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Items: 1 to 20 of 67

1.
Regulation of BDNF Release by ARMS/Kidins220 through Modulation of Synaptotagmin-IV Levels
Saray López-Benito, Julia Sánchez-Sánchez, Verónica Brito, Laura Calvo, Silvia Lisa, María Torres-Valle, Mary E. Palko, Cristina Vicente-García, Seila Fernández-Fernández, Juan P. Bolaños, Silvia Ginés, Lino Tessarollo, Juan C. Arévalo
J Neurosci. 2018 Jun 6; 38(23): 5415–5428. doi: 10.1523/JNEUROSCI.1653-17.2018
PMCID:
PMC5990986
AbstractArticlePDF–3.7M
2.
Stepping Out of the Shade: Control of Neuronal Activity by the Scaffold Protein Kidins220/ARMS
Joachim Scholz-Starke, Fabrizia Cesca
Front Cell Neurosci. 2016; 10: 68. Published online 2016 Mar 14. doi: 10.3389/fncel.2016.00068
PMCID:
PMC4789535
AbstractArticlePDF–1021K
3.
Development of a neuroprotective peptide that preserves survival pathways by preventing Kidins220/ARMS calpain processing induced by excitotoxicity
A Gamir-Morralla, C López-Menéndez, S Ayuso-Dolado, G S Tejeda, J Montaner, A Rosell, T Iglesias, M Díaz-Guerra
Cell Death Dis. 2015 Oct; 6(10): e1939. Published online 2015 Oct 22. doi: 10.1038/cddis.2015.307
PMCID:
PMC4632323
AbstractArticlePDF–2.7M
4.
Kidins220/ARMS is expressed in neuroblastoma tumors and stabilizes neurotrophic signaling in a human neuroblastoma cell line
Danny A. Rogers, Nina F. Schor
Pediatr Res. Author manuscript; available in PMC 2014 May 1.
Published in final edited form as: Pediatr Res. 2013 Nov; 74(5): 517–524. Published online 2013 Sep 2. doi: 10.1038/pr.2013.146
PMCID:
PMC3968798
AbstractArticlePDF–1.1M
5.
Upregulated ankyrin repeat-rich membrane spanning protein contributes to tumour progression in cutaneous melanoma
Y H Liao, S M Hsu, H L Yang, M S Tsai, P H Huang
Br J Cancer. 2011 Mar 15; 104(6): 982–988. Published online 2011 Feb 22. doi: 10.1038/bjc.2011.18
PMCID:
PMC3065267
AbstractArticlePDF–691K
6.
Ankyrin-rich Membrane Spanning Protein Plays a Critical Role in Nuclear Factor-κB Signaling
Lynn F. Sniderhan, Angela Stout, Yuanan Lu, Moses V. Chao, Sanjay B. Maggirwar
Mol Cell Neurosci. Author manuscript; available in PMC 2009 Jul 1.
Published in final edited form as: Mol Cell Neurosci. 2008 Jul; 38(3): 404–416. Published online 2008 Apr 16. doi: 10.1016/j.mcn.2008.04.001
PMCID:
PMC2577916
AbstractArticlePDF–789K
7.
Phosphate dysregulation via the XPR1:KIDINS220 protein complex is a therapeutic vulnerability in ovarian cancer
Daniel P Bondeson, Brenton R Paolella, Adhana Asfaw, Michael V Rothberg, Thomas A Skipper, Carly Langan, Gabriel Mesa, Alfredo Gonzalez, Lauren E Surface, Kentaro Ito, Mariya Kazachkova, William N Colgan, Allison Warren, Josh M Dempster, John M Krill-Burger, Maria Ericsson, Andrew A Tang, Iris Fung, Emily S Chambers, Mai Abdusamad, Nancy Dumont, John G Doench, Federica Piccioni, David E Root, Jesse Boehm, William C Hahn, Michael Mannstadt, James M McFarland, Francisca Vazquez, Todd R Golub
Nat Cancer. Author manuscript; available in PMC 2022 Oct 18.
Published in final edited form as: Nat Cancer. 2022 Jun; 3(6): 681–695. Published online 2022 Apr 18. doi: 10.1038/s43018-022-00360-7
PMCID:
PMC9246846
AbstractArticlePDF–4.9M
8.
Kidins220 and tumour development: Insights into a complexity of cross-talk among signalling pathways (Review)
Shuo Cai, Jun Cai, Wen G. Jiang, Lin Ye
Int J Mol Med. 2017 Oct; 40(4): 965–971. Published online 2017 Aug 9. doi: 10.3892/ijmm.2017.3093
PMCID:
PMC5593494
AbstractArticlePDF–540K
9.
MiR-4638-5p inhibits castration resistance of prostate cancer through repressing Kidins220 expression and PI3K/AKT pathway activity
Yang Wang, Ning Shao, Xueying Mao, Minmin Zhu, Weifei Fan, Zhixiang Shen, Rong Xiao, Chuncai Wang, Wenping Bao, Xinyu Xu, Chun Yang, Jian Dong, Deshui Yu, Yan Wu, Caixia Zhu, Liting Wen, Xiaojie Lu, Yong-Jie Lu, Ninghan Feng
Oncotarget. 2016 Jul 26; 7(30): 47444–47464. Published online 2016 Jun 18. doi: 10.18632/oncotarget.10165
PMCID:
PMC5216953
AbstractArticlePDF–17M
10.
Functional Interaction between the Scaffold Protein Kidins220/ARMS and Neuronal Voltage-Gated Na+ Channels
Fabrizia Cesca, Annyesha Satapathy, Enrico Ferrea, Thierry Nieus, Fabio Benfenati, Joachim Scholz-Starke
J Biol Chem. 2015 Jul 17; 290(29): 18045–18055. Published online 2015 Jun 2. doi: 10.1074/jbc.M115.654699
PMCID:
PMC4505050
AbstractArticlePDF–1.5M
11.
