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Items: 1 to 20 of 48

1.
An iTRAQ-based proteomic analysis reveals dysregulation of neocortical synaptopodin in Lewy body dementias
Arnab Datta, Yuek Ling Chai, Jing Min Tan, Jasinda H. Lee, Paul T. Francis, Christopher P. Chen, Siu Kwan Sze, Mitchell K. P. Lai
Mol Brain. 2017; 10: 36. Published online 2017 Aug 11. doi: 10.1186/s13041-017-0316-9
PMCID:
PMC5553757
AbstractArticlePDF–829K
2.
Urine synaptopodin excretion is an important marker of glomerular disease progression
Soon Kil Kwon, Seung Jung Kim, Hye-Young Kim
Korean J Intern Med. 2016 Sep; 31(5): 938–943. Published online 2016 Sep 1. doi: 10.3904/kjim.2015.226
PMCID:
PMC5016285
AbstractArticlePDF–344K
3.
Microbiota-derived butyrate dynamically regulates intestinal homeostasis through regulation of actin-associated protein synaptopodin
Ruth X. Wang, J. Scott Lee, Eric L. Campbell, Sean P. Colgan
Proc Natl Acad Sci U S A. 2020 May 26; 117(21): 11648–11657. Published online 2020 May 12. doi: 10.1073/pnas.1917597117
PMCID:
PMC7260972
AbstractArticlePDF–1.8M
4.
Intrinsic disorder and amino acid specificity modulate binding of the WW2 domain in kidney and brain protein (KIBRA) to synaptopodin
Ethiene Kwok, Diego J. Rodriguez, Joachim Kremerskothen, Afua Nyarko
J Biol Chem. 2019 Nov 15; 294(46): 17383–17394. Published online 2019 Oct 9. doi: 10.1074/jbc.RA119.009589
PMCID:
PMC6873182
AbstractArticlePDF–1.8M
5.
Exome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk
Mark Z. Kos, Melanie A. Carless, Juan Peralta, August Blackburn, Marcio Almeida, David Roalf, Michael F. Pogue-Geile, Konasale Prasad, Ruben C. Gur, Vishwajit Nimgaonkar, Joanne E. Curran, Ravi Duggirala, David C. Glahn, John Blangero, Raquel E. Gur, Laura Almasy
Schizophr Bull. 2016 Mar; 42(2): 288–300. Published online 2015 Sep 24. doi: 10.1093/schbul/sbv135
PMCID:
PMC4753604
AbstractArticlePDF–1.0M
6.
Synaptopodin Regulates Spine Plasticity: Mediation by Calcium Stores
Eduard Korkotian, Michael Frotscher, Menahem Segal
J Neurosci. 2014 Aug 27; 34(35): 11641–11651. doi: 10.1523/JNEUROSCI.0381-14.2014
PMCID:
PMC6608418
AbstractArticlePDF–5.3M
7.
A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS
Gentzon Hall, Rasheed A. Gbadegesin, Peter Lavin, Guanghong Wu, Yangfan Liu, Edwin C. Oh, Liming Wang, Robert F. Spurney, Jason Eckel, Thomas Lindsey, Alison Homstad, Andrew F. Malone, Paul J. Phelan, Andrey Shaw, David N. Howell, Peter J. Conlon, Nicholas Katsanis, Michelle P. Winn
J Am Soc Nephrol. 2015 Apr; 26(4): 831–843. Published online 2014 Aug 21. doi: 10.1681/ASN.2013101053
PMCID:
PMC4378093
AbstractArticle
8.
Synaptopodin: An Actin-associated Protein in Telencephalic Dendrites and Renal Podocytes
Peter Mundel, Hans W. Heid, Thomas M. Mundel, Meike Krüger, Jochen Reiser, Wilhelm Kriz
J Cell Biol. 1997 Oct 6; 139(1): 193–204. doi: 10.1083/jcb.139.1.193
PMCID:
PMC2139823
AbstractArticlePDF–1.2M
9.
BAG3 and SYNPO (synaptopodin) facilitate phospho-MAPT/Tau degradation via autophagy in neuronal processes
Changyi Ji, Maoping Tang, Claudia Zeidler, Jörg Höhfeld, Gail VW Johnson
Autophagy. 2019; 15(7): 1199–1213. Published online 2019 Mar 1. doi: 10.1080/15548627.2019.1580096
PMCID:
PMC6613891
AbstractArticlePDF–7.5M
10.
Urinary Podocyte-Associated mRNA profile in Various Stages of Diabetic Nephropathy
Min Zheng, Lin-Li Lv, Jie Ni, Hai-Feng Ni, Qing Li, Kun-Ling Ma, Bi-Cheng Liu
PLoS One. 2011; 6(5): e20431. Published online 2011 May 31. doi: 10.1371/journal.pone.0020431
PMCID:
PMC3105067
AbstractArticlePDF–285K
11.
KIBRA Modulates Directional Migration of Podocytes
Kerstin Duning, Eva-Maria Schurek, Marc Schlüter, Michael Bayer, Hans-Christian Reinhardt, Albrecht Schwab, Liliana Schaefer, Thomas Benzing, Bernhard Schermer, Moin A. Saleem, Tobias B. Huber, Sebastian Bachmann, Joachim Kremerskothen, Thomas Weide, Hermann Pavenstädt
J Am Soc Nephrol. 2008 Oct; 19(10): 1891–1903. doi: 10.1681/ASN.2007080916
PMCID:
PMC2551571
AbstractArticle
12.
