Papers associated with cell part (and mapt)

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	Mitochondrial cellular organization and shape fluctuations are differentially modulated by cytoskeletal networks., Fernández Casafuz AB., Sci Rep. March 11, 2023; 13 (1): 4065.
	Proteomic screen reveals diverse protein transport between connected neurons in the visual system., Schiapparelli LM., Cell Rep. January 25, 2022; 38 (4): 110287.
	Tau, XMAP215/Msps and Eb1 co-operate interdependently to regulate microtubule polymerisation and bundle formation in axons., Hahn I., PLoS Genet. July 1, 2021; 17 (7): e1009647.
	Co-movement of astral microtubules, organelles and F-actin by dynein and actomyosin forces in frog egg cytoplasm., Pelletier JF., Elife. December 7, 2020; 9
	Retraction of rod-like mitochondria during microtubule-dependent transport., De Rossi MC., Biosci Rep. June 29, 2018; 38 (3):
	Tau-based fluorescent protein fusions to visualize microtubules., Mooney P., Cytoskeleton (Hoboken). June 1, 2017; 74 (6): 221-232.
	Malaria parasite CelTOS targets the inner leaflet of cell membranes for pore-dependent disruption., Jimah JR., Elife. December 1, 2016; 5
	Stochasticity in the miR-9/Hes1 oscillatory network can account for clonal heterogeneity in the timing of differentiation., Phillips NE., Elife. January 28, 2016; 5
	Tau Tubulin Kinase TTBK2 Sensitivity of Glutamate Receptor GluK2., Nieding K., Cell Physiol Biochem. January 1, 2016; 39 (4): 1444-52.
	The active Hsc70/tau complex can be exploited to enhance tau turnover without damaging microtubule dynamics., Fontaine SN., Hum Mol Genet. July 15, 2015; 24 (14): 3971-81.
	Microtubule-associated protein tau promotes neuronal class II β-tubulin microtubule formation and axon elongation in embryonic Xenopus laevis., Liu Y., Eur J Neurosci. May 1, 2015; 41 (10): 1263-75.
	Lateral motion and bending of microtubules studied with a new single-filament tracking routine in living cells., Pallavicini C., Biophys J. June 17, 2014; 106 (12): 2625-35.
	Domain-domain interactions determine the gating, permeation, pharmacology, and subunit modulation of the IKs ion channel., Zaydman MA., Elife. March 12, 2014; 3 e03606.
	c-Jun N-terminal kinase phosphorylation of heterogeneous nuclear ribonucleoprotein K regulates vertebrate axon outgrowth via a posttranscriptional mechanism., Hutchins EJ., J Neurosci. September 11, 2013; 33 (37): 14666-80.
	Imbalance of Hsp70 family variants fosters tau accumulation., Jinwal UK., FASEB J. April 1, 2013; 27 (4): 1450-9.
	Upregulation of Na+,Cl(-)-coupled betaine/γ-amino-butyric acid transporter BGT1 by Tau tubulin kinase 2., Almilaji A., Cell Physiol Biochem. January 1, 2013; 32 (2): 334-43.
	HIRA dependent H3.3 deposition is required for transcriptional reprogramming following nuclear transfer to Xenopus oocytes., Jullien J., Epigenetics Chromatin. October 29, 2012; 5 (1): 17.
	Heterogeneous nuclear ribonucleoprotein K, an RNA-binding protein, is required for optic axon regeneration in Xenopus laevis., Liu Y., J Neurosci. March 7, 2012; 32 (10): 3563-74.
	State-independent intracellular access of quaternary ammonium blockers to the pore of TREK-1., Rapedius M., Channels (Austin). January 1, 2012; 6 (6): 473-8.
	hnRNP K post-transcriptionally co-regulates multiple cytoskeletal genes needed for axonogenesis., Liu Y., Development. July 1, 2011; 138 (14): 3079-90.
	Alzheimer Aβ disrupts the mitotic spindle and directly inhibits mitotic microtubule motors., Borysov SI., Cell Cycle. May 1, 2011; 10 (9): 1397-410.
	TRESK background K(+) channel is inhibited by PAR-1/MARK microtubule affinity-regulating kinases in Xenopus oocytes., Braun G., PLoS One. January 1, 2011; 6 (12): e28119.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	Hsc70 rapidly engages tau after microtubule destabilization., Jinwal UK., J Biol Chem. May 28, 2010; 285 (22): 16798-805.
	The Hsp90 cochaperone, FKBP51, increases Tau stability and polymerizes microtubules., Jinwal UK., J Neurosci. January 13, 2010; 30 (2): 591-9.
