Pages that link to "Q44219636"

The following pages link to Accumulation of somatic mutation in mitochondrial DNA extracted from peripheral blood cells in diabetic patients (Q44219636):

Displaying 21 items.

• Quantitative cellular level analysis of mitochondrial DNA 3243A > G mutations in individual tissues from the archival temporal bones of a MELAS patient (Q33494096) (← links)
• Correlation study on adiponectin gene SNP45 and long-term oxidative stress in patients with diabetes and carotid atherosclerosis (Q33962104) (← links)
• Role of somatic mutations in vascular disease formation (Q34059841) (← links)
• Somatic DNA damages in cardiovascular autonomic neuropathy (Q34747306) (← links)
• Rapid and sensitive real-time polymerase chain reaction method for detection and quantification of 3243A>G mitochondrial point mutation (Q35790141) (← links)
• Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approach (Q35988151) (← links)
• Mitochondrial dysfunction and mitochondrial DNA mutations in atherosclerotic complications in diabetes (Q35999426) (← links)
• Molecular mechanisms of mitochondrial diabetes (MIDD). (Q36194894) (← links)
• Linking the metabolic state and mitochondrial DNA in chronic disease, health, and aging (Q36635352) (← links)
• Mitochondrial disease: maintenance of mitochondrial genome and molecular diagnostics (Q36666800) (← links)
• Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation (Q37092297) (← links)
• Whole blood genome-wide expression profiling and network analysis suggest MELAS master regulators (Q38333915) (← links)
• Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men. (Q38889446) (← links)
• Bioinformatics Study of m.9053G>A Mutation at the ATP6 Gene in Relation to Type 2 Diabetes Mellitus and Cataract Diseases. (Q41079051) (← links)
• Dipeptidyl peptidase-4 inhibitor linagliptin attenuates neointima formation after vascular injury (Q43023352) (← links)
• Associations between hyperglycaemia and somatic transversion mutations in mitochondrial DNA of people with diabetes mellitus (Q44609199) (← links)
• Sperm Mitochondrial Mutations as a Cause of Low Sperm Motility (Q56689113) (← links)
• Heteroplasmy Detection of Mitochondrial DNA A3243G Mutation Using Quantitative Real-Time PCR Assay Based on TaqMan-MGB Probes (Q59808129) (← links)
• Current literature in diabetes (Q73210876) (← links)
• Acute metabolic cataract as a first manifestation of diabetes mellitus in a 12-year-old girl (Q80003588) (← links)
• TaqMan-MGB probe quantitative PCR assays to genotype and quantify three mtDNA mutations of Leber hereditary optic neuropathy (Q97681292) (← links)