Zobrazeno 1 - 10
of 282
pro vyhledávání: '"A. G. Sweeney"'
Autor:
Baoliang Peng, Zhaoling Yao, Xiaocong Wang, Mitchel Crombeen, Dalton G. Sweeney, Kam Chiu Tam
Publikováno v:
Green Energy & Environment, Vol 5, Iss 1, Pp 37-49 (2020)
The most abundant natural biopolymer on earth, cellulose fiber, may offer a highly efficient, low-cost, and chemical-free option for wastewater treatment. Cellulose is widely distributed in plants and several marine animals. It is a carbohydrate poly
Externí odkaz:
https://doaj.org/article/61394d7ee08d40a9bcbf99f0622f94b2
Autor:
S. W. Tobin, S. Hashemi, K. Dadson, S. Turdi, K. Ebrahimian, J. Zhao, G. Sweeney, J. Grigull, J. C. McDermott
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
Abstract Myocyte Enhancer Factor 2 (MEF2) mediates cardiac remodelling in heart failure (HF) and is also a target of β-adrenergic signalling, a front-line treatment for HF. We identified global gene transcription networks involved in HF with and wit
Externí odkaz:
https://doaj.org/article/d8d5bdb28cbb420387d3534659928246
Autor:
Emily G. Sweeney, Andrew Nishida, Alexandra Weston, Maria S. Bañuelos, Kristin Potter, John Conery, Karen Guillemin
Publikováno v:
mSphere, Vol 4, Iss 3 (2019)
ABSTRACT Bacteria are often found living in aggregated multicellular communities known as biofilms. Biofilms are three-dimensional structures that confer distinct physical and biological properties to the collective of cells living within them. We us
Externí odkaz:
https://doaj.org/article/d3c261acaab04c50b6951dc6de6ec08f
Publikováno v:
Lateness and Modernity in Medieval Architecture ISBN: 9789004538436
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38a8e40c8e4fa62bd4c0c53a4ad1aead
https://doi.org/10.1163/9789004538467_002
https://doi.org/10.1163/9789004538467_002
Autor:
Kyle G. Sweeney
Publikováno v:
Journal of the Society of Architectural Historians. 81:236-238
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c700de24ad96e97f19b0a3369ff58d6d
https://doi.org/10.1525/jsah.2022.81.2.236
https://doi.org/10.1525/jsah.2022.81.2.236
Autor:
Suran Nethisinghe, Wei N. Lim, Heather Ging, Anna Zeitlberger, Rosella Abeti, Sally Pemble, Mary G. Sweeney, Robyn Labrum, Charisse Cervera, Henry Houlden, Elisabeth Rosser, Patricia Limousin, Angus Kennedy, Michael P. Lunn, Kailash P. Bhatia, Nicholas W. Wood, John Hardy, James M. Polke, Liana Veneziano, Alfredo Brusco, Mary B. Davis, Paola Giunti
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 12 (2018)
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused by a CAG repeat expansion in the TATA-box binding protein gene (TBP). The disease has a varied age at onset and clinical presentation. It is distinct
Externí odkaz:
https://doaj.org/article/15eee59640234cc3a342ef919bb83ae9
Autor:
Suran Nethisinghe, Maria Lucia Pigazzini, Sally Pemble, Mary G. Sweeney, Robyn Labrum, Katarina Manso, David Moore, Jon Warner, Mary B. Davis, Paola Giunti
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 12 (2018)
Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative disorder caused by an expansion of a polyglutamine tract within the ATXN1 gene. Normal alleles have been reported to range from 6 to 35 repeats, intermediate alleles from
Externí odkaz:
https://doaj.org/article/a75bd019892b41b583329a8dee9d1f85
Autor:
Dimitri M. Kullmann, Mary G. Sweeney, Andrea Haworth, Richa Sud, S. McCall, Roope Männikkö, K. Suetterlin, Dipa Jayaseelan, Emma Matthews, James Burge, Stephanie Schorge, Doreen Fialho, Michael G. Hanna
Publikováno v:
Brain. 145:607-620
High-throughput DNA sequencing is increasingly employed to diagnose single gene neurological and neuromuscular disorders. Large volumes of data present new challenges in data interpretation and its useful translation into clinical and genetic counsel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a76a7b88fa5905d1062ef0d1c63167a0
https://doi.org/10.1093/brain/awab344
https://doi.org/10.1093/brain/awab344
Autor:
Robert D.S. Pitceathly, Shamima Rahman, Yehani Wedatilake, James M. Polke, Sebahattin Cirak, A. Reghan Foley, Anna Sailer, Matthew E. Hurles, Jim Stalker, Iain Hargreaves, Cathy E. Woodward, Mary G. Sweeney, Francesco Muntoni, Henry Houlden, Jan-Willem Taanman, Michael G. Hanna
Publikováno v:
Cell Reports, Vol 3, Iss 6, Pp 1795-1805 (2013)
The molecular basis of cytochrome c oxidase (COX, complex IV) deficiency remains genetically undetermined in many cases. Homozygosity mapping and whole-exome sequencing were performed in a consanguineous pedigree with isolated COX deficiency linked t
Externí odkaz:
https://doaj.org/article/7f50ed1f094e41fea13e5a8a8b52cb0f