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Items: 1 to 20 of 95

1.
The Contribution of PDCD6 Polymorphisms to Oral Cancer Risk
LIANG-CHUN SHIH, JIE-LONG HE, WEN-SHIN CHANG, CHE-LUN HSU, TE-CHUN HSIA, YUN-CHI WANG, JIA-SING YANG, MEI-CHIN MONG, CHIA-WEN TSAI, DA-TIAN BAU
Cancer Genomics Proteomics. 2022 Jul-Aug; 19(4): 456–463. Published online 2022 Jul 3. doi: 10.21873/cgp.20332
PMCID:
PMC9247878
ArticlePDF–151K
2.
PDCD6 cooperates with C-Raf to facilitate colorectal cancer progression via Raf/MEK/ERK activation
Xiaojuan Wang, Fan Wu, Han Wang, Xiaoyuan Duan, Rong Huang, Amannisa Tuersuntuoheti, Luying Su, Shida Yan, Yuechao Zhao, Yan Lu, Kai Li, Jinjie Yao, Zhiwen Luo, Lei Guo, Jianmei Liu, Xiao Chen, Yalan Lu, Hanjie Hu, Xingchen Li, Mandula Bao, Xinyu Bi, Boyu Du, Shiying Miao, Jianqiang Cai, Linfang Wang, Haitao Zhou, Jianming Ying, Wei Song, Hong Zhao
J Exp Clin Cancer Res. 2020; 39: 147. Published online 2020 Aug 3. doi: 10.1186/s13046-020-01632-9
PMCID:
PMC7398064
ArticlePDF–8.4M
3.
The apoptosis linked gene ALG‐2 is dysregulated in tumors of various origin and contributes to cancer cell viability
Jonas M. la Cour, Berit R. Høj, Jens Mollerup, Ronald Simon, Guido Sauter, Martin W. Berchtold
Mol Oncol. 2008 Apr; 1(4): 431–439. Published online 2007 Aug 19. doi: 10.1016/j.molonc.2007.08.002
PMCID:
PMC5543837
ArticlePDF–1.6M
4.
Apoptosis-linked gene 2 promotes breast cancer growth and metastasis by regulating the cytoskeleton
Juan Qin, Dengwen Li, Yunqiang Zhou, Songbo Xie, Xin Du, Ziwei Hao, Ruming Liu, Xinqi Liu, Min Liu, Jun Zhou
Oncotarget. 2017 Jan 10; 8(2): 2745–2757. Published online 2016 Dec 1. doi: 10.18632/oncotarget.13740
PMCID:
PMC5356838
ArticlePDF–19M
5.
Variations in the PDCD6 Gene Are Associated with Increased Uterine Leiomyoma Risk in the Chinese
Kui Zhang, Bin Zhou, Shaoqing Shi, Yaping Song, Lin Zhang
Genet Test Mol Biomarkers. 2013 Jul; 17(7): 524–528. doi: 10.1089/gtmb.2012.0461
PMCID:
PMC3700461
ArticlePDF–123K
6.
PDCD6 is an independent predictor of progression free survival in epithelial ovarian cancer
Dan Su, Haiyan Xu, Jianguo Feng, Yun Gao, Linhui Gu, Lisha Ying, Dionyssios Katsaros, Herbert Yu, Shenhua Xu, Ming Qi
J Transl Med. 2012; 10: 31. Published online 2012 Feb 27. doi: 10.1186/1479-5876-10-31
PMCID:
PMC3305474
ArticlePDF–638K
7.
Crystallization and X-ray diffraction analysis of N-­terminally truncated human ALG-2
Hironori Suzuki, Masato Kawasaki, Takeshi Kakiuchi, Hideki Shibata, Soichi Wakatsuki, Masatoshi Maki
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2008 Nov 1; 64(Pt 11): 974–977. Published online 2008 Oct 31. doi: 10.1107/S1744309108030297
PMCID:
PMC2581688
ArticlePDF–733K
8.
Up-Regulation of ALG-2 in Hepatomas and Lung Cancer Tissue
Jonas M. la Cour, Jens Mollerup, Pernille Winding, Svetlana Tarabykina, Maxwell Sehested, Martin W. Berchtold
Am J Pathol. 2003 Jul; 163(1): 81–89. doi: 10.1016/S0002-9440(10)63632-2
PMCID:
PMC1868153
ArticlePDF–857K
9.
Ca2+ Binding to EF Hands 1 and 3 Is Essential for the Interaction of Apoptosis-Linked Gene-2 with Alix/AIP1 in Ocular Melanoma
Lalita Subramanian, Arthur S. Polans, Teresa M. Walker, Paul R. van Ginkel, Saswati Bhattacharya, Julia M. Dellaria, John W. Crabb, Jos Cox, Isabelle Durussel, Krzysztof Palczewski
Biochemistry. Author manuscript; available in PMC 2006 Jan 26.
Published in final edited form as: Biochemistry. 2004 Sep 7; 43(35): 11175–11186. doi: 10.1021/bi048848d
PMCID:
PMC1351334
ArticlePDF–853K
10.
Programmed cell death 6, a novel p53‐responsive gene, targets to the nucleus in the apoptotic response to DNA damage
Kazuho Suzuki, Nurmaa Dashzeveg, Zheng‐Guang Lu, Naoe Taira, Yoshio Miki, Kiyotsugu Yoshida
Cancer Sci. 2012 Oct; 103(10): 1788–1794. Published online 2012 Aug 7. doi: 10.1111/j.1349-7006.2012.02362.x
PMCID:
PMC7659207
ArticlePDF–718K
11.
