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For: Peng M, Falk MJ, Haase VH, King R, Polyak E, Selak M, Yudkoff M, Hancock WW, Meade R, Saiki R. Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease. PLoS Genet. 2008;4:e1000061. [PMID: 18437205 DOI: 10.1371/journal.pgen.1000061] [Cited by in Crossref: 95] [Cited by in F6Publishing: 100] [Article Influence: 6.3] [Reference Citation Analysis]
Number Citing Articles
1 Chang CF, Gunawan AL, Liparulo I, Zushin PH, Bertholet AM, Kirichok Y, Stahl A. CoQ Regulates Brown Adipose Tissue Respiration and Uncoupling Protein 1 Expression. Antioxidants (Basel) 2022;12. [PMID: 36670876 DOI: 10.3390/antiox12010014] [Reference Citation Analysis]
2 Banerjee R, Purhonen J, Kallijärvi J. The mitochondrial coenzyme Q junction and complex III: biochemistry and pathophysiology. FEBS J 2022;289:6936-58. [PMID: 34428349 DOI: 10.1111/febs.16164] [Cited by in Crossref: 17] [Cited by in F6Publishing: 15] [Article Influence: 17.0] [Reference Citation Analysis]
3 Wang Y, Hekimi S. The efficacy of coenzyme Q10 treatment in alleviating the symptoms of primary coenzyme Q10 deficiency: A systematic review. J Cell Mol Med 2022. [PMID: 35985679 DOI: 10.1111/jcmm.17488] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Jiang Z, Hao F, Zhu F, Yuan F, Ma L, Li G, Chen J, Tong T. RSL1D1 modulates cell senescence and proliferation via regulation of PPARγ mRNA stability. Life Sciences 2022. [DOI: 10.1016/j.lfs.2022.120848] [Reference Citation Analysis]
5 Rahnavard A, Mann B, Giri A, Chatterjee R, Crandall KA. Metabolite, protein, and tissue dysfunction associated with COVID-19 disease severity. Sci Rep 2022;12:12204. [PMID: 35842456 DOI: 10.1038/s41598-022-16396-9] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Wang Y, Gumus E, Hekimi S. A novel COQ7 mutation causing primarily neuromuscular pathology and its treatment options. Molecular Genetics and Metabolism Reports 2022;31:100877. [DOI: 10.1016/j.ymgmr.2022.100877] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Wang Y, Hekimi S. The efficacy of coenzyme Q10 treatment in alleviating the symptoms of primary coenzyme Q10 deficiency: a systematic review.. [DOI: 10.1101/2022.05.21.22275418] [Reference Citation Analysis]
8 Feng YQ, Wang JJ, Li MH, Tian Y, Zhao AH, Li L, De Felici M, Shen W. Impaired primordial follicle assembly in offspring ovaries from zearalenone-exposed mothers involves reduced mitochondrial activity and altered epigenetics in oocytes. Cell Mol Life Sci 2022;79:258. [PMID: 35469021 DOI: 10.1007/s00018-022-04288-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Barutta F, Bellini S, Gruden G. Mechanisms of podocyte injury and implications for diabetic nephropathy. Clin Sci (Lond) 2022;136:493-520. [PMID: 35415751 DOI: 10.1042/CS20210625] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
10 Chang C, Gunawan AL, Zushin PH, Timblin GA, Bertholet AM, Wang B, Sajio K, Kirichok Y, Stahl A. Coenzyme Q regulates UCP1 expression and thermogenesis through the integrated stress responses.. [DOI: 10.1101/2022.03.18.484957] [Reference Citation Analysis]
11 Braga PC, Alves MG, Rodrigues AS, Oliveira PF. Mitochondrial Pathophysiology on Chronic Kidney Disease. Int J Mol Sci 2022;23:1776. [PMID: 35163697 DOI: 10.3390/ijms23031776] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
