Filamentous Fungi and Yeasts as Sources of Coenzyme Q10 and Its Applications
P Tokdar, P Ranadive, S George - Fungal Biotechnology, 2022 - taylorfrancis.com
Coenzyme Q or CoQ is also known as ubiquinone is a benzoquinone that is present in
human, animals and most living beings but its isoprene units varies in different living entities …
human, animals and most living beings but its isoprene units varies in different living entities …
Coenzyme Q10 deficiency in children: Frequent type 2C muscle fibers with normal morphology
RB Sommerville, CM Zaidman, A Pestronk - Muscle & nerve, 2013 - Wiley Online Library
Introduction: Neurological disorders with low tissue coenzyme Q10 (CoQ10) levels are
important to identify, as they may be treatable. Methods: We evaluated retrospectively …
important to identify, as they may be treatable. Methods: We evaluated retrospectively …
The Effect of Alhagi maurorum Medik on Mitochondrial Function
J Zulfiqar - 2023 - westminsterresearch.westminster.ac …
Mitochondrial bioenergetics are crucial for the optimal activity of the cell and are emerging
therapeutic targets for the treatment of several metabolic syndromes and cancer. Alhagi …
therapeutic targets for the treatment of several metabolic syndromes and cancer. Alhagi …
[HTML][HTML] Coenzyme Q10: Current Overview
K Erdoğan, MS Macit, NT Şanlıer… - Türk Kadın Sağlığı ve …, 2022 - dergipark.org.tr
Coenzyme Q10 (CoQ10) is a lipid-soluble component from benzoquinones. The oxidized
form of Coenzyme Q10 is ubiquinone, and the reduced form is ubiquinol. As well to its …
form of Coenzyme Q10 is ubiquinone, and the reduced form is ubiquinol. As well to its …
Hereditary Neuromuscular Diseases. Part 3. Muscular Dystrophies: Pathogenesis, Diagnosis and Attempts of Trial Treatments
VM Kazakov, AA Skoromets, DI Rudenko… - Russian neurological …, 2020 - rnj.com
Membrane theory of muscle weakness in hereditary muscular dystrophy was described with
accent of predominated Ca 2+ ions in skeletal muscle due to destruction of the sarcolemma …
accent of predominated Ca 2+ ions in skeletal muscle due to destruction of the sarcolemma …
Current biochemical treatments of mitochondrial respiratory chain disorders
R Heaton, L Millichap, F Saleem, J Gannon… - Expert Opinion on …, 2019 - Taylor & Francis
Introduction: The clinical heterogeneity and unpredictable clinical course of mitochondrial
respiratory chain (MRC) disorders have hindered the development of effective therapeutic …
respiratory chain (MRC) disorders have hindered the development of effective therapeutic …
Studying the role of coenzyme Q10 in mitochondrial calcium and redox signaling
Z Bonilla del Río - 2022 - ediss.uni-goettingen.de
LETM1: leucine zipper-EF-hand-containing transmembrane protein 1 LPO: lipid
peroxidation mΔΨ: mitochondrial membrane potential mCa2+: mitochondrial matrix Ca2+ …
peroxidation mΔΨ: mitochondrial membrane potential mCa2+: mitochondrial matrix Ca2+ …
核黄素反应性多种酰基辅酶A 脱氢酶缺乏症
伏红霞， 朱润秀 - 中国医师杂志, 2015 - cqvip.com
核黄素反应性多种酰基辅酶A 脱氢酶缺乏症(riboflavin responsive-multiple acyl-CoA
dehydrogenase deficiency, RRMADD) 是由于缺乏ETF (electron transfer flavoprotein) …
dehydrogenase deficiency, RRMADD) 是由于缺乏ETF (electron transfer flavoprotein) …
[HTML][HTML] Диагностическое значение показателя коэнзима q 10 в крови у детей с митохондриальными заболеваниями
ЕА Николаева, МН Харабадзе… - Российский вестник …, 2015 - cyberleninka.ru
С целью установления диагностической значимости изменения показателя коэнзима Q
10 проведено исследование его уровня в крови у 15 детей с митохондриальными …
10 проведено исследование его уровня в крови у 15 детей с митохондриальными …
[PDF][PDF] Studying the Role of Coenzyme Q10 in Mitochondrial Calcium and Redox Signaling
ZB del Río - 2022 - d-nb.info
LETM1: leucine zipper-EF-hand-containing transmembrane protein 1 LPO: lipid
peroxidation mΔΨ: mitochondrial membrane potential mCa2+: mitochondrial matrix Ca2+ …
peroxidation mΔΨ: mitochondrial membrane potential mCa2+: mitochondrial matrix Ca2+ …