supported by a grant from the Zhejiang Provincial Natural Science Foundation of China(No.LY22H050002)
Over the past decade,mitochondrial dysfunction has been investigated as a key contributor to acute and chronic kidney disease.However,the precise molecular mechanisms linking mitochondrial damage to kidney disease rem...
the Capital Clinic Research and Demonstration Application of Diagnosis and Treatment Project(No.Z201100005520038).
To the Editor:Both pathogen-associated molecular patterns and damage-associated molecular patterns(DAMPs)are known to enhance levels of inflammation and tissue injury during sepsis.Mitochondria are a major source of D...
To the Editor: Mitochondrial diseases are a common group of human genetic diseases that can occur at any decade of life. Mitochondrial DNA (mtDNA) mutations are responsible for most adult-onset mitochondrial diseases....
grants from the National Natural Science Foundation of China (No. 81671235 and No. 81701237);People's Benefit Project of Science and Technology in Qingdao (No. 16-6-2-1-nsh) and the Taishan Scholars Program of Shandong Province.
To the Editor: Mitochondrial encephalomyopathy with lactate acidosis and stroke-like episodes (MELAS) is one of the most common multisystem mitochondrial disorders with broad clinical manifestations.[1] It is usually ...
This study was supported by grants from the National Natural Science Foundation of China (No. 81271256 and No. 81471153) and Beijing Municipal Science and Technology Commission (No. Z 131107002213062).
Background: Mitocbondrial DNA (mtDNA) content measured by different techniques cannot be compared between studies, and age- and tissue-related control values are hardly available. In the present study, we aimed to ...
Thank you for your valuable comments on our paper, "A Mitochondrial DNAA8701G Mutation Associated with Maternally Inherited Hypertension and Dilated Cardiomyopathy in a Chinese Pedigree."We agree with this conclusio...
This study was supported by grants from National Natural Science Foundation of China (No. 81271256 and No. 81471153) and the Capital Characteristic Clinical Application Research Projects (No. Z 1311070022 13062).
Background: Mitochondrial diseases are a group of energy metabolic disorders with multisystem involvements. Variable clinical features present a major challenge in pediatric diagnoses. We summarized the clinical spec...
Background: Cardiovascular diseases, including dilated cardiomyopathy (DCM) and hypertension, are the leading cause of death worldwide.The role of mitochondrial DNA (mtDNA) in the pathogenesis of these diseases h...
This work was supported by the grant 81322017 from the National Natural Science Foundation of China, grant NCET-13-0736 from Program for New Century Excellent Talents in University, National Key Clinical Specialty Discipline Construction Program and Key Clinical Specialty Discipline Construction Program of Fujian.
Background: Mitochondrial dysflmction is linked to the pathogenesis of Parkinson's disease (PD). However, the precise role of mitochondrial DNA (mtDNA) variations is obscure. On the other hand, mtDNA haplogroups...
Background The mitochondrial displacement loop (D-loop) accumulates mutations and single nucleotide polymorphisms (SNPs) at a higher frequency than other regions of mitochondrial DNA (mtDNA).We previously identi...