12 Wang R, Kairen C, Li L, Zhang L, Gong H, Huang X. Overexpression of NDUFV1 alleviates renal damage by improving mitochondrial function in unilateral ureteral obstruction model mice. Cell Biol Int 2021. [PMID: 34936716 DOI: 10.1002/cbin.11736] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 González-García P, Barriocanal-Casado E, Díaz-Casado ME, López-Herrador S, Hidalgo-Gutiérrez A, López LC. Animal Models of Coenzyme Q Deficiency: Mechanistic and Translational Learnings. Antioxidants (Basel) 2021;10:1687. [PMID: 34829558 DOI: 10.3390/antiox10111687] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
14 Galvan DL, Mise K, Danesh FR. Mitochondrial Regulation of Diabetic Kidney Disease. Front Med (Lausanne) 2021;8:745279. [PMID: 34646847 DOI: 10.3389/fmed.2021.745279] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
15 Wang P, Castellani CA, Yao J, Huan T, Bielak LF, Zhao W, Haessler J, Roby J, Sun X, Guo X, Longchamps RJ, Manson JE, Grove ML, Bressler J, Taylor KD, Lappalainen T, Kasela S, Van Den Berg DJ, Hou L, Reiner A, Liu Y, Boerwinkle E, Smith JA, Peyser PA, Fornage M, Rich SS, Rotter JI, Kooperberg C, Arking DE, Levy D, Liu C; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium. Epigenome-wide association study of mitochondrial genome copy number. Hum Mol Genet 2021:ddab240. [PMID: 34415308 DOI: 10.1093/hmg/ddab240] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
16 Sidhom EH, Kim C, Kost-Alimova M, Ting MT, Keller K, Avila-Pacheco J, Watts AJ, Vernon KA, Marshall JL, Reyes-Bricio E, Racette M, Wieder N, Kleiner G, Grinkevich EJ, Chen F, Weins A, Clish CB, Shaw JL, Quinzii CM, Greka A. Targeting a Braf/Mapk pathway rescues podocyte lipid peroxidation in CoQ-deficiency kidney disease. J Clin Invest 2021;131:141380. [PMID: 33444290 DOI: 10.1172/JCI141380] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
17 Tan W, Airik R. Primary coenzyme Q10 nephropathy, a potentially treatable form of steroid-resistant nephrotic syndrome. Pediatr Nephrol 2021. [PMID: 33479824 DOI: 10.1007/s00467-020-04914-8] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
18 Galvan DL, Perico L. Mitochondrial dysfunction in kidney diseases. Clinical Bioenergetics 2021. [DOI: 10.1016/b978-0-12-819621-2.00005-x] [Reference Citation Analysis]
19 Stefanatos R, Sanz A, Fernandez-ayala DJM. Model Cells and Organisms in Mitochondrial Diseases. Mitochondrial Diseases 2021. [DOI: 10.1007/978-3-030-70147-5_10] [Reference Citation Analysis]
20 De Giorgi M, Jarrett KE, Burton JC, Doerfler AM, Hurley A, Li A, Hsu RH, Furgurson M, Patel KR, Han J, Borchers CH, Lagor WR. Depletion of essential isoprenoids and ER stress induction following acute liver-specific deletion of HMG-CoA reductase. J Lipid Res 2020;61:1675-86. [PMID: 33109681 DOI: 10.1194/jlr.RA120001006] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.7] [Reference Citation Analysis]
21 Maeoka Y, Doi T, Aizawa M, Miyasako K, Hirashio S, Masuda Y, Kishita Y, Okazaki Y, Murayama K, Imasawa T, Hara S, Masaki T. A case report of adult-onset COQ8B nephropathy presenting focal segmental glomerulosclerosis with granular swollen podocytes. BMC Nephrol 2020;21:376. [PMID: 32859164 DOI: 10.1186/s12882-020-02040-z] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
22 Wang Y, Hekimi S. Micellization of coenzyme Q by the fungicide caspofungin allows for safe intravenous administration to reach extreme supraphysiological concentrations. Redox Biol 2020;36:101680. [PMID: 32810741 DOI: 10.1016/j.redox.2020.101680] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
23 Quinzii CM, Lopez LC. Abnormalities of hydrogen sulfide and glutathione pathways in mitochondrial dysfunction. J Adv Res 2021;27:79-84. [PMID: 33318868 DOI: 10.1016/j.jare.2020.04.002] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
