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For: Sztul E, Chen PW, Casanova JE, Cherfils J, Dacks JB, Lambright DG, Lee FS, Randazzo PA, Santy LC, Schürmann A, Wilhelmi I, Yohe ME, Kahn RA. ARF GTPases and their GEFs and GAPs: concepts and challenges. Mol Biol Cell 2019;30:1249-71. [PMID: 31084567 DOI: 10.1091/mbc.E18-12-0820] [Cited by in Crossref: 125] [Cited by in F6Publishing: 127] [Article Influence: 41.7] [Reference Citation Analysis]
Number Citing Articles
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6 Ali Shad M, Wang Y, Zhang H, Zhai S, Shalmani A, Li Y. Genetic analysis of GEFs and GDIs in rice reveals the roles of OsGEF5, OsGDI1, and OsGEF3 in the regulation of grain size and plant height. The Crop Journal 2022. [DOI: 10.1016/j.cj.2022.07.018] [Reference Citation Analysis]
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10 Khakurel A, Kudlyk T, Pokrovskaya I, D’souza Z, Lupashin VV. GARP complex controls Golgi physiology by stabilizing COPI machinery and Golgi v-SNAREs.. [DOI: 10.1101/2022.07.22.501184] [Reference Citation Analysis]
11 Paone S, Olivieri A. Role of Host Small GTPases in Apicomplexan Parasite Infection. Microorganisms 2022;10:1370. [DOI: 10.3390/microorganisms10071370] [Reference Citation Analysis]
12 Purkanti R, Thattai M. Genome doubling enabled the expansion of yeast vesicle traffic pathways. Sci Rep 2022;12:11213. [PMID: 35780185 DOI: 10.1038/s41598-022-15419-9] [Reference Citation Analysis]
13 Gallardo CM, Nguyen AT, Routh AL, Torbett BE. Selective ablation of 3' RNA ends and processive RTs facilitate direct cDNA sequencing of full-length host cell and viral transcripts. Nucleic Acids Res 2022:gkac516. [PMID: 35736235 DOI: 10.1093/nar/gkac516] [Reference Citation Analysis]
14 Fiola-Masson E, Artigalas J, Campbell S, Claing A. Activation of the GTPase ARF6 regulates invasion of human vascular smooth muscle cells by stimulating MMP14 activity. Sci Rep 2022;12:9532. [PMID: 35680971 DOI: 10.1038/s41598-022-13574-7] [Reference Citation Analysis]
15 Wong-dilworth L, Rodilla-ramirez C, Fox E, Restel SD, Stockhammer A, Adarska P, Bottanelli F. Gene editing and super-resolution microscopy reveal multiple distinct roles for ARF GTPases in cellular membrane organization.. [DOI: 10.1101/2022.05.31.494106] [Reference Citation Analysis]
16 Yang S, Liu Y, Brown A, Schaks M, Ding B, Kramer DA, Ding L, Alekhina O, Billadeau DD, Chowdhury S, Wang J, Rottner K, Chen B. Arf GTPase activates the WAVE Regulatory Complex through a novel binding site.. [DOI: 10.1101/2022.05.13.491857] [Reference Citation Analysis]
17 Ito A, Fukaya M, Okamoto H, Sakagami H. Physiological and Pathological Roles of the Cytohesin Family in Neurons. Int J Mol Sci 2022;23:5087. [PMID: 35563476 DOI: 10.3390/ijms23095087] [Reference Citation Analysis]
18 Drastichova Z, Trubacova R, Novotny J. β-Arrestin2 Is Critically Involved in the Differential Regulation of Phosphosignaling Pathways by Thyrotropin-Releasing Hormone and Taltirelin. Cells 2022;11:1473. [PMID: 35563779 DOI: 10.3390/cells11091473] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Yemenici M, Kartal Sural B, Karaer Uzuner S, Palabiyik B. Involvement of Sec71 and Ubp2 in tunicamycin-induced ER stress response in the fission yeast. Mol Biol Rep 2022. [PMID: 35474054 DOI: 10.1007/s11033-022-07321-4] [Reference Citation Analysis]
20 Sandilands E, Freckmann EC, Román-fernández A, Mcgarry L, Galbraith L, Mason S, Patel R, Anand J, Cartwright J, Leung HY, Blyth K, Bryant DM. The small GTPase ARF3 controls metastasis and invasion modality by regulating N-cadherin levels.. [DOI: 10.1101/2022.04.25.489355] [Reference Citation Analysis]
