Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hannah L. Best"'
Autor:
Hannah L. Best, Lainey J. Williamson, Magdalena Lipka-Lloyd, Helen Waller-Evans, Emyr Lloyd-Evans, Pierre J. Rizkallah, Colin Berry
Publikováno v:
Toxins, Vol 14, Iss 12, p 863 (2022)
Tpp80Aa1 from Bacillus thuringiensis is a Toxin_10 family protein (Tpp) with reported action against Culex mosquitoes. Here, we demonstrate an expanded target range, showing Tpp80Aa1 is also active against the larvae of Anopheles gambiae and Aedes ae
Externí odkaz:
https://doaj.org/article/464c13bcf6e14c4481bcdbf83c7d7ac0
Autor:
Hannah L Best, Nicole J Neverman, Hollie E Wicky, Nadia L Mitchell, Beulah Leitch, Stephanie M Hughes
Publikováno v:
Neurobiology of Disease, Vol 100, Iss , Pp 62-74 (2017)
Batten disease (neuronal ceroid lipofuscinosis) refers to a group of neurodegenerative lysosomal storage diseases predominantly affecting children. There are currently no effective treatments, and the functions of many of the associated gene products
Externí odkaz:
https://doaj.org/article/d41179562f024cc48573499b633dc120
Autor:
Ian Andrew Fallis, Eman A. H. Al-Wattar, Adam H. Day, Nathaniel I. Keymer, Emyr Lloyd-Evans, Martin H. Ubler, Rudolf Konrad Allemann, Robert J. Mart, Niklaas J. Buurma, Hannah L. Best, Simon J. A. Pope
Publikováno v:
Chemical Science
Visualising a c-Myc nuclear localisation signal peptide using an organometallic complex.
A nuclear localisation sequence (NLS) peptide, PAAKRVKLD, derived from the human c-Myc regulator gene, has been functionalised with a long wavelength (λex
A nuclear localisation sequence (NLS) peptide, PAAKRVKLD, derived from the human c-Myc regulator gene, has been functionalised with a long wavelength (λex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3109e401e6e322107c93fafe96363317
https://doi.org/10.1039/c9sc05568a
https://doi.org/10.1039/c9sc05568a
Autor:
Lainey J. Williamson, Marina Galchenkova, Hannah L. Best, Richard J. Bean, Anna Munke, Salah Awel, Gisel Pena, Juraj Knoska, Robin Schubert, Katerina Doerner, Hyun-Woo Park, Dennis K. Bideshi, Alessandra Henkel, Viviane Kremling, Bjarne Klopprogge, Emyr Lloyd-Evans, Mark Young, Joana Valerio, Marco Kloos, Marcin Sikorski, Grant Mills, Johan Bielecki, Henry Kirkwood, Chan Kim, Raphael de Wijn, Kristina Lorenzen, P. Lourdu Xavier, Aida Rahmani, Luca Gelisio, Oleksandr Yefanov, Adrian P. Mancuso, Brian Federici, Henry N. Chapman, Neil Crickmore, Pierre J. Rizkallah, Colin Berry, Dominik Oberthür
Tpp49Aa1 fromLysinibacillus sphaericusis a Toxin_10 family protein that – in combination with Cry48Aa1, a 3-domain crystal protein - has potent mosquitocidal activity, specifically againstCulex quinquefasciatusmosquitoes. MHz serial femtosecond cry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46fb447bc0ed67262e42b24808246b41
https://doi.org/10.1101/2022.01.14.476343
https://doi.org/10.1101/2022.01.14.476343
Publikováno v:
Molecular Genetics and Metabolism. 138:107212
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b69407c123c13b77359a405a577b7e0b
https://doi.org/10.1016/j.ymgme.2022.107212
https://doi.org/10.1016/j.ymgme.2022.107212
Autor:
Hannah L. Best, Rafael A. Badell-Grau, Katie Shipley, Abdullah S. Alshehri, Helen Waller-Evans, Emyr Lloyd-Evans
Publikováno v:
Molecular Genetics and Metabolism. 138:107029
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84fcf6126f2fb14b59582b42c4546b28
https://doi.org/10.1016/j.ymgme.2022.107029
https://doi.org/10.1016/j.ymgme.2022.107029
Publikováno v:
Journal of neurochemistryReferences. 157(3)
Neuronal ceroid lipofuscinoses (NCLs) are a group of inherited childhood neurodegenerative disorders. In addition to the accumulation of auto-fluorescent storage material in lysosomes, NCLs are largely characterised by region-specific neuroinflammati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19cdf85f95ef559386ef3566d84d3cd5
https://pubmed.ncbi.nlm.nih.gov/33368303
https://pubmed.ncbi.nlm.nih.gov/33368303
Autor:
Beulah Leitch, Stephanie M. Hughes, Hollie E Wicky, Nadia L. Mitchell, Hannah L Best, Nicole J. Neverman
Publikováno v:
Neurobiology of Disease, Vol 100, Iss, Pp 62-74 (2017)
Batten disease (neuronal ceroid lipofuscinosis) refers to a group of neurodegenerative lysosomal storage diseases predominantly affecting children. There are currently no effective treatments, and the functions of many of the associated gene products
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::928ad7fc17535c510d404ba8a840da7c
https://doi.org/10.1016/j.nbd.2017.01.001
https://doi.org/10.1016/j.nbd.2017.01.001
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1852:2292-2300
The neuronal ceroid lipofuscinoses represent a group of severe childhood lysosomal storage diseases. With at least 13 identified variants they are the most common cause of inherited neurodegeneration in children. These diseases share common pathologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::feb9876f71f1efaf5b74f8da9a25e4e1
https://doi.org/10.1016/j.bbadis.2015.04.026
https://doi.org/10.1016/j.bbadis.2015.04.026