Items where authors include "Webster, C.P."

Export as [feed] Atom [feed] RSS
Number of items: 11.

Article

Scarrott, J.M. orcid.org/0000-0002-6046-7687, Alves-Cruzeiro, J., Marchi, P.M. et al. (7 more authors) (2023) Ap4b1-knockout mouse model of hereditary spastic paraplegia type 47 displays motor dysfunction, aberrant brain morphology and ATG9A mislocalization. Brain Communications, 5 (1). fcac335.

Bauer, C.S., Webster, C.P., Shaw, A.C. et al. (12 more authors) (2022) Loss of TMEM106B exacerbates C9ALS/FTD DPR pathology by disrupting autophagosome maturation. Frontiers in Cellular Neuroscience, 16. 1061559. ISSN 1662-5102

Marchi, P.M. orcid.org/0000-0002-8893-3790, Marrone, L., Brasseur, L. et al. (19 more authors) (2022) C9ORF72-derived poly-GA DPRs undergo endocytic uptake in iAstrocytes and spread to motor neurons. Life Science Alliance, 5 (9). e202101276. ISSN 2575-1077

Bauer, C.S., Cohen, R.N., Sironi, F. et al. (11 more authors) (2022) An interaction between synapsin and C9orf72 regulates excitatory synapses and is impaired in ALS/FTD. Acta Neuropathologica, 144 (3). pp. 437-464. ISSN 0001-6322

Marrone, L., Marchi, P.M. orcid.org/0000-0002-8893-3790, Webster, C.P. orcid.org/0000-0003-4197-2036 et al. (11 more authors) (2022) SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction. Human Molecular Genetics, 31 (16). pp. 2693-2710. ISSN 0964-6906

Karyka, E., Berrueta Ramirez, N., Webster, C.P. orcid.org/0000-0003-4197-2036 et al. (11 more authors) (2022) SMN-deficient cells exhibit increased ribosomal DNA damage. Life Science Alliance, 5 (8). e202101145. ISSN 2575-1077

Alves-Cruzeiro, J., Webster, C.P. and Azzouz, M. orcid.org/0000-0001-6564-5967 (2019) The hybrid AAVP tool gets an upgrade. Proceedings of the National Academy of Sciences, 116 (37). pp. 18162-18164. ISSN 0027-8424

Webster, C.P., Smith, E.F., Grierson, A.J. et al. (1 more author) (2018) C9orf72 plays a central role in Rab GTPase-dependent regulation of autophagy. Small GTPases, 9 (5). ISSN 2154-1248

Moller, A., Bauer, C.S., Cohen, R.N. et al. (2 more authors) (2017) Amyotrophic lateral sclerosis-associated mutant SOD1 inhibits anterograde axonal transport of mitochondria by reducing Miro1 levels. Human Molecular Genetics, 26 (23). pp. 4668-4679. ISSN 0964-6906

Webster, C.P., Smith, E.F., Bauer, C.S. et al. (12 more authors) (2016) The C9orf72 protein interacts with Rab1a and the ULK1 complex to regulate initiation of autophagy. EMBO Journal, 35 (15). pp. 1656-1676.

Proceedings Paper

Allen, S.P., Hall, B., Castelli, L. orcid.org/0000-0003-3620-4219 et al. (11 more authors) (2018) Inosine reverses motor neuron toxicity observed in amyotrophic lateral sclerosis patient astrocytes with an adenosine deaminase deficiency. In: Biochimica et Biophysica Acta (BBA) - Bioenergetics. 20th European Bioenergetics Conference, 25-30 Aug 2018, Budapest, Hungary. Elsevier BV , e23-e23.

This list was generated on Mon Mar 25 01:24:04 2024 GMT.