The role of CELF proteins in neurological disorders

Por Gallo, Jean-Marc, Spickett, Carl
Publicado em 2010

Trans-splicing correction of tau isoform imbalance in a mouse model of tau mis-splicing

Por Avale, María Elena, Rodríguez-Martín, Teresa, Gallo, Jean-Marc
Publicado em 2013

Tau mis-splicing in the pathogenesis of neurodegenerative disorders

Por Park, Sun Ah, Ahn, Sang Il, Gallo, Jean-Marc
Publicado no BMB Rep (2016)

Focal distortion of the nuclear envelope by huntingtin aggregates revealed by lamin immunostaining

Por Chapple, J. Paul, Bros-Facer, Virginie, Butler, Rachel, Gallo, Jean-Marc
Publicado em 2008

Correction of tau mis-splicing caused by FTDP-17 MAPT mutations by spliceosome-mediated RNA trans-splicing

Por Rodriguez-Martin, Teresa, Anthony, Karen, Garcia-Blanco, Mariano A., Mansfield, S. Gary, Anderton, Brian H., Gallo, Jean-Marc
Publicado em 2009

Dipeptide repeat protein inclusions are rare in the spinal cord and almost absent from motor neurons in C9ORF72 mutant amyotrophic lateral sclerosis and are unlikely to cause their...

Por Gomez-Deza, Jorge, Lee, Youn-bok, Troakes, Claire, Nolan, Matthew, Al-Sarraj, Safa, Gallo, Jean-Marc, Shaw, Christopher E.
Publicado no Acta Neuropathol Commun (2015)

Lack of association between TDP-43 pathology and tau mis-splicing in Alzheimer's disease

Por Niblock, Michael, Hortobágyi, Tibor, Troakes, Claire, Al-Sarraj, Safa, Spickett, Carl, Jones, Rebecca, Shaw, Christopher E., Gallo, Jean-Marc
Publicado no Neurobiol Aging (2016)

Absence of disturbed axonal transport in spinal and bulbar muscular atrophy

Por Malik, Bilal, Nirmalananthan, Niranjanan, Bilsland, Lynsey G., La Spada, Albert R., Hanna, Michael G., Schiavo, Giampietro, Gallo, Jean-Marc, Greensmith, Linda
Publicado em 2011

Reprogramming of tau alternative splicing by spliceosome-mediated RNA trans-splicing: Implications for tauopathies

Por Rodriguez-Martin, Teresa, Garcia-Blanco, Mariano A., Mansfield, S. Gary, Grover, Andrew C., Hutton, Michael, Yu, Qingming, Zhou, Jianhua, Anderton, Brian H., Gallo, Jean-Marc
Publicado em 2005

The ataxia protein sacsin is a functional co-chaperone that protects against polyglutamine-expanded ataxin-1

Por Parfitt, David A., Michael, Gregory J., Vermeulen, Esmeralda G.M., Prodromou, Natalia V., Webb, Tom R., Gallo, Jean-Marc, Cheetham, Michael E., Nicoll, William S., Blatch, Gregory L., Chapple, J. Paul
Publicado em 2009

Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD

Por Niblock, Michael, Smith, Bradley N., Lee, Youn-Bok, Sardone, Valentina, Topp, Simon, Troakes, Claire, Al-Sarraj, Safa, Leblond, Claire S., Dion, Patrick A., Rouleau, Guy A., Shaw, Christopher E., Gallo, Jean-Marc
Publicado no Acta Neuropathol Commun (2016)

Allele-Specific Knockdown of ALS-Associated Mutant TDP-43 in Neural Stem Cells Derived from Induced Pluripotent Stem Cells

Por Nishimura, Agnes L., Shum, Carole, Scotter, Emma L., Abdelgany, Amr, Sardone, Valentina, Wright, Jamie, Lee, Youn-Bok, Chen, Han-Jou, Bilican, Bilada, Carrasco, Monica, Maniatis, Tom, Chandran, Siddharthan, Rogelj, Boris, Gallo, Jean-Marc, Shaw, Christopher E.
Publicado em 2014

Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups

Por Parfitt, David A., Lane, Amelia, Ramsden, Conor M., Carr, Amanda-Jayne F., Munro, Peter M., Jovanovic, Katarina, Schwarz, Nele, Kanuga, Naheed, Muthiah, Manickam N., Hull, Sarah, Gallo, Jean-Marc, da Cruz, Lyndon, Moore, Anthony T., Hardcastle, Alison J., Coffey, Peter J., Cheetham, Michael E.
Publicado no Cell Stem Cell (2016)

Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease

Por Sassi, Celeste, Guerreiro, Rita, Gibbs, Raphael, Ding, Jinhui, Lupton, Michelle K., Troakes, Claire, Al-Sarraj, Safa, Niblock, Michael, Gallo, Jean-Marc, Adnan, Jihad, Killick, Richard, Brown, Kristelle S., Medway, Christopher, Lord, Jenny, Turton, James, Bras, Jose, Morgan, Kevin, Powell, John F., Singleton, Andrew, Hardy, John
Publicado no Neurobiol Aging (2014)

Hexanucleotide Repeats in ALS/FTD Form Length-Dependent RNA Foci, Sequester RNA Binding Proteins, and Are Neurotoxic

Por Lee, Youn-Bok, Chen, Han-Jou, Peres, João N., Gomez-Deza, Jorge, Attig, Jan, Štalekar, Maja, Troakes, Claire, Nishimura, Agnes L., Scotter, Emma L., Vance, Caroline, Adachi, Yoshitsugu, Sardone, Valentina, Miller, Jack W., Smith, Bradley N., Gallo, Jean-Marc, Ule, Jernej, Hirth, Frank, Rogelj, Boris, Houart, Corinne, Shaw, Christopher E.
Publicado em 2013

Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

Por Vance, Caroline, Rogelj, Boris, Hortobágyi, Tibor, De Vos, Kurt J., Nishimura, Agnes Lumi, Sreedharan, Jemeen, Hu, Xun, Smith, Bradley, Ruddy, Deborah, Wright, Paul, Ganesalingam, Jeban, Williams, Kelly L., Tripathi, Vineeta, Al-Saraj, Safa, Al-Chalabi, Ammar, Leigh, P. Nigel, Blair, Ian P., Nicholson, Garth, de Belleroche, Jackie, Gallo, Jean-Marc, Miller, Christopher C., Shaw, Christopher E.
Publicado no Science (2009)