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Items: 1 to 20 of 36

1.
Association of the SHOX2 and RASSF1A methylation levels with the pathological evolution of early-stage lung adenocarcinoma
Jiaping Zhao, Yu Lu, Xiaosha Ren, Tingting Bian, Jia Feng, Hui Sun, Lei Liu, Bin She, Yifei Liu, Honggang Ke
BMC Cancer. 2024; 24: 687. Published online 2024 Jun 5. doi: 10.1186/s12885-024-12452-x
PMCID:
PMC11154976
AbstractArticlePDF–2.4M
2.
SHOX2 cooperates with STAT3 to promote breast cancer metastasis through the transcriptional activation of WASF3
Yong Teng, Reid Loveless, Elayne M Benson, Li Sun, Austin Y Shull, Chloe Shay
J Exp Clin Cancer Res. 2021; 40: 274. Published online 2021 Aug 31. doi: 10.1186/s13046-021-02083-6
PMCID:
PMC8406721
AbstractArticlePDF–4.8M
3.
SHOX2体外增强膀胱癌细胞的迁移、侵袭和干细胞特性
植 曦, 周 俊豪, 田 湖, 周 冉冉, 黄 振辉, 刘 存东
Nan Fang Yi Ke Da Xue Xue Bao. 2021 Jul 20; 41(7): 995–1001. Chinese. doi: 10.12122/j.issn.1673-4254.2021.07.05
PMCID:
PMC8329670
AbstractArticlePDF–1.9M
4.
矮小同源盒基因启动子区域甲基化诊断肺癌价值的meta分析
刘 强, 王 帅, 裴 国田, 杨 影顺, 黄 宇清
Zhongguo Fei Ai Za Zhi. 2021 Jul 20; 24(7): 490–496. Chinese. doi: 10.3779/j.issn.1009-3419.2021.101.27
PMCID:
PMC8317090
AbstractArticlePDF–5.8M
5.
A Novel Diagnosis Method Based on Methylation Analysis of SHOX2 and Serum Biomarker for Early Stage Lung Cancer
Wenhai Huang, Hao Huang, Shuishen Zhang, Xueping Wang, Juan Ouyang, Zhichao Lin, Peisong Chen
Cancer Control. 2020 Jan-Dec; 27(1): 1073274820969703. Published online 2020 Nov 10. doi: 10.1177/1073274820969703
PMCID:
PMC7791477
AbstractArticlePDF–424K
6.
A SHOX2 loss-of-function mutation underlying familial atrial fibrillation
Ning Li, Zhang-Sheng Wang, Xin-Hua Wang, Ying-Jia Xu, Qi Qiao, Xiu-Mei Li, Ruo-Min Di, Xiao-Juan Guo, Ruo-Gu Li, Min Zhang, Xing-Biao Qiu, Yi-Qing Yang
Int J Med Sci. 2018; 15(13): 1564–1572. Published online 2018 Oct 20. doi: 10.7150/ijms.27424
PMCID:
PMC6216059
AbstractArticlePDF–736K
7.
Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei
Domenico Fasci, Hugo van Ingen, Richard A. Scheltema, Albert J. R. Heck
Mol Cell Proteomics. 2018 Oct; 17(10): 2018–2033. Published online 2018 Jul 18. doi: 10.1074/mcp.RA118.000924
PMCID:
PMC6166682
AbstractArticlePDF–3.8M
8.
Potential of quantitative SEPT9 and SHOX2 methylation in plasmatic circulating cell-free DNA as auxiliary staging parameter in colorectal cancer: a prospective observational cohort study
Julia Bergheim, Alexander Semaan, Heidrun Gevensleben, Susanne Groening, Andreas Knoblich, Jörn Dietrich, Julia Weber, Jörg C. Kalff, Friedrich Bootz, Glen Kristiansen, Dimo Dietrich
Br J Cancer. 2018 May 1; 118(9): 1217–1228. Published online 2018 Apr 3. doi: 10.1038/s41416-018-0035-8
PMCID:
PMC5943265
AbstractArticlePDF–569K
9.
