Coby Van den Bogert

Academic Medical Center — Netherlands

Biochemistry, Genetics and Molecular Biology · Life Sciences

24h-index1.9kcitations65works0.02yr avg
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Research Topics

Mitochondrial Function and Pathology(48), Metabolism and Genetic Disorders(27), ATP Synthase and ATPases Research(20), RNA modifications and cancer(7), Photosynthetic Processes and Mechanisms(6)

Publications65 total

Assembly of cytochrome‐<i>c</i> oxidase in cultured human cells
European Journal of Biochemistry·1998· 233 citedOpen Access
Familial mitochondrial DNA depletion in liver: haplotype analysis of candidate genes
Human Genetics·1998· 36 cited
Preferential amplification and phenotypic selection in a population of deleted and wild-type mitochondrial DNA in cultured cells
Current Genetics·1997· 19 cited
Cerebellar Hypoplasia in Respiratory Chain Dysfunction
Neuropediatrics·1996· 23 cited
Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia
The Journal of Pediatrics·1996· 63 cited
X‐linked cardioskeletal myopathy and neutropenia (Barth syndrome): Respiratory‐chain abnormalities in cultured fibroblasts
Journal of Inherited Metabolic Disease·1996· 99 citedOpen Access
Fatal neonatal liver failure and depletion of mitochondrial DNA in three children of one family
Journal of Inherited Metabolic Disease·1996· 10 cited
Progressive generalized brain atrophy and infantile spasms associated with cytochrome<i>c</i> oxidase deficiency
Journal of Inherited Metabolic Disease·1996· 7 citedOpen Access
Assembly of mitochondrial ATP synthase in cultured human cells: implications for mitochondrial diseases
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease·1995· 87 cited
Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findings.
PubMed·1995· 9 cited
[Diseases caused by mitochondrial DNA mutations].
PubMed·1995
Altered properties of mitochondrial ATP-synthase in patients with a T → G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease·1995· 105 cited
Altered kinetics of cytochrome c oxidase in a patient with severe mitochondrial encephalomyopathy
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease·1995· 18 cited
Expression and fate of the nuclearly encoded subunits of cytochrome-c oxidase in cultured human cells depleted of mitochondrial gene products
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research·1995· 43 cited
Meta-iodobenzylguanidine inhibits complex I and III of the respiratory chain in the human cell line molt-4
Biochemical Pharmacology·1995· 21 cited
The pre-mRNA of nuclear respiratory factor 1, a regulator of mitochondrial biogenesis, is alternatively spliced in human tissues and cell lines
Human Molecular Genetics·1995· 7 citedOpen Access
Deficiëntie van de adenine-nucleotide-translocator in spierweefsel: een mitochondriale ziekte, behandeld met vitamine E
Radboud Repository (Radboud University)·1995Open Access
Meta-iodobenzylguanidine (MIBG) inhibits malate and succinate driven mitochondrial ATP synthesis in the human neuroblastoma cell line SK-N-BE(2c)
European Journal of Cancer·1995· 17 cited
Signals on proteins, intracellular targeting and inborn errors of organellar metabolism
Journal of Inherited Metabolic Disease·1994· 4 cited
Permanent increase of immunocytochemical reactivity for γ-aminobutyric acid (GABA), glutamic acid decarboxylase, mitochondrial enzymes, and glial fibrillary acidic protein in rat cerebral cortex damaged by early postnatal hypoxia-ischemia
Acta Neuropathologica·1994· 17 cited
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Frequent Co-authors

A.M. Kroon(17), Trudi E. Melis(8), Marijke Holtrop(7), Ronald J. A. Wanders(7), Johannes N. Spelbrink(7), Leo Nijtmans(6), Bert H.J. Dontje(6), Mieke J. M. Van Galen(6), Anton O. Muijsers(5), Rob Zwart(5), H. de Vries(5), H. D. Bakker(5), Petr Klement(4), P. G. Barth(4), Pieter A. Bolhuis(4), H.R. Scholte(4), Lukas Dekker(4), André B. P. Kuilenburg(4), Jan‐Willem Taanman(3), A. H. van Gennip(3)