about
TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathyElastic network models capture the motions apparent within ensembles of RNA structuresRecessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection Fraction.Free energies for coarse-grained proteins by integrating multibody statistical contact potentials with entropies from elastic network models.Factors correlating with significant differences between X-ray structures of myoglobin.Ribosome Mechanics Informs about Mechanism.PANDA: pathway and annotation explorer for visualizing and interpreting gene-centric data.Computational and experimental characterization of RNA cubic nanoscaffolds.Integration of Immune Cell Populations, mRNA-Seq, and CpG Methylation to Better Predict Humoral Immunity to Influenza Vaccination: Dependence of mRNA-Seq/CpG Methylation on Immune Cell PopulationsUnderstanding protein-nanoparticle interaction: a new gateway to disease therapeutics.A computational investigation on the connection between dynamics properties of ribosomal proteins and ribosome assemblyMACE: model based analysis of ChIP-exo.Human telomerase model shows the role of the TEN domain in advancing the double helix for the next polymerization step.System-Wide Associations between DNA-Methylation, Gene Expression, and Humoral Immune Response to Influenza Vaccination.The Non-Coding RNA Ontology (NCRO): a comprehensive resource for the unification of non-coding RNA biology.Whole-exome analysis reveals novel somatic genomic alterations associated with outcome in immunochemotherapy-treated diffuse large B-cell lymphoma.Structural origins of misfolding propensity in the platelet adhesive von Willebrand factor A1 domain.Molecular modeling and molecular dynamic simulation of the effects of variants in the TGFBR2 kinase domain as a paradigm for interpretation of variants obtained by next generation sequencing.Recursive Indirect-Paths Modularity (RIP-M) for Detecting Community Structure in RNA-Seq Co-expression Networks.Gene signatures associated with adaptive humoral immunity following seasonal influenza A/H1N1 vaccination.The development of non-coding RNA ontology.A Novel Kleefstra Syndrome-associated Variant That Affects the Conserved TPLX Motif within the Ankyrin Repeat of EHMT1 Leads to Abnormal Protein Folding.Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine.De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy."The molecule's the thing:" the promise of molecular modeling and dynamic simulations in aiding the prioritization and interpretation of genomic testing results.Short paths in protein structure space originate in graph structure.Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidoses.Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CII.Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates with Unique Phenotype.Revealing rotational modes of functionalized gold nanorods on live cell membranes.ICGA-PSO-ELM approach for accurate multiclass cancer classification resulting in reduced gene sets in which genes encoding secreted proteins are highly represented.Molecular modeling of LDLR aids interpretation of genomic variantsRecurrent MSC E116K mutations in ALK-negative anaplastic large cell lymphomaRITAN: rapid integration of term annotation and network resourcesAurora kinase B-phosphorylated HP1α functions in chromosomal instability
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Michael T. Zimmermann
@ast
Michael T. Zimmermann
@en
Michael T. Zimmermann
@es
Michael T. Zimmermann
@sl
type
label
Michael T. Zimmermann
@ast
Michael T. Zimmermann
@en
Michael T. Zimmermann
@es
Michael T. Zimmermann
@sl
prefLabel
Michael T. Zimmermann
@ast
Michael T. Zimmermann
@en
Michael T. Zimmermann
@es
Michael T. Zimmermann
@sl
P106
P1153
35785314000
P21
P31
P496
0000-0001-7073-0525