21 Dewees SI, Vargová R, Hardin KR, Turn RE, Devi S, Linnert J, Wolfrum U, Caspary T, Eliáš M, Kahn RA. Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E. Mol Biol Cell 2022;33:ar33. [PMID: 35196065 DOI: 10.1091/mbc.E21-10-0509-T] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Keren-kaplan T, Sarić A, Ghosh S, Williamson CD, Jia R, Li Y, Bonifacino JS. RUFY3 and RUFY4 are ARL8 effectors that promote coupling of endolysosomes to dynein-dynactin. Nat Commun 2022;13. [DOI: 10.1038/s41467-022-28952-y] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 6.0] [Reference Citation Analysis]
23 Kendall AK, Chandra M, Xie B, Wan W, Jackson LP. Improved mammalian retromer cryo-EM structures reveal a new assembly interface.. [DOI: 10.1101/2022.03.04.482375] [Reference Citation Analysis]
24 Li T, Guo Y. ADP-Ribosylation Factor Family of Small GTP-Binding Proteins: Their Membrane Recruitment, Activation, Crosstalk and Functions. Front Cell Dev Biol 2022;10:813353. [DOI: 10.3389/fcell.2022.813353] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
25 Gallardo CM, Nguyen AT, Routh AL, Torbett BE. Selective Ablation of 3’ RNA ends and Processive RTs Facilitate Direct cDNA Sequencing of Full-length Host Cell and Viral Transcripts.. [DOI: 10.1101/2022.01.27.478099] [Reference Citation Analysis]
26 Miyamoto Y, Torii T, Homma K, Oizumi H, Ohbuchi K, Mizoguchi K, Takashima S, Yamauchi J. The adaptor SH2B1 and the phosphatase PTP4A1 regulate the phosphorylation of cytohesin-2 in myelinating Schwann cells in mice. Sci Signal 2022;15:eabi5276. [PMID: 35077201 DOI: 10.1126/scisignal.abi5276] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Mani S, Krishnan K, Thattai M. Graph-theoretic constraints on vesicle traffic networks. J Biosci 2022;47. [DOI: 10.1007/s12038-021-00252-5] [Reference Citation Analysis]
28 Tamaddon-jahromi S, Murphy K, Walker W, Kanamarlapudi V. EFA6R suppresses ovarian cancer cell migration and invasion.. [DOI: 10.1101/2022.01.21.477266] [Reference Citation Analysis]
29 Bailetti D, Sentinelli F, Prudente S, Cimini FA, Barchetta I, Totaro M, Di Costanzo A, Barbonetti A, Leonetti F, Cavallo MG, Baroni MG. Deep Resequencing of 9 Candidate Genes Identifies a Role for ARAP1 and IGF2BP2 in Modulating Insulin Secretion Adjusted for Insulin Resistance in Obese Southern Europeans. Int J Mol Sci 2022;23:1221. [PMID: 35163144 DOI: 10.3390/ijms23031221] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 Riffo-Campos AL, Perez-Hernandez J, Ortega A, Martinez-Arroyo O, Flores-Chova A, Redon J, Cortes R. Exosomal and Plasma Non-Coding RNA Signature Associated with Urinary Albumin Excretion in Hypertension. Int J Mol Sci 2022;23:823. [PMID: 35055008 DOI: 10.3390/ijms23020823] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
31 Yin G, Lv G, Zhang J, Jiang H, Lai T, Yang Y, Ren Y, Wang J, Yi C, Chen H, Huang Y, Xiao C. Early-stage structure-based drug discovery for small GTPases by NMR spectroscopy. Pharmacol Ther 2022;236:108110. [PMID: 35007659 DOI: 10.1016/j.pharmthera.2022.108110] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
32 Pennauer M, Buczak K, Prescianotto-Baschong C, Spiess M. Shared and specific functions of Arfs 1-5 at the Golgi revealed by systematic knockouts. J Cell Biol 2022;221:e202106100. [PMID: 34749397 DOI: 10.1083/jcb.202106100] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
33 Hellicar J, Stevenson NL, Stephens DJ, Lowe M. Supply chain logistics - the role of the Golgi complex in extracellular matrix production and maintenance. J Cell Sci 2022;135:jcs258879. [PMID: 35023559 DOI: 10.1242/jcs.258879] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
