Reply: The role of DNAJB2 in amyotrophic lateral sclerosis

od Chen, Han-Jou, Shaw, Christopher E.
Izdano u Brain (2016)

Disease Mechanisms and Therapeutic Approaches in C9orf72 ALS-FTD

od Mayl, Keith, Shaw, Christopher E., Lee, Youn-Bok
Izdano u Biomedicines (2021)

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

od Scotter, Emma L., Chen, Han-Jou, Shaw, Christopher E.
Izdano u Neurotherapeutics (2015)

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

od Scotter, Emma L., Chen, Han-Jou, Shaw, Christopher E.
Izdano u Neurotherapeutics (2015)

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

od Tripathi, Vineeta Bhasker, Baskaran, Pranetha, Shaw, Christopher E., Guthrie, Sarah
Izdano 2014

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

od Bilican, Bilada, Serio, Andrea, Shaw, Christopher E, Maniatis, Tom, Chandran, Siddharthan
Izdano 2013

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

od Hedges, Erin C., Topp, Simon, Shaw, Christopher E., Nishimura, Agnes L.
Izdano u Stem Cell Res (2021)

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

od Ganesalingam, Jeban, An, Jiyan, Shaw, Christopher E, Shaw, Gerry, Lacomis, David, Bowser, Robert
Izdano 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

od Kattuah, Wejdan, Rogelj, Boris, King, Andrew, Shaw, Christopher E., Hortobágyi, Tibor, Troakes, Claire
Izdano u Front Neurosci (2019)

RNA Misprocessing in C9orf72-Linked Neurodegeneration

od Barker, Holly V., Niblock, Michael, Lee, Youn-Bok, Shaw, Christopher E., Gallo, Jean-Marc
Izdano u Front Cell Neurosci (2017)

Latent Cluster Analysis of ALS Phenotypes Identifies Prognostically Differing Groups

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

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

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

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

od Mórotz, Gábor M., De Vos, Kurt J., Vagnoni, Alessio, Ackerley, Steven, Shaw, Christopher E., Miller, Christopher C.J.
Izdano 2012

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

od King, Andrew, Troakes, Claire, Smith, Bradley, Nolan, Matthew, Curran, Olimpia, Vance, Caroline, Shaw, Christopher E., Al-Sarraj, Safa
Izdano u 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...

od Gomez-Deza, Jorge, Lee, Youn-bok, Troakes, Claire, Nolan, Matthew, Al-Sarraj, Safa, Gallo, Jean-Marc, Shaw, Christopher E.
Izdano u Acta Neuropathol Commun (2015)

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

od Niblock, Michael, Hortobágyi, Tibor, Troakes, Claire, Al-Sarraj, Safa, Spickett, Carl, Jones, Rebecca, Shaw, Christopher E., Gallo, Jean-Marc
Izdano u Neurobiol Aging (2016)

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

od So, Eva, Mitchell, Jacqueline C, Memmi, Caroline, Chennell, George, Vizcay-Barrena, Gema, Allison, Leanne, Shaw, Christopher E, Vance, Caroline
Izdano u Hum Mol Genet (2018)

A clinical tool for predicting survival in ALS

od Knibb, Jonathan A, Keren, Noa, Kulka, Anna, Leigh, P Nigel, Martin, Sarah, Shaw, Christopher E, Tsuda, Miho, Al-Chalabi, Ammar
Izdano u J Neurol Neurosurg Psychiatry (2016)

ALS-linked FUS mutants affect the localization of U7 snRNP and replication-dependent histone gene expression in human cells

od Gadgil, Ankur, Walczak, Agnieszka, Stępień, Agata, Mechtersheimer, Jonas, Nishimura, Agnes Lumi, Shaw, Christopher E., Ruepp, Marc-David, Raczyńska, Katarzyna Dorota
Izdano u Sci Rep (2021)

Glutamate Slows Axonal Transport of Neurofilaments in Transfected Neurons

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