298 related articles for article (PubMed ID: 26438524)
1. UNC-45A Is a Nonmuscle Myosin IIA Chaperone Required for NK Cell Cytotoxicity via Control of Lytic Granule Secretion.
Iizuka Y; Cichocki F; Sieben A; Sforza F; Karim R; Coughlin K; Isaksson Vogel R; Gavioli R; McCullar V; Lenvik T; Lee M; Miller J; Bazzaro M
J Immunol; 2015 Nov; 195(10):4760-70. PubMed ID: 26438524
[TBL] [Abstract][Full Text] [Related]
2. UNC-45A is required for neurite extension via controlling NMII activation.
Iizuka Y; Mooneyham A; Sieben A; Chen K; Maile M; Hellweg R; Schütz F; Teckle K; Starr T; Thayanithy V; Vogel RI; Lou E; Lee MK; Bazzaro M
Mol Biol Cell; 2017 May; 28(10):1337-1346. PubMed ID: 28356421
[TBL] [Abstract][Full Text] [Related]
3. Myosin IIA is required for cytolytic granule exocytosis in human NK cells.
Andzelm MM; Chen X; Krzewski K; Orange JS; Strominger JL
J Exp Med; 2007 Oct; 204(10):2285-91. PubMed ID: 17875677
[TBL] [Abstract][Full Text] [Related]
4. Myosin IIA associates with NK cell lytic granules to enable their interaction with F-actin and function at the immunological synapse.
Sanborn KB; Rak GD; Maru SY; Demers K; Difeo A; Martignetti JA; Betts MR; Favier R; Banerjee PP; Orange JS
J Immunol; 2009 Jun; 182(11):6969-84. PubMed ID: 19454694
[TBL] [Abstract][Full Text] [Related]
5. Navigating barriers: the challenge of directed secretion at the natural killer cell lytic immunological synapse.
Sanborn KB; Orange JS
J Clin Immunol; 2010 May; 30(3):358-63. PubMed ID: 20191315
[TBL] [Abstract][Full Text] [Related]
6. NK cell lytic granules are highly motile at the immunological synapse and require F-actin for post-degranulation persistence.
Mace EM; Wu WW; Ho T; Mann SS; Hsu HT; Orange JS
J Immunol; 2012 Nov; 189(10):4870-80. PubMed ID: 23066148
[TBL] [Abstract][Full Text] [Related]
7. Formation of a WIP-, WASp-, actin-, and myosin IIA-containing multiprotein complex in activated NK cells and its alteration by KIR inhibitory signaling.
Krzewski K; Chen X; Orange JS; Strominger JL
J Cell Biol; 2006 Apr; 173(1):121-32. PubMed ID: 16606694
[TBL] [Abstract][Full Text] [Related]
8. Phosphorylation of the myosin IIA tailpiece regulates single myosin IIA molecule association with lytic granules to promote NK-cell cytotoxicity.
Sanborn KB; Mace EM; Rak GD; Difeo A; Martignetti JA; Pecci A; Bussel JB; Favier R; Orange JS
Blood; 2011 Nov; 118(22):5862-71. PubMed ID: 22123909
[TBL] [Abstract][Full Text] [Related]
9. An actin cytoskeletal barrier inhibits lytic granule release from natural killer cells in patients with Chediak-Higashi syndrome.
Gil-Krzewska A; Saeed MB; Oszmiana A; Fischer ER; Lagrue K; Gahl WA; Introne WJ; Coligan JE; Davis DM; Krzewski K
J Allergy Clin Immunol; 2018 Sep; 142(3):914-927.e6. PubMed ID: 29241728
[TBL] [Abstract][Full Text] [Related]
10. Nanoscale Dynamism of Actin Enables Secretory Function in Cytolytic Cells.
Carisey AF; Mace EM; Saeed MB; Davis DM; Orange JS
Curr Biol; 2018 Feb; 28(4):489-502.e9. PubMed ID: 29398219
[TBL] [Abstract][Full Text] [Related]
