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 *

203 related articles for article (PubMed ID: 10893194)

  • 1. Actin disruption alters the localization of tau in the growth cones of cerebellar granule neurons.
    Zmuda JF; Rivas RJ
    J Cell Sci; 2000 Aug; 113 ( Pt 15)():2797-809. PubMed ID: 10893194
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Actin filament disruption blocks cerebellar granule neurons at the unipolar stage of differentiation in vitro.
    Zmuda JF; Rivas RJ
    J Neurobiol; 2000 Jun; 43(4):313-28. PubMed ID: 10861558
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Microtubule-Associated Protein Tau Mediates the Organization of Microtubules and Their Dynamic Exploration of Actin-Rich Lamellipodia and Filopodia of Cortical Growth Cones.
    Biswas S; Kalil K
    J Neurosci; 2018 Jan; 38(2):291-307. PubMed ID: 29167405
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Developmental regulation of sensory axon regeneration in the absence of growth cones.
    Jones SL; Selzer ME; Gallo G
    J Neurobiol; 2006 Dec; 66(14):1630-45. PubMed ID: 17058187
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Tau is enriched on dynamic microtubules in the distal region of growing axons.
    Black MM; Slaughter T; Moshiach S; Obrocka M; Fischer I
    J Neurosci; 1996 Jun; 16(11):3601-19. PubMed ID: 8642405
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The role of local actin instability in axon formation.
    Bradke F; Dotti CG
    Science; 1999 Mar; 283(5409):1931-4. PubMed ID: 10082468
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Microtubule and Rac 1-dependent F-actin in growth cones.
    Grabham PW; Reznik B; Goldberg DJ
    J Cell Sci; 2003 Sep; 116(Pt 18):3739-48. PubMed ID: 12890754
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Role of microtubules and actin filaments in the movement of mitochondria in the axons and dendrites of cultured hippocampal neurons.
    Ligon LA; Steward O
    J Comp Neurol; 2000 Nov; 427(3):351-61. PubMed ID: 11054698
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Differential requirement of F-actin and microtubule cytoskeleton in cue-induced local protein synthesis in axonal growth cones.
    Piper M; Lee AC; van Horck FP; McNeilly H; Lu TB; Harris WA; Holt CE
    Neural Dev; 2015 Feb; 10():3. PubMed ID: 25886013
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Collapsin response mediator protein 4 regulates growth cone dynamics through the actin and microtubule cytoskeleton.
    Khazaei MR; Girouard MP; Alchini R; Ong Tone S; Shimada T; Bechstedt S; Cowan M; Guillet D; Wiseman PW; Brouhard G; Cloutier JF; Fournier AE
    J Biol Chem; 2014 Oct; 289(43):30133-43. PubMed ID: 25225289
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Golgi apparatus and the centrosome are localized to the sites of newly emerging axons in cerebellar granule neurons in vitro.
    Zmuda JF; Rivas RJ
    Cell Motil Cytoskeleton; 1998; 41(1):18-38. PubMed ID: 9744296
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Microfilament-associated growth cone component depends upon Tau for its intracellular localization.
    DiTella M; Feiguin F; Morfini G; Cáceres A
    Cell Motil Cytoskeleton; 1994; 29(2):117-30. PubMed ID: 7820862
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The role of cytoskeleton in organizing growth cones: a microfilament-associated growth cone component depends upon microtubules for its localization.
    Goslin K; Birgbauer E; Banker G; Solomon F
    J Cell Biol; 1989 Oct; 109(4 Pt 1):1621-31. PubMed ID: 2677024
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Axon branching requires interactions between dynamic microtubules and actin filaments.
    Dent EW; Kalil K
    J Neurosci; 2001 Dec; 21(24):9757-69. PubMed ID: 11739584
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Doublecortin associates with microtubules preferentially in regions of the axon displaying actin-rich protrusive structures.
    Tint I; Jean D; Baas PW; Black MM
    J Neurosci; 2009 Sep; 29(35):10995-1010. PubMed ID: 19726658
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Growth cones are not required for initial establishment of polarity or differential axon branch growth in cultured hippocampal neurons.
    Ruthel G; Hollenbeck PJ
    J Neurosci; 2000 Mar; 20(6):2266-74. PubMed ID: 10704502
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Control of growth cone motility and neurite outgrowth by SPIN90.
    Kim SM; Bae J; Cho IH; Choi KY; Park YJ; Ryu JH; Chun JS; Song WK
    Exp Cell Res; 2011 Oct; 317(16):2276-87. PubMed ID: 21763308
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evidence that actin and myosin are involved in the poleward flux of tubulin in metaphase kinetochore microtubules of crane-fly spermatocytes.
    Silverman-Gavrila RV; Forer A
    J Cell Sci; 2000 Feb; 113 ( Pt 4)():597-609. PubMed ID: 10652253
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Microtubules, actin and cytolinkers: how to connect cytoskeletons in the neuronal growth cone.
    Pinto-Costa R; Sousa MM
    Neurosci Lett; 2021 Mar; 747():135693. PubMed ID: 33529653
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Growth cone collapse through coincident loss of actin bundles and leading edge actin without actin depolymerization.
    Zhou FQ; Cohan CS
    J Cell Biol; 2001 May; 153(5):1071-84. PubMed ID: 11381091
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.