Sarcopenia: aging-related loss of muscle mass and function
Sarcopenia is a loss of muscle mass and function in the elderly that reduces mobility,
diminishes quality of life, and can lead to fall-related injuries, which require costly …
diminishes quality of life, and can lead to fall-related injuries, which require costly …
[HTML][HTML] Coenzyme Q biosynthesis in health and disease
MJ Acosta, LV Fonseca, MA Desbats, C Cerqua… - … et Biophysica Acta (BBA …, 2016 - Elsevier
Coenzyme Q (CoQ, or ubiquinone) is a remarkable lipid that plays an essential role in
mitochondria as an electron shuttle between complexes I and II of the respiratory chain, and …
mitochondria as an electron shuttle between complexes I and II of the respiratory chain, and …
[HTML][HTML] ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption
S Ashraf, HY Gee, S Woerner, LX Xie… - The Journal of …, 2013 - Am Soc Clin Investig
Identification of single-gene causes of steroid-resistant nephrotic syndrome (SRNS) has
furthered the understanding of the pathogenesis of this disease. Here, using a combination …
furthered the understanding of the pathogenesis of this disease. Here, using a combination …
[HTML][HTML] COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
SF Heeringa, G Chernin, M Chaki… - The Journal of …, 2011 - Am Soc Clin Investig
Steroid-resistant nephrotic syndrome (SRNS) is a frequent cause of end-stage renal failure.
Identification of single-gene causes of SRNS has generated some insights into its …
Identification of single-gene causes of SRNS has generated some insights into its …
Identification of UBIAD1 as a novel human menaquinone-4 biosynthetic enzyme
K Nakagawa, Y Hirota, N Sawada, N Yuge… - Nature, 2010 - nature.com
Vitamin K occurs in the natural world in several forms, including a plant form, phylloquinone
(PK), and a bacterial form, menaquinones (MKs). In many species, including humans, PK is …
(PK), and a bacterial form, menaquinones (MKs). In many species, including humans, PK is …
Genetic bases and clinical manifestations of coenzyme Q10 (CoQ10) deficiency
MA Desbats, G Lunardi, M Doimo, E Trevisson… - Journal of inherited …, 2015 - Springer
Coenzyme Q 10 is a remarkable lipid involved in many cellular processes such as energy
production through the mitochondrial respiratory chain (RC), beta-oxidation of fatty acids …
production through the mitochondrial respiratory chain (RC), beta-oxidation of fatty acids …
Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy
Multiple-System Atrophy Research … - New England Journal …, 2013 - Mass Medical Soc
Background Multiple-system atrophy is an intractable neurodegenerative disease
characterized by autonomic failure in addition to various combinations of parkinsonism …
characterized by autonomic failure in addition to various combinations of parkinsonism …
[HTML][HTML] Coenzyme Q biosynthesis and its role in the respiratory chain structure
M Alcázar-Fabra, P Navas, G Brea-Calvo - Biochimica et Biophysica Acta …, 2016 - Elsevier
Coenzyme Q (CoQ) is a unique electron carrier in the mitochondrial respiratory chain, which
is synthesized on-site by a nuclear encoded multiprotein complex. CoQ receives electrons …
is synthesized on-site by a nuclear encoded multiprotein complex. CoQ receives electrons …
[HTML][HTML] Mitochondrial neurodegeneration
M Zeviani, C Viscomi - Cells, 2022 - mdpi.com
Mitochondria are cytoplasmic organelles, which generate energy as heat and ATP, the
universal energy currency of the cell. This process is carried out by coupling electron …
universal energy currency of the cell. This process is carried out by coupling electron …
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement
F Diomedi-Camassei, S Di Giandomenico… - Journal of the …, 2007 - journals.lww.com
Abstract Primary coenzyme Q 10 (CoQ 10) deficiency includes a group of rare autosomal
recessive disorders primarily characterized by neurological and muscular symptoms. Rarely …
recessive disorders primarily characterized by neurological and muscular symptoms. Rarely …