about
Profile-profile comparisons by COMPASS predict intricate homologies between protein familiesEstimates of statistical significance for comparison of individual positions in multiple sequence alignmentsChromatin topology is coupled to Polycomb group protein subnuclear organization.CASP5 assessment of fold recognition target predictions.Exploring dynamics of protein structure determination and homology-based prediction to estimate the number of superfamilies and folds.COMPASS server for remote homology inference.Using homology relations within a database markedly boosts protein sequence similarity search.PROCAIN: protein profile comparison with assisting information.COMPASS server for homology detection: improved statistical accuracy, speed and functionality.Discrete-continuous duality of protein structure space.PROCAIN server for remote protein sequence similarity searchConsidering scores between unrelated proteins in the search database improves profile comparison.Analysis of CASP8 targets, predictions and assessment methods.A comprehensive system for evaluation of remote sequence similarity detectionA tale of two ferredoxins: sequence similarity and structural differences.BRCA1 establishes DNA damage signaling and pericentric heterochromatin of the X chromosome in male meiosis.H3K27 modifications define segmental regulatory domains in the Drosophila bithorax complex.A boundary element between Tsix and Xist binds the chromatin insulator Ctcf and contributes to initiation of X-chromosome inactivationSpreading of X chromosome inactivation via a hierarchy of defined Polycomb stations.Single-cell transcriptional analysis of normal, aberrant, and malignant hematopoiesis in zebrafishSIRT6 Suppresses Pancreatic Cancer through Control of Lin28bTumor cells can follow distinct evolutionary paths to become resistant to epidermal growth factor receptor inhibition.X-chromosome hyperactivation in mammals via nonlinear relationships between chromatin states and transcriptionStructure similarity measure with penalty for close non-equivalent residues.Phenotypic categorization of genetic skin diseases reveals new relations between phenotypes, genes and pathways.T cell immune deficiency in zap70 mutant zebrafishXist RNA is a potent suppressor of hematologic cancer in mice.Influence of maternal breast milk ingestion on acquisition of the intestinal microbiome in preterm infants.Informatics for molecular biologists.Prolonged Mek1/2 suppression impairs the developmental potential of embryonic stem cells.Genome-wide identification of autosomal genes with allelic imbalance of chromatin state.A Specialized Mechanism of Translation Mediated by FXR1a-Associated MicroRNP in Cellular Quiescence.Survival in Quiescence Requires the Euchromatic Deployment of Clr4/SUV39H by Argonaute-Associated Small RNAs.Accurate statistical model of comparison between multiple sequence alignments.Effects of glutamate agonists on the isolated neurons from the locomotor network of the mollusc Clione limacina.Phenotypic and genotypic analyses of genetic skin disease through the Online Mendelian Inheritance in Man (OMIM) database.Polycomb Repressive Complex 2 Methylates Elongin A to Regulate Transcription.Genetic Intersection of Tsix and Hedgehog Signaling during the Initiation of X-Chromosome Inactivation.TOX Regulates Growth, DNA Repair, and Genomic Instability in T-cell Acute Lymphoblastic Leukemia.Quality of alignment comparison by COMPASS improves with inclusion of diverse confident homologs.
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description
researcher ORCID ID = 0000-0002-4240-5466
@en
wetenschapper
@nl
name
Ruslan I Sadreyev
@ast
Ruslan I Sadreyev
@en
Ruslan I Sadreyev
@nl
type
label
Ruslan I Sadreyev
@ast
Ruslan I Sadreyev
@en
Ruslan I Sadreyev
@nl
prefLabel
Ruslan I Sadreyev
@ast
Ruslan I Sadreyev
@en
Ruslan I Sadreyev
@nl
P106
P21
P31
P496
0000-0002-4240-5466