Cytoplasmic dynein could be key to understanding neurodegeneration

Por Banks, Gareth T, Fisher, Elizabeth MC
Publicado em 2008

Reciprocal interactions between circadian clocks and aging

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

TDP-43 is a culprit in human neurodegeneration, and not just an innocent bystander

Por Banks, Gareth T., Kuta, Anna, Isaacs, Adrian M., Fisher, Elizabeth M. C.
Publicado em 2008

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

Mouse Cytoplasmic Dynein Intermediate Chains: Identification of New Isoforms, Alternative Splicing and Tissue Distribution of Transcripts

Por Kuta, Anna, Deng, Wenhan, Morsi El-Kadi, Ali, Banks, Gareth T., Hafezparast, Majid, Pfister, K. Kevin, Fisher, Elizabeth M. C.
Publicado em 2010

Correction: Mouse Cytoplasmic Dynein Intermediate Chains: Identification of New Isoforms, Alternative Splicing and Tissue Distribution of Transcripts

Por Kuta, Anna, Deng, Wenhan, Morsi El-Kadi, Ali, Banks, Gareth T., Hafezparast, Majid, Pfister, K. Kevin, Fisher, Elizabeth M. C.
Publicado em 2010

Mutant Glycyl-tRNA Synthetase (Gars) Ameliorates SOD1(G93A) Motor Neuron Degeneration Phenotype but Has Little Affect on Loa Dynein Heavy Chain Mutant Mice

Por Banks, Gareth T., Bros-Facer, Virginie, Williams, Hazel P., Chia, Ruth, Achilli, Francesca, Bryson, J. Barney, Greensmith, Linda, Fisher, Elizabeth M. C.
Publicado em 2009

Correction: Mutant Glycyl-tRNA Synthetase (Gars) Ameliorates SOD1(G93A) Motor Neuron Degeneration Phenotype but Has Little Affect on Loa Dynein Heavy Chain Mutant Mice

Por Banks, Gareth T., Bros-Facer, Virginie, Williams, Hazel P., Chia, Ruth, Achilli, Francesca, Bryson, J. Barney, Greensmith, Linda, Fisher, Elizabeth M. C.
Publicado em 2009

Neurodegenerative Mutation in Cytoplasmic Dynein Alters Its Organization and Dynein-Dynactin and Dynein-Kinesin Interactions

Por Deng, Wenhan, Garrett, Caroline, Dombert, Benjamin, Soura, Violetta, Banks, Gareth, Fisher, Elizabeth M. C., van der Brug, Marcel P., Hafezparast, Majid
Publicado em 2010

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)

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

The Legs at odd angles (Loa) Mutation in Cytoplasmic Dynein Ameliorates Mitochondrial Function in SOD1(G93A) Mouse Model for Motor Neuron Disease

Por El-Kadi, Ali Morsi, Bros-Facer, Virginie, Deng, Wenhan, Philpott, Amelia, Stoddart, Eleanor, Banks, Gareth, Jackson, Graham S., Fisher, Elizabeth M. C., Duchen, Michael R., Greensmith, Linda, Moore, Anthony L., Hafezparast, Majid
Publicado em 2010

Behavioral and Other Phenotypes in a Cytoplasmic Dynein Light Intermediate Chain 1 Mutant Mouse

Por Banks, Gareth T., Haas, Matilda A., Line, Samantha, Shepherd, Hazel L., AlQatari, Mona, Stewart, Sammy, Rishal, Ida, Philpott, Amelia, Kalmar, Bernadett, Kuta, Anna, Groves, Michael, Parkinson, Nicholas, Acevedo-Arozena, Abraham, Brandner, Sebastian, Bannerman, David, Greensmith, Linda, Hafezparast, Majid, Koltzenburg, Martin, Deacon, Robert, Fainzilber, Mike, Fisher, Elizabeth M. C.
Publicado em 2011

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

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease

Por Potter, Paul K., Bowl, Michael R., Jeyarajan, Prashanthini, Wisby, Laura, Blease, Andrew, Goldsworthy, Michelle E., Simon, Michelle M., Greenaway, Simon, Michel, Vincent, Barnard, Alun, Aguilar, Carlos, Agnew, Thomas, Banks, Gareth, Blake, Andrew, Chessum, Lauren, Dorning, Joanne, Falcone, Sara, Goosey, Laurence, Harris, Shelley, Haynes, Andy, Heise, Ines, Hillier, Rosie, Hough, Tertius, Hoslin, Angela, Hutchison, Marie, King, Ruairidh, Kumar, Saumya, Lad, Heena V., Law, Gemma, MacLaren, Robert E., Morse, Susan, Nicol, Thomas, Parker, Andrew, Pickford, Karen, Sethi, Siddharth, Starbuck, Becky, Stelma, Femke, Cheeseman, Michael, Cross, Sally H., Foster, Russell G., Jackson, Ian J., Peirson, Stuart N., Thakker, Rajesh V., Vincent, Tonia, Scudamore, Cheryl, Wells, Sara, El-Amraoui, Aziz, Petit, Christine, Acevedo-Arozena, Abraham, Nolan, Patrick M., Cox, Roger, Mallon, Anne-Marie, Brown, Steve D. M.
Publicado no Nat Commun (2016)