Nef stimulates proliferation of glomerular podocytes through activation of Src-dependent Stat3 and MAPK1,2 pathways
John Cijiang He, Mohammad Husain, Masaaki Sunamoto, Vivette D. D’Agati, Mary E. Klotman, Ravi Iyengar, Paul E. Klotman
J Clin Invest. 2004 Sep 1; 114(5): 643–651. doi: 10.1172/JCI21004
PMCID:
PMC514582
AbstractArticlePDF–918K
13.
TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways
Guillaume Dorval, Valeryia Kuzmuk, Olivier Gribouval, Gavin I. Welsh, Agnieszka Bierzynska, Alain Schmitt, Stéphanie Miserey-Lenkei, Ania Koziell, Shuman Haq, Alexandre Benmerah, Géraldine Mollet, Olivia Boyer, Moin A. Saleem, Corinne Antignac
Am J Hum Genet. 2019 Feb 7; 104(2): 348–355. Published online 2019 Jan 17. doi: 10.1016/j.ajhg.2018.12.016
PMCID:
PMC6369567
AbstractArticlePDF–2.0M
14.
Proteasomal degradation of Nck1 but not Nck2 regulates RhoA activation and actin dynamics
Lisa Buvall, Priyanka Rashmi, Esther Lopez-Rivera, Svetlana Andreeva, Astrid Weins, Hanna Wallentin, Anna Greka, Peter Mundel
Nat Commun. Author manuscript; available in PMC 2016 Jan 2.
Published in final edited form as: Nat Commun. 2013; 4: 2863. doi: 10.1038/ncomms3863
PMCID:
PMC4698162
AbstractArticlePDF–1008K
15.
Regulation of podocyte BKCa channels by synaptopodin, Rho, and actin microfilaments
Eun Young Kim, Jae Mi Suh, Yu-Hsin Chiu, Stuart E. Dryer
Am J Physiol Renal Physiol. 2010 Sep; 299(3): F594–F604. Published online 2010 Jul 14. doi: 10.1152/ajprenal.00206.2010
PMCID:
PMC2944294
AbstractArticle
16.
Synaptopodin regulates the actin-bundling activity of α-actinin in an isoform-specific manner
Katsuhiko Asanuma, Kwanghee Kim, Jun Oh, Laura Giardino, Sophie Chabanis, Christian Faul, Jochen Reiser, Peter Mundel
J Clin Invest. 2005 May 2; 115(5): 1188–1198. Published online 2005 Apr 1. doi: 10.1172/JCI23371
Correction in:
J Clin Invest. 2012 Feb 1; 122(2): 781.
PMCID:
PMC1070637
AbstractArticlePDF–1.4M
17.
HIV-1 Subtypes B and C Tat Differentially Impact Synaptic Plasticity Expression and Implicates HIV-Associated Neurocognitive Disorders
Thangavel Samikkannu, Venkata S.R. Atluri, Adriana Y. Arias, Kesava V.K. Rao, Carmen T. Mulet, Rahul D. Jayant, Madhavan P.N. Nair
Curr HIV Res. Author manuscript; available in PMC 2015 Aug 31.
Published in final edited form as: Curr HIV Res. 2014; 12(6): 397–405. doi: 10.2174/1570162x13666150121104720
PMCID:
PMC4554345
AbstractArticlePDF–1.5M
18.
Proteins recruited by SH3 domains of Ruk/CIN85 adaptor identified by LC-MS/MS
Serhiy Havrylov, Yuriy Rzhepetskyy, Agata Malinowska, Lyudmyla Drobot, Maria Jolanta Redowicz
Proteome Sci. 2009; 7: 21. Published online 2009 Jun 16. doi: 10.1186/1477-5956-7-21
PMCID:
PMC2702278
AbstractArticlePDF–2.5M
19.
Alterations in the brain interactome of the intrinsically disordered N-terminal domain of the cellular prion protein (PrPC) in Alzheimer’s disease
Sarah Ulbrich, Petra Janning, Ralf Seidel, Jakob Matschke, Anika Gonsberg, Sebastian Jung, Markus Glatzel, Martin Engelhard, Konstanze F. Winklhofer, Jörg Tatzelt
PLoS One. 2018; 13(5): e0197659. Published online 2018 May 23. doi: 10.1371/journal.pone.0197659
PMCID:
PMC5965872
AbstractArticlePDF–2.4M
20.
A trimeric Rab7 GEF controls NPC1-dependent lysosomal cholesterol export
Dick J. H. van den Boomen, Agata Sienkiewicz, Ilana Berlin, Marlieke L. M. Jongsma, Daphne M. van Elsland, J. Paul Luzio, Jacques J. C. Neefjes, Paul J. Lehner
Nat Commun. 2020; 11: 5559. Published online 2020 Nov 3. doi: 10.1038/s41467-020-19032-0
PMCID:
PMC7642327
AbstractArticlePDF–12M

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