When Clocks Go Bad: Neurobehavioural Consequences of Disrupted Circadian Timing

Por Barnard, Alun R., Nolan, Patrick M.
Publicado em 2008

Primary Xanthoma of the Mandible: Report of a Rare Case

Por Morel, Dominic, Kelsch, Robert D., Nolan, Patrick J.
Publicado no Head Neck Pathol (2015)

Reciprocal interactions between circadian clocks and aging

Por Banks, Gareth, Nolan, Patrick M., Peirson, Stuart N.
Publicado no Mamm Genome (2016)

Cognitive assessment of mice strains heterozygous for cell-adhesion genes reveals strain-specific alterations in timing

Por Gallistel, C. R., Tucci, Valter, Nolan, Patrick M., Schachner, Melitta, Jakovcevski, Igor, Kheifets, Aaron, Barboza, Luendro
Publicado em 2014

Early motor deficits in mouse disease models are reliably uncovered using an automated home-cage wheel-running system: a cross-laboratory validation

Por Mandillo, Silvia, Heise, Ines, Garbugino, Luciana, Tocchini-Valentini, Glauco P., Giuliani, Alessandro, Wells, Sara, Nolan, Patrick M.
Publicado em 2014

Distinct and Separable Roles for Endogenous CRY1 and CRY2 within the Circadian Molecular Clockwork of the Suprachiasmatic Nucleus, as Revealed by the Fbxl3(Afh) Mutation

Por Anand, Sneha N., Maywood, Elizabeth S., Chesham, Johanna E., Joynson, Greg, Banks, Gareth T., Hastings, Michael H., Nolan, Patrick M.
Publicado em 2013

A twin and molecular genetics study of sleep paralysis and associated factors

Por Denis, Dan, French, Christopher C., Rowe, Richard, Zavos, Helena M. S., Nolan, Patrick M., Parsons, Michael J., Gregory, Alice M.
Publicado no J Sleep Res (2015)

Polymorphisms in the circadian expressed genes PER3 and ARNTL2 are associated with diurnal preference and GNβ3 with sleep measures

Por Parsons, Michael J, Lester, Kathryn J, Barclay, Nicola L, Archer, Simon N, Nolan, Patrick M, Eley, Thalia C, Gregory, Alice M
Publicado no J Sleep Res (2014)

Reduced Anxiety and Depression-Like Behaviours in the Circadian Period Mutant Mouse Afterhours

Por Keers, Robert, Pedroso, Inti, Breen, Gerome, Aitchison, Kathy J., Nolan, Patrick M., Cichon, Sven, Nöthen, Markus M., Rietschel, Marcella, Schalkwyk, Leonard C., Fernandes, Cathy
Publicado em 2012

Genetic background influences age-related decline in visual and nonvisual retinal responses, circadian rhythms, and sleep()

Por Banks, Gareth, Heise, Ines, Starbuck, Becky, Osborne, Tamzin, Wisby, Laura, Potter, Paul, Jackson, Ian J., Foster, Russell G., Peirson, Stuart N., Nolan, Patrick M.
Publicado no Neurobiol Aging (2015)

Defining the Cause of Skewed X-Chromosome Inactivation in X-Linked Mental Retardation by Use of a Mouse Model

Por Muers, Mary R. , Sharpe, Jacqueline A. , Garrick, David , Sloane-Stanley, Jacqueline , Nolan, Patrick M. , Hacker, Terry , Wood, William G. , Higgs, Douglas R. , Gibbons, Richard J. 
Publicado em 2007

A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice

Por Becker, Esther B. E., Oliver, Peter L., Glitsch, Maike D., Banks, Gareth T., Achilli, Francesca, Hardy, Andrea, Nolan, Patrick M., Fisher, Elizabeth M. C., Davies, Kay E.
Publicado em 2009

Overexpression of Fto leads to increased food intake and results in obesity

Por Church, Chris, Moir, Lee, McMurray, Fiona, Girard, Christophe, Banks, Gareth T, Teboul, Lydia, Wells, Sara, Bruning, Jens C., Nolan, Patrick M, Ashcroft, Frances M., Cox, Roger D.
Publicado em 2010

