Brian H. Robinson spends much of his time researching Biochemistry, Internal medicine, Respiratory chain, Molecular biology and Endocrinology. His studies in Superoxide, Radical, Mitochondrion, Leigh disease and Reactive oxygen species are all subfields of Biochemistry research. His Internal medicine study integrates concerns from other disciplines, such as Pyruvate dehydrogenase deficiency, Pyruvate dehydrogenase complex and Mitochondrial Encephalomyopathies, Mitochondrial myopathy.
His work deals with themes such as Adenosine triphosphate, Mitochondrial disease, Mitochondrial respiratory chain, Fibroblast and Metabolism, which intersect with Respiratory chain. His research integrates issues of Genetics, Polymerase chain reaction, Gene, Biotin and Genomic library in his study of Molecular biology. His Endocrinology study combines topics from a wide range of disciplines, such as Pyruvate Dehydrogenase Complex Deficiency Disease, Oxoglutarate dehydrogenase complex, Physiology and Proportionate short stature.
Brian H. Robinson focuses on Biochemistry, Molecular biology, Internal medicine, Pyruvate dehydrogenase complex and Endocrinology. His Biochemistry research focuses on Mitochondrion, Pyruvate carboxylase, Pyruvate dehydrogenase kinase, Oxoglutarate dehydrogenase complex and Pyruvate decarboxylation. His studies in Mitochondrion integrate themes in fields like Citrate synthase, Enzyme and Pathology.
His Molecular biology research incorporates elements of Complementary DNA, Genetics, Gene, Mutation and Cytochrome c oxidase. His study focuses on the intersection of Cytochrome c oxidase and fields such as Respiratory chain with connections in the field of Mitochondrial respiratory chain. His Endocrinology research is multidisciplinary, relying on both Hypotonia and Dihydrolipoamide dehydrogenase.
His primary areas of study are Mitochondrion, Molecular biology, Mitochondrial DNA, Biochemistry and Internal medicine. The Mitochondrion study combines topics in areas such as Citrate synthase and Bioinformatics. He interconnects Missense mutation, Pyruvate dehydrogenase phosphatase, Mutant and Cytochrome c oxidase in the investigation of issues within Molecular biology.
The various areas that Brian H. Robinson examines in his Mitochondrial DNA study include Mutation, Respiratory chain and Skeletal muscle. Brian H. Robinson has included themes like Gastroenterology, Congenital lactic acidosis, Endocrinology and Pathology in his Internal medicine study. His work on Lactic acidosis as part of general Endocrinology research is often related to Scad, thus linking different fields of science.
His scientific interests lie mostly in Mitochondrion, Molecular biology, Internal medicine, Biochemistry and Respiratory chain. His study in Mitochondrion is interdisciplinary in nature, drawing from both Leukemia, Cancer research, BCL2-related protein A1 and Citrate synthase. His work focuses on many connections between Molecular biology and other disciplines, such as Missense mutation, that overlap with his field of interest in Point mutation, Mutant and Heteroplasmy.
His Internal medicine research includes themes of Gastroenterology, Congenital lactic acidosis, Endocrinology and Pathology. His Biochemistry study is mostly concerned with Pyruvate dehydrogenase phosphatase, Pyruvate dehydrogenase complex, Gene product and Pyruvate decarboxylation. His Respiratory chain study contributes to a more complete understanding of Genetics.
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Mitochondria, oxygen free radicals, disease and ageing
Sandeep Raha;Brian H Robinson.
Trends in Biochemical Sciences (2000)
Approaches to DNA Mutagenesis: An Overview
Michael Mingfu Ling;Brian H. Robinson.
Analytical Biochemistry (1997)
Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high.
Y Tatuch;J Christodoulou;A Feigenbaum;J T Clarke.
American Journal of Human Genetics (1992)
Inhibition of Mitochondrial Translation as a Therapeutic Strategy for Human Acute Myeloid Leukemia
Marko Škrtić;Shrivani Sriskanthadevan;Bozhena Jhas;Marinella Gebbia.
Cancer Cell (2011)
Mitochondria, oxygen free radicals, and apoptosis
Sandeep Raha;Brian H. Robinson.
American Journal of Medical Genetics (2001)
Mutations in Iron-Sulfur Cluster Scaffold Genes NFU1 and BOLA3 Cause a Fatal Deficiency of Multiple Respiratory Chain and 2-Oxoacid Dehydrogenase Enzymes
Jessie M. Cameron;Alexandre Janer;Valeriy Levandovskiy;Nevena MacKay.
American Journal of Human Genetics (2011)
Human Complex I deficiency: Clinical spectrum and involvement of oxygen free radicals in the pathogenicity of the defect
Brian H Robinson.
Biochimica et Biophysica Acta (1998)
Superoxides from mitochondrial complex III: the role of manganese superoxide dismutase
Sandeep Raha;Gillian E McEachern;A.Tomoko Myint;Brian H Robinson.
Free Radical Biology and Medicine (2000)
Mutations in the X-linked pyruvate dehydrogenase (E1) alpha subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency.
Willy Lissens;Linda De Meirleir;Sara Seneca;Inge Liebaers.
Human Mutation (2000)
Variable clinical presentation in patients with defective E1 component of pyruvate dehydrogenase complex.
Brian H. Robinson;Harriet MacMillan;Roumyana Petrova-Benedict;W. Geoffrey Sherwood.
The Journal of Pediatrics (1987)
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