24 Ren J, Dai C. Pathophysiology of Chronic Kidney Disease. Chronic Kidney Disease 2020. [DOI: 10.1007/978-981-32-9131-7_2] [Reference Citation Analysis]
25 Han Q, Yang C, Lu J, Zhang Y, Li J. Metabolism of Oxalate in Humans: A Potential Role Kynurenine Aminotransferase/Glutamine Transaminase/Cysteine Conjugate Beta-lyase Plays in Hyperoxaluria. Curr Med Chem 2019. [PMID: 30907303 DOI: 10.2174/0929867326666190325095223] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
26 Ben-Meir A, Kim K, McQuaid R, Esfandiari N, Bentov Y, Casper RF, Jurisicova A. Co-Enzyme Q10 Supplementation Rescues Cumulus Cells Dysfunction in a Maternal Aging Model. Antioxidants (Basel) 2019;8:E58. [PMID: 30857157 DOI: 10.3390/antiox8030058] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 5.8] [Reference Citation Analysis]
27 Widmeier E, Airik M, Hugo H, Schapiro D, Wedel J, Ghosh CC, Nakayama M, Schneider R, Awad AM, Nag A, Cho J, Schueler M, Clarke CF, Airik R, Hildebrandt F. Treatment with 2,4-Dihydroxybenzoic Acid Prevents FSGS Progression and Renal Fibrosis in Podocyte-Specific Coq6 Knockout Mice. J Am Soc Nephrol 2019;30:393-405. [PMID: 30737270 DOI: 10.1681/ASN.2018060625] [Cited by in Crossref: 27] [Cited by in F6Publishing: 29] [Article Influence: 6.8] [Reference Citation Analysis]
28 Song CC, Hong Q, Geng XD, Wang X, Wang SQ, Cui SY, Guo MD, Li O, Cai GY, Chen XM, Wu D. New Mutation of Coenzyme Q10 Monooxygenase 6 Causing Podocyte Injury in a Focal Segmental Glomerulosclerosis Patient. Chin Med J (Engl) 2018;131:2666-75. [PMID: 30425193 DOI: 10.4103/0366-6999.245158] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
29 Kleiner G, Barca E, Ziosi M, Emmanuele V, Xu Y, Hidalgo-Gutierrez A, Qiao C, Tadesse S, Area-Gomez E, Lopez LC, Quinzii CM. CoQ10 supplementation rescues nephrotic syndrome through normalization of H2S oxidation pathway. Biochim Biophys Acta Mol Basis Dis 2018;1864:3708-22. [PMID: 30251690 DOI: 10.1016/j.bbadis.2018.09.002] [Cited by in Crossref: 28] [Cited by in F6Publishing: 29] [Article Influence: 5.6] [Reference Citation Analysis]
30 Cauvi D, Hultman P, Pollard K. Autoimmune Models. Comprehensive Toxicology 2018. [DOI: 10.1016/b978-0-08-100601-6.02004-4] [Reference Citation Analysis]
31 Hughes BG, Harrison PM, Hekimi S. Estimating the occurrence of primary ubiquinone deficiency by analysis of large-scale sequencing data. Sci Rep 2017;7:17744. [PMID: 29255295 DOI: 10.1038/s41598-017-17564-y] [Cited by in Crossref: 25] [Cited by in F6Publishing: 25] [Article Influence: 4.2] [Reference Citation Analysis]
32 Kuszak AJ, Espey MG, Falk MJ, Holmbeck MA, Manfredi G, Shadel GS, Vernon HJ, Zolkipli-Cunningham Z. Nutritional Interventions for Mitochondrial OXPHOS Deficiencies: Mechanisms and Model Systems. Annu Rev Pathol 2018;13:163-91. [PMID: 29099651 DOI: 10.1146/annurev-pathol-020117-043644] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 2.8] [Reference Citation Analysis]
33 Quinzii CM, Luna-Sanchez M, Ziosi M, Hidalgo-Gutierrez A, Kleiner G, Lopez LC. The Role of Sulfide Oxidation Impairment in the Pathogenesis of Primary CoQ Deficiency. Front Physiol 2017;8:525. [PMID: 28790927 DOI: 10.3389/fphys.2017.00525] [Cited by in Crossref: 30] [Cited by in F6Publishing: 30] [Article Influence: 5.0] [Reference Citation Analysis]
34 González-Mariscal I, Martín-Montalvo A, Ojeda-González C, Rodríguez-Eguren A, Gutiérrez-Ríos P, Navas P, Santos-Ocaña C. Balanced CoQ6 biosynthesis is required for lifespan and mitophagy in yeast. Microb Cell 2017;4:38-51. [PMID: 28357388 DOI: 10.15698/mic2017.02.556] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 2.0] [Reference Citation Analysis]
