Items where authors include "Blanco, Gonzalo"
Article
Stonadge, Amy, Genzor, Aitana V, Russell, Alex et al. (6 more authors) (2023) Myofibrillar myopathy hallmarks associated with ZAK deficiency. Human Molecular Genetics. pp. 2751-2770. ISSN 0964-6906
Blanco, Gonzalo orcid.org/0000-0003-3827-3111, Brown, Amy and Li, Xiang (2022) ZAK-beta is activated by cell compression and mediates contraction-induced MAPK signaling in muscle. EMBO Journal. e111650. ISSN 0261-4189
Cracknell, Tobias, Mannsverk, Steinar, Nichols, Angus et al. (2 more authors) (2020) Proteomic resolution of IGFN1 complexes reveals a functional interaction with the actin nucleating protein COBL. Experimental cell research. 112179. ISSN 0014-4827
Blanco, Gonzalo orcid.org/0000-0003-3827-3111, Corrochano, Silvia and Acevedo-Arozena, Abraham (2018) Skeletal Muscle Modulates Huntington's Disease Pathogenesis in Mice: Role of Physical Exercise. Journal of Experimental Neuroscience. PMC6210627. ISSN 1179-0695
Jokl, Elliot James, Hughes, Gideon Llywelyn, Cracknell, Tobias Rowland et al. (2 more authors) (2018) Transcriptional up-regulation of BAG3, a Chaperone Assisted Selective Autophagy factor, in animal models of KY-deficient hereditary myopathy. Disease Models & Mechanisms. ISSN 1754-8411
Blanco, Gonzalo orcid.org/0000-0003-3827-3111 (2018) A genetic modifier suggests that endurance exercise exacerbates Huntington's disease. Human Molecular Genetics. pp. 1-9. ISSN 0964-6906
Li, Xiang, Baker, Jane, Cracknell, Tobias Rowland et al. (2 more authors) (2017) IGFN1_v1 is required for myoblast fusion and differentiation. PLosOne.
Vasli, Nasim, Harris, Elizabeth, Karamchandani, Jason et al. (22 more authors) (2017) Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion. Brain : a journal of neurology. pp. 37-48. ISSN 1460-2156
Jokl, Elliot J and Blanco, Gonzalo orcid.org/0000-0003-3827-3111 (2016) Disrupted autophagy undermines skeletal muscle adaptation and integrity. Mammalian genome : official journal of the International Mammalian Genome Society. ISSN 1432-1777