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Items: 1 to 20 of 27

1.
Loss of Dok-3 in Non-tumor Cells Induces Malignant Transformation of Benign Epithelial Tumor Cells of the Intestine
Sumimasa Arimura, Akane Inoue-Yamauchi, Kotoe Katayama, Tatsuo Kanno, Hiroki Jozawa, Seiya Imoto, Yuji Yamanashi
Cancer Res Commun. 2022 Dec; 2(12): 1590–1600. Published online 2022 Dec 8. doi: 10.1158/2767-9764.CRC-22-0347
PMCID:
PMC10035524
AbstractArticlePDF–12M
2.
DOK3 is involved in microglial cell activation in neuropathic pain by interacting with GPR84
Wen-Shuang Gao, Yu-Juan Qu, Juan Huai, Hui Wei, Yang Zhang, Shou-Wei Yue
Aging (Albany NY) 2021 Jan 15; 13(1): 389–410. Published online 2020 Dec 3. doi: 10.18632/aging.202144
PMCID:
PMC7835011
AbstractArticlePDF–2.5M
3.
DOK3 Modulates Bone Remodeling by Negatively Regulating Osteoclastogenesis and Positively Regulating Osteoblastogenesis
Xiaofeng Cai, Junjie Xing, Courtney L Long, Qisheng Peng, Mary Beth Humphrey
J Bone Miner Res. Author manuscript; available in PMC 2017 Nov 15.
Published in final edited form as: J Bone Miner Res. 2017 Nov; 32(11): 2207–2218. Published online 2017 Aug 2. doi: 10.1002/jbmr.3205
PMCID:
PMC5685877
AbstractArticlePDF–1.1M
4.
Dok3 restrains neutrophil production of calprotectin during TLR4 sensing of SARS-CoV-2 spike protein
Jia Tong Loh, Joey Kay Hui Teo, Kong-Peng Lam
Front Immunol. 2022; 13: 996637. Published online 2022 Sep 12. doi: 10.3389/fimmu.2022.996637
PMCID:
PMC9510782
AbstractArticlePDF–6.9M
5.
Dok-3 deficient mice display different immune clustering and Tim-3 expression
Wenjiang Yan, Yijia Tian, Peng Sun, Jingjing Yang, Na Li, Yuanyuan Sun, Shuangxi Wang, Cheng Zhang
Eur J Med Res. 2019; 24: 26. Published online 2019 Jul 27. doi: 10.1186/s40001-019-0384-7
PMCID:
PMC6660655
AbstractArticlePDF–2.8M
6.
Dok3–protein phosphatase 1 interaction attenuates Card9 signaling and neutrophil-dependent antifungal immunity
Jia Tong Loh, Shengli Xu, Jian Xin Huo, Susana Soo-Yeon Kim, Yue Wang, Kong-Peng Lam
J Clin Invest. 2019 Jul 1; 129(7): 2717–2729. Published online 2019 Jun 10. doi: 10.1172/JCI126341
PMCID:
PMC6597244
AbstractArticlePDF–10M
7.
DOK3 Negatively Regulates LPS Responses and Endotoxin Tolerance
Qisheng Peng, Jason L. O’Loughlin, Mary Beth Humphrey
PLoS One. 2012; 7(6): e39967. Published online 2012 Jun 27. doi: 10.1371/journal.pone.0039967
PMCID:
PMC3384629
AbstractArticlePDF–4.5M
8.
Interaction of Moloney murine leukemia virus matrix protein with IQGAP
Juliana Leung, Andrew Yueh, Frank S K Appah, Jr, Bing Yuan, Kenia de los Santos, Stephen P Goff
EMBO J. 2006 May 17; 25(10): 2155–2166. Published online 2006 Apr 20. doi: 10.1038/sj.emboj.7601097
PMCID:
PMC1462987
AbstractArticlePDF–231K
9.
DOK3 maintains intestinal homeostasis by suppressing JAK2/STAT3 signaling and S100a8/9 production in neutrophils
Jia Tong Loh, Koon-Guan Lee, Alison P. Lee, Joey Kay Hui Teo, Hsueh Lee Lim, Susana Soo-Yeon Kim, Andy Hee-Meng Tan, Kong-Peng Lam
Cell Death Dis. 2021 Nov; 12(11): 1054. Published online 2021 Nov 6. doi: 10.1038/s41419-021-04357-5
PMCID:
PMC8572282
AbstractArticlePDF–2.9M
10.
Vitamin B6 inhibits macrophage activation to prevent lipopolysaccharide‐induced acute pneumonia in mice
Mei‐Rong Shan, Sheng‐Nan Zhou, Chang‐Ning Fu, Jia‐Wen Song, Xue‐Qing Wang, Wen‐Wu Bai, Peng Li, Ping Song, Mo‐Li Zhu, Zhi‐Min Ma, Zhan Liu, Jian Xu, Bo Dong, Chao Liu, Tao Guo, Cheng Zhang, Shuang‐Xi Wang
J Cell Mol Med. 2020 Mar; 24(5): 3139–3148. Published online 2020 Jan 22. doi: 10.1111/jcmm.14983
PMCID:
PMC7077594
AbstractArticlePDF–1.1M
11.
A Physical Interaction Between the Adaptor Proteins DOK3 and DAP12 Is Required to Inhibit Lipopolysaccharide Signaling in Macrophages
Qisheng Peng, Courtney L. Long, Shikha Malhotra, Mary Beth Humphrey
Sci Signal. Author manuscript; available in PMC 2014 Feb 13.