35 Duann P, Lin PH. Mitochondria Damage and Kidney Disease. Adv Exp Med Biol 2017;982:529-51. [PMID: 28551805 DOI: 10.1007/978-3-319-55330-6_27] [Cited by in Crossref: 72] [Cited by in F6Publishing: 75] [Article Influence: 12.0] [Reference Citation Analysis]
36 Quinzii C, Hirano M. Ataxia (Familial Cerebellar) With Muscle CoQ10 Deficiency☆. Reference Module in Neuroscience and Biobehavioral Psychology 2017. [DOI: 10.1016/b978-0-12-809324-5.00484-3] [Reference Citation Analysis]
37 Bora NM, Garg R, Kumari SS, Devineni K, Agrawal V. CoQ10-Mitochondrial Energizer in Ageing Oocytes and female infertility. Journal of South Asian Federation of Obstetrics and Gynaecology 2016;8:253-255. [DOI: 10.5005/jp-journals-10006-1429] [Reference Citation Analysis]
38 Wang Y, Hekimi S. Understanding Ubiquinone. Trends in Cell Biology 2016;26:367-78. [DOI: 10.1016/j.tcb.2015.12.007] [Cited by in Crossref: 126] [Cited by in F6Publishing: 130] [Article Influence: 18.0] [Reference Citation Analysis]
39 Emma F, Montini G, Parikh SM, Salviati L. Mitochondrial dysfunction in inherited renal disease and acute kidney injury. Nat Rev Nephrol 2016;12:267-80. [PMID: 26804019 DOI: 10.1038/nrneph.2015.214] [Cited by in Crossref: 196] [Cited by in F6Publishing: 208] [Article Influence: 28.0] [Reference Citation Analysis]
40 Luna-Sánchez M, Díaz-Casado E, Barca E, Tejada MÁ, Montilla-García Á, Cobos EJ, Escames G, Acuña-Castroviejo D, Quinzii CM, López LC. The clinical heterogeneity of coenzyme Q10 deficiency results from genotypic differences in the Coq9 gene. EMBO Mol Med 2015;7:670-87. [PMID: 25802402 DOI: 10.15252/emmm.201404632] [Cited by in Crossref: 60] [Cited by in F6Publishing: 64] [Article Influence: 8.6] [Reference Citation Analysis]
41 Quinzii CM, Loos M. Multisystemic Infantile CoQ10 Deficiency with Renal Involvement. Mitochondrial Case Studies 2016. [DOI: 10.1016/b978-0-12-800877-5.00035-8] [Reference Citation Analysis]
42 Shiobara Y, Harada C, Shiota T, Sakamoto K, Kita K, Tanaka S, Tabata K, Sekie K, Yamamoto Y, Sugiyama T. Knockdown of the coenzyme Q synthesis gene Smed-dlp1 affects planarian regeneration and tissue homeostasis. Redox Biol 2015;6:599-606. [PMID: 26516985 DOI: 10.1016/j.redox.2015.10.004] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
43 Ben-Meir A, Burstein E, Borrego-Alvarez A, Chong J, Wong E, Yavorska T, Naranian T, Chi M, Wang Y, Bentov Y, Alexis J, Meriano J, Sung HK, Gasser DL, Moley KH, Hekimi S, Casper RF, Jurisicova A. Coenzyme Q10 restores oocyte mitochondrial function and fertility during reproductive aging. Aging Cell 2015;14:887-95. [PMID: 26111777 DOI: 10.1111/acel.12368] [Cited by in Crossref: 216] [Cited by in F6Publishing: 232] [Article Influence: 27.0] [Reference Citation Analysis]
44 Freyer C, Stranneheim H, Naess K, Mourier A, Felser A, Maffezzini C, Lesko N, Bruhn H, Engvall M, Wibom R, Barbaro M, Hinze Y, Magnusson M, Andeer R, Zetterström RH, von Döbeln U, Wredenberg A, Wedell A. Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid. J Med Genet 2015;52:779-83. [PMID: 26084283 DOI: 10.1136/jmedgenet-2015-102986] [Cited by in Crossref: 70] [Cited by in F6Publishing: 74] [Article Influence: 8.8] [Reference Citation Analysis]
45 Elguindy MM, Nakamaru-Ogiso E. Apoptosis-inducing Factor (AIF) and Its Family Member Protein, AMID, Are Rotenone-sensitive NADH:Ubiquinone Oxidoreductases (NDH-2). J Biol Chem 2015;290:20815-26. [PMID: 26063804 DOI: 10.1074/jbc.M115.641498] [Cited by in Crossref: 63] [Cited by in F6Publishing: 66] [Article Influence: 7.9] [Reference Citation Analysis]
