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 *

248 related articles for article (PubMed ID: 16685646)

  • 1. A mutation of beta -actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia.
    Procaccio V; Salazar G; Ono S; Styers ML; Gearing M; Davila A; Jimenez R; Juncos J; Gutekunst CA; Meroni G; Fontanella B; Sontag E; Sontag JM; Faundez V; Wainer BH
    Am J Hum Genet; 2006 Jun; 78(6):947-60. PubMed ID: 16685646
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Actin-depolymerizing factor and cofilin-1 play overlapping roles in promoting rapid F-actin depolymerization in mammalian nonmuscle cells.
    Hotulainen P; Paunola E; Vartiainen MK; Lappalainen P
    Mol Biol Cell; 2005 Feb; 16(2):649-64. PubMed ID: 15548599
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Establishment of latrunculin-A resistance in HeLa cells by expression of R183A D184A mutant beta-actin.
    Fujita M; Ichinose S; Kiyono T; Tsurumi T; Omori A
    Oncogene; 2003 Jan; 22(4):627-31. PubMed ID: 12555075
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Use of latrunculin-A, an actin monomer-binding drug.
    Ayscough K
    Methods Enzymol; 1998; 298():18-25. PubMed ID: 9751867
    [No Abstract]   [Full Text] [Related]  

  • 5. Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).
    Zhu M; Yang T; Wei S; DeWan AT; Morell RJ; Elfenbein JL; Fisher RA; Leal SM; Smith RJ; Friderici KH
    Am J Hum Genet; 2003 Nov; 73(5):1082-91. PubMed ID: 13680526
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Thoracic aortic aneurysm (TAAD)-causing mutation in actin affects formin regulation of polymerization.
    Malloy LE; Wen KK; Pierick AR; Wedemeyer EW; Bergeron SE; Vanderpool ND; McKane M; Rubenstein PA; Bartlett HL
    J Biol Chem; 2012 Aug; 287(34):28398-408. PubMed ID: 22753406
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dephosphorylation-dependent inhibitory activity of juxtanodin on filamentous actin disassembly.
    Meng J; Xia W; Tang J; Tang BL; Liang F
    J Biol Chem; 2010 Sep; 285(37):28838-49. PubMed ID: 20610382
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Differential effects of Latrunculin-A on myofibrils in cultures of skeletal muscle cells: insights into mechanisms of myofibrillogenesis.
    Wang J; Sanger JM; Sanger JW
    Cell Motil Cytoskeleton; 2005 Sep; 62(1):35-47. PubMed ID: 16080205
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.
    Rendtorff ND; Zhu M; Fagerheim T; Antal TL; Jones M; Teslovich TM; Gillanders EM; Barmada M; Teig E; Trent JM; Friderici KH; Stephan DA; Tranebjaerg L
    Eur J Hum Genet; 2006 Oct; 14(10):1097-105. PubMed ID: 16773128
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Xin repeats define a novel actin-binding motif.
    Pacholsky D; Vakeel P; Himmel M; Löwe T; Stradal T; Rottner K; Fürst DO; van der Ven PF
    J Cell Sci; 2004 Oct; 117(Pt 22):5257-68. PubMed ID: 15454575
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Latrunculin alters the actin-monomer subunit interface to prevent polymerization.
    Morton WM; Ayscough KR; McLaughlin PJ
    Nat Cell Biol; 2000 Jun; 2(6):376-8. PubMed ID: 10854330
    [No Abstract]   [Full Text] [Related]  

  • 12. Dystonia-deafness syndrome caused by a β-actin gene mutation and response to deep brain stimulation.
    Eggink H; van Egmond ME; Verschuuren-Bemelmans CC; Schönherr MC; de Koning TJ; Oterdoom DL; van Dijk JM; Tijssen MA
    Mov Disord; 2017 Jan; 32(1):162-165. PubMed ID: 27862284
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Regulation of the mesangial cell myofibroblast phenotype by actin polymerization.
    Patel K; Harding P; Haney LB; Glass WF
    J Cell Physiol; 2003 Jun; 195(3):435-45. PubMed ID: 12704653
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Disruption of the actin cytoskeleton regulates cytokine-induced iNOS expression.
    Zeng C; Morrison AR
    Am J Physiol Cell Physiol; 2001 Sep; 281(3):C932-40. PubMed ID: 11502570
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Acto-myosin drug effects and aqueous outflow function.
    Epstein DL; Rowlette LL; Roberts BC
    Invest Ophthalmol Vis Sci; 1999 Jan; 40(1):74-81. PubMed ID: 9888429
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Latrunculin B has different effects on pollen germination and tube growth.
    Gibbon BC; Kovar DR; Staiger CJ
    Plant Cell; 1999 Dec; 11(12):2349-63. PubMed ID: 10590163
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome.
    Tranebjaerg L; Hamel BC; Gabreels FJ; Renier WO; Van Ghelue M
    Eur J Hum Genet; 2000 Jun; 8(6):464-7. PubMed ID: 10878669
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Early molecular events in the assembly of the focal adhesion-stress fiber complex during fibroblast spreading.
    Zimerman B; Volberg T; Geiger B
    Cell Motil Cytoskeleton; 2004 Jul; 58(3):143-59. PubMed ID: 15146534
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The yeast dynamin-related GTPase Vps1p functions in the organization of the actin cytoskeleton via interaction with Sla1p.
    Yu X; Cai M
    J Cell Sci; 2004 Aug; 117(Pt 17):3839-53. PubMed ID: 15265985
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autoregulation of actin synthesis requires the 3'-UTR of actin mRNA and protects cells from actin overproduction.
    Lyubimova A; Bershadsky AD; Ben-Ze'ev A
    J Cell Biochem; 1999 Nov; 76(1):1-12. PubMed ID: 10580995
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.