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XB--480505
Papers associated with tf (and OMIM)
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AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia., Diarra S, Ghosh S, Cissé L, Coulibaly T, Yalcouyé A, Harmison G, Diallo S, Diallo SH, Coulibaly O, Schindler A, Cissé CAK, Maiga AB, Bamba S, Samassekou O, Khokha MK, Mis EK, Lahkani SA, Donovan FX, Jacobson S, Blackstone C, Guinto CO, Landouré G, Bonifacino JS, Fischbeck KH, Grunseich C., Neurobiol Dis. May 19, 2024; 106537. |
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Control of actin polymerization via the coincidence of phosphoinositides and high membrane curvature., Daste F, Walrant A, Holst MR, Gadsby JR, Mason J, Lee JE, Brook D, Mettlen M, Larsson E, Lee SF, Lundmark R, Gallop JL., J Cell Biol. November 6, 2017; 216 (11): 3745-3765. ![]() |
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In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations., Schimanski LM, Drakesmith H, Merryweather-Clarke AT, Viprakasit V, Edwards JP, Sweetland E, Bastin JM, Cowley D, Chinthammitr Y, Robson KJ, Townsend AR., Blood. May 15, 2005; 105 (10): 4096-102. |
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