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Items: 1 to 20 of 53

1.
肌球蛋白轻链9在恶性肿瘤中的研究进展
游 伊梦, 刘 庭波, 沈 建箴
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2021 Oct 28; 46(10): 1153–1158. Chinese. doi: 10.11817/j.issn.1672-7347.2021.200814
PMCID:
PMC10930228
AbstractArticlePDF–542K
2.
MYL9 promotes squamous cervical cancer migration and invasion by enhancing aerobic glycolysis
Bin Wen, Limei Luo, Zhaoyang Zeng, Xiping Luo
J Int Med Res. 2023 Nov; 51(11): 03000605231208582. Published online 2023 Nov 11. doi: 10.1177/03000605231208582
PMCID:
PMC10640809
AbstractArticlePDF–839K
3.
MYL9 expressed in cancer-associated fibroblasts regulate the immune microenvironment of colorectal cancer and promotes tumor progression in an autocrine manner
Shenghe Deng, Denglong Cheng, Jun Wang, Junnan Gu, Yifan Xue, Zhenxing Jiang, Le Qin, Fuwei Mao, Yinghao Cao, Kailin Cai
J Exp Clin Cancer Res. 2023; 42: 294. Published online 2023 Nov 6. doi: 10.1186/s13046-023-02863-2
PMCID:
PMC10626665
AbstractArticlePDF–6.3M
4.
Increased Myosin light chain 9 expression during Kawasaki disease vasculitis
Hironobu Kobayashi, Motoko Y. Kimura, Ichita Hasegawa, Eisuke Suganuma, Yuzuru Ikehara, Kazuhiko Azuma, Toshihiro Ito, Ryota Ebata, Yosuke Kurashima, Yohei Kawasaki, Yuki Shiko, Naoki Saito, Hirotaro Iwase, Youngho Lee, Magali Noval Rivas, Moshe Arditi, Masahiko Zuka, Hiromichi Hamada, Toshinori Nakayama
Front Immunol. 2022; 13: 1036672. Published online 2023 Jan 6. doi: 10.3389/fimmu.2022.1036672
PMCID:
PMC9853906
AbstractArticlePDF–21M
5.
Clinicopathological significance of MYL9 expression in pancreatic ductal adenocarcinoma
Katsunori Matsushita, Shogo Kobayashi, Hirofumi Akita, Masamitsu Konno, Ayumu Asai, Takehiro Noda, Yoshifumi Iwagami, Tadafumi Asaoka, Kunihito Gotoh, Masaki Mori, Yuichiro Doki, Hidetoshi Eguchi, Hideshi Ishii
Cancer Rep (Hoboken) 2022 Oct; 5(10): e1582. Published online 2021 Nov 24. doi: 10.1002/cnr2.1582
PMCID:
PMC9575502
AbstractArticlePDF–2.7M
6.
Elevated Myl9 reflects the Myl9-containing microthrombi in SARS-CoV-2–induced lung exudative vasculitis and predicts COVID-19 severity
Chiaki Iwamura, Kiyoshi Hirahara, Masahiro Kiuchi, Sanae Ikehara, Kazuhiko Azuma, Tadanaga Shimada, Sachiko Kuriyama, Syota Ohki, Emiri Yamamoto, Yosuke Inaba, Yuki Shiko, Ami Aoki, Kota Kokubo, Rui Hirasawa, Takahisa Hishiya, Kaori Tsuji, Tetsutaro Nagaoka, Satoru Ishikawa, Akira Kojima, Haruki Mito, Ryota Hase, Yasunori Kasahara, Naohide Kuriyama, Tetsuya Tsukamoto, Sukeyuki Nakamura, Takashi Urushibara, Satoru Kaneda, Seiichiro Sakao, Minoru Tobiume, Yoshio Suzuki, Mitsuhiro Tsujiwaki, Terufumi Kubo, Tadashi Hasegawa, Hiroshi Nakase, Osamu Nishida, Kazuhisa Takahashi, Komei Baba, Yoko Iizumi, Toshiya Okazaki, Motoko Y. Kimura, Ichiro Yoshino, Hidetoshi Igari, Hiroshi Nakajima, Takuji Suzuki, Hideki Hanaoka, Taka-aki Nakada, Yuzuru Ikehara, Koutaro Yokote, Toshinori Nakayama
Proc Natl Acad Sci U S A. 2022 Aug 16; 119(33): e2203437119. Published online 2022 Jul 27. doi: 10.1073/pnas.2203437119
PMCID:
PMC9388124
AbstractArticlePDF–2.8M
7.
