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Year | Number of Results |
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2005 | 1 |
2007 | 1 |
2013 | 1 |
2018 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 55614
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KIF16B is a candidate gene for a novel autosomal-recessive intellectual disability syndrome.
Am J Med Genet A. 2018 Jul;176(7):1602-1609. doi: 10.1002/ajmg.a.38723. Epub 2018 May 7.
Am J Med Genet A. 2018.
PMID: 29736960
The kinesin KIF16B mediates apical transcytosis of transferrin receptor in AP-1B-deficient epithelia.
Perez Bay AE, Schreiner R, Mazzoni F, Carvajal-Gonzalez JM, Gravotta D, Perret E, Lehmann Mantaras G, Zhu YS, Rodriguez-Boulan EJ.
Perez Bay AE, et al.
EMBO J. 2013 Jul 31;32(15):2125-39. doi: 10.1038/emboj.2013.130. Epub 2013 Jun 7.
EMBO J. 2013.
PMID: 23749212
Free PMC article.
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The structural basis of novel endosome anchoring activity of KIF16B kinesin.
Blatner NR, Wilson MI, Lei C, Hong W, Murray D, Williams RL, Cho W.
Blatner NR, et al.
EMBO J. 2007 Aug 8;26(15):3709-19. doi: 10.1038/sj.emboj.7601800. Epub 2007 Jul 19.
EMBO J. 2007.
PMID: 17641687
Free PMC article.
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Modulation of receptor recycling and degradation by the endosomal kinesin KIF16B.
Hoepfner S, Severin F, Cabezas A, Habermann B, Runge A, Gillooly D, Stenmark H, Zerial M.
Hoepfner S, et al.
Cell. 2005 May 6;121(3):437-50. doi: 10.1016/j.cell.2005.02.017.
Cell. 2005.
PMID: 15882625
Free article.
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