	Activators of G proteins inhibit GSK-3beta and stabilize beta-Catenin in Xenopus oocytes., Najafi SM., Biochem Biophys Res Commun. May 1, 2009; 382 (2): 365-9.
	How DASPMI reveals mitochondrial membrane potential: fluorescence decay kinetics and steady-state anisotropy in living cells., Ramadass R., Biophys J. October 1, 2008; 95 (8): 4068-76.
	Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells., Park TJ., Nat Genet. July 1, 2008; 40 (7): 871-9.
	LRP6 transduces a canonical Wnt signal independently of Axin degradation by inhibiting GSK3's phosphorylation of beta-catenin., Cselenyi CS., Proc Natl Acad Sci U S A. June 10, 2008; 105 (23): 8032-7.
	NMR observation of Tau in Xenopus oocytes., Bodart JF., J Magn Reson. June 1, 2008; 192 (2): 252-7.
	Developmental regulation of central spindle assembly and cytokinesis during vertebrate embryogenesis., Kieserman EK., Curr Biol. January 22, 2008; 18 (2): 116-23.
	Expression and functional characterization of the human ether-à-go-go-related gene (HERG) K+ channel cardiac splice variant in Xenopus laevis oocytes., Aydar E., J Membr Biol. January 1, 2006; 211 (2): 115-26.
	The circadian clock-containing photoreceptor cells in Xenopus laevis express several isoforms of casein kinase I., Constance CM., Brain Res Mol Brain Res. May 20, 2005; 136 (1-2): 199-211.
	A comparison of the ability of XMAP215 and tau to inhibit the microtubule destabilizing activity of XKCM1., Noetzel TL., Philos Trans R Soc Lond B Biol Sci. March 29, 2005; 360 (1455): 591-4.
	Perturbation analysis of the voltage-sensitive conformational changes of the Na+/glucose cotransporter., Loo DD., J Gen Physiol. January 1, 2005; 125 (1): 13-36.
	Tau interaction with microtubules in vivo., Samsonov A., J Cell Sci. December 1, 2004; 117 (Pt 25): 6129-41.
	Abnormal Tau phosphorylation of the Alzheimer-type also occurs during mitosis., Delobel P., J Neurochem. October 1, 2002; 83 (2): 412-20.
	Functional characterization of FTDP-17 tau gene mutations through their effects on Xenopus oocyte maturation., Delobel P., J Biol Chem. March 15, 2002; 277 (11): 9199-205.
	Drosophila Aurora A kinase is required to localize D-TACC to centrosomes and to regulate astral microtubules., Giet R., J Cell Biol. February 4, 2002; 156 (3): 437-51.
	Molecular cloning of XTP, a tau-like microtubule-associated protein from Xenopus laevis tadpoles., Olesen OF., Gene. January 23, 2002; 283 (1-2): 299-309.
	RNA anchoring in the vegetal cortex of the Xenopus oocyte., Alarcón VB., J Cell Sci. May 1, 2001; 114 (Pt 9): 1731-41.
	The prolyl isomerase Pin1 restores the function of Alzheimer-associated phosphorylated tau protein., Lu PJ., Nature. June 24, 1999; 399 (6738): 784-8.
	Nuclear glycogen and glycogen synthase kinase 3., Ragano-Caracciolo M., Biochem Biophys Res Commun. August 19, 1998; 249 (2): 422-7.
	Identification of regions that regulate the expression and activity of G protein-gated inward rectifier K+ channels in Xenopus oocytes., Stevens EB., J Physiol. September 15, 1997; 503 ( Pt 3) 547-62.
	Single-channel kinetics, inactivation, and spatial distribution of inositol trisphosphate (IP3) receptors in Xenopus oocyte nucleus., Mak DO., J Gen Physiol. May 1, 1997; 109 (5): 571-87.
	Lithium inhibits glycogen synthase kinase-3 activity and mimics wingless signalling in intact cells., Stambolic V., Curr Biol. December 1, 1996; 6 (12): 1664-8.
	Exogenous tau RNA is localized in oocytes: possible evidence for evolutionary conservation of localization mechanisms., Litman P., Dev Biol. May 25, 1996; 176 (1): 86-94.
	Estimation of water content and water mobility in the nucleus and cytoplasm of Xenopus laevis oocytes by NMR microscopy., Päuser S., Magn Reson Imaging. January 1, 1995; 13 (2): 269-76.
	The expression of phosphorylated and non-phosphorylated forms of MAP5 in the amphibian CNS., Viereck C., Dev Biol. February 5, 1990; 508 (2): 257-64.
	Microtubule-associated proteins and the determination of neuronal form., Matus A., J Physiol (Paris). January 1, 1990; 84 (1): 134-7.

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