11. UNC-45a promotes myosin folding and stress fiber assembly.
Lehtimäki JI; Fenix AM; Kotila TM; Balistreri G; Paavolainen L; Varjosalo M; Burnette DT; Lappalainen P
J Cell Biol; 2017 Dec; 216(12):4053-4072. PubMed ID: 29055011
[TBL] [Abstract][Full Text] [Related]
12. UNC-45A Is a Novel Microtubule-Associated Protein and Regulator of Paclitaxel Sensitivity in Ovarian Cancer Cells.
Mooneyham A; Iizuka Y; Yang Q; Coombes C; McClellan M; Shridhar V; Emmings E; Shetty M; Chen L; Ai T; Meints J; Lee MK; Gardner M; Bazzaro M
Mol Cancer Res; 2019 Feb; 17(2):370-383. PubMed ID: 30322860
[TBL] [Abstract][Full Text] [Related]
13. Measurement of Lytic Granule Convergence After Formation of an NK Cell Immunological Synapse.
Hsu HT; Carisey AF; Orange JS
Methods Mol Biol; 2017; 1584():497-515. PubMed ID: 28255722
[TBL] [Abstract][Full Text] [Related]
14. WIP is essential for lytic granule polarization and NK cell cytotoxicity.
Krzewski K; Chen X; Strominger JL
Proc Natl Acad Sci U S A; 2008 Feb; 105(7):2568-73. PubMed ID: 18258743
[TBL] [Abstract][Full Text] [Related]
15. Concerted actions of distinct nonmuscle myosin II isoforms drive intracellular membrane remodeling in live animals.
Milberg O; Shitara A; Ebrahim S; Masedunskas A; Tora M; Tran DT; Chen Y; Conti MA; Adelstein RS; Ten Hagen KG; Weigert R
J Cell Biol; 2017 Jul; 216(7):1925-1936. PubMed ID: 28600434
[TBL] [Abstract][Full Text] [Related]
16. PPP1R9B (Neurabin 2): involvement and dynamics in the NK immunological synapse.
Meng X; Kanwar N; Du Q; Goping IS; Bleackley RC; Wilkins JA
Eur J Immunol; 2009 Feb; 39(2):552-60. PubMed ID: 19130477
[TBL] [Abstract][Full Text] [Related]
17. Chediak-Higashi syndrome: Lysosomal trafficking regulator domains regulate exocytosis of lytic granules but not cytokine secretion by natural killer cells.
Gil-Krzewska A; Wood SM; Murakami Y; Nguyen V; Chiang SCC; Cullinane AR; Peruzzi G; Gahl WA; Coligan JE; Introne WJ; Bryceson YT; Krzewski K
J Allergy Clin Immunol; 2016 Apr; 137(4):1165-1177. PubMed ID: 26478006
[TBL] [Abstract][Full Text] [Related]
18. Dynamin 2 regulates granule exocytosis during NK cell-mediated cytotoxicity.
Arneson LN; Segovis CM; Gomez TS; Schoon RA; Dick CJ; Lou Z; Billadeau DD; Leibson PJ
J Immunol; 2008 Nov; 181(10):6995-7001. PubMed ID: 18981119
[TBL] [Abstract][Full Text] [Related]
19. The septin cytoskeleton regulates natural killer cell lytic granule release.
Phatarpekar PV; Overlee BL; Leehan A; Wilton KM; Ham H; Billadeau DD
J Cell Biol; 2020 Nov; 219(11):. PubMed ID: 32841357
[TBL] [Abstract][Full Text] [Related]
20. The Wiskott-Aldrich syndrome protein regulates nuclear translocation of NFAT2 and NF-kappa B (RelA) independently of its role in filamentous actin polymerization and actin cytoskeletal rearrangement.
Huang W; Ochs HD; Dupont B; Vyas YM
J Immunol; 2005 Mar; 174(5):2602-11. PubMed ID: 15728466
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
