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Items: 1 to 20 of 38

1.
Recurring EPHB1 mutations in human cancers alter receptor signalling and compartmentalisation of colorectal cancer cells
Snehangshu Kundu, Luís Nunes, Jeremy Adler, Lucy Mathot, Ivaylo Stoimenov, Tobias Sjöblom
Cell Commun Signal. 2023; 21: 354. Published online 2023 Dec 15. doi: 10.1186/s12964-023-01378-9
PMCID:
PMC10722860
AbstractArticlePDF–2.9M
2.
EphB1 Suppression in Acute Myelogenous Leukemia: Regulating the DNA Damage Control System
K.R. Kampen, F.J.G. Scherpen, G. Garcia-Manero, H. Yang, G.J.L. Kaspers, J. Cloos, C.M. Zwaan, M.M. van den Heuvel-Eibrink, S.M. Kornblau, E.S.J.M. De Bont
Mol Cancer Res. Author manuscript; available in PMC 2016 Aug 15.
Published in final edited form as: Mol Cancer Res. 2015 Jun; 13(6): 982–992. Published online 2015 May 5. doi: 10.1158/1541-7786.MCR-14-0660-T
PMCID:
PMC4983719
AbstractArticlePDF–1.3M
3.
Decreased expression of receptor tyrosine kinase of EphB1 protein in renal cell carcinomas
Shuigen Zhou, Longxin Wang, Guimei Li, Zhengyu Zhang, Jiandong Wang
Int J Clin Exp Pathol. 2014; 7(7): 4254–4260. Published online 2014 Jun 15.
PMCID:
PMC4129041
AbstractArticlePDF–1.0M
4.
Loss of expression of EphB1 protein in serous carcinoma of ovary associated with metastasis and poor survival
Haiyan Wang, Juanjuan Wen, Hai Wang, Qinq Guo, Shanshan Shi, Qunli Shi, Xiaojun Zhou, Qi Liu, Guangming Lu, Jiandong Wang
Int J Clin Exp Pathol. 2014; 7(1): 313–321. Published online 2013 Dec 15.
PMCID:
PMC3885486
AbstractArticlePDF–699K
5.
Identification of tetracycline combinations as EphB1 tyrosine kinase inhibitors for treatment of neuropathic pain
Mahmoud S. Ahmed, Ping Wang, Ngoc Uyen Nhi Nguyen, Yuji Nakada, Ivan Menendez-Montes, Muhammad Ismail, Robert Bachoo, Mark Henkemeyer, Hesham A. Sadek, Enas S. Kandil
Proc Natl Acad Sci U S A. 2021 Mar 9; 118(10): e2016265118. Published online 2021 Feb 24. doi: 10.1073/pnas.2016265118
PMCID:
PMC7958374
AbstractArticlePDF–1.9M
6.
Knockdown of EphB1 receptor decreases medulloblastoma cell growth and migration and increases cellular radiosensitization
Shilpa Bhatia, Nimrah A. Baig, Olga Timofeeva, Elena B. Pasquale, Kellen Hirsch, Tobey J. MacDonald, Anatoly Dritschilo, Yi Chien Lee, Mark Henkemeyer, Brian Rood, Mira Jung, Xiao-Jing Wang, Marcel Kool, Olga Rodriguez, Chris Albanese, Sana D. Karam
Oncotarget. 2015 Apr 20; 6(11): 8929–8946. Published online 2015 Mar 30. doi: 10.18632/oncotarget.3369
PMCID:
PMC4496193
AbstractArticlePDF–4.7M
7.
A genome-wide association study points to multiple loci predicting antidepressant treatment outcome in depression
Marcus Ising, Susanne Lucae, Elisabeth B. Binder, Thomas Bettecken, Manfred Uhr, Stephan Ripke, Martin A. Kohli, Johannes M. Hennings, Sonja Horstmann, Stefan Kloiber, Andreas Menke, Brigitta Bondy, Rainer Rupprecht, Katharina Domschke, Bernhard T. Baune, Volker Arolt, A. John Rush, Florian Holsboer, Bertram Müller-Myhsok
Arch Gen Psychiatry. Author manuscript; available in PMC 2015 Jun 14.
Published in final edited form as: Arch Gen Psychiatry. 2009 Sep; 66(9): 966–975. doi: 10.1001/archgenpsychiatry.2009.95
PMCID:
PMC4465570
AbstractArticlePDF–2.3M
8.
Ligand-dependent EphB1 signaling suppresses glioma invasion and correlates with patient survival
Lei Teng, Mitsutoshi Nakada, Natsuki Furuyama, Hemragul Sabit, Takuya Furuta, Yutaka Hayashi, Takahisa Takino, Yu Dong, Hiroshi Sato, Yoshimichi Sai, Ken-ichi Miyamoto, Michael E. Berens, Shi-Guang Zhao, Jun-Ichiro Hamada
Neuro Oncol. 2013 Dec; 15(12): 1710–1720. Published online 2013 Oct 11. doi: 10.1093/neuonc/not128
PMCID:
PMC3829595
AbstractArticlePDF–866K
9.
Resequencing and Association Analysis of the KALRN and EPHB1 Genes And Their Contribution to Schizophrenia Susceptibility
Itaru Kushima, Yukako Nakamura, Branko Aleksic, Masashi Ikeda, Yoshihito Ito, Tomoko Shiino, Tomo Okochi, Yasuhisa Fukuo, Hiroshi Ujike, Michio Suzuki, Toshiya Inada, Ryota Hashimoto, Masatoshi Takeda, Kozo Kaibuchi, Nakao Iwata, Norio Ozaki
Schizophr Bull. 2012 May; 38(3): 552–560. Published online 2010 Nov 1. doi: 10.1093/schbul/sbq118
PMCID:
PMC3329972
AbstractArticlePDF–212K
10.
