham, Sally L. Dunwoodie, M. Bax, David W.M. Muller
Publikováno v:
European Heart Journal. 42
Background/Introduction SCAD typically affects women in their fifth or sixth decade with a paucity of cardiovascular risk factors.(1) It is caused by a coronary artery intramural haematoma with or without intimal tear. Resultant luminal occlusion man
Autor:
Ram Maharjan, Lyndal Henden, Kelly L. Williams, Alison L. Hogan, Benjamin Heng, Ian P. Blair, Sandrine Chan Moi Fat, Ingrid S. Tarr, Natalie Grima, Shu Yang, Katharine Y. Zhang, Amy K. Cain, Qiongyi Zhao, Sharlynn Wu, Marco Morsch, Amanda L. Wright, Jennifer A. Fifita, Albert Lee, Stephanie L. Rayner, Zong-Hong Zhang, Emily P. McCann
Publikováno v:
Neuropathology and applied neurobiologyREFERENCES. 47(7)
Aim Splicing factor proline and glutamine rich (SFPQ) is an RNA-DNA binding protein that is dysregulated in Alzheimer's disease and frontotemporal dementia. Dysregulation of SFPQ, specifically increased intron retention and nuclear depletion, has bee
Autor:
Sally L. Dunwoodie, Lucy McGrath-Cadell, Abtehale Al-Hussaini, Slavé Petrovski, Eleni Giannoulatou, Sri V V Deevi, Nabila Bouatia-Naji, Keren J Carss, David Adlam, Tom R. Webb, Ingrid S. Tarr, Diluka Premawardhana, Nilesh J. Samani, Stephen E. Hamby, Alice Wood, Carolina Haefliger, David W.M. Muller, Robert M. Graham, Javier Armisen, Samuel H. Lewis, Deevia Kotecha, Quanli Wang, Anna A Baranowska, Dimitrios Vitsios, Diane Fatkin, S. Hesselson, Siiri E. Iismaa
Publikováno v:
Circulation. Genomic and Precision Medicine
Supplemental Digital Content is available in the text.
Background: Spontaneous coronary artery dissection (SCAD) occurs when an epicardial coronary artery is narrowed or occluded by an intramural hematoma. SCAD mainly affects women and is associ
Background: Spontaneous coronary artery dissection (SCAD) occurs when an epicardial coronary artery is narrowed or occluded by an intramural hematoma. SCAD mainly affects women and is associ
Autor:
Lyndal Henden, Qiongyi Zhao, Benjamin Heng, Ram Maharjan, Shu Yang, Sharlynn Wu, Ian P. Blair, Amy K. Cain, Ingrid S. Tarr, Zong-Hong Zhang, Natalie Grima, Katharine Y. Zang, Emily P. McCann, Kelly L. Williams, Sandrine Chan Moi Fat, Alison L. Hogan, Jennifer A. Fifita, Marco Morsch, Amanda L. Wright
BackgroundSplicing factor proline and glutamine rich (SFPQ, also known as polypyrimidine tract-binding protein-associated-splicing factor, PSF) is a RNA-DNA binding protein with roles in key cellular pathways such as DNA transcription and repair, RNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aef207e003688cad0957ec184671e642
https://doi.org/10.1101/2020.09.22.309062
https://doi.org/10.1101/2020.09.22.309062
Akademický článek
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Autor:
Ingrid S. Tarr, Roger Pamphlett, Shu Yang, Emily P. McCann, Garth A. Nicholson, Jennifer A. Fifita, Dominic B. Rowe, Ian P. Blair, Alison L. Hogan, Denis C. Bauer, Neil F. W. Saunders, Katharine Y. Zhang, Jasmin Galper, Kelly L. Williams
Publikováno v:
Neurodegenerative Diseases. 17:304-312
Background: Mutations in the genes encoding the heterogeneous nuclear ribonucleoproteins hnRNPA1 and hnRNPA2/B1 have been reported in a multisystem proteinopathy that includes amyotrophic lateral sclerosis (ALS) and inclusion body myopathy associated
Autor:
Ingrid S. Tarr, Beben Benyamin, Natalie A. Twine, Denis C. Bauer, Emily P. McCann, Garth A. Nicholson, Qiongyi Zhao, Dominic B. Rowe, Tim J Peters, Ian P. Blair, Susan J. Clark, Kelly L. Williams, Katharine Y. Zhang, Zong Hong Zhang
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-17 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-17 (2019)
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterised by the loss of upper and lower motor neurons. ALS exhibits high phenotypic variability including age and site of onset, and disease duration. To uncover epigenetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6107b8d49a98eab6aca8fb86ca28622
https://hdl.handle.net/11541.2/138138
https://hdl.handle.net/11541.2/138138