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pro vyhledávání: '"Hills, Rachel"'
Akademický článek
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Akademický článek
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Autor:
Lane, Emma L., Harrison, David J., Ramos‐Varas, Elena, Hills, Rachel, Turner, Sophie, Lelos, Mariah J.
Publikováno v:
Movement Disorders; Mar2022, Vol. 37 Issue 3, p613-619, 7p
Autor:
Muha, Villo, Williamson, Ritchie, Hills, Rachel, McNeilly, Alison D, McWilliams, Thomas G, Alonso, Jana, Schimpl, Marianne, Leney, Aneika C, Heck, Albert J R, Sutherland, Calum, Read, Kevin D, McCrimmon, Rory J, Brooks, Simon P, van Aalten, Daan M F, Afd Biomol.Mass Spect. and Proteomics, Sub Biomol.Mass Spect. and Proteomics, Sub Biomol.Mass Spectrometry & Proteom., Biomolecular Mass Spectrometry and Proteomics
Publikováno v:
Open Biology
Biology Open, 9(11). Company of Biologists Ltd
Open Biology, Vol 9, Iss 11 (2019)
Biology Open, 9(11). Company of Biologists Ltd
Open Biology, Vol 9, Iss 11 (2019)
O-GlcNAcylation is an abundant post-translational modification in the nervous system, linked to both neurodevelopmental and neurodegenerative disease. However, the mechanistic links between these phenotypes and site-specific O-GlcNAcylation remain la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cccbbead2f89b493137c41378706ef7b
https://pubmed.ncbi.nlm.nih.gov/31771416
https://pubmed.ncbi.nlm.nih.gov/31771416
Autor:
Villo Muha, Williamson, Ritchie, Hills, Rachel, McNeilly, Alison D., McWilliams, Thomas G., Alonso, Jana, Schimpl, Marianne, Aneika C. Leney, Heck, Albert J. R., Sutherland, Calum, Read, Kevin D., McCrimmon, Rory J., Brooks, Simon P., Aalten, Daan M. F. Van
O-GlcNAcylation is an abundant post-translational modification in the nervous system, linked to both neurodevelopmental and neurodegenerative disease. However, the mechanistic links between these phenotypes and site-specific O-GlcNAcylation remains l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::497830a3c607b71ecc105a09710e734c
Autor:
Villo Muha, Williamson, Ritchie, Hills, Rachel, McNeilly, Alison D., McWilliams, Thomas G., Alonso, Jana, Schimpl, Marianne, Aneika C. Leney, Heck, Albert J. R., Sutherland, Calum, Read, Kevin D., McCrimmon, Rory J., Brooks, Simon P., Aalten, Daan M. F. Van
Figure S7: Behavioural characterisation of Crmp2S517A mice. (a)–(c) Open filed test, (male, WT, n = 12; Crmp2S517A, n = 10; mean ± SD) 15 minutes of testing. (a) Open filed test. (b) WT (20 ± 8) and Crmp2S517A (22 ± 7) mice spent similar amounts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9df8cec9d52bfc539439e244a1c6e3dc
Autor:
Villo Muha, Williamson, Ritchie, Hills, Rachel, McNeilly, Alison D., McWilliams, Thomas G., Alonso, Jana, Schimpl, Marianne, Aneika C. Leney, Heck, Albert J. R., Sutherland, Calum, Read, Kevin D., McCrimmon, Rory J., Brooks, Simon P., Aalten, Daan M. F. Van
Figure S1: Purification and site mapping of O-GlcNAc CRMP2 (a) CRMP2 purified via ion exchange chromatography was subjected to O-GlcNAc enrichment using CpOGAD298N-GST fusion protein. O-GlcNAcylated CRMP2 is approximately 2000-fold enriched via this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1523baaf1f5366cd0ac0c93a29aa7543
Autor:
McWilliams, Thomas G., Barini, Erica, Pohjolan-Pirhonen, Risto, Brooks, Simon P., Singh, François, Burel, Sophie, Balk, Kristin, Kumar, Atul, Montava-Garriga, Lambert, Prescott, Alan R., Hassoun, Sidi Mohamed, Mouton-Liger, François, Ball, Graeme, Hills, Rachel, Knebel, Axel, Ayse Ulusoy, Monte, Donato A. Di, Tamjar, Jevgenia, Antico, Odetta, Fears, Kyle, Smith, Laura, Brambilla, Riccardo, Palin, Eino, Valori, Miko, Eerola-Rautio, Johanna, Tienari, Pentti, Corti, Olga, Dunnett, Stephen B., Ganley, Ian G., Suomalainen, Anu, Miratul M. K. Muqit
Mutations in PINK1 and Parkin result in autosomal recessive Parkinson's disease (PD). Cell culture and in vitro studies have elaborated the PINK1-dependent regulation of Parkin and defined how this dyad orchestrates the elimination of damaged mitocho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d5a135bafe5f64e4d92e4e3f511536c
Autor:
McWilliams, Thomas G., Barini, Erica, Pohjolan-Pirhonen, Risto, Brooks, Simon P., Singh, François, Burel, Sophie, Balk, Kristin, Kumar, Atul, Montava-Garriga, Lambert, Prescott, Alan R., Hassoun, Sidi Mohamed, Mouton-Liger, François, Ball, Graeme, Hills, Rachel, Knebel, Axel, Ayse Ulusoy, Monte, Donato A. Di, Tamjar, Jevgenia, Antico, Odetta, Fears, Kyle, Smith, Laura, Brambilla, Riccardo, Palin, Eino, Valori, Miko, Eerola-Rautio, Johanna, Tienari, Pentti, Corti, Olga, Dunnett, Stephen B., Ganley, Ian G., Suomalainen, Anu, Miratul M. K. Muqit
Mutations in PINK1 and Parkin result in autosomal recessive Parkinson's disease (PD). Cell culture and in vitro studies have elaborated the PINK1-dependent regulation of Parkin and defined how this dyad orchestrates the elimination of damaged mitocho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::016f2d494cc8a03b640a220dec466668
Autor:
McWilliams, Thomas G., Barini, Erica, Pohjolan-Pirhonen, Risto, Brooks, Simon P., Singh, François, Burel, Sophie, Balk, Kristin, Kumar, Atul, Montava-Garriga, Lambert, Prescott, Alan R., Hassoun, Sidi Mohamed, Mouton-Liger, François, Ball, Graeme, Hills, Rachel, Knebel, Axel, Ayse Ulusoy, Monte, Donato A. Di, Tamjar, Jevgenia, Antico, Odetta, Fears, Kyle, Smith, Laura, Brambilla, Riccardo, Palin, Eino, Valori, Miko, Eerola-Rautio, Johanna, Tienari, Pentti, Corti, Olga, Dunnett, Stephen B., Ganley, Ian G., Suomalainen, Anu, Miratul M. K. Muqit
Mutations in PINK1 and Parkin result in autosomal recessive Parkinson's disease (PD). Cell culture and in vitro studies have elaborated the PINK1-dependent regulation of Parkin and defined how this dyad orchestrates the elimination of damaged mitocho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3576d774c3b239f4ece2e746dc2c602c