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Evolutionary Divergence of Enzymatic Mechanisms for Tubulin Detyrosination.
Cell Rep. 2019 Dec 17;29(12):4159-4171.e6. doi: 10.1016/j.celrep.2019.11.074.
Cell Rep. 2019.
PMID: 31851940
Free article.
Tubulin glutamylation: a skeleton key for neurodegenerative diseases.
van der Laan S, Dubra G, Rogowski K.
van der Laan S, et al. Among authors: dubra g.
Neural Regen Res. 2019 Nov;14(11):1899-1900. doi: 10.4103/1673-5374.259611.
Neural Regen Res. 2019.
PMID: 31290441
Free PMC article.
No abstract available.
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Ki-67 regulates global gene expression and promotes sequential stages of carcinogenesis.
Mrouj K, Andrés-Sánchez N, Dubra G, Singh P, Sobecki M, Chahar D, Al Ghoul E, Aznar AB, Prieto S, Pirot N, Bernex F, Bordignon B, Hassen-Khodja C, Villalba M, Krasinska L, Fisher D.
Mrouj K, et al. Among authors: dubra g.
Proc Natl Acad Sci U S A. 2021 Mar 9;118(10):e2026507118. doi: 10.1073/pnas.2026507118.
Proc Natl Acad Sci U S A. 2021.
PMID: 33658388
Free PMC article.
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A cyclin-dependent kinase-mediated phosphorylation switch of disordered protein condensation.
Valverde JM, Dubra G, Phillips M, Haider A, Elena-Real C, Fournet A, Alghoul E, Chahar D, Andrés-Sanchez N, Paloni M, Bernadó P, van Mierlo G, Vermeulen M, van den Toorn H, Heck AJR, Constantinou A, Barducci A, Ghosh K, Sibille N, Knipscheer P, Krasinska L, Fisher D, Altelaar M.
Valverde JM, et al. Among authors: dubra g.
Nat Commun. 2023 Oct 9;14(1):6316. doi: 10.1038/s41467-023-42049-0.
Nat Commun. 2023.
PMID: 37813838
Free PMC article.
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CDK8 and CDK19 act redundantly to control the CFTR pathway in the intestinal epithelium.
Prieto S, Dubra G, Camasses A, Aznar AB, Begon-Pescia C, Simboeck E, Pirot N, Gerbe F, Angevin L, Jay P, Krasinska L, Fisher D.
Prieto S, et al. Among authors: dubra g.
EMBO Rep. 2023 Feb 6;24(2):e54261. doi: 10.15252/embr.202154261. Epub 2022 Dec 22.
EMBO Rep. 2023.
PMID: 36545778
Free PMC article.
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Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease.
Ma CA, Stinson JR, Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR, Lyons JJ, Nelson CG, Ruffo E, Dorjbal B, Glauzy S, Yamakawa N, Arjunaraja S, Voss K, Stoddard J, Niemela J, Zhang Y, Rosenzweig SD, McElwee JJ, DiMaggio T, Matthews HF, Jones N, Stone KD, Palma A, Oleastro M, Prieto E, Bernasconi AR, Dubra G, Danielian S, Zaiat J, Marti MA, Kim B, Cooper MA, Romberg ND, Meffre E, Gelfand EW, Snow AL, Milner JD.
Ma CA, et al. Among authors: dubra g.
Nat Genet. 2017 Oct 27;49(11):1661. doi: 10.1038/ng1117-1661b.
Nat Genet. 2017.
PMID: 29074947
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Germline hypomorphic CARD11 mutations in severe atopic disease.
Ma CA, Stinson JR, Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR, Lyons JJ, Nelson CG, Ruffo E, Dorjbal B, Glauzy S, Yamakawa N, Arjunaraja S, Voss K, Stoddard J, Niemela J, Zhang Y, Rosenzweig SD, McElwee JJ, DiMaggio T, Matthews HF, Jones N, Stone KD, Palma A, Oleastro M, Prieto E, Bernasconi AR, Dubra G, Danielian S, Zaiat J, Marti MA, Kim B, Cooper MA, Romberg N, Meffre E, Gelfand EW, Snow AL, Milner JD.
Ma CA, et al. Among authors: dubra g.
Nat Genet. 2017 Aug;49(8):1192-1201. doi: 10.1038/ng.3898. Epub 2017 Jun 19.
Nat Genet. 2017.
PMID: 28628108
Free PMC article.
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