ALG-2 couples T cell activation and apoptosis by regulating proteasome activity and influencing MCL1 stability
Tian-Sheng He, Wangsheng Ji, Junqi Zhang, Jing Lu, Xinqi Liu
Cell Death Dis. 2020 Jan; 11(1): 5. Published online 2020 Jan 2. doi: 10.1038/s41419-019-2199-4
PMCID:
PMC6952393
ArticlePDF–4.9M
12.
ALG2 regulates glioblastoma cell proliferation, migration and tumorigenicity
Dunke Zhang, Feng Wang, Yi Pang, Erhu Zhao, Sunqin Zhu, Fei Chen, Hongjuan Cui
Biochem Biophys Res Commun. Author manuscript; available in PMC 2019 Dec 2.
Published in final edited form as: Biochem Biophys Res Commun. 2017 Apr 29; 486(2): 300–306. Published online 2017 Mar 12. doi: 10.1016/j.bbrc.2017.03.032
PMCID:
PMC6886229
ArticlePDF–1.5M
13.
RUNX1-PDCD6 fusion resulting from a novel t(5;21)(p15;q22) chromosome translocation in myelodysplastic syndrome secondary to chronic lymphocytic leukemia
Ioannis Panagopoulos, Ludmila Gorunova, Eva-Marie Jacobsen, Kristin Andersen, Francesca Micci, Sverre Heim
PLoS One. 2018; 13(4): e0196181. Published online 2018 Apr 19. doi: 10.1371/journal.pone.0196181
PMCID:
PMC5908135
ArticlePDF–2.7M
14.
The calcium-binding protein ALG-2 regulates protein secretion and trafficking via interactions with MISSL and MAP1B proteins
Terunao Takahara, Kuniko Inoue, Yumika Arai, Keiko Kuwata, Hideki Shibata, Masatoshi Maki
J Biol Chem. 2017 Oct 13; 292(41): 17057–17072. Published online 2017 Sep 1. doi: 10.1074/jbc.M117.800201
PMCID:
PMC5641880
ArticlePDF–3.6M
15.
Apoptosis-linked Gene-2 (ALG-2)/Sec31 Interactions Regulate Endoplasmic Reticulum (ER)-to-Golgi Transport: A POTENTIAL EFFECTOR PATHWAY FOR LUMINAL CALCIUM
Jared R. Helm, Marvin Bentley, Kevin D. Thorsen, Ting Wang, Lauren Foltz, Viola Oorschot, Judith Klumperman, Jesse C. Hay
J Biol Chem. 2014 Aug 22; 289(34): 23609–23628. Published online 2014 Jul 8. doi: 10.1074/jbc.M114.561829
PMCID:
PMC4156086
ArticlePDF–5.6M
16.
ALG-2-interacting Tubby-like protein superfamily member PLSCR3 is secreted by an exosomal pathway and taken up by recipient cultured cells
Tatsutoshi Inuzuka, Akira Inokawa, Cen Chen, Kumiko Kizu, Hiroshi Narita, Hideki Shibata, Masatoshi Maki
Biosci Rep. 2013; 33(2): e00026. Prepublished online 2013 Jan 26. Published online 2013 Mar 7. doi: 10.1042/BSR20120123
PMCID:
PMC3590573
ArticlePDF–1.6M
17.
Identification of the Penta-EF-hand Protein ALG-2 as a Ca2+-dependent Interactor of Mucolipin-1
Silvia Vergarajauregui, Jose A. Martina, Rosa Puertollano
J Biol Chem. 2009 Dec 25; 284(52): 36357–36366. Published online 2009 Oct 28. doi: 10.1074/jbc.M109.047241
PMCID:
PMC2794751
ArticlePDF–1.8M
18.
Expression level of NEAT1 differentiates benign and malignant thyroid nodules by regulating NEAT1/miR-9/PTEN and NEAT1/miR-124/PDCD6 signalling
Li Zhao, Na Zhou, Ping Zhao
Int J Mol Med. 2020 Nov; 46(5): 1661–1670. Published online 2020 Sep 4. doi: 10.3892/ijmm.2020.4721
PMCID:
PMC7521579
ArticlePDF–725K
19.
Structural and Functional Study of Apoptosis-linked Gene-2·Heme-binding Protein 2 Interactions in HIV-1 Production
Jing Ma, Xianfeng Zhang, Yanbin Feng, Hui Zhang, Xiaojun Wang, Yonghui Zheng, Wentao Qiao, Xinqi Liu
J Biol Chem. 2016 Dec 23; 291(52): 26670–26685. Published online 2016 Oct 26. doi: 10.1074/jbc.M116.752444
PMCID:
PMC5207177
ArticlePDF–4.6M
20.
Nuclear ALG-2 Protein Interacts with Ca2+ Homeostasis Endoplasmic Reticulum Protein (CHERP) Ca2+-dependently and Participates in Regulation of Alternative Splicing of Inositol Trisphosphate Receptor Type 1 (IP3R1) Pre-mRNA
Kanae Sasaki-Osugi, Chiaki Imoto, Terunao Takahara, Hideki Shibata, Masatoshi Maki
J Biol Chem. 2013 Nov 15; 288(46): 33361–33375. Published online 2013 Sep 27. doi: 10.1074/jbc.M113.497479
PMCID:
PMC3829183
ArticlePDF–3.1M

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