The landscape of prognostic and immunological role of myosin light chain 9 (MYL9) in human tumors
Minghe Lv, Lumeng Luo, Xue Chen
Immun Inflamm Dis. 2022 Feb; 10(2): 241–254. Published online 2021 Nov 2. doi: 10.1002/iid3.557
PMCID:
PMC8767521
AbstractArticlePDF–4.9M
8.
Myosin Light Chain 9/12 Regulates the Pathogenesis of Inflammatory Bowel Disease
Masaya Yokoyama, Motoko Y. Kimura, Toshihiro Ito, Koji Hayashizaki, Yukihiro Endo, Yangsong Wang, Ryoji Yagi, Tomoo Nakagawa, Naoya Kato, Hisahiro Matsubara, Toshinori Nakayama
Front Immunol. 2020; 11: 594297. Published online 2021 Jan 29. doi: 10.3389/fimmu.2020.594297
PMCID:
PMC7878395
AbstractArticlePDF–17M
9.
Homozygous deletion in MYL9 expands the molecular basis of megacystis–microcolon–intestinal hypoperistalsis syndrome
Carolina Araujo Moreno, Nara Sobreira, Elizabeth Pugh, Peng Zhang, Gary Steel, Fábio Rossi Torres, Denise Pontes Cavalcanti
Eur J Hum Genet. 2018 May; 26(5): 669–675. Published online 2018 Feb 16. doi: 10.1038/s41431-017-0055-5
PMCID:
PMC5945668
AbstractArticlePDF–864K
10.
Expression and prognostic significance of MYL9 in esophageal squamous cell carcinoma
Jian-Hua Wang, Lan Zhang, Shu-Ting Huang, Jing Xu, Yun Zhou, Xing-Juan Yu, Rong-Zhen Luo, Zhe-Sheng Wen, Wei-Hua Jia, Min Zheng
PLoS One. 2017; 12(4): e0175280. Published online 2017 Apr 7. doi: 10.1371/journal.pone.0175280
PMCID:
PMC5384754
AbstractArticlePDF–1.7M
11.
Myosin light chain 9 promotes the proliferation, invasion, migration and angiogenesis of colorectal cancer cells by binding to Yes-associated protein 1 and regulating Hippo signaling
Min Feng, Ningfei Dong, Xin Zhou, Lihong Ma, Rui Xiang
Bioengineered. 2022; 13(1): 96–106. Published online 2022 Jan 3. doi: 10.1080/21655979.2021.2008641
PMCID:
PMC8805887
AbstractArticlePDF–2.9M
12.
Intermolecular and Intramolecular Interactions Regulate Catalytic Activity of Myotonic Dystrophy Kinase-Related Cdc42-Binding Kinase α
Ivan Tan, Kah Tong Seow, Louis Lim, Thomas Leung
Mol Cell Biol. 2001 Apr; 21(8): 2767–2778. doi: 10.1128/MCB.21.8.2767-2778.2001
PMCID:
PMC86907
AbstractArticlePDF–557K
13.
LAMB3 Promotes Myofibrogenesis and Cytoskeletal Reorganization in Endometrial Stromal Cells via the RhoA/ROCK1/MYL9 Pathway
Xiaomei Qin, Bin Zeng, Suren R. Sooranna, Mujun Li
Cell Biochem Biophys. 2024; 82(1): 127–137. Published online 2023 Oct 6. doi: 10.1007/s12013-023-01186-5
PMCID:
PMC10867058
AbstractArticlePDF–2.1M
14.