SHOX2 is a Potent Independent Biomarker to Predict Survival of WHO Grade II–III Diffuse Gliomas
Yu-An Zhang, Yunyun Zhou, Xin Luo, Kai Song, Xiaotu Ma, Adwait Sathe, Luc Girard, Guanghua Xiao, Adi F Gazdar
EBioMedicine. 2016 Nov; 13: 80–89. Published online 2016 Oct 28. doi: 10.1016/j.ebiom.2016.10.040
PMCID:
PMC5264450
AbstractArticlePDF–1.7M
10.
Validation of the SHOX2/PTGER4 DNA Methylation Marker Panel for Plasma-Based Discrimination between Patients with Malignant and Nonmalignant Lung Disease
Gunter Weiss, Anne Schlegel, Denise Kottwitz, Thomas König, Reimo Tetzner
J Thorac Oncol. 2017 Jan; 12(1): 77–84. doi: 10.1016/j.jtho.2016.08.123
PMCID:
PMC5226366
AbstractArticle
11.
Promoter hypermethylation of SHOX2 and SEPT9 is a potential biomarker for minimally invasive diagnosis in adenocarcinomas of the biliary tract
V. Branchi, P. Schaefer, A. Semaan, A. Kania, P. Lingohr, J. C. Kalff, N. Schäfer, G. Kristiansen, D. Dietrich, H. Matthaei
Clin Epigenetics. 2016; 8: 133. Published online 2016 Dec 12. doi: 10.1186/s13148-016-0299-x
PMCID:
PMC5153824
AbstractArticlePDF–687K
12.
SEPT9 and SHOX2 DNA methylation status and its utility in the diagnosis of colonic adenomas and colorectal adenocarcinomas
Alexander Semaan, Anne van Ellen, Sebastian Meller, Dominik Bergheim, Vittorio Branchi, Philipp Lingohr, Diane Goltz, Jörg C. Kalff, Glen Kristiansen, Hanno Matthaei, Dimitrios Pantelis, Dimo Dietrich
Clin Epigenetics. 2016; 8: 100. Published online 2016 Sep 20. doi: 10.1186/s13148-016-0267-5
PMCID:
PMC5028994
AbstractArticlePDF–878K
13.
Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation
Sandra Hoffmann, Sebastian Clauss, Ina M. Berger, Birgit Weiß, Antonino Montalbano, Ralph Röth, Madeline Bucher, Ina Klier, Reza Wakili, Hervé Seitz, Eric Schulze-Bahr, Hugo A. Katus, Friederike Flachsbart, Almut Nebel, Sabina PW. Guenther, Erik Bagaev, Wolfgang Rottbauer, Stefan Kääb, Steffen Just, Gudrun A. Rappold
Basic Res Cardiol. 2016; 111: 36. Published online 2016 Apr 30. doi: 10.1007/s00395-016-0557-2
PMCID:
PMC4853439
AbstractArticlePDF–3.2M
14.
Myofibroblasts are distinguished from activated skin fibroblasts by the expression of AOC3 and other associated markers
Lin-ting Hsia, Neil Ashley, Djamila Ouaret, Lai Mun Wang, Jennifer Wilding, Walter F. Bodmer
Proc Natl Acad Sci U S A. 2016 Apr 12; 113(15): E2162–E2171. Published online 2016 Mar 28. doi: 10.1073/pnas.1603534113
PMCID:
PMC4839407
AbstractArticlePDF–2.3M
15.
