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Cited by in CrossRef
For: Rahajeng J, Giridharan SSP, Cai B, Naslavsky N, Caplan S. Important relationships between Rab and MICAL proteins in endocytic trafficking. World J Biol Chem 2010; 1(8): 254-264 [PMID: 21537482 DOI: 10.4331/wjbc.v1.i8.254]
URL: https://www.wjgnet.com/1949-8454/full/v1/i8/254.htm
Number Citing Articles
1
Y. Wang, W. Deng, Y. Zhang, S. Sun, S. Zhao, Y. Chen, X. Zhao, L. Liu, J. Du. MICAL2 promotes breast cancer cell migration by maintaining epidermal growth factor receptor (EGFR) stability and EGFR/P38 signalling activationActa Physiologica 2018; 222(2) doi: 10.1111/apha.12920
2
Yixing Yang, Fengwen Ye, Tianxiang Xia, Qianwen Wang, Yujie Zhang, Jun Du. High MICAL-L2 expression and its role in the prognosis of colon adenocarcinomaBMC Cancer 2022; 22(1) doi: 10.1186/s12885-022-09614-0
3
Modian Liu, Chun Huang, Rongfeng Dai, Wenwen Ren, Xinyi Li, Xiaoyun Wu, Xiaoming Ma, Min Chu, Pengjia Bao, Xian Guo, Jie Pei, Lin Xiong, Ping Yan, Chunnian Liang. Copy Number Variations in the MICALL2 and MOGAT2 Genes Are Associated with Ashidan Yak Growth TraitsAnimals 2022; 12(20): 2779 doi: 10.3390/ani12202779
4
Pengxiang Min, Lin Zhang, Yueyuan Wang, Chenxiang Qi, Yixuan Song, Maria Bibi, Yujie Zhang, Yadong Ma, Xuyang Zhao, Minjie Yu, Jun Du. MICAL-L2 Is Essential for c-Myc Deubiquitination and Stability in Non-small Cell Lung Cancer CellsFrontiers in Cell and Developmental Biology 2021; 8 doi: 10.3389/fcell.2020.575903
5
Atsuhiro Nakajo, Shin-ichiro Yoshimura, Hiroko Togawa, Masataka Kunii, Tomohiko Iwano, Ayaka Izumi, Yuria Noguchi, Ayako Watanabe, Ayako Goto, Toshiro Sato, Akihiro Harada. EHBP1L1 coordinates Rab8 and Bin1 to regulate apical-directed transport in polarized epithelial cellsJournal of Cell Biology 2016; 212(3): 297 doi: 10.1083/jcb.201508086
6
Jachen A. Solinger, Anne Spang. Sorting of cargo in the tubular endosomal networkBioEssays 2022; 44(12) doi: 10.1002/bies.202200158
7
Ayuko Sakane, Ahmed Alamir Mahmoud Abdallah, Kiyoshi Nakano, Kazufumi Honda, Wataru Ikeda, Yumiko Nishikawa, Mitsuru Matsumoto, Natsuki Matsushita, Toshio Kitamura, Takuya Sasaki. Rab13 Small G Protein and Junctional Rab13-binding Protein (JRAB) Orchestrate Actin Cytoskeletal Organization during Epithelial Junctional DevelopmentJournal of Biological Chemistry 2012; 287(51): 42455 doi: 10.1074/jbc.M112.383653
8
Maria Antonietta Vanoni. Structure-function studies of MICAL, the unusual multidomain flavoenzyme involved in actin cytoskeleton dynamicsArchives of Biochemistry and Biophysics 2017; 632: 118 doi: 10.1016/j.abb.2017.06.004
9
Emi Mizuno-Yamasaki, Felix Rivera-Molina, Peter Novick. GTPase Networks in Membrane TrafficAnnual Review of Biochemistry 2012; 81(1): 637 doi: 10.1146/annurev-biochem-052810-093700
10
