Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Petrina Lau"'
Publikováno v:
STAR Protocols, Vol 4, Iss 4, Pp 102618- (2023)
Summary: The mammalian suprachiasmatic nucleus (SCN) is the principal circadian clock that synchronizes daily behavioral and physiological responses in response to environmental cues. Here, we present a protocol for harvesting mouse SCN by vibrating
Externí odkaz:
https://doaj.org/article/94c20f39e26246e1bbbe024f75e229f0
Autor:
Michelle Stewart, Petrina Lau, Gareth Banks, Rasneer Sonia Bains, Enrico Castroflorio, Peter L. Oliver, Christine L. Dixon, Michael C. Kruer, Dimitri M. Kullmann, Abraham Acevedo-Arozena, Sara E. Wells, Silvia Corrochano, Patrick M. Nolan
Publikováno v:
Disease Models & Mechanisms, Vol 12, Iss 2 (2019)
Loss-of-function mutations in a human AMPA receptor-associated protein, ferric chelate reductase 1-like (FRRS1L), are associated with a devastating neurological condition incorporating choreoathetosis, cognitive deficits and epileptic encephalopathie
Externí odkaz:
https://doaj.org/article/d76387fa133742d3bce48ece5c214c9b
Autor:
Elizabeth Nicholson, Mathilde C. C. Guillaumin, Michael R. Bowl, Patrick M. Nolan, Stuart N. Peirson, Laurence A. Brown, Sibah Hasan, Nora Bourbia, Minghui Yin, Sara Wells, Vladyslav V. Vyazovskiy, Gareth Banks, Rasneer Sonia Bains, Kirill E. Volynski, Ines Heise, Carlos A. Aguilar, Christopher T. Esapa, Petrina Lau, Erica Tagliatti
Publikováno v:
Science Advances
Science Advances, 6 (33)
Science Advances, 6 (33)
Switches between global sleep and wakefulness states are believed to be dictated by top-down influences arising from subcortical nuclei. Using forward genetics and in vivo electrophysiology, we identified a recessive mouse mutant line characterized b
Autor:
Mathilde C. C. Guillaumin, Sara Wells, Nora Bourbia, Erica Tagliatti, Laurence A. Brown, Kirill E. Volynski, Petrina Lau, Christopher T. Esapa, Minghui Yin, Rasneer Sonia Bains, Michael R. Bowl, Sibah Hasan, Patrick M. Nolan, Stuart N. Peirson, Vladyslav V. Vyazovskiy, Gareth Banks, Elizabeth Nicholson, Carlos A. Aguilar, Ines Heise
Sleep-wake transitions are modulated through extensive subcortical networks although the precise roles of their individual components remain elusive. Using forward genetics and in vivo electrophysiology, we identified a recessive mouse mutant line ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9f324851ec90178f50bb570203790b3
https://doi.org/10.1101/2020.01.09.900233
https://doi.org/10.1101/2020.01.09.900233
Autor:
Petrina Lau, Michelle Simon, Anna Hoerder-Suabedissen, Federico Tinarelli, Andrew Rutman, Patrick M. Nolan, Neil R. Horner, Matthew Sweeting, Johanna E. Chesham, Sara Johnson, Henrik Westerberg, Gareth Banks, Ashleigh G. Wilcox, Zoltán Molnár, Alun R. Barnard, Valter Tucci, Robert A. Hirst, Glenda Lassi, Lee B. Smith, Michael H. Hastings, Thomas N. Lawson
Publikováno v:
Molecular Psychiatry
Banks, G, Lassi, G, Hoerder-Suabedissen, A, Tinarelli, F, Simon, M M, Wilcox, A, Lau, P, Lawson, T N, Johnson, S, Rutman, A, Sweeting, M, Chesham, J E, Barnard, A R, Horner, N R, Westerberg, H, Smith, L B, Molnar, Z, Hastings, M H, Hirst, R A, Tucci, V & Nolan, P 2017, ' A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies ', Molecular Psychiatry . https://doi.org/10.1038/mp.2017.54
Banks, G, Lassi, G, Hoerder-Suabedissen, A, Tinarelli, F, Simon, M M, Wilcox, A, Lau, P, Lawson, T N, Johnson, S, Rutman, A, Sweeting, M, Chesham, J E, Barnard, A R, Horner, N R, Westerberg, H, Smith, L B, Molnar, Z, Hastings, M H, Hirst, R A, Tucci, V & Nolan, P 2017, ' A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies ', Molecular Psychiatry . https://doi.org/10.1038/mp.2017.54
Microtubule severing enzymes implement a diverse range of tissue-specific molecular functions throughout development and into adulthood. Although microtubule severing is fundamental to many dynamic neural processes, little is known regarding the role
Autor:
Silvia Corrochano, Sara Wells, Abraham Acevedo-Arozena, Dimitri M. Kullmann, Peter L. Oliver, Patrick M. Nolan, Gareth Banks, Enrico Castroflorio, Petrina Lau, Rasneer Sonia Bains, Michael C. Kruer, Michelle Stewart, Christine L Dixon
Publikováno v:
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 12, Iss 2 (2019)
Disease Models & Mechanisms, Vol 12, Iss 2 (2019)
Loss-of-function mutations in a human AMPA receptor-associated protein, ferric chelate reductase 1-like (FRRS1L), are associated with a devastating neurological condition incorporating choreoathetosis, cognitive deficits and epileptic encephalopathie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d14f530cbd5c933f19a74cb4e510b60
https://doi.org/10.1101/388561
https://doi.org/10.1101/388561
Publikováno v:
IBRO Reports. 6:S508