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
Meian He, Min Xu, Ben Zhang, Jun Liang, Peng Chen, Jong-Young Lee, Todd A. Johnson, Huaixing Li, Xiaobo Yang, Juncheng Dai, Liming Liang, Lixuan Gui, Qibin Qi, Jinyan Huang, Yanping Li, Linda S. Adair, Tin Aung, Qiuyin Cai, Ching-Yu Cheng, Myeong-Chan Cho, Yoon Shin Cho, Minjie Chu, Bin Cui, Yu-Tang Gao, Min Jin Go, Dongfeng Gu, Weiqiong Gu, Huan Guo, Yongchen Hao, Jie Hong, Zhibin Hu, Yanling Hu, Jianfeng Huang, Joo-Yeon Hwang, Mohammad Kamran Ikram, Guangfu Jin, Dae-Hee Kang, Chiea Chuen Khor, Bong-Jo Kim, Hung Tae Kim, Michiaki Kubo, Jeannette Lee, Juyoung Lee, Nanette R. Lee, Ruoying Li, Jun Li, JianJun Liu, Jirong Longe, Wei Lu, Xiangfeng Lu, Xiaoping Miao, Yukinori Okada, Rick Twee-Hee Ong, Gaokun Qiu, Mark Seielstad, Xueling Sim, Huaidong Song, Fumihiko Takeuchi, Toshihiro Tanaka, Phil R. Taylor, Laiyuan Wang, Weiqing Wang, Yiqin Wang, Chen Wu, Ying Wu, Yong-Bing Xiang, Ken Yamamoto, Handong Yang, Ming Liao, Mitsuhiro Yokota, Terri Young, Xiaomin Zhang, Norihiro Kato, Qing K. Wang, Wei Zheng, Frank B. Hu, Dongxin Lin, Hongbing Shen, Yik Ying Teo, Zengnan Mo, Tien Yin Wong, Xu Lin, Karen L. Mohlke, Guang Ning, Tatsuhiko Tsunoda, Bok-Ghee Han, Xiao-Ou Shu, E. Shyong Tai, Tangchun Wu, Lu Qi
Hum Mol Genet. 2015 Mar 15; 24(6): 1791–1800. Published online 2014 Nov 26. doi: 10.1093/hmg/ddu583
PMCID:
PMC4351379
AbstractArticlePDF–436K
16.
Quantification of Cell-Free mSHOX2 Plasma DNA for Therapy Monitoring in Advanced Stage Non-Small Cell (NSCLC) and Small-Cell Lung Cancer (SCLC) Patients
Bernd Schmidt, Julia Beyer, Dimo Dietrich, Ines Bork, Volker Liebenberg, Michael Fleischhacker
PLoS One. 2015; 10(2): e0118195. Published online 2015 Feb 12. doi: 10.1371/journal.pone.0118195
PMCID:
PMC4326280
AbstractArticlePDF–318K
17.
SHOX2 Overexpression Favors Differentiation of Embryonic Stem Cells into Cardiac Pacemaker Cells, Improving Biological Pacing Ability
Vittoria Ionta, Wenbin Liang, Elizabeth H. Kim, Reza Rafie, Alessandro Giacomello, Eduardo Marbán, Hee Cheol Cho
Stem Cell Reports. 2015 Jan 13; 4(1): 129–142. Published online 2014 Dec 18. doi: 10.1016/j.stemcr.2014.11.004
PMCID:
PMC4297875
AbstractArticlePDF–2.4M
18.
14-3-3ε and NAV2 interact to regulate neurite outgrowth and axon elongation
Mark A. Marzinke, Terri Mavencamp, Joseph Duratinsky, Margaret Clagett-Dame
Arch Biochem Biophys. Author manuscript; available in PMC 2014 Aug 4.
Published in final edited form as: Arch Biochem Biophys. 2013 Dec; 540(0): 94–100. Published online 2013 Oct 23. doi: 10.1016/j.abb.2013.10.012
PMCID:
PMC4120646
AbstractArticlePDF–1.9M
19.
SHOX2 Is a Direct miR-375 Target and a Novel Epithelial-to-Mesenchymal Transition Inducer in Breast Cancer Cells
Sungguan Hong, Hyangsoon Noh, Yong Teng, Jing Shao, Hina Rehmani, Han-Fei Ding, Zheng Dong, Shi-Bing Su, Huidong Shi, Jaejik Kim, Shuang Huang
Neoplasia. 2014 Apr; 16(4): 279–290.e5. Published online 2014 Apr 18. doi: 10.1016/j.neo.2014.03.010
PMCID:
PMC4094831
AbstractArticlePDF–3.0M
20.
The palmitoyl acyltransferase HIP14 shares a high proportion of interactors with huntingtin: implications for a role in the pathogenesis of Huntington's disease
Stefanie L. Butland, Shaun S. Sanders, Mandi E. Schmidt, Sean-Patrick Riechers, David T.S. Lin, Dale D.O. Martin, Kuljeet Vaid, Rona K. Graham, Roshni R. Singaraja, Erich E. Wanker, Elizabeth Conibear, Michael R. Hayden
Hum Mol Genet. 2014 Aug 1; 23(15): 4142–4160. Published online 2014 Apr 4. doi: 10.1093/hmg/ddu137
PMCID:
PMC4082372
AbstractArticlePDF–1.7M

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