34 Krahn AH, Glick BS. Intra-Golgi Transport. Reference Module in Life Sciences 2022. [DOI: 10.1016/b978-0-12-821618-7.00075-4] [Reference Citation Analysis]
35 Haines A, Wesolowski J, Ryan NM, Monteiro-Brás T, Paumet F. Cross Talk between ARF1 and RhoA Coordinates the Formation of Cytoskeletal Scaffolds during Chlamydia Infection. mBio 2021;12:e0239721. [PMID: 34903051 DOI: 10.1128/mBio.02397-21] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
36 Shi M, Tie HC, Mahajan D, Sun X, Zhou Y, Boh BK, Vardy LA, Lu L. Arl15 upregulates the TGFβ family signaling by promoting the assembly of the Smad-complex.. [DOI: 10.1101/2021.12.14.472727] [Reference Citation Analysis]
37 Chia J, Wang SC, Wee S, Gill DJ, Tay F, Kannan S, Verma CS, Gunaratne J, Bard FA. Src activates retrograde membrane traffic through phosphorylation of GBF1. Elife 2021;10:e68678. [PMID: 34870592 DOI: 10.7554/eLife.68678] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
38 Araki M, Yoshimoto K, Ohta M, Katada T, Kontani K. Development of a versatile HPLC-based method to evaluate the activation status of small GTPases. J Biol Chem 2021;297:101428. [PMID: 34801548 DOI: 10.1016/j.jbc.2021.101428] [Reference Citation Analysis]
39 Chen K, Hsu J, Lee FS. AMPK promotes Arf6 activation in a kinase-independent manner upon energy deprivation.. [DOI: 10.1101/2021.11.18.469188] [Reference Citation Analysis]
40 Chen PW, Gasilina A, Yadav MP, Randazzo PA. Control of cell signaling by Arf GTPases and their regulators: Focus on links to cancer and other GTPase families. Biochim Biophys Acta Mol Cell Res 2021;1869:119171. [PMID: 34774605 DOI: 10.1016/j.bbamcr.2021.119171] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
41 Dewees SI, Vargová R, Hardin KR, Turn RE, Devi S, Linnert J, Wolfrum U, Caspary T, Eliáš M, Kahn RA. Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E.. [DOI: 10.1101/2021.10.14.464442] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
42 Zhou Y, Amom P, Reeder SH, Lee BH, Helton A, Dobritsa AA. Members of the ELMOD protein family specify formation of distinct aperture domains on the Arabidopsis pollen surface. Elife 2021;10:e71061. [PMID: 34591014 DOI: 10.7554/eLife.71061] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
43 Turn RE, Hu Y, Dewees SI, Devi N, East MP, Hardin KR, Khatib T, Linnert J, Wolfrum U, Lim MJ, Casanova JE, Caspary T, Kahn RA. The ARF GAPs ELMOD1 and ELMOD3 act at the Golgi and Cilia to Regulate Ciliogenesis and Ciliary Protein Traffic.. [DOI: 10.1101/2021.09.15.460558] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
44 Mima J. Self-assemblies of Rab- and Arf-family small GTPases on lipid bilayers in membrane tethering. Biophys Rev 2021;13:531-9. [PMID: 34471437 DOI: 10.1007/s12551-021-00819-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
45 Brito C, Costa-Silva B, Barral DC, Pojo M. Unraveling the Relevance of ARL GTPases in Cutaneous Melanoma Prognosis through Integrated Bioinformatics Analysis. Int J Mol Sci 2021;22:9260. [PMID: 34502169 DOI: 10.3390/ijms22179260] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
46 Pavišić V, Mahmutefendić Lučin H, Blagojević Zagorac G, Lučin P. Arf GTPases Are Required for the Establishment of the Pre-Assembly Compartment in the Early Phase of Cytomegalovirus Infection. Life (Basel) 2021;11:867. [PMID: 34440611 DOI: 10.3390/life11080867] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
47 Borchers AC, Langemeyer L, Ungermann C. Who's in control? Principles of Rab GTPase activation in endolysosomal membrane trafficking and beyond. J Cell Biol 2021;220:e202105120. [PMID: 34383013 DOI: 10.1083/jcb.202105120] [Cited by in Crossref: 13] [Cited by in F6Publishing: 18] [Article Influence: 13.0] [Reference Citation Analysis]
