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Spatial genomic heterogeneity in diffuse intrinsic pontine and midline high-grade glioma: implications for diagnostic biopsy and targeted therapeuticsIntegrated Genomic Analysis of Diverse Induced Pluripotent Stem Cells from the Progenitor Cell Biology ConsortiumExome sequencing supports a de novo mutational paradigm for schizophrenia.Lung Gene Expression Analysis (LGEA): an integrative web portal for comprehensive gene expression data analysis in lung developmentComplementary RNA amplification methods enhance microarray identification of transcripts expressed in the C. elegans nervous system.Increased protein-coding mutations in the mitochondrial genome of African American women with preeclampsia.Identification of genes and pathways involved in retinal neovascularization by microarray analysis of two animal models of retinal angiogenesisPediatric Crohn disease patients exhibit specific ileal transcriptome and microbiome signature.Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.Analysis and expansion of the eosinophilic esophagitis transcriptome by RNA sequencingTransdifferentiation of human fibroblasts to endothelial cells: role of innate immunity.A gene expression atlas of early craniofacial developmentPigtailed macaques as a model to study long-term safety of lentivirus vector-mediated gene therapy for hemoglobinopathies.Cytokinesis failure in RhoA-deficient mouse erythroblasts involves actomyosin and midbody dysregulation and triggers p53 activationIntrinsic Age-Dependent Changes and Cell-Cell Contacts Regulate Nephron Progenitor Lifespan.Molecular, phenotypic, and sample-associated data to describe pluripotent stem cell lines and derivatives.The complex genetics of hypoplastic left heart syndrome.Increased frequency of double and triple heterozygous gene variants in children with intrahepatic cholestasis.IRAK1 is a novel DEK transcriptional target and is essential for head and neck cancer cell survival.Vertical sleeve gastrectomy reduces hepatic steatosis while increasing serum bile acids in a weight-loss-independent manner.Foamy Virus Vector Carries a Strong Insulator in Its Long Terminal Repeat Which Reduces Its Genotoxic Potential.Long ncRNA Landscape in the Ileum of Treatment-Naive Early-Onset Crohn Disease.Whole exome sequencing for familial bicuspid aortic valve identifies putative variants.Whole-exome sequencing uncovers oxidoreductases DHTKD1 and OGDHL as linkers between mitochondrial dysfunction and eosinophilic esophagitis.KIT blockade is sufficient for donor hematopoietic stem cell engraftment in Fanconi anemia mice.Ulcerative colitis mucosal transcriptomes reveal mitochondriopathy and personalized mechanisms underlying disease severity and treatment responseAge-of-diagnosis dependent ileal immune intensification and reduced alpha-defensin in older versus younger pediatric Crohn Disease patients despite already established dysbiosisGenetic Variation and Gene DiscoverySingle cell RNA sequencing reveals regional heterogeneity of hepatobiliary innate lymphoid cells in a tissue-enriched fashioncellHarmony: cell-level matching and holistic comparison of single-cell transcriptomesSingle-cell RNA sequencing identifies inflammatory tissue T cells in eosinophilic esophagitis
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P50
description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Phillip Dexheimer
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Phillip Dexheimer
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Phillip Dexheimer
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Phillip Dexheimer
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Phillip Dexheimer
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type
label
Phillip Dexheimer
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Phillip Dexheimer
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Phillip Dexheimer
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Phillip Dexheimer
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Phillip Dexheimer
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prefLabel
Phillip Dexheimer
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Phillip Dexheimer
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Phillip Dexheimer
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Phillip Dexheimer
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Phillip Dexheimer
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P106
P21
P31
P496
0000-0003-3965-6894