PKD1, PKD2 and their substrate Kidins220 regulate neurotensin secretion in the BON human endocrine cell line
Jing Li, L. Andy Chen, Courtney M. Townsend, Jr., B. Mark Evers
J Biol Chem. Author manuscript; available in PMC 2009 Feb 1.
Published in final edited form as: J Biol Chem. 2008 Feb 1; 283(5): 2614–2621. Published online 2007 Nov 29. doi: 10.1074/jbc.M707513200
PMCID:
PMC2427157
AbstractArticlePDF–1.5M
12.
Novel Kidins220/ARMS Splice Isoforms: Potential Specific Regulators of Neuronal and Cardiovascular Development
Nathalie Schmieg, Claire Thomas, Arisa Yabe, David S. Lynch, Teresa Iglesias, Probir Chakravarty, Giampietro Schiavo
PLoS One. 2015; 10(6): e0129944. Published online 2015 Jun 17. doi: 10.1371/journal.pone.0129944
PMCID:
PMC4470590
AbstractArticlePDF–4.4M
13.
Role of Sigma-1 Receptor C-terminal Segment in Inositol 1,4,5-Trisphosphate Receptor Activation: CONSTITUTIVE ENHANCEMENT OF CALCIUM SIGNALING IN MCF-7 TUMOR CELLS
Zhiping Wu, Wayne D. Bowen
J Biol Chem. 2008 Oct 17; 283(42): 28198–28215. doi: 10.1074/jbc.M802099200
PMCID:
PMC2661391
AbstractArticlePDF–951K
14.
Kidins220/ARMS Is Transported by a Kinesin-1–based Mechanism Likely to be Involved in Neuronal Differentiation
Aurora Bracale, Fabrizia Cesca, Veronika E. Neubrand, Timothy P. Newsome, Michael Way, Giampietro Schiavo
Mol Biol Cell. 2007 Jan; 18(1): 142–152. doi: 10.1091/mbc.E06-05-0453
PMCID:
PMC1751333
AbstractArticlePDF–1.1M
15.
An Evolutionarily Conserved Transmembrane Protein That Is a Novel Downstream Target of Neurotrophin and Ephrin Receptors
Haeyoung Kong, Jim Boulter, Janet L. Weber, Cary Lai, Moses V. Chao
J Neurosci. 2001 Jan 1; 21(1): 176–185. doi: 10.1523/JNEUROSCI.21-01-00176.2001
PMCID:
PMC6762419
AbstractArticlePDF–1.0M
16.
Kidins220/ARMS binds to the B cell antigen receptor and regulates B cell development and activation
Gina J. Fiala, Iga Janowska, Fabiola Prutek, Elias Hobeika, Annyesha Satapathy, Adrian Sprenger, Thomas Plum, Maximilian Seidl, Jörn Dengjel, Michael Reth, Fabrizia Cesca, Tilman Brummer, Susana Minguet, Wolfgang W.A. Schamel
J Exp Med. 2015 Sep 21; 212(10): 1693–1708. doi: 10.1084/jem.20141271
PMCID:
PMC4577850
AbstractArticlePDF–3.3M
17.
Investigating the role of ankyrin-rich membrane spanning protein in Human Immunodeficiency Virus Type-1 Tat-induced microglia activation
Vir B. Singh, Alicia K. Wooten, Joseph W. Jackson, Sanjay B. Maggirwar, Michelle Kiebala
J Neurovirol. Author manuscript; available in PMC 2016 Apr 1.
Published in final edited form as: J Neurovirol. 2015 Apr; 21(2): 186–198. Published online 2015 Jan 31. doi: 10.1007/s13365-015-0318-2
PMCID:
PMC4375029
AbstractArticlePDF–1.4M
18.
A unique pathway for sustained neurotrophin signaling through an ankyrin-rich membrane-spanning protein
Juan Carlos Arévalo, Hiroko Yano, Kenneth K Teng, Moses V Chao
EMBO J. 2004 Jun 16; 23(12): 2358–2368. Published online 2004 May 27. doi: 10.1038/sj.emboj.7600253
PMCID:
PMC423292
AbstractArticlePDF–600K
19.
Regulation of the endosomal SNX27-retromer by OTULIN
Aurelia Stangl, Paul R. Elliott, Adan Pinto-Fernandez, Sarah Bonham, Luke Harrison, Annalisa Schaub, Kerstin Kutzner, Kirstin Keusekotten, Paul T. Pfluger, Farid El Oualid, Benedikt M. Kessler, David Komander, Daniel Krappmann
Nat Commun. 2019; 10: 4320. Published online 2019 Sep 20. doi: 10.1038/s41467-019-12309-z
PMCID:
PMC6754446
AbstractArticlePDF–6.0M
20.
Duffy-Null–Associated Low Neutrophil Counts Influence HIV-1 Susceptibility in High-Risk South African Black Women
Veron Ramsuran, Hemant Kulkarni, Weijing He, Koleka Mlisana, Edwina J. Wright, Lise Werner, John Castiblanco, Rahul Dhanda, Tuan Le, Matthew J. Dolan, Weihua Guan, Robin A. Weiss, Robert A. Clark, Salim S. Abdool Karim, Sunil K. Ahuja, Thumbi Ndung'u
Clin Infect Dis. 2011 May 15; 52(10): 1248–1256. doi: 10.1093/cid/cir119
PMCID:
PMC3115278
AbstractArticlePDF–543K

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