48 Giubilaro J, Schuetz DA, Stepniewski TM, Namkung Y, Khoury E, Lara-Márquez M, Campbell S, Beautrait A, Armando S, Radresa O, Duchaine J, Lamarche-Vane N, Claing A, Selent J, Bouvier M, Marinier A, Laporte SA. Discovery of a dual Ras and ARF6 inhibitor from a GPCR endocytosis screen. Nat Commun 2021;12:4688. [PMID: 34344896 DOI: 10.1038/s41467-021-24968-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
49 Adarska P, Wong-Dilworth L, Bottanelli F. ARF GTPases and Their Ubiquitous Role in Intracellular Trafficking Beyond the Golgi. Front Cell Dev Biol 2021;9:679046. [PMID: 34368129 DOI: 10.3389/fcell.2021.679046] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 13.0] [Reference Citation Analysis]
50 Trillet K, Jacobs KA, André-Grégoire G, Thys A, Maghe C, Cruard J, Minvielle S, Diest SG, Montagnac G, Bidère N, Gavard J. The glycoprotein GP130 governs the surface presentation of the G protein-coupled receptor APLNR. J Cell Biol 2021;220:e202004114. [PMID: 34287648 DOI: 10.1083/jcb.202004114] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
51 Iraburu MJ, Garner T, Montiel-Duarte C. Revising Endosomal Trafficking under Insulin Receptor Activation. Int J Mol Sci 2021;22:6978. [PMID: 34209489 DOI: 10.3390/ijms22136978] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
52 Xu WK, Gou Y, Lozano MM, Dudley JP. Unconventional p97/VCP-Mediated Endoplasmic Reticulum-to-Endosome Trafficking of a Retroviral Protein. J Virol 2021;95:e0053121. [PMID: 33952644 DOI: 10.1128/JVI.00531-21] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
53 Su MY, Fromm SA, Remis J, Toso DB, Hurley JH. Structural basis for the ARF GAP activity and specificity of the C9orf72 complex. Nat Commun 2021;12:3786. [PMID: 34145292 DOI: 10.1038/s41467-021-24081-0] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
54 Zhou Y, Amom P, Reeder SH, Lee BH, Helton A, Dobritsa AA. Members of the ELMOD protein family specify formation of distinct aperture domains on the Arabidopsis pollen surface.. [DOI: 10.1101/2021.06.15.448545] [Reference Citation Analysis]
55 Lauri A, Fasano G, Venditti M, Dallapiccola B, Tartaglia M. In vivo Functional Genomics for Undiagnosed Patients: The Impact of Small GTPases Signaling Dysregulation at Pan-Embryo Developmental Scale. Front Cell Dev Biol 2021;9:642235. [PMID: 34124035 DOI: 10.3389/fcell.2021.642235] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
56 Suo Y, Hu F, Zhu H, Li D, Qi R, Huang J, Wu W. BIG3 and BIG5 Redundantly Mediate Vesicle Trafficking in Arabidopsis. Biomolecules 2021;11:732. [PMID: 34069034 DOI: 10.3390/biom11050732] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
57 Rasmussen ML, Robertson GL, Gama V. Break on Through: Golgi-Derived Vesicles Aid in Mitochondrial Fission. Cell Metab 2020;31:1047-9. [PMID: 32492390 DOI: 10.1016/j.cmet.2020.05.010] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
58 Smeyers J, Banchi EG, Latouche M. C9ORF72: What It Is, What It Does, and Why It Matters. Front Cell Neurosci 2021;15:661447. [PMID: 34025358 DOI: 10.3389/fncel.2021.661447] [Cited by in Crossref: 14] [Cited by in F6Publishing: 18] [Article Influence: 14.0] [Reference Citation Analysis]
59 Qadeer A, Giri BR, Ullah H, Cheng G. Transcriptional profiles of genes potentially involved in extracellular vesicle biogenesis in Schistosoma japonicum. Acta Trop 2021;217:105851. [PMID: 33524382 DOI: 10.1016/j.actatropica.2021.105851] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
