| human | Q5 |
| P496 | ORCID iD | 0000-0003-3965-6894 |
| P734 | family name | Dexheimer | Q37531273 |
| Dexheimer | Q37531273 | ||
| Dexheimer | Q37531273 | ||
| P735 | given name | Phillip | Q19816553 |
| Phillip | Q19816553 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q35159515 | A gene expression atlas of early craniofacial development |
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| Q34143183 | Analysis and expansion of the eosinophilic esophagitis transcriptome by RNA sequencing |
| Q33320351 | Complementary RNA amplification methods enhance microarray identification of transcripts expressed in the C. elegans nervous system |
| Q43189216 | Corrigendum. Pediatric Crohn disease patients exhibit specific ileal transcriptome and microbiome signature |
| Q36070467 | Cytokinesis failure in RhoA-deficient mouse erythroblasts involves actomyosin and midbody dysregulation and triggers p53 activation |
| Q30405748 | Exome sequencing supports a de novo mutational paradigm for schizophrenia. |
| Q45326104 | Foamy Virus Vector Carries a Strong Insulator in Its Long Terminal Repeat Which Reduces Its Genotoxic Potential |
| Q61865735 | Genetic Variation and Gene Discovery |
| Q28748452 | Genome-Wide Analysis of Copy Number Variation in Type 1 Diabetes |
| Q34003041 | Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease |
| Q38295578 | IRAK1 is a novel DEK transcriptional target and is essential for head and neck cancer cell survival. |
| Q33845347 | Identification of genes and pathways involved in retinal neovascularization by microarray analysis of two animal models of retinal angiogenesis |
| Q36753645 | Increased frequency of double and triple heterozygous gene variants in children with intrahepatic cholestasis |
| Q33714774 | Increased protein-coding mutations in the mitochondrial genome of African American women with preeclampsia |
| Q28596287 | Integrated Genomic Analysis of Diverse Induced Pluripotent Stem Cells from the Progenitor Cell Biology Consortium |
| Q36191159 | Intrinsic Age-Dependent Changes and Cell-Cell Contacts Regulate Nephron Progenitor Lifespan |
| Q52811444 | KIT blockade is sufficient for donor hematopoietic stem cell engraftment in Fanconi anemia mice. |
| Q50089710 | Long ncRNA Landscape in the Ileum of Treatment-Naive Early-Onset Crohn Disease. |
| Q31153794 | Lung Gene Expression Analysis (LGEA): an integrative web portal for comprehensive gene expression data analysis in lung development |
| Q36325186 | Molecular, phenotypic, and sample-associated data to describe pluripotent stem cell lines and derivatives |
| Q98281134 | Mucosal Inflammatory and Wound Healing Gene Programs Reveal Targets for Stricturing Behavior in Pediatric Crohn's Disease |
| Q112639198 | Nuclear Vav3 is required for polycomb repression complex-1 activity in B-cell lymphoblastic leukemogenesis |
| Q33944190 | Pediatric Crohn disease patients exhibit specific ileal transcriptome and microbiome signature |
| Q35664334 | Pigtailed macaques as a model to study long-term safety of lentivirus vector-mediated gene therapy for hemoglobinopathies |
| Q64090386 | Single cell RNA sequencing reveals regional heterogeneity of hepatobiliary innate lymphoid cells in a tissue-enriched fashion |
| Q92928315 | Single-cell RNA sequencing identifies inflammatory tissue T cells in eosinophilic esophagitis |
| Q27317083 | Spatial genomic heterogeneity in diffuse intrinsic pontine and midline high-grade glioma: implications for diagnostic biopsy and targeted therapeutics |
| Q36377531 | The complex genetics of hypoplastic left heart syndrome. |
| Q35022859 | Transdifferentiation of human fibroblasts to endothelial cells: role of innate immunity |
| Q60921844 | Ulcerative colitis mucosal transcriptomes reveal mitochondriopathy and personalized mechanisms underlying disease severity and treatment response |
| Q42873394 | Vertical sleeve gastrectomy reduces hepatic steatosis while increasing serum bile acids in a weight-loss-independent manner |
| Q51064957 | Whole exome sequencing for familial bicuspid aortic valve identifies putative variants. |
| Q52691460 | Whole-exome sequencing uncovers oxidoreductases DHTKD1 and OGDHL as linkers between mitochondrial dysfunction and eosinophilic esophagitis. |
| Q90139918 | cellHarmony: cell-level matching and holistic comparison of single-cell transcriptomes |
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