Published in final edited form as: Sci Signal. 2013 Aug 20; 6(289): ra72. Published online 2013 Aug 20. doi: 10.1126/scisignal.2003801
PMCID:
PMC3923308
AbstractArticlePDF–3.7M
12.
Inhibition of the Jun N-Terminal Protein Kinase Pathway by SHIP-1, a Lipid Phosphatase That Interacts with the Adaptor Molecule Dok-3
Jeffrey D. Robson, Dominique Davidson, André Veillette
Mol Cell Biol. 2004 Mar; 24(6): 2332–2343. doi: 10.1128/MCB.24.6.2332-2343.2004
PMCID:
PMC355862
AbstractArticlePDF–691K
13.
A functional genomics predictive network model identifies regulators of inflammatory bowel disease
Lauren A Peters, Jacqueline Perrigoue, Arthur Mortha, Alina Iuga, Won-min Song, Eric M Neiman, Sean R Llewellyn, Antonio Di Narzo, Brian A Kidd, Shannon E Telesco, Yongzhong Zhao, Aleksandar Stojmirovic, Jocelyn Sendecki, Khader Shameer, Riccardo Miotto, Bojan Losic, Hardik Shah, Eunjee Lee, Minghui Wang, Jeremiah J Faith, Andrew Kasarskis, Carrie Brodmerkel, Mark Curran, Anuk Das, Joshua R Friedman, Yoshinori Fukui, Mary Beth Humphrey, Brian M Iritani, Nicholas Sibinga, Teresa K Tarrant, Carmen Argmann, Ke Hao, Panos Roussos, Jun Zhu, Bin Zhang, Radu Dobrin, Lloyd F Mayer, Eric E Schadt
Nat Genet. Author manuscript; available in PMC 2018 Oct 1.
Published in final edited form as: Nat Genet. 2017 Oct; 49(10): 1437–1449. Published online 2017 Sep 11. doi: 10.1038/ng.3947
PMCID:
PMC5660607
AbstractArticlePDF–1.6M
14.
Adaptor protein DOK3 promotes plasma cell differentiation by regulating the expression of programmed cell death 1 ligands
Xijun Ou, Shengli Xu, Yan-Feng Li, Kong-Peng Lam
Proc Natl Acad Sci U S A. 2014 Aug 5; 111(31): 11431–11436. Published online 2014 Jul 22. doi: 10.1073/pnas.1400539111
PMCID:
PMC4128136
AbstractArticlePDF–1.4M
15.
Subcellular localization of Grb2 by the adaptor protein Dok-3 restricts the intensity of Ca2+ signaling in B cells
Björn Stork, Konstantin Neumann, Ingo Goldbeck, Sebastian Alers, Thilo Kähne, Michael Naumann, Michael Engelke, Jürgen Wienands
EMBO J. 2007 Feb 21; 26(4): 1140–1149. Published online 2007 Feb 8. doi: 10.1038/sj.emboj.7601557
PMCID:
PMC1852829
AbstractArticlePDF–396K
16.
Dok-3, a Novel Adapter Molecule Involved in the Negative Regulation of Immunoreceptor Signaling
Serge Lemay, Dominique Davidson, Sylvain Latour, André Veillette
Mol Cell Biol. 2000 Apr; 20(8): 2743–2754. doi: 10.1128/mcb.20.8.2743-2754.2000
PMCID:
PMC85490
AbstractArticlePDF–1.0M
17.
Identification of DOK family genes as lung tumor suppressors
Alice H. Berger, Masaru Niki, Alessandro Morotti, Barry S. Taylor, Nicholas D. Socci, Agnes Viale, Cameron Brennan, Janos Szoke, Noriko Motoi, Paul B. Rothman, Julie Teruya-Feldstein, William L. Gerald, Marc Ladanyi, Pier Paolo Pandolfi
Nat Genet. Author manuscript; available in PMC 2010 Oct 18.
Published in final edited form as: Nat Genet. 2010 Mar; 42(3): 216–223. Published online 2010 Feb 7. doi: 10.1038/ng.527
PMCID:
PMC2956443
AbstractArticlePDF–3.5M
18.
Characterization of a Novel Member of the DOK Family That Binds and Modulates Abl Signaling
Feng Cong, Bing Yuan, Stephen P. Goff
Mol Cell Biol. 1999 Dec; 19(12): 8314–8325. doi: 10.1128/mcb.19.12.8314
PMCID:
PMC84915
AbstractArticlePDF–2.4M
19.
Novel p62dok family members, dok-4 and dok-5, are substrates of the c-Ret receptor tyrosine kinase and mediate neuronal differentiation
Jan Grimm, Martin Sachs, Stefan Britsch, Silvana Di Cesare, Thomas Schwarz-Romond, Kari Alitalo, Walter Birchmeier
J Cell Biol. 2001 Jul 23; 154(2): 345–354. doi: 10.1083/jcb.200102032
PMCID:
PMC2150770
AbstractArticlePDF–545K
20.
Database resources of the National Center for Biotechnology Information
David L. Wheeler, Deanna M. Church, Alex E. Lash, Detlef D. Leipe, Thomas L. Madden, Joan U. Pontius, Gregory D. Schuler, Lynn M. Schriml, Tatiana A. Tatusova, Lukas Wagner, Barbara A. Rapp
Nucleic Acids Res. 2001 Jan 1; 29(1): 11–16. doi: 10.1093/nar/29.1.11
PMCID:
PMC29800
AbstractArticlePDF–101K

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