60 Arrazola Sastre A, Luque Montoro M, Lacerda HM, Llavero F, Zugaza JL. Small GTPases of the Rab and Arf Families: Key Regulators of Intracellular Trafficking in Neurodegeneration. Int J Mol Sci 2021;22:4425. [PMID: 33922618 DOI: 10.3390/ijms22094425] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 11.0] [Reference Citation Analysis]
61 Pennauer M, Buczak K, Prescianotto-baschong C, Spiess M. Shared and specific functions of Arfs 1–5 at the Golgi revealed by systematic knockouts.. [DOI: 10.1101/2021.04.19.440443] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
62 Creekmore BC, Chang YW, Lee EB. The Cryo-EM Effect: Structural Biology of Neurodegenerative Disease Proteostasis Factors. J Neuropathol Exp Neurol 2021;80:494-513. [PMID: 33860329 DOI: 10.1093/jnen/nlab029] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
63 Su M, Fromm SA, Remis J, Toso DB, Hurley JH. Structural basis for the ARF GAP activity and specificity of the C9orf72 complex.. [DOI: 10.1101/2021.04.13.439632] [Reference Citation Analysis]
64 Watanabe A, Hataida H, Inoue N, Kamon K, Baba K, Sasaki K, Kimura R, Sasaki H, Eura Y, Ni W, Shibasaki Y, Waguri S, Kokame K, Shiba Y. Arf GTPase-Activating proteins SMAP1 and AGFG2 regulate the size of Weibel-Palade bodies and exocytosis of von Willebrand factor.. [DOI: 10.1101/2021.03.29.437631] [Reference Citation Analysis]
65 Brandi V, Polticelli F. In Silico Analysis of Huntingtin Homologs in Lower Eukaryotes. Int J Mol Sci 2021;22:3214. [PMID: 33809947 DOI: 10.3390/ijms22063214] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
66 Jackson T, Belsham GJ. Picornaviruses: A View from 3A. Viruses 2021;13:456. [PMID: 33799649 DOI: 10.3390/v13030456] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
67 Lepelley A, Martin-Niclós MJ, Le Bihan M, Marsh JA, Uggenti C, Rice GI, Bondet V, Duffy D, Hertzog J, Rehwinkel J, Amselem S, Boulisfane-El Khalifi S, Brennan M, Carter E, Chatenoud L, Chhun S, Coulomb l'Hermine A, Depp M, Legendre M, Mackenzie KJ, Marey J, McDougall C, McKenzie KJ, Molina TJ, Neven B, Seabra L, Thumerelle C, Wislez M, Nathan N, Manel N, Crow YJ, Frémond ML. Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling. J Exp Med 2020;217:e20200600. [PMID: 32725128 DOI: 10.1084/jem.20200600] [Cited by in Crossref: 67] [Cited by in F6Publishing: 69] [Article Influence: 67.0] [Reference Citation Analysis]
68 Purkanti R, Thattai M. Paralogous gene modules derived from ancient hybridization drive vesicle traffic evolution in yeast.. [DOI: 10.1101/2021.03.03.433305] [Reference Citation Analysis]
69 Turn RE, Linnert J, Gigante ED, Wolfrum U, Caspary T, Kahn RA. Roles for ELMOD2 and Rootletin in ciliogenesis. Mol Biol Cell 2021;32:800-22. [PMID: 33596093 DOI: 10.1091/mbc.E20-10-0635] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
70 Fujibayashi K, Mima J. The Small GTPase Arf6 Functions as a Membrane Tether in a Chemically-Defined Reconstitution System. Front Cell Dev Biol 2021;9:628910. [PMID: 33585484 DOI: 10.3389/fcell.2021.628910] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
71 Sager G, Szul T, Lee E, Kawai R, Presley JF, Sztul E. Modeling the dynamic behaviors of the COPI vesicle formation regulators, the small GTPase Arf1 and its activating Sec7 guanine nucleotide exchange factor GBF1 on Golgi membranes. Mol Biol Cell 2021;32:446-59. [PMID: 33405949 DOI: 10.1091/mbc.E20-09-0587] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
72 Duellberg C, Auer A, Canigova N, Loibl K, Loose M. In vitro reconstitution reveals phosphoinositides as cargo-release factors and activators of the ARF6 GAP ADAP1. Proc Natl Acad Sci U S A 2021;118:e2010054118. [PMID: 33443153 DOI: 10.1073/pnas.2010054118] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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