University College London-ko ikertzaileekin lankidetzan egindako argitalpenak (11)

2024

  1. TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43

    Neurobiology of Disease, Vol. 193

2021

  1. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

2018

  1. A genetic modifier suggests that endurance exercise exacerbates Huntington's disease

    Human Molecular Genetics, Vol. 27, Núm. 10, pp. 1723-1731

  2. Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis

    EMBO Journal, Vol. 37, Núm. 11

  3. TDP-43 mutations increase HNRNP A1-7B through gain of splicing function

    Brain

2017

  1. Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in 'FUSDelta14' knockin mice

    Brain, Vol. 140, Núm. 11, pp. 2797-2805

2016

  1. Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration

    Human Molecular Genetics, Vol. 25, Núm. 2, pp. 291-307

  2. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

    Autophagy

  3. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Autophagy, Vol. 12, Núm. 1, pp. 1-222

2014

  1. Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy

    Neurobiology of Aging, Vol. 35, Núm. 6, pp. 1491-1498

2012

  1. Guidelines for the use and interpretation of assays for monitoring autophagy

    Autophagy, Vol. 8, Núm. 4, pp. 445-544