Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Thomas M, Bennett"'
Autor:
Yuefang Zhou, Thomas M. Bennett, Philip A. Ruzycki, Zhaohua Guo, Yu-Qing Cao, Mohammad Shahidullah, Nicholas A. Delamere, Alan Shiels
Publikováno v:
Cells, Vol 13, Iss 3, p 257 (2024)
TRPM3 belongs to the melastatin sub-family of transient receptor potential (TRPM) cation channels and has been shown to function as a steroid-activated, heat-sensitive calcium ion (Ca2+) channel. A missense substitution (p.I65M) in the TRPM3 gene of
Externí odkaz:
https://doaj.org/article/a31be883560d4d9e9cf79bb437091d5a
Whole-exome sequencing prioritizes candidate genes for hereditary cataract in the Emory mouse mutant
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 13, Iss 5 (2023)
AbstractThe Emory cataract (EmEmEmEmPrxAdamts10Abhd12In silicoPrxAdamts10Abhd12Adamts10Abhd12PrxAdamts10Abhd12Em
Externí odkaz:
https://doaj.org/article/0e18a85e753a4c35974ac868d6346077
Publikováno v:
Global Challenges, Vol 6, Iss 4, Pp n/a-n/a (2022)
Abstract Insulating materials are ubiquitous in a built environment and play a critical role in reducing the energy consumed to maintain habitable indoor environments. Mineral wool insulation (MWI) products, including glass, stone, and slag variants,
Externí odkaz:
https://doaj.org/article/6b6b1ba928ff4cdc8332b22b8411b4b5
Publikováno v:
Cells, Vol 10, Iss 10, p 2606 (2021)
Genetic variations in ephrin type-A receptor 2 (EPHA2) have been associated with inherited and age-related forms of cataract in humans. Here, we have characterized the eye lens phenotype and transcript profile of germline Epha2 knock-in mutant mice h
Externí odkaz:
https://doaj.org/article/07822e8786b74a26b2feaa1aa7b9de47
Publikováno v:
FASEB J
Charged multivesicular-body protein 4b (CHMP4B) is a core sub-unit of the endosomal sorting complex required for transport-III (ESCRT-III) machinery that serves myriad remodeling and scission processes of biological membranes. Mutation of the human C
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189881 (2017)
Rare germ-line mutations in the coding regions of the human EPHA2 gene (EPHA2) have been associated with inherited forms of pediatric cataract, whereas, frequent, non-coding, single nucleotide variants (SNVs) have been associated with age-related cat
Externí odkaz:
https://doaj.org/article/864b0990507a48ca9ee003f9800b3287
Publikováno v:
ACS sustainable chemistryengineering. 10(38)
The linearity of the plastics economy is wasteful and polluting. To encourage recycling and decrease diversion to landfill, new legislation within the EU and UK will tax single-use plastic products made with less than 30% recycled plastic. At present
Autor:
Alice J. Haddleton, Thomas M. Bennett, Xinyong Chen, Steven M. Howdle, Vincenzo Taresco, Rachel L. Atkinson
Publikováno v:
Polymer Chemistry. 11:5029-5039
The synthesis of particles with discrete phases using traditional emulsion polymerisation is a well-established process. Phase-separated particles have a wide range of applications, such as in coatings, drug delivery, impact modification and as suppo
Publikováno v:
Bennett, T M, Allan, J F, Garden, J A & Shaver, M P 2022, ' Low Formaldehyde Binders for Mineral Wool Insulation: A Review ', Global Challenges . https://doi.org/10.1002/gch2.202100110
Bennett, T M, Allan, J F, Garden, J A & Shaver, M P 2022, ' Low Formaldehyde Binders for Mineral Wool Insulation: A Review ', Global Challenges, pp. 2100110 . https://doi.org/10.1002/gch2.202100110
Bennett, T M, Allan, J F, Garden, J A & Shaver, M P 2022, ' Low Formaldehyde Binders for Mineral Wool Insulation: A Review ', Global Challenges, pp. 2100110 . https://doi.org/10.1002/gch2.202100110
Insulating materials are ubiquitous in a built environment and play a critical role in reducing the energy consumed to maintain habitable indoor environments. Mineral wool insulation (MWI) products, including glass, stone, and slag variants, are the
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0132529 (2015)
Primary open-angle glaucoma (POAG) is a clinically important and genetically heterogeneous cause of progressive vision loss as a result of retinal ganglion cell death. Here we have utilized trio-based, whole-exome sequencing to identify the genetic d
Externí odkaz:
https://doaj.org/article/0c39439e1ade4a329ec25c72cbe886b2