Zhang L, Hall G, Han P, Li C, Cui J
Front Pediatr. 2025; 12:1378083.
PMID: 39877334
PMC: 11772357.
DOI: 10.3389/fped.2024.1378083.
Park P, Choi S, Ahn Y, Kim S, Kim C, Kim H
Pediatr Nephrol. 2025; .
PMID: 39805995
DOI: 10.1007/s00467-024-06611-2.
Wahedi A, Sudhakar S, Lam A, Ciancio J, Mills P, Gissen P
Neurol Genet. 2024; 10(6):e200209.
PMID: 39601013
PMC: 11595325.
DOI: 10.1212/NXG.0000000000200209.
Pan P, Zhou N, Sun Y, Chen Z, Han J, Zhou W
Front Pediatr. 2024; 12:1410133.
PMID: 39398416
PMC: 11466766.
DOI: 10.3389/fped.2024.1410133.
Hernandez-Camacho J, Vicente-Garcia C, Ardila-Garcia L, Padilla-Campos A, Lopez-Lluch G, Santos-Ocana C
J Cachexia Sarcopenia Muscle. 2024; 15(6):2402-2416.
PMID: 39354863
PMC: 11634497.
DOI: 10.1002/jcsm.13574.
Primary Coenzyme Q10 Deficiency-Related Ataxias.
Lopriore P, Vista M, Tessa A, Giuntini M, Caldarazzo Ienco E, Mancuso M
J Clin Med. 2024; 13(8).
PMID: 38673663
PMC: 11050807.
DOI: 10.3390/jcm13082391.
Diverse retinal-kidney phenotypes associated with homozygous whole-gene deletions in patients with kidney failure.
Esson G, Logan I, Wood K, Browning A, Sayer J
J Rare Dis (Berlin). 2024; 3(1):7.
PMID: 38433745
PMC: 10904492.
DOI: 10.1007/s44162-024-00031-4.
Focus on Mitochondrial Respiratory Chain: Potential Therapeutic Target for Chronic Renal Failure.
Wang Y, Yang J, Zhang Y, Zhou J
Int J Mol Sci. 2024; 25(2).
PMID: 38256023
PMC: 10815764.
DOI: 10.3390/ijms25020949.
Mitochondrial electron transport chain, ceramide, and coenzyme Q are linked in a pathway that drives insulin resistance in skeletal muscle.
Diaz-Vegas A, Madsen S, Cooke K, Carroll L, Khor J, Turner N
Elife. 2023; 12.
PMID: 38149844
PMC: 10752590.
DOI: 10.7554/eLife.87340.
Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease.
Marasa M, Ahram D, Rehman A, Mitrotti A, Abhyankar A, Jain N
Kidney Int Rep. 2023; 8(8):1638-1647.
PMID: 37547535
PMC: 10403677.
DOI: 10.1016/j.ekir.2023.05.021.
Biosynthesis, Deficiency, and Supplementation of Coenzyme Q.
Staiano C, Garcia-Corzo L, Mantle D, Turton N, Millichap L, Brea-Calvo G
Antioxidants (Basel). 2023; 12(7).
PMID: 37508007
PMC: 10375973.
DOI: 10.3390/antiox12071469.
New Insights on the Uptake and Trafficking of Coenzyme Q.
Guile M, Jain A, Anderson K, Clarke C
Antioxidants (Basel). 2023; 12(7).
PMID: 37507930
PMC: 10376127.
DOI: 10.3390/antiox12071391.
New insights from trio whole-exome sequencing in the children with kidney disease: A single-center retrospective cohort study.
Chen Y, Zhang Y, Huang J, Zeng Y, Qian Y, Chen J
Mol Genet Genomic Med. 2023; 11(7):e2163.
PMID: 37248651
PMC: 10337271.
DOI: 10.1002/mgg3.2163.
Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases.
Liang R, Chen X, Zhang Y, Law C, Yu S, Jiao J
Front Pediatr. 2023; 10:1030191.
PMID: 36843884
PMC: 9948246.
DOI: 10.3389/fped.2022.1030191.
Mitochondria regulate intracellular coenzyme Q transport and ferroptotic resistance via STARD7.
Deshwal S, Onishi M, Tatsuta T, Bartsch T, Cors E, Ried K
Nat Cell Biol. 2023; 25(2):246-257.
PMID: 36658222
PMC: 9928583.
DOI: 10.1038/s41556-022-01071-y.
Total and reduced/oxidized forms of coenzyme Q in fibroblasts of patients with mitochondrial disease.
Watanabe C, Osaka H, Watanabe M, Miyauchi A, Jimbo E, Tokuyama T
Mol Genet Metab Rep. 2023; 34:100951.
PMID: 36632326
PMC: 9826971.
DOI: 10.1016/j.ymgmr.2022.100951.
Predicting and Understanding the Pathology of Single Nucleotide Variants in Human Genes.
Wang S, Jain A, Novales N, Nashner A, Tran F, Clarke C
Antioxidants (Basel). 2022; 11(12).
PMID: 36552517
PMC: 9774615.
DOI: 10.3390/antiox11122308.
Role of abnormal energy metabolism in the progression of chronic kidney disease and drug intervention.
Liu X, Du H, Sun Y, Shao L
Ren Fail. 2022; 44(1):790-805.
PMID: 35535500
PMC: 9103584.
DOI: 10.1080/0886022X.2022.2072743.
Mechanisms of podocyte injury and implications for diabetic nephropathy.
Barutta F, Bellini S, Gruden G
Clin Sci (Lond). 2022; 136(7):493-520.
PMID: 35415751
PMC: 9008595.
DOI: 10.1042/CS20210625.
Primary Coenzyme Q10 Deficiency-7 and Pathogenic Variants: Clinical Presentation, Biochemical Analyses, and Treatment.
Xie J, Jiang J, Guo Q
Front Genet. 2022; 12:776807.
PMID: 35154243
PMC: 8826242.
DOI: 10.3389/fgene.2021.776807.
