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Year Number of Results
1996 2
1997 1
1998 2
2016 1
2017 1
2019 1
2020 1
2022 1
2023 1
2024 0

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PubMed for id: 568215738

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Page 1
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations.
Sbardella D, Tundo GR, Cunsolo V, Grasso G, Cascella R, Caputo V, Santoro AM, Milardi D, Pecorelli A, Ciaccio C, Di Pierro D, Leoncini S, Campagnolo L, Pironi V, Oddone F, Manni P, Foti S, Giardina E, De Felice C, Hayek J, Curatolo P, Galasso C, Valacchi G, Coletta M, Graziani G, Marini S. Sbardella D, et al. Biochim Biophys Acta Mol Basis Dis. 2020 Jul 1;1866(7):165793. doi: 10.1016/j.bbadis.2020.165793. Epub 2020 Apr 8. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 32275946 Free article.
Biallelic TBCD Mutations Cause Early-Onset Neurodegenerative Encephalopathy.
Miyake N, Fukai R, Ohba C, Chihara T, Miura M, Shimizu H, Kakita A, Imagawa E, Shiina M, Ogata K, Okuno-Yuguchi J, Fueki N, Ogiso Y, Suzumura H, Watabe Y, Imataka G, Leong HY, Fattal-Valevski A, Kramer U, Miyatake S, Kato M, Okamoto N, Sato Y, Mitsuhashi S, Nishino I, Kaneko N, Nishiyama A, Tamura T, Mizuguchi T, Nakashima M, Tanaka F, Saitsu H, Matsumoto N. Miyake N, et al. Am J Hum Genet. 2016 Oct 6;99(4):950-961. doi: 10.1016/j.ajhg.2016.08.005. Epub 2016 Sep 22. Am J Hum Genet. 2016. PMID: 27666374 Free PMC article.
Pathway leading to correctly folded beta-tubulin.
Tian G, Huang Y, Rommelaere H, Vandekerckhove J, Ampe C, Cowan NJ. Tian G, et al. Cell. 1996 Jul 26;86(2):287-96. doi: 10.1016/s0092-8674(00)80100-2. Cell. 1996. PMID: 8706133 Free article.
Chaperonin-mediated folding of actin and tubulin.
Lewis SA, Tian G, Vainberg IE, Cowan NJ. Lewis SA, et al. J Cell Biol. 1996 Jan;132(1-2):1-4. doi: 10.1083/jcb.132.1.1. J Cell Biol. 1996. PMID: 8567715 Free PMC article. Review. No abstract available.