about
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesFibrinogen beta variants confer protection against coronary artery disease in a Greek case-control studyComprehensive mapping of the effects of azacitidine on DNA methylation, repressive/permissive histone marks and gene expression in primary cells from patients with MDS and MDS-related disease.Complementary seminovaginal microbiome in couples.Gene-Expression Profiling Suggests Impaired Signaling via the Interferon Pathway in Cstb-/- MicrogliaCharacterization and target genes of nine human PRD-like homeobox domain genes expressed exclusively in early embryos.Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation.Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes.Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays.Corrigendum: Characterization and target genes of nine human PRD-like homeobox domain genes expressed exclusively in early embryos.Meta-signature of human endometrial receptivity: a meta-analysis and validation study of transcriptomic biomarkers.The human PRD-like homeobox gene LEUTX has a central role in embryo genome activation.Tissue-specific mitochondrial heteroplasmy at position 16,093 within the same individualGlobin mRNA reduction for whole-blood transcriptome sequencing.Estrogen receptor β, a regulator of androgen receptor signaling in the mouse ventral prostate.MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate.Analysis of allele and haplotype diversity across 25 genomic regions in three Eastern European populations.A novel amplification strategy for genotyping with liquid chromatography-electrospray ionization mass spectrometry.The pruritus- and TH2-associated cytokine IL-31 promotes growth of sensory nerves.Whole-exome sequencing identifies a polymorphism in the BMP5 gene associated with SSRI treatment response in major depression.Combined immunodeficiency and hypoglycemia associated with mutations in hypoxia upregulated 1.Optimizing bone morphogenic protein 4-mediated human embryonic stem cell differentiation into trophoblast-like cells using fibroblast growth factor 2 and transforming growth factor-β/activin/nodal signalling inhibition.Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies.Evaluation of the 124-plex SNP typing microarray for forensic testing.Comparison of DNA extraction methods for multiplex polymerase chain reaction.Human pluripotent reprogramming with CRISPR activators.Genetic evidence of assortative mating in humansTAC-seq: targeted DNA and RNA sequencing for precise biomarker molecule counting
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-1297-1464
@en
name
Kaarel Krjutškov
@ast
Kaarel Krjutškov
@en
Kaarel Krjutškov
@sl
type
label
Kaarel Krjutškov
@ast
Kaarel Krjutškov
@en
Kaarel Krjutškov
@sl
altLabel
Kaarel Krjutskov
@en
prefLabel
Kaarel Krjutškov
@ast
Kaarel Krjutškov
@en
Kaarel Krjutškov
@sl
P1053
H-8401-2015
P106
P21
P214
73149542872200302222
P2953
Kaarel_Krjutškov
P31
P3829
P496
0000-0003-1297-1464
P569
1981-03-14T00:00:00Z
P735
P7859
viaf-73149542872200302222