Stéphane Frémont, Guillaume Romet-Lemonne, Anne Houdusse, Arnaud Echard. Emerging roles of MICAL family proteins – from actin oxidation to membrane trafficking during cytokinesisJournal of Cell Science 2017; 130(9): 1509 doi: 10.1242/jcs.202028
11
Maria Vanoni, Teresa Vitali, Daniela Zucchini. MICAL, the Flavoenzyme Participating in Cytoskeleton DynamicsInternational Journal of Molecular Sciences 2013; 14(4): 6920 doi: 10.3390/ijms14046920
12
Eljo Y. Van Battum, Rou-Afza F. Gunput, Suzanne Lemstra, Ewout J.N. Groen, Ka Lou Yu, Youri Adolfs, Yeping Zhou, Casper C. Hoogenraad, Yukata Yoshida, Melitta Schachner, Anna Akhmanova, R. Jeroen Pasterkamp. The intracellular redox protein MICAL-1 regulates the development of hippocampal mossy fibre connectionsNature Communications 2014; 5(1) doi: 10.1038/ncomms5317
13
Yeping Zhou, Rou-Afza F. Gunput, Youri Adolfs, R. Jeroen Pasterkamp. MICALs in control of the cytoskeleton, exocytosis, and cell deathCellular and Molecular Life Sciences 2011; 68(24): 4033 doi: 10.1007/s00018-011-0787-2
14
Wenjie Deng, Yueyuan Wang, Luo Gu, Biao Duan, Jie Cui, Yujie Zhang, Yan Chen, Shixiu Sun, Jing Dong, Jun Du. MICAL1 controls cell invasive phenotype via regulating oxidative stress in breast cancer cellsBMC Cancer 2016; 16(1) doi: 10.1186/s12885-016-2553-1
15
Sebastian Montealegre, Peter M. van Endert. Endocytic Recycling of MHC Class I Molecules in Non-professional Antigen Presenting and Dendritic CellsFrontiers in Immunology 2019; 9 doi: 10.3389/fimmu.2018.03098
16
Heather H. Ward, Angela Wandinger-Ness. Encyclopedia of Signaling Molecules2012; : 1547 doi: 10.1007/978-1-4419-0461-4_19
17
Yi Sun, Javier Jaldin-Fincati, Zhi Liu, Philip J. Bilan, Amira Klip, Patrick J. Brennwald. A complex of Rab13 with MICAL-L2 and α-actinin-4 is essential for insulin-dependent GLUT4 exocytosisMolecular Biology of the Cell 2016; 27(1): 75 doi: 10.1091/mbc.E15-05-0319
18
Tabitha A. Peterson, Robert C. Piper. Rab GTPasesMethods in Molecular Biology 2021; 2293: 117 doi: 10.1007/978-1-0716-1346-7_9
19
Bernard J. Koch, Joseph F. Ryan, Andreas D. Baxevanis, Olivier Lespinet. The Diversification of the LIM Superclass at the Base of the Metazoa Increased Subcellular Complexity and Promoted Multicellular SpecializationPLoS ONE 2012; 7(3): e33261 doi: 10.1371/journal.pone.0033261
20
David Villarroel‐Campos, Francisca C. Bronfman, Christian Gonzalez‐Billault. Rab GTPase signaling in neurite outgrowth and axon specificationCytoskeleton 2016; 73(9): 498 doi: 10.1002/cm.21303
21
Heather H. Ward, Angela Wandinger-Ness. Encyclopedia of Signaling Molecules2018; : 4396 doi: 10.1007/978-3-319-67199-4_19
22
Xi Qiao, Duy Ngo, Bilinda Straight, Belinda L. Needham, Charles E. Hilton, Amy Naugle. A Bayesian high-dimensional mediation analysis for multilevel genome-wide epigenetic dataJournal of Applied Statistics 2024; : 1 doi: 10.1080/02664763.2024.2367148
23
Mathilde Chaineau, Maria S. Ioannou, Peter S. McPherson. Rab35: GEFs, GAPs and EffectorsTraffic 2013; 14(11): 1109 doi: 10.1111/tra.12096