46 Peng M, Ostrovsky J, Kwon YJ, Polyak E, Licata J, Tsukikawa M, Marty E, Thomas J, Felix CA, Xiao R, Zhang Z, Gasser DL, Argon Y, Falk MJ. Inhibiting cytosolic translation and autophagy improves health in mitochondrial disease. Hum Mol Genet 2015;24:4829-47. [PMID: 26041819 DOI: 10.1093/hmg/ddv207] [Cited by in Crossref: 50] [Cited by in F6Publishing: 52] [Article Influence: 6.3] [Reference Citation Analysis]
47 Huang W, Gao F, Li K, Wang W, Lai YR, Tang SH, Yang DH. Decaprenyl diphosphate synthase subunit 2 as a prognosis factor in hepatocellular carcinoma. World J Gastroenterol 2015; 21(10): 3055-3065 [PMID: 25780306 DOI: 10.3748/wjg.v21.i10.3055] [Cited by in CrossRef: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
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50 Cauvi D, Hultman P, Pollard K. Autoimmune Models☆. Reference Module in Biomedical Sciences 2015. [DOI: 10.1016/b978-0-12-801238-3.02004-3] [Reference Citation Analysis]
51 Mondini A, Messa P, Rastaldi MP. The sclerosing glomerulus in mice and man: novel insights. Curr Opin Nephrol Hypertens 2014;23:239-44. [PMID: 24709948 DOI: 10.1097/01.mnh.0000444817.95496.40] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.6] [Reference Citation Analysis]
52 Feng C, Gao Y, Dorshorst B, Song C, Gu X, Li Q, Li J, Liu T, Rubin CJ, Zhao Y, Wang Y, Fei J, Li H, Chen K, Qu H, Shu D, Ashwell C, Da Y, Andersson L, Hu X, Li N. A cis-regulatory mutation of PDSS2 causes silky-feather in chickens. PLoS Genet 2014;10:e1004576. [PMID: 25166907 DOI: 10.1371/journal.pgen.1004576] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 2.2] [Reference Citation Analysis]
53 Licitra F, Puccio H. An overview of current mouse models recapitulating coenzyme q10 deficiency syndrome. Mol Syndromol 2014;5:180-6. [PMID: 25126051 DOI: 10.1159/000362942] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 1.8] [Reference Citation Analysis]
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55 Fernández-Ayala DJ, Jiménez-Gancedo S, Guerra I, Navas P. Invertebrate models for coenzyme q10 deficiency. Mol Syndromol 2014;5:170-9. [PMID: 25126050 DOI: 10.1159/000362751] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.8] [Reference Citation Analysis]
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60 Zhang Z, Falk MJ. Integrated transcriptome analysis across mitochondrial disease etiologies and tissues improves understanding of common cellular adaptations to respiratory chain dysfunction. Int J Biochem Cell Biol 2014;50:106-11. [PMID: 24569120 DOI: 10.1016/j.biocel.2014.02.012] [Cited by in Crossref: 28] [Cited by in F6Publishing: 28] [Article Influence: 3.1] [Reference Citation Analysis]
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63 Doimo M, Trevisson E, Airik R, Bergdoll M, Santos-Ocaña C, Hildebrandt F, Navas P, Pierrel F, Salviati L. Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiency. Biochim Biophys Acta 2014;1842:1-6. [PMID: 24140869 DOI: 10.1016/j.bbadis.2013.10.007] [Cited by in Crossref: 56] [Cited by in F6Publishing: 60] [Article Influence: 5.6] [Reference Citation Analysis]
64 Manoli I, Sysol JR, Li L, Houillier P, Garone C, Wang C, Zerfas PM, Cusmano-Ozog K, Young S, Trivedi NS, Cheng J, Sloan JL, Chandler RJ, Abu-Asab M, Tsokos M, Elkahloun AG, Rosen S, Enns GM, Berry GT, Hoffmann V, DiMauro S, Schnermann J, Venditti CP. Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia. Proc Natl Acad Sci U S A 2013;110:13552-7. [PMID: 23898205 DOI: 10.1073/pnas.1302764110] [Cited by in Crossref: 76] [Cited by in F6Publishing: 79] [Article Influence: 7.6] [Reference Citation Analysis]
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