Reply: The role of DNAJB2 in amyotrophic lateral sclerosis

Por Chen, Han-Jou, Shaw, Christopher E.
Publicado no Brain (2016)

Erratum to: TDP-43 Proteinopathy and ALS: Insights into Disease Mechanisms and Therapeutic Targets

Por Scotter, Emma L., Chen, Han-Jou, Shaw, Christopher E.
Publicado no Neurotherapeutics (2015)

TDP-43 Proteinopathy and ALS: Insights into Disease Mechanisms and Therapeutic Targets

Por Scotter, Emma L., Chen, Han-Jou, Shaw, Christopher E.
Publicado no Neurotherapeutics (2015)

Tar DNA-binding protein-43 (TDP-43) regulates axon growth in vitro and in vivo()

Por Tripathi, Vineeta Bhasker, Baskaran, Pranetha, Shaw, Christopher E., Guthrie, Sarah
Publicado em 2014

Unpicking neurodegeneration in a dish with human pluripotent stem cells: One cell type at a time

Por Bilican, Bilada, Serio, Andrea, Shaw, Christopher E, Maniatis, Tom, Chandran, Siddharthan
Publicado em 2013

Generation of six induced pluripotent stem cell lines from patients with amyotrophic lateral sclerosis with associated genetic mutations in either FUS or ANXA11

Por Hedges, Erin C., Topp, Simon, Shaw, Christopher E., Nishimura, Agnes L.
Publicado no Stem Cell Res (2021)

Combination of neurofilament heavy chain and complement c3 as CSF biomarkers for ALS

Por Ganesalingam, Jeban, An, Jiyan, Shaw, Christopher E, Shaw, Gerry, Lacomis, David, Bowser, Robert
Publicado em 2011

Heterogeneous Nuclear Ribonucleoprotein E2 (hnRNP E2) Is a Component of TDP-43 Aggregates Specifically in the A and C Pathological Subtypes of Frontotemporal Lobar Degeneration

Por Kattuah, Wejdan, Rogelj, Boris, King, Andrew, Shaw, Christopher E., Hortobágyi, Tibor, Troakes, Claire
Publicado no Front Neurosci (2019)

RNA Misprocessing in C9orf72-Linked Neurodegeneration

Por Barker, Holly V., Niblock, Michael, Lee, Youn-Bok, Shaw, Christopher E., Gallo, Jean-Marc
Publicado no Front Cell Neurosci (2017)

Latent Cluster Analysis of ALS Phenotypes Identifies Prognostically Differing Groups

Por Ganesalingam, Jeban, Stahl, Daniel, Wijesekera, Lokesh, Galtrey, Clare, Shaw, Christopher E., Leigh, P. Nigel, Al-Chalabi, Ammar
Publicado em 2009

Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?

Por Isaacs, Jeremy D, Dean, Andrew F, Shaw, Christopher E, Al‐Chalabi, Ammar, Mills, Kerry R, Leigh, P Nigel
Publicado em 2007

Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria

Por Mórotz, Gábor M., De Vos, Kurt J., Vagnoni, Alessio, Ackerley, Steven, Shaw, Christopher E., Miller, Christopher C.J.
Publicado em 2012

ALS-FUS pathology revisited: singleton FUS mutations and an unusual case with both a FUS and TARDBP mutation

Por King, Andrew, Troakes, Claire, Smith, Bradley, Nolan, Matthew, Curran, Olimpia, Vance, Caroline, Shaw, Christopher E., Al-Sarraj, Safa
Publicado no Acta Neuropathol Commun (2015)

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)

Mitochondrial abnormalities and disruption of the neuromuscular junction precede the clinical phenotype and motor neuron loss in hFUS(WT) transgenic mice

Por So, Eva, Mitchell, Jacqueline C, Memmi, Caroline, Chennell, George, Vizcay-Barrena, Gema, Allison, Leanne, Shaw, Christopher E, Vance, Caroline
Publicado no Hum Mol Genet (2018)

A clinical tool for predicting survival in ALS

Por Knibb, Jonathan A, Keren, Noa, Kulka, Anna, Leigh, P Nigel, Martin, Sarah, Shaw, Christopher E, Tsuda, Miho, Al-Chalabi, Ammar
Publicado no J Neurol Neurosurg Psychiatry (2016)

Glutamate Slows Axonal Transport of Neurofilaments in Transfected Neurons

Por Ackerley, Steven, Grierson, Andrew J., Brownlees, Janet, Thornhill, Paul, Anderton, Brian H., Leigh, P. Nigel, Shaw, Christopher E., Miller, Christopher C.J.
Publicado em 2000

Neurofilament heavy chain side arm phosphorylation regulates axonal transport of neurofilaments

Por Ackerley, Steven, Thornhill, Paul, Grierson, Andrew J., Brownlees, Janet, Anderton, Brian H., Leigh, P. Nigel, Shaw, Christopher E., Miller, Christopher C.J.
Publicado em 2003

The risk to relatives of patients with sporadic amyotrophic lateral sclerosis

Por Hanby, Martha F., Scott, Kirsten M., Scotton, William, Wijesekera, Lokesh, Mole, Thomas, Ellis, Catherine E., Nigel Leigh, P., Shaw, Christopher E., Al-Chalabi, Ammar
Publicado em 2011