These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 38675612)

  • 21. The kinesin-5 tail domain directly modulates the mechanochemical cycle of the motor domain for anti-parallel microtubule sliding.
    Bodrug T; Wilson-Kubalek EM; Nithianantham S; Thompson AF; Alfieri A; Gaska I; Major J; Debs G; Inagaki S; Gutierrez P; Gheber L; McKenney RJ; Sindelar CV; Milligan R; Stumpff J; Rosenfeld SS; Forth ST; Al-Bassam J
    Elife; 2020 Jan; 9():. PubMed ID: 31958056
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Accumulation of cytoplasmic dynein and dynactin at microtubule plus ends in Aspergillus nidulans is kinesin dependent.
    Zhang J; Li S; Fischer R; Xiang X
    Mol Biol Cell; 2003 Apr; 14(4):1479-88. PubMed ID: 12686603
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A bidirectional kinesin motor in live Drosophila embryos.
    Sciambi CJ; Komma DJ; Sköld HN; Hirose K; Endow SA
    Traffic; 2005 Nov; 6(11):1036-46. PubMed ID: 16190984
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The Aspergillus nidulans kinesin-3 UncA motor moves vesicles along a subpopulation of microtubules.
    Zekert N; Fischer R
    Mol Biol Cell; 2009 Jan; 20(2):673-84. PubMed ID: 19037104
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Processivity of the motor protein kinesin requires two heads.
    Hancock WO; Howard J
    J Cell Biol; 1998 Mar; 140(6):1395-405. PubMed ID: 9508772
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Human kinesin-5 KIF11 drives the helical motion of anti-parallel and parallel microtubules around each other.
    Meißner L; Niese L; Schüring I; Mitra A; Diez S
    EMBO J; 2024 Apr; 43(7):1244-1256. PubMed ID: 38424239
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Flexible microtubule anchoring modulates the bi-directional motility of the kinesin-5 Cin8.
    Pandey H; Singh SK; Sadan M; Popov M; Singh M; Davidov G; Inagaki S; Al-Bassam J; Zarivach R; Rosenfeld SS; Gheber L
    Cell Mol Life Sci; 2021 Aug; 78(16):6051-6068. PubMed ID: 34274977
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Dynamic positioning of mitotic spindles in yeast: role of microtubule motors and cortical determinants.
    Yeh E; Yang C; Chin E; Maddox P; Salmon ED; Lew DJ; Bloom K
    Mol Biol Cell; 2000 Nov; 11(11):3949-61. PubMed ID: 11071919
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Essential kinesins: characterization of Caenorhabditis elegans KLP-15.
    Robin G; DeBonis S; Dornier A; Cappello G; Ebel C; Wade RH; Thierry-Mieg D; Kozielski F
    Biochemistry; 2005 May; 44(17):6526-36. PubMed ID: 15850386
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A lever-arm rotation drives motility of the minus-end-directed kinesin Ncd.
    Endres NF; Yoshioka C; Milligan RA; Vale RD
    Nature; 2006 Feb; 439(7078):875-8. PubMed ID: 16382238
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A potential physiological role for bi-directional motility and motor clustering of mitotic kinesin-5 Cin8 in yeast mitosis.
    Shapira O; Goldstein A; Al-Bassam J; Gheber L
    J Cell Sci; 2017 Feb; 130(4):725-734. PubMed ID: 28069834
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Role of the kinesin neck region in processive microtubule-based motility.
    Romberg L; Pierce DW; Vale RD
    J Cell Biol; 1998 Mar; 140(6):1407-16. PubMed ID: 9508773
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Minus-end-directed motor Ncd exhibits processive movement that is enhanced by microtubule bundling in vitro.
    Furuta K; Toyoshima YY
    Curr Biol; 2008 Jan; 18(2):152-7. PubMed ID: 18207739
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Neck-motor interactions trigger rotation of the kinesin stalk.
    Liu HL; Pemble CW; Endow SA
    Sci Rep; 2012; 2():236. PubMed ID: 22355749
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The microtubule plus-end localization of Aspergillus dynein is important for dynein-early-endosome interaction but not for dynein ATPase activation.
    Zhang J; Zhuang L; Lee Y; Abenza JF; Peñalva MA; Xiang X
    J Cell Sci; 2010 Oct; 123(Pt 20):3596-604. PubMed ID: 20876661
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Gamma-tubulin and the C-terminal motor domain kinesin-like protein, KLPA, function in the establishment of spindle bipolarity in Aspergillus nidulans.
    Prigozhina NL; Walker RA; Oakley CE; Oakley BR
    Mol Biol Cell; 2001 Oct; 12(10):3161-74. PubMed ID: 11598200
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Aspergillus nidulans kinesin-3 tail is necessary and sufficient to recognize modified microtubules.
    Seidel C; Zekert N; Fischer R
    PLoS One; 2012; 7(2):e30976. PubMed ID: 22363525
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Directional switching of the kinesin Cin8 through motor coupling.
    Roostalu J; Hentrich C; Bieling P; Telley IA; Schiebel E; Surrey T
    Science; 2011 Apr; 332(6025):94-9. PubMed ID: 21350123
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Directionality of dynein is controlled by the angle and length of its stalk.
    Can S; Lacey S; Gur M; Carter AP; Yildiz A
    Nature; 2019 Feb; 566(7744):407-410. PubMed ID: 30728497
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Kinesin's neck-linker determines its ability to navigate obstacles on the microtubule surface.
    Hoeprich GJ; Thompson AR; McVicker DP; Hancock WO; Berger CL
    Biophys J; 2014 Apr; 106(8):1691-700. PubMed ID: 24739168
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.