Výsledky vyhledávání - "Casey, O'Farrell"

Dehalobium species implicated in 2,3,7,8-tetrachlorodibenzo-p-dioxin dechlorination in the contaminated sediments of Sydney Harbour Estuary

Autor: Matthew Lee, Gan Liang, Sophie I. Holland, Casey O'Farrell, Keith Osborne, Michael J. Manefield

Publikováno v: Marine pollution bulletin. 179

Polychlorinated dibenzo-p-dioxins and furans (PCDD/F) are some of the most environmentally recalcitrant and toxic compounds. They occur naturally and as by-products of anthropogenic activity. Sydney Harbour Estuary (Sydney, Australia), is heavily con

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ab3ed84bf1cb6604bb664fda107cc9e
https://pubmed.ncbi.nlm.nih.gov/35504213

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Aerobic biotransformation of 6:2 fluorotelomer sulfonate by Dietzia aurantiaca J3 under sulfur-limiting conditions

Autor: Valentina Méndez, Sophie Holland, Shefali Bhardwaj, James McDonald, Stuart Khan, Denis O'Carroll, Russell Pickford, Sarah Richards, Casey O'Farrell, Nicholas Coleman, Matthew Lee, Michael J. Manefield

Publikováno v: The Science of the total environment. 829

The polyfluorinated alkyl substance 6:2 fluorotelomer sulfonate (6:2 FTS) has been detected in diverse environments impacted by aqueous film-forming foams used for firefighting. In this study, a bacterial strain (J3) using 6:2 FTS as a sulfur source

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a21f990f399081ea04c273b3fbecc909
https://pubmed.ncbi.nlm.nih.gov/35306084

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Dehalobium species implicated in 2,3,7,8-tetrachloro-p-dioxin dechlorination in the contaminated sediments of Sydney Harbour Estuary

Autor: Matthew Lee, Gan Liang, Sophie I. Holland, Casey O’Farrell, Keith Osbourne, Michael J. Manefield

Polychlorinated dibenzo-p-dioxins and furans (PCDD/F) are some of the most environmentally recalcitrant and toxic compounds. They are naturally occurring and by-products of anthropogenic activity. Sydney Harbour Estuary (Sydney, Australia), is heavil

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2b37e806a3417a7959822843ec650398
https://doi.org/10.1101/2021.12.12.472303

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Mutant torsinA interacts with tyrosine hydroxylase in cultured cells

Autor: Martin B. Delatycki, Mark R. Cookson, Paul J. Lockhart, Michael Hutton, Kirstee Martin, Casey O'Farrell

Publikováno v: Neuroscience. 164:1127-1137

A specific mutation (DeltaE302/303) in the torsinA gene underlies most cases of dominantly inherited early-onset torsion dystonia. This mutation causes the protein to aggregate and form intracellular inclusion bodies in cultured cells and animal mode

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a8329b1e8a3dd1099c95286a3600c4
https://doi.org/10.1016/j.neuroscience.2009.09.017

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Biochemical characterization of torsinB

Autor: Dennis W. Dickson, Paul J. Lockhart, Sarah Lincoln, Andrew B. Singleton, Casey O'Farrell, Michael De Lucia, Mark R. Cookson

Publikováno v: Molecular Brain Research. 127:1-9

Mutations in torsinA, a member of the AAA+ family of ATPases, are associated with early onset-dystonia. A closely related homologue, torsinB, has also been described but the significance of this second form is not clear. Here, we demonstrate that in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23efbe513030dd0c1f3b5c0572febc59
https://doi.org/10.1016/j.molbrainres.2004.05.005

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N-myc Regulates Parkin Expression

Autor: Gregory Kapatos, Fanny Gonzalez-de-Chavez, Nigel T. Maidment, Casey O'Farrell, Kelvin Chiu, Matthew J. Farrer, Andrew B. West

Publikováno v: Journal of Biological Chemistry. 279:28896-28902

Mutations in the parkin gene are common in early-onset and familial Parkinson's disease (PD), and the parkin protein interacts in the ubiquitin-proteasome system as an E3 ligase. However, the regulatory pathways that govern parkin expression are unkn

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2812db2e091ef5c828127a4616e40f04
https://doi.org/10.1074/jbc.m400126200

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It's a double knock-out! The quaking mouse is a spontaneous deletion of parkin and parkin co-regulated gene (PACRG)

Autor: Paul J. Lockhart, Matthew J. Farrer, Casey O'Farrell

Publikováno v: Movement Disorders. 19:101-104

Mutations in the parkin gene (PRKN) are the commonest cause of juvenile and early-onset parkinsonism. However, the pathogenic mechanism by which loss of parkin protein results in degeneration of dopaminergic neurons remains elusive. Animal models pro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c18544e3bf5be52a3ba7e6c5a9712bc4
https://doi.org/10.1002/mds.20000

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RING finger 1 mutations in Parkin produce altered localization of the protein

Autor: Chris McLendon, Michael G. Schlossmacher, Casey O'Farrell, Paul J. Lockhart, Mark R. Cookson, Matthew J. Farrer

Publikováno v: Human Molecular Genetics. 12:2957-2965

The Parkin gene (PRKN) encodes an E3 protein-ubiquitin ligase for which loss of function is associated with autosomal-recessive juvenile (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22f365b0bf86bbe574fbe4bdfb8cfd9b
https://doi.org/10.1093/hmg/ddg328

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