Arv1 promotes cell division by recruiting IQGAP1 and myosin to the cleavage furrow
Hilde Sundvold, Vibeke Sundvold-Gjerstad, Helle Malerød-Fjeld, Kaisa Haglund, Harald Stenmark, Lene Malerød
Cell Cycle. 2016; 15(5): 628–643. Published online 2016 Mar 30. doi: 10.1080/15384101.2016.1146834
PMCID:
PMC4845929
AbstractArticlePDF–1.6M
15.
Nogo-B regulates migration and contraction of airway smooth muscle cells by decreasing ARPC 2/3 and increasing MYL-9 expression
Wujian Xu, Weijun Hong, Yan Shao, Yunye Ning, Zailong Cai, Qiang Li
Respir Res. 2011; 12(1): 14. Published online 2011 Jan 21. doi: 10.1186/1465-9921-12-14
PMCID:
PMC3037873
AbstractArticlePDF–835K
16.
PRPF19 facilitates colorectal cancer liver metastasis through activation of the Src-YAP1 pathway via K63-linked ubiquitination of MYL9
Rui Zhou, Jie Chen, Yunxiuxiu Xu, Yibiao Ye, Guoping Zhong, Tao Chen, Lin Qiu
Cell Death Dis. 2023 Apr; 14(4): 258. Published online 2023 Apr 8. doi: 10.1038/s41419-023-05776-2
PMCID:
PMC10082770
AbstractArticlePDF–5.9M
17.
Intact lipid rafts regulate HIV-1 Tat protein-induced activation of the Rho signaling and upregulation of P-glycoprotein in brain endothelial cells
Yu Zhong, Bernhard Hennig, Michal Toborek
J Cereb Blood Flow Metab. 2010 Mar; 30(3): 522–533. Published online 2009 Sep 30. doi: 10.1038/jcbfm.2009.214
PMCID:
PMC2949153
AbstractArticlePDF–758K
18.
A QUICK Screen for Lrrk2 Interaction Partners – Leucine-rich Repeat Kinase 2 is Involved in Actin Cytoskeleton Dynamics
Andrea Meixner, Karsten Boldt, Marleen Van Troys, Manor Askenazi, Christian J. Gloeckner, Matthias Bauer, Jarrod A. Marto, Christophe Ampe, Norbert Kinkl, Marius Ueffing
Mol Cell Proteomics. 2011 Jan; 10(1): M110.001172. Published online 2010 Sep 27. doi: 10.1074/mcp.M110.001172
PMCID:
PMC3013447
AbstractArticlePDF–958K
19.
SIK2 orchestrates actin-dependent host response upon Salmonella infection
Marcel Hahn, Adriana Covarrubias-Pinto, Lina Herhaus, Shankha Satpathy, Kevin Klann, Keith B. Boyle, Christian Münch, Krishnaraj Rajalingam, Felix Randow, Chunaram Choudhary, Ivan Dikic
Proc Natl Acad Sci U S A. 2021 May 11; 118(19): e2024144118. Published online 2021 May 4. doi: 10.1073/pnas.2024144118
PMCID:
PMC8126862
AbstractArticlePDF–3.0M
20.
Platelet Proteome Analysis Reveals Integrin-dependent Aggregation Defects in Patients with Myelodysplastic Syndromes
Julia Fröbel, Ron-Patrick Cadeddu, Sonja Hartwig, Ingmar Bruns, Christian M. Wilk, Andrea Kündgen, Johannes C. Fischer, Thomas Schroeder, Ulrich G. Steidl, Ulrich Germing, Stefan Lehr, Rainer Haas, Akos Czibere
Mol Cell Proteomics. 2013 May; 12(5): 1272–1280. Published online 2013 Feb 4. doi: 10.1074/mcp.M112.023168
PMCID:
PMC3650338
AbstractArticlePDF–346K

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