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Year | Number of Results |
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2005 | 1 |
2009 | 1 |
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Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
Nat Genet. 2005 Mar;37(3):289-94. doi: 10.1038/ng1514. Epub 2005 Jan 30.
Nat Genet. 2005.
PMID: 15731758
Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis.
Bitoun M, Durieux AC, Prudhon B, Bevilacqua JA, Herledan A, Sakanyan V, Urtizberea A, Cartier L, Romero NB, Guicheney P.
Bitoun M, et al.
Hum Mutat. 2009 Oct;30(10):1419-27. doi: 10.1002/humu.21086.
Hum Mutat. 2009.
PMID: 19623537
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GSK3α phosphorylates dynamin-2 to promote GLUT4 endocytosis in muscle cells.
Laiman J, Hsu YJ, Loh J, Tang WC, Chuang MC, Liu HK, Yang WS, Chen BC, Chuang LM, Chang YC, Liu YW.
Laiman J, et al.
J Cell Biol. 2023 Feb 6;222(2):e202102119. doi: 10.1083/jcb.202102119. Epub 2022 Nov 29.
J Cell Biol. 2023.
PMID: 36445308
Free PMC article.
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