Search details
1.
Coenzyme Q10 and Autoimmune Disorders: An Overview.
Int J Mol Sci
; 25(8)2024 Apr 22.
Article
in English
| MEDLINE | ID: mdl-38674161
2.
Potential Biomarkers of Mitochondrial Dysfunction Associated with COVID-19 Infection.
Adv Exp Med Biol
; 1412: 211-224, 2023.
Article
in English
| MEDLINE | ID: mdl-37378769
3.
Maternal but not fetoplacental health can be improved by metformin in a murine diet-induced model of maternal obesity and glucose intolerance.
J Physiol
; 600(4): 903-919, 2022 02.
Article
in English
| MEDLINE | ID: mdl-34505282
4.
Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies.
Int J Mol Sci
; 23(18)2022 Sep 12.
Article
in English
| MEDLINE | ID: mdl-36142486
5.
The Biochemical Assessment of Mitochondrial Respiratory Chain Disorders.
Int J Mol Sci
; 23(13)2022 Jul 05.
Article
in English
| MEDLINE | ID: mdl-35806492
6.
Expression of mutant exon 1 huntingtin fragments in human neural stem cells and neurons causes inclusion formation and mitochondrial dysfunction.
FASEB J
; 34(6): 8139-8154, 2020 06.
Article
in English
| MEDLINE | ID: mdl-32329133
7.
The Effect of Organophosphate Exposure on Neuronal Cell Coenzyme Q10 Status.
Neurochem Res
; 46(1): 131-139, 2021 Jan.
Article
in English
| MEDLINE | ID: mdl-32306167
8.
Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial disease.
Mol Biol Rep
; 48(3): 2093-2104, 2021 Mar.
Article
in English
| MEDLINE | ID: mdl-33742325
9.
Targeted Treatment of Age-Related Fibromyalgia with Supplemental Coenzyme Q10.
Adv Exp Med Biol
; 1286: 77-85, 2021.
Article
in English
| MEDLINE | ID: mdl-33725346
10.
Targetable Pathways for Alleviating Mitochondrial Dysfunction in Neurodegeneration of Metabolic and Non-Metabolic Diseases.
Int J Mol Sci
; 22(21)2021 Oct 23.
Article
in English
| MEDLINE | ID: mdl-34768878
11.
The Effect of Methylmalonic Acid Treatment on Human Neuronal Cell Coenzyme Q10 Status and Mitochondrial Function.
Int J Mol Sci
; 21(23)2020 Nov 30.
Article
in English
| MEDLINE | ID: mdl-33266298
12.
Differential phenotypic expression of a novel PDHA1 mutation in a female monozygotic twin pair.
Hum Genet
; 138(11-12): 1313-1322, 2019 Dec.
Article
in English
| MEDLINE | ID: mdl-31673819
13.
Coenzyme Q10 Supplementation in Fibrosis and Aging.
Adv Exp Med Biol
; 1178: 103-112, 2019.
Article
in English
| MEDLINE | ID: mdl-31493224
14.
Assessment of Mitochondrial Dysfunction in Experimental Autoimmune Encephalomyelitis (EAE) Models of Multiple Sclerosis.
Int J Mol Sci
; 20(20)2019 Oct 09.
Article
in English
| MEDLINE | ID: mdl-31600882
15.
Integrated Approach Reveals Role of Mitochondrial Germ-Line Mutation F18L in Respiratory Chain, Oxidative Alterations, Drug Sensitivity, and Patient Prognosis in Glioblastoma.
Int J Mol Sci
; 20(13)2019 Jul 09.
Article
in English
| MEDLINE | ID: mdl-31323957
16.
A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype.
J Med Genet
; 53(9): 634-41, 2016 09.
Article
in English
| MEDLINE | ID: mdl-27091925
17.
A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency.
Hum Genet
; 134(8): 869-79, 2015 Aug.
Article
in English
| MEDLINE | ID: mdl-26008905
18.
Nutritional programming of coenzyme Q: potential for prevention and intervention?
FASEB J
; 28(12): 5398-405, 2014 Dec.
Article
in English
| MEDLINE | ID: mdl-25172893
19.
Zellweger syndrome and secondary mitochondrial myopathy.
Eur J Pediatr
; 174(4): 557-63, 2015 Apr.
Article
in English
| MEDLINE | ID: mdl-25287621
20.
The ketogenic diet component decanoic acid increases mitochondrial citrate synthase and complex I activity in neuronal cells.
J Neurochem
; 129(3): 426-33, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24383952