about
Evolutionary patterns of the mitochondrial genome in Metazoa: exploring the role of mutation and selection in mitochondrial protein coding genesThe RHNumtS compilation: features and bioinformatics approaches to locate and quantify Human NumtSA solid quality-control analysis of AB SOLiD short-read sequencing data.Multifaceted enrichment analysis of RNA-RNA crosstalk reveals cooperating micro-societies in human colorectal cancerHigh-confidence assessment of functional impact of human mitochondrial non-synonymous genome variations by APOGEEStepwise analysis of MIR9 loci identifies miR-9-5p to be involved in Oestrogen regulated pathways in breast cancer patients.The biological clock and the molecular basis of lysosomal storage diseases.Inflammatory Bowel Disease Meets Systems Biology: A Multi-Omics Challenge and Frontier.Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing.Infantile and childhood onset PLA2G6-associated neurodegeneration in a large North African cohort.Identification of p53-target genes in Danio rerioMutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.A primary tumor gene expression signature identifies a crucial role played by tumor stroma myofibroblasts in lymph node involvement in oral squamous cell carcinoma.A Broad Overview of Computational Methods for Predicting the Pathophysiological Effects of Non-synonymous Variants.Molecular dynamics recipes for genome research.Expanding the mutation spectrum in 130 probands with ARPKD: identification of 62 novel PKHD1 mutations by sanger sequencing and MLPA analysis.Systematic Analysis of Mouse Genome Reveals Distinct Evolutionary and Functional Properties Among Circadian and Ultradian GenesA novel mutation in CDH11 , encoding cadherin-11, cause Branchioskeletogenital (Elsahy-Waters) syndromeGene code CD274/PD-L1: from molecular basis toward cancer immunotherapyMitImpact: an exhaustive collection of pre-computed pathogenicity predictions of human mitochondrial non-synonymous variants.Double missense mutations in cardiac myosin-binding protein C and myopalladin genes: A case report with diffuse coronary disease, complete atrioventricular block, and progression to dilated cardiomyopathyA Multi-Layered Study on Harmonic Oscillations in Mammalian Genomics and ProteomicsTRIM8-driven transcriptomic profile of neural stem cells identified glioma-related nodal genes and pathwaysA single-center study on 140 patients with cerebral cavernous malformations: 28 new pathogenic variants and functional characterization of a PDCD10 large deletionSudden cardiac death in J wave syndrome with short QT associated to a novel mutation in Nav 1.8 coding gene SCN10A: First case report for a possible pharmacogenomic roleSudden death in mild hypertrophic cardiomyopathy with compound DSG2/DSC2/MYH6 mutations: Revisiting phenotype after genetic assessment in a master runner athleteAssociation of a homozygous GCK missense mutation with mild diabetesAre Gaming-Enabled Graphic Processing Unit Cards Convenient for Molecular Dynamics Simulation?
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description
onderzoeker
@nl
researcher
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հետազոտող
@hy
name
Stefano Castellana
@ast
Stefano Castellana
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Stefano Castellana
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Stefano Castellana
@nl
Stefano Castellana
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type
label
Stefano Castellana
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Stefano Castellana
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Stefano Castellana
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Stefano Castellana
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Stefano Castellana
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prefLabel
Stefano Castellana
@ast
Stefano Castellana
@en
Stefano Castellana
@es
Stefano Castellana
@nl
Stefano Castellana
@sl
P106
P1153
24467247900
P21
P2456
P31
P496
0000-0001-8688-9530