Specification of Distinct Dopaminergic Neural Pathways: Roles of the Eph Family Receptor EphB1 and Ligand Ephrin-B2
Yong Yue, David A. J. Widmer, Alycia K. Halladay, Douglas Pat Cerretti, George C. Wagner, Jean-Luc Dreyer, Renping Zhou
J Neurosci. 1999 Mar 15; 19(6): 2090–2101. doi: 10.1523/JNEUROSCI.19-06-02090.1999
PMCID:
PMC6782574
AbstractArticlePDF–1.3M
11.
Completing the structural family portrait of the human EphB tyrosine kinase domains
Ross C Overman, Judit E Debreczeni, Caroline M Truman, Mark S McAlister, Teresa K Attwood
Protein Sci. 2014 May; 23(5): 627–638. Published online 2014 Mar 11. doi: 10.1002/pro.2445
PMCID:
PMC4005714
AbstractArticlePDF–405K
12.
Exploring the Link between Germline and Somatic Genetic Alterations in Breast Carcinogenesis
Núria Bonifaci, Bohdan Górski, Bartlomiej Masojć, Dominika Wokołorczyk, Anna Jakubowska, Tadeusz Dębniak, Antoni Berenguer, Jordi Serra Musach, Joan Brunet, Joaquín Dopazo, Steven A. Narod, Jan Lubiński, Conxi Lázaro, Cezary Cybulski, Miguel Angel Pujana
PLoS One. 2010; 5(11): e14078. Published online 2010 Nov 22. doi: 10.1371/journal.pone.0014078
PMCID:
PMC2989917
AbstractArticlePDF–272K
13.
Peripheral EphrinB1/EphB1 signalling attenuates muscle hyperalgesia in MPS patients and a rat model of taut band-associated persistent muscle pain
Feihong Jin, Lianying Zhao, Qiya Hu, Feng Qi
Mol Pain. 2020; 16: 1744806920984079. Published online 2020 Dec 27. doi: 10.1177/1744806920984079
PMCID:
PMC7780166
AbstractArticlePDF–849K
14.
Eph receptors discriminate specific ligand oligomers to determine alternative signaling complexes, attachment, and assembly responses
Elke Stein, Andrew A. Lane, Douglas Pat Cerretti, Harald O. Schoecklmann, Alfred D. Schroff, Robert L. Van Etten, Thomas O. Daniel
Genes Dev. 1998 Mar 1; 12(5): 667–678. doi: 10.1101/gad.12.5.667
PMCID:
PMC316584
AbstractArticlePDF–3.0M
15.
Molecular characterization of a family of ligands for eph-related tyrosine kinase receptors.
M P Beckmann, D P Cerretti, P Baum, T Vanden Bos, L James, T Farrah, C Kozlosky, T Hollingsworth, H Shilling, E Maraskovsky, et al.
EMBO J. 1994 Aug 15; 13(16): 3757–3762. doi: 10.1002/j.1460-2075.1994.tb06685.x
PMCID:
PMC395287
SummaryPage BrowsePDF–1.6M
16.
Interactions between Eph kinases and ephrins provide a mechanism to support platelet aggregation once cell-to-cell contact has occurred
Nicolas Prevost, Donna Woulfe, Takako Tanaka, Lawrence F. Brass
Proc Natl Acad Sci U S A. 2002 Jul 9; 99(14): 9219–9224. Published online 2002 Jun 25. doi: 10.1073/pnas.142053899
PMCID:
PMC123121
AbstractArticlePDF–290K
17.
EphB Receptors Regulate Stem/Progenitor Cell Proliferation, Migration, and Polarity during Hippocampal Neurogenesis
Michael J. Chumley, Timothy Catchpole, Robert E. Silvany, Steven G. Kernie, Mark Henkemeyer
J Neurosci. 2007 Dec 5; 27(49): 13481–13490. doi: 10.1523/JNEUROSCI.4158-07.2007
PMCID:
PMC6673089
AbstractArticlePDF–598K
18.
Hsp90 is an essential regulator of EphA2 receptor stability and signaling: Implications for cancer cell migration and metastasis
Balasubramaniam Annamalai, Xueguang Liu, Udhayakumar Gopal, Jennifer Isaacs
Mol Cancer Res. Author manuscript; available in PMC 2011 Aug 12.
Published in final edited form as: Mol Cancer Res. 2009 Jul; 7(7): 1021–1032. Published online 2009 Jun 30. doi: 10.1158/1541-7786.MCR-08-0582
PMCID:
PMC3155284
AbstractArticlePDF–1.8M
19.
Regulation of Connexin32 by ephrin receptors and T-cell protein-tyrosine phosphatase
Andrew J. Trease, Hanjun Li, Gaelle Spagnol, Li Zheng, Kelly L. Stauch, Paul L. Sorgen
J Biol Chem. 2019 Jan 4; 294(1): 341–350. Published online 2018 Nov 6. doi: 10.1074/jbc.RA118.003883
PMCID:
PMC6322898
AbstractArticlePDF–1.6M
20.
Nck-Interacting Ste20 Kinase Couples Eph Receptors to c-Jun N-Terminal Kinase and Integrin Activation
Elena Becker, Uyen Huynh-Do, Sacha Holland, Tony Pawson, Tom O. Daniel, Edward Y. Skolnik
Mol Cell Biol. 2000 Mar; 20(5): 1537–1545. doi: 10.1128/mcb.20.5.1537-1545.2000
PMCID:
PMC85333
AbstractArticlePDF–1.2M

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