about
The pattern of polymorphism in Arabidopsis thalianaA multiprotein complex necessary for both transcription and DNA replication at the β-globin locusAltered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitmentSaccharomyces Rrm3p, a 5' to 3' DNA helicase that promotes replication fork progression through telomeric and subtelomeric DNA.Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiationAllelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative resultsTcf7 is an important regulator of the switch of self-renewal and differentiation in a multipotential hematopoietic cell lineMolecular phenotypes in triple negative breast cancer from African American patients suggest targets for therapySerum response factor is an essential transcription factor in megakaryocytic maturationIdentification of biologically relevant enhancers in human erythroid cells.Single-lineage transcriptome analysis reveals key regulatory pathways in primitive erythroid progenitors in the mouse embryoRole for MKL1 in megakaryocytic maturation.MKL1 and MKL2 play redundant and crucial roles in megakaryocyte maturation and platelet formation.EBNA1 regulates cellular gene expression by binding cellular promotersMixHMM: inferring copy number variation and allelic imbalance using SNP arrays and tumor samples mixed with stromal cellsX chromosome-wide analyses of genomic DNA methylation states and gene expression in male and female neutrophils.Schizosaccharomyces pombe pfh1+ encodes an essential 5' to 3' DNA helicase that is a member of the PIF1 subfamily of DNA helicases.Downstream targets of HOXB4 in a cell line model of primitive hematopoietic progenitor cellsMutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis.Neuronal mechanism for acute mechanosensitivity in tactile-foraging waterfowl.Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytes.Functional genomic screen of human stem cell differentiation reveals pathways involved in neurodevelopment and neurodegeneration.GPHMM: an integrated hidden Markov model for identification of copy number alteration and loss of heterozygosity in complex tumor samples using whole genome SNP arraysPatterns of histone H3 lysine 27 monomethylation and erythroid cell type-specific gene expressionCTCF and CohesinSA-1 Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid CellsMutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis.The blood transcriptional signature of chronic hepatitis C virus is consistent with an ongoing interferon-mediated antiviral response.DNA polymerase β variant Ile260Met generates global gene expression changes related to cellular transformation.A procedure for highly specific, sensitive, and unbiased whole-genome amplification.Chromatin architecture and transcription factor binding regulate expression of erythrocyte membrane protein genesWhole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemia.Favorable outcome associated with an IGF-1 ligand signature in breast cancer.Estrogen Drives Cellular Transformation and Mutagenesis in Cells Expressing the Breast Cancer-Associated R438W DNA Polymerase Lambda Protein.NFBD1/MDC1 regulates Cav1 and Cav2 independently of DNA damage and p53.Valproic acid antagonizes the capacity of other histone deacetylase inhibitors to activate the Epstein-barr virus lytic cycle.Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability.Nonstochastic reprogramming from a privileged somatic cell state.Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus.Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosis.STAT4 and T-bet control follicular helper T cell development in viral infections.
P50
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P50
description
hulumtues
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researcher
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հետազոտող
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name
Vincent Schulz
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Vincent Schulz
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Vincent Schulz
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Vincent Schulz
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Vincent Schulz
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Викентий Шульц
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type
label
Vincent Schulz
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Vincent Schulz
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Vincent Schulz
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Vincent Schulz
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Vincent Schulz
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Викентий Шульц
@ru
prefLabel
Vincent Schulz
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Vincent Schulz
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Vincent Schulz
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Vincent Schulz
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Vincent Schulz
@sl
Викентий Шульц
@ru
P106
P21
P31
P496
0000-0001-6333-4284