Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and mice

Autor: Pagnamenta, AT, Heemeryck, P, Martin, HC, Bosc, C, Peris, L, Uszynski, I, Gory-Fauré, S, Couly, S, Deshpande, C, Siddiqui, A, Elmonairy, AA, Consortium, WGS500, Consortium, Genomics England Research, Jayawant, S, Murthy, S, Walker, I, Loong, L, Bauer, P, Vossier, F, Denarier, E, Maurice, T, Barbier, EL, Deloulme, J-C, Taylor, JC, Blair, EM, Andrieux, A, Moutin, M-J

Publikováno v: Hum Mol Genet
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2019, ⟨10.1093/hmg/ddz186⟩
Human Molecular Genetics, 2019, ⟨10.1093/hmg/ddz186⟩

Reversible detyrosination of tubulin, the building block of microtubules, is crucial for neuronal physiology. Enzymes responsible for detyrosination were recently identified as complexes of vasohibins (VASHs) one or two with small VASH-binding protei

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7d34fc643d09769823472ee19c051e30
https://pubmed.ncbi.nlm.nih.gov/31363758

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