Pages that link to "Q36532577"
Jump to navigation
Jump to search
The following pages link to Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease (Q36532577):
Displaying 50 items.
- The rise of mitochondria in medicine (Q26740014) (← links)
- Genetic manipulation for inherited neurodegenerative diseases: myth or reality? (Q26752831) (← links)
- Mitochondrial disease in adults: what's old and what's new? (Q26776417) (← links)
- Prevalence of neurogenetic disorders in the North of England (Q26784050) (← links)
- Resources, challenges and way forward in rare mitochondrial diseases research (Q26800675) (← links)
- A neurodegenerative perspective on mitochondrial optic neuropathies (Q28072026) (← links)
- Genetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum Disorder (Q28553061) (← links)
- Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutation: data from the German mitoNET registry (Q31060952) (← links)
- Autonomic, functional, skeletal muscle, and cardiac abnormalities are associated with increased ergoreflex sensitivity in mitochondrial disease (Q31165571) (← links)
- Quantification of gait in mitochondrial m.3243A > G patients: a validation study (Q33691343) (← links)
- Disease-associated mitochondrial mutations and the evolution of primate mitogenomes. (Q33693717) (← links)
- Hypoxia treatment reverses neurodegenerative disease in a mouse model of Leigh syndrome. (Q33737837) (← links)
- Mitochondrial dysfunction in inherited renal disease and acute kidney injury (Q33793389) (← links)
- Short-term serum deprivation causes no significant mitochondrial DNA mutation in vascular smooth muscle cells revealed by a new next generation sequencing technology (Q34529641) (← links)
- A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency (Q35829584) (← links)
- Potential compounds for the treatment of mitochondrial disease. (Q35847813) (← links)
- A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis. (Q36164488) (← links)
- A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease (Q36277419) (← links)
- Nucleotide pools dictate the identity and frequency of ribonucleotide incorporation in mitochondrial DNA. (Q36282442) (← links)
- LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population. (Q36305492) (← links)
- Clinically proven mtDNA mutations are not common in those with chronic fatigue syndrome. (Q36311088) (← links)
- Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project. (Q36311644) (← links)
- Mitochondrial functions modulate neuroendocrine, metabolic, inflammatory, and transcriptional responses to acute psychological stress (Q36354896) (← links)
- Mitochondrial disease: genetics and management (Q36492283) (← links)
- Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck (Q36581411) (← links)
- Attitudes toward prevention of mtDNA-related diseases through oocyte mitochondrial replacement therapy (Q36823140) (← links)
- Hypoxia as a therapy for mitochondrial disease. (Q36882394) (← links)
- Modifying the Mitochondrial Genome (Q36894373) (← links)
- Clinical and Molecular Characteristics in 100 Chinese Pediatric Patients with m.3243A>G Mutation in Mitochondrial DNA (Q37185443) (← links)
- Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults (Q37225729) (← links)
- A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype (Q37235772) (← links)
- Clinical features of the pathogenic m.5540G>A mitochondrial transfer RNA tryptophan gene mutation. (Q37343266) (← links)
- The genetics and pathology of mitochondrial disease. (Q37560946) (← links)
- Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination. (Q37561288) (← links)
- Adult Onset Leigh Syndrome in the Intensive Care Setting: A Novel Presentation of a C12orf65 Related Mitochondrial Disease (Q37589775) (← links)
- Identification of miRNA, lncRNA and mRNA-associated ceRNA networks and potential biomarker for MELAS with mitochondrial DNA A3243G mutation (Q37615347) (← links)
- Mitochondrial Myopathy in Follow-up of a Patient With Chronic Fatigue Syndrome (Q38338320) (← links)
- Hospitalizations for mitochondrial disease across the lifespan in the U.S. (Q38401402) (← links)
- Mutations causing mitochondrial disease: What is new and what challenges remain? (Q38592664) (← links)
- Pharmacologic modeling of primary mitochondrial respiratory chain dysfunction in zebrafish (Q38653585) (← links)
- Mitochondrial Mutations in Cardiac Disorders (Q38678063) (← links)
- Novel reproductive technologies to prevent mitochondrial disease (Q38708531) (← links)
- Mitochondrial DNA mutations and cardiovascular disease (Q38760397) (← links)
- Review: Central nervous system involvement in mitochondrial disease (Q38861730) (← links)
- Presentation and Diagnostic Evaluation of Mitochondrial Disease. (Q39022446) (← links)
- Clinical Features, Molecular Heterogeneity, and Prognostic Implications in YARS2-Related Mitochondrial Myopathy (Q39232047) (← links)
- Genetic Counselling for Maternally Inherited Mitochondrial Disorders. (Q39325696) (← links)
- Concise Review: Induced Pluripotent Stem Cell-Based Drug Discovery for Mitochondrial Disease. (Q39330002) (← links)
- Mitochondrial disease patients' perception of dietary supplements' use. (Q39573813) (← links)
- Sustained AMPK activation improves muscle function in a mitochondrial myopathy mouse model by promoting muscle fiber regeneration (Q39732168) (← links)