about
The hydrogenosomes of Psalteriomonas lanternaStructure based hypothesis of a mitochondrial ribosome rescue mechanismOrigin and evolution of the peroxisomal proteome.Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex IMPV17L2 is required for ribosome assembly in mitochondriaA mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stabilityA functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosomeMutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial diseaseMutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expressionSTRING: a web-server to retrieve and display the repeatedly occurring neighbourhood of a geneThe yeast coexpression network has a small-world, scale-free architecture and can be explained by a simple modelSTRING: known and predicted protein-protein associations, integrated and transferred across organismsFACIL: Fast and Accurate Genetic Code Inference and LogoPOMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeOrthology prediction at scalable resolution by phylogenetic tree analysisSTRING: a database of predicted functional associations between proteinsCorrelation between sequence conservation and the genomic context after gene duplication.Correlation between sequence conservation and the genomic context after gene duplicationA global definition of expression context is conserved between orthologs, but does not correlate with sequence conservation.KIAA0556 is a novel ciliary basal body component mutated in Joubert syndromeTMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndromeTMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal GlycosylationReconstruction of the proto-mitochondrial metabolismDiscovery of a HapE mutation that causes azole resistance in Aspergillus fumigatus through whole genome sequencing and sexual crossingInferring metabolic states in uncharacterized environments using gene-expression measurementsPredicting human genetic interactions from cancer genome evolutionSignature genes as a phylogenomic toolMeasuring genome evolutionAn siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genesAn organelle-specific protein landscape identifies novel diseases and molecular mechanismsGenome phylogeny based on gene contentThe PinkThing for analysing ChIP profiling data in their genomic contextLoss, replacement and gain of proteins at the origin of the mitochondria.Comparative genomics for reliable protein-function prediction from genomic data.Benchmarking ortholog identification methods using functional genomics data.Horizontal gene transfer from Bacteria to rumen Ciliates indicates adaptation to their anaerobic, carbohydrates-rich environment.Development of the first marmoset-specific DNA microarray (EUMAMA): a new genetic tool for large-scale expression profiling in a non-human primate.From endosymbiont to host-controlled organelle: the hijacking of mitochondrial protein synthesis and metabolismThe [FeFe] hydrogenase of Nyctotherus ovalis has a chimeric origin.Conserved co-expression for candidate disease gene prioritization.
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Martijn A Huynen
@ast
Martijn A Huynen
@en
Martijn A Huynen
@es
Martijn A Huynen
@nl
Martijn A Huynen
@sl
type
label
Martijn A Huynen
@ast
Martijn A Huynen
@en
Martijn A Huynen
@es
Martijn A Huynen
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Martijn A Huynen
@sl
altLabel
Martijn Huynen
@en
prefLabel
Martijn A Huynen
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Martijn A Huynen
@en
Martijn A Huynen
@es
Martijn A Huynen
@nl
Martijn A Huynen
@sl
P1053
A-1530-2014
P106
P21
P2456
P31
P496
0000-0001-6189-5491