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The MELAS mutation m.3243A>G promotes reactivation of fetal cardiac genes and an epithelial-mesenchymal transition-like program via dysregulation of miRNAs - ScienceDirect
The MELAS mutation m.3243A>G promotes reactivation of fetal cardiac genes and an epithelial-mesenchymal transition-like program via dysregulation of miRNAs - ScienceDirect

LHON/MELAS overlap syndrome associated with a mitochondrial MTND1 gene mutation | European Journal of Human Genetics
LHON/MELAS overlap syndrome associated with a mitochondrial MTND1 gene mutation | European Journal of Human Genetics

JCI - Neuronal degeneration and mitochondrial dysfunction
JCI - Neuronal degeneration and mitochondrial dysfunction

Nitric Oxide Deficiency: potential cause and therapeutic target for SLEs in MELAS - YouTube
Nitric Oxide Deficiency: potential cause and therapeutic target for SLEs in MELAS - YouTube

Gene organization of the human mt genome (center), in which MELAS... | Download Scientific Diagram
Gene organization of the human mt genome (center), in which MELAS... | Download Scientific Diagram

Current advances in gene therapy of mitochondrial diseases | Journal of Translational Medicine | Full Text
Current advances in gene therapy of mitochondrial diseases | Journal of Translational Medicine | Full Text

MELAS Syndrome | Hereditary Ocular Diseases
MELAS Syndrome | Hereditary Ocular Diseases

What is MT-TS1 Gene MERRF/MELAS overlap syndrome, MT-TS1 related NGS Genetic DNA Test ?
What is MT-TS1 Gene MERRF/MELAS overlap syndrome, MT-TS1 related NGS Genetic DNA Test ?

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes: MedlinePlus Genetics
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes: MedlinePlus Genetics

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes: MedlinePlus Genetics
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes: MedlinePlus Genetics

Late-onset MELAS syndrome with mtDNA 14453G→A mutation masquerading as an acute encephalitis: a case report | BMC Neurology | Full Text
Late-onset MELAS syndrome with mtDNA 14453G→A mutation masquerading as an acute encephalitis: a case report | BMC Neurology | Full Text

MELAS syndrome causes, symptoms, diagnosis, treatment & prognosis
MELAS syndrome causes, symptoms, diagnosis, treatment & prognosis

MELAS syndrome causes, symptoms, diagnosis, treatment & prognosis
MELAS syndrome causes, symptoms, diagnosis, treatment & prognosis

MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity | Journal of Neurology, Neurosurgery & Psychiatry
MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity | Journal of Neurology, Neurosurgery & Psychiatry

MELAS Syndrome Symptoms and Treatment
MELAS Syndrome Symptoms and Treatment

MELAS (V) - World Stroke Academy
MELAS (V) - World Stroke Academy

Non-random distribution of mitochondrial m.3243A>G heteroplasmy in human retina and its impact on cellular phenotype | bioRxiv
Non-random distribution of mitochondrial m.3243A>G heteroplasmy in human retina and its impact on cellular phenotype | bioRxiv

A) Map of the human mitochondrial genome and the secondary structure... | Download Scientific Diagram
A) Map of the human mitochondrial genome and the secondary structure... | Download Scientific Diagram

Prime time for base editing in the mitochondria | Signal Transduction and Targeted Therapy
Prime time for base editing in the mitochondria | Signal Transduction and Targeted Therapy

Characteristics of iPSCs derived from a MELAS patient. (A) The sequence... | Download Scientific Diagram
Characteristics of iPSCs derived from a MELAS patient. (A) The sequence... | Download Scientific Diagram

Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome | Journal of Neurology
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome | Journal of Neurology

Frontiers | Advances in mt-tRNA Mutation-Caused Mitochondrial Disease Modeling: Patients' Brain in a Dish
Frontiers | Advances in mt-tRNA Mutation-Caused Mitochondrial Disease Modeling: Patients' Brain in a Dish

Gene therapy for primary mitochondrial diseases: experimental advances and clinical challenges | Nature Reviews Neurology
Gene therapy for primary mitochondrial diseases: experimental advances and clinical challenges | Nature Reviews Neurology

MERRF and MELAS: current gene therapy trends and approaches
MERRF and MELAS: current gene therapy trends and approaches

The MELAS mutation m.3243A>G alters the expression of mitochondrial tRNA fragments - ScienceDirect
The MELAS mutation m.3243A>G alters the expression of mitochondrial tRNA fragments - ScienceDirect

MELAS Syndrome - Khondrion
MELAS Syndrome - Khondrion

MELAS syndrome is an inherited disease caused by a mutation in a gene loc..
MELAS syndrome is an inherited disease caused by a mutation in a gene loc..