Early doors (Edo) mutant mouse reveals the importance of period 2 (PER2) PAS domain structure for circadian pacemaking

Por Militi, Stefania, Maywood, Elizabeth S., Sandate, Colby R., Chesham, Johanna E., Barnard, Alun R., Parsons, Michael J., Vibert, Jennifer L., Joynson, Greg M., Partch, Carrie L., Hastings, Michael H., Nolan, Patrick M.
Publicado no Proc Natl Acad Sci U S A (2016)

Analysis of Individual Mouse Activity in Group Housed Animals of Different Inbred Strains using a Novel Automated Home Cage Analysis System

Por Bains, Rasneer S., Cater, Heather L., Sillito, Rowland R., Chartsias, Agisilaos, Sneddon, Duncan, Concas, Danilo, Keskivali-Bond, Piia, Lukins, Timothy C., Wells, Sara, Acevedo Arozena, Abraham, Nolan, Patrick M., Armstrong, J. Douglas
Publicado no Front Behav Neurosci (2016)

KATNAL1 Regulation of Sertoli Cell Microtubule Dynamics Is Essential for Spermiogenesis and Male Fertility

Por Smith, Lee B., Milne, Laura, Nelson, Nancy, Eddie, Sharon, Brown, Pamela, Atanassova, Nina, O'Bryan, Moira K., O'Donnell, Liza, Rhodes, Danielle, Wells, Sara, Napper, Diane, Nolan, Patrick, Lalanne, Zuzanna, Cheeseman, Michael, Peters, Josephine
Publicado em 2012

Melanopsin Regulates Both Sleep-Promoting and Arousal-Promoting Responses to Light

Por Pilorz, Violetta, Tam, Shu K. E., Hughes, Steven, Pothecary, Carina A., Jagannath, Aarti, Hankins, Mark W., Bannerman, David M., Lightman, Stafford L., Vyazovskiy, Vladyslav V., Nolan, Patrick M., Foster, Russell G., Peirson, Stuart N.
Publicado no PLoS Biol (2016)

Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans

Por Keays, David A., Tian, Guoling, Poirier, Karine, Huang, Guo-Jen, Siebold, Christian, Cleak, James, Oliver, Peter L., Fray, Martin, Harvey, Robert J., Molnár, Zoltán, Piñon, Maria C., Dear, Neil, Valdar, William, Brown, Steve D.M., Davies, Kay E., Rawlins, J. Nicholas P., Cowan, Nicholas J., Nolan, Patrick, Chelly, Jamel, Flint, Jonathan
Publicado em 2007

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

Por Bogani, Debora, Willoughby, Catherine, Davies, Jennifer, Kaur, Kulvinder, Mirza, Ghazala, Paudyal, Anju, Haines, Heather, McKeone, Richard, Cadman, Matthew, Pieles, Guido, Schneider, Jürgen E., Bhattacharya, Shoumo, Hardy, Andrea, Nolan, Patrick M., Tripodis, Nikos, Depew, Michael J., Chandrasekara, Ramya, Duncan, Gimara, Sharpe, Paul T., Greenfield, Andy, Denny, Paul, Brown, Steve D. M., Ragoussis, Jiannis, Arkell, Ruth M.
Publicado em 2005

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy

Por Achilli, Francesca, Bros-Facer, Virginie, Williams, Hazel P., Banks, Gareth T., AlQatari, Mona, Chia, Ruth, Tucci, Valter, Groves, Michael, Nickols, Carole D., Seburn, Kevin L., Kendall, Rachel, Cader, Muhammed Z., Talbot, Kevin, van Minnen, Jan, Burgess, Robert W., Brandner, Sebastian, Martin, Joanne E., Koltzenburg, Martin, Greensmith, Linda, Nolan, Patrick M., Fisher, Elizabeth M. C.
Publicado em 2009