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Publications by Yolanda CAMPOS
Comparative Analysis of the Pathogenic Mechanisms Associated With the G8363A and A8296G Mutations in the Mitochondrial tRNALysgene
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
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The Impact of Pathogenic Mitochondrial DNA Mutations on Substantia Nigra Neurons
Journal of Neuroscience
Neuroscience
Mitochondrial DNA Mutations Associated With Neuromuscular Diseases: Analysis and Diagnosis Using the Polymerase Chain Reaction
Pediatric Research
Child Health
Pediatrics
Perinatology
Two Pathogenic Point Mutations Exist in the Authentic Mitochondrial Genome, Not in the Nuclear Pseudogene
Journal of Human Genetics
Genetics
Peripheral Neuropathy With Ataxia in Childhood as a Result of the G8363A Mutation in Mitochondrial DNA
Pediatric Research
Child Health
Pediatrics
Perinatology
Pathogenic Mitochondrial tRNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease
Human Mutation
Genetics
Insights on the Mechanisms of Ca2+regulation of Connexin26 Hemichannels Revealed by Human Pathogenic Mutations (D50n/Y)
Journal of General Physiology
Physiology
Dynein Mutations Associated With Hereditary Motor Neuropathies Impair Mitochondrial Morphology and Function With Age
Neurobiology of Disease
Neurology
The Effect of Mitochondrial DNA Mutations in Brain Tumors
Journal of Basic and Clinical Health Sciences
Mutations in the Highly Conserved SLQYLA Motif of Vif in a Simian–human Immunodeficiency Virus Result in a Less Pathogenic Virus and Are Associated With G-To-A Mutations in the Viral Genome
Virology
Virology
