1529 検索結果 in 遺伝子発現
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Publications
TGF-β1 and TGF-β2 abundance in liver diseases of mice and men
TGF-β1 is a major player in chronic liver diseases promoting fibrogenesis and tumorigenesis through various mechanisms …
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Publications
High fat diet enhances stemness and tumorigenicity of intestinal progenitors
Little is known about how pro-obesity diets regulate tissue stem and progenitor cell function. …
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Toll-like receptors in maraena whitefish: Evolutionary relationship among salmonid fishes and patterns of response to Aeromonas salmonicida
Toll-like receptors (TLRs) interact directly with particular pathogenic structures and are thus highly important to innate immunity. …
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Publications
Postnatal Pancreas of Mice Contains Tripotent Progenitors Capable of Giving Rise to Duct, Acinar, and Endocrine Cells In Vitro
Postnatal pancreas is a potential source for progenitor cells to generate endocrine β-cells for treating type 1 diabetes. …
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Expression-based GWAS identifies variants, gene interactions and key regulators affecting intramuscular fatty acid content and composition in porcine meat
The aim of this work is to better understand the genetic mechanisms determining two complex traits affecting porcine meat quality: intramuscular fat (IMF) content and its fatty acid (FA) composition. …
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Analysis of dysplasia in patients with Barrett's esophagus based on expression pattern of 90 genes
Diagnoses of dysplasia, based on histologic analyses, dictate management decisions for patients with Barrett's esophagus (BE). …
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Publications
Comparison of microRNA profiles between benign and malignant salivary gland tumors in tissue, blood and saliva samples: a prospective, case-control study
Salivary gland tumors (SGTs) are rare head and neck malignancies consisting of a spectrum of tumors with different biological behaviors. …
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Gene Expression
Advance your translational and clinical research with TaqMan or Delta Gene assays …
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Publications
Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization
Cranial malformations are a significant cause of perinatal morbidity and mortality. …
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Publications
The molecular basis for sonographic cervical shortening at term: identification of differentially expressed genes and the epithelial-mesenchymal transition as a function of cervical length
The purpose of this study was to determine whether cervical shortening of a ripe cervix at term is associated with changes in the cervical transcriptome. …
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Publications
Lipidomic Profiling of Influenza Infection Identifies Mediators that Induce and Resolve Inflammation
Bioactive lipid mediators play a crucial role in the induction and resolution of inflammation. …
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Publications
Identification and functional analysis of novel facial patterning genes in the duplicated beak chicken embryo
Cranial neural crest cells form the majority of the facial skeleton. …
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Publications
Molecular signatures at imminent death: Hemocyte gene expression profiling of shrimp succumbing to viral and fungal infections
Infectious diseases represent the most serious threat to shrimp farming worldwide. …
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Cells with surface expression of CD133highCD71low are enriched for tripotent colony-forming progenitor cells in the adult murine pancreas
Progenitor cells in the adult pancreas are potential sources of endocrine beta cells for treating type 1 diabetes. …
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Publications
Creatine reduces hepatic TG accumulation in hepatocytes by stimulating fatty acid oxidation
Non-alcoholic fatty liver disease encompasses a wide spectrum of liver damage including steatosis, non-alcoholic steatohepatitis, fibrosis and cirrhosis. …
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Publications
Direct Induction and Functional Maturation of Forebrain GABAergic Neurons from Human Pluripotent Stem Cells
Gamma-aminobutyric acid (GABA)-releasing interneurons play an important modulatory role in the cortex and have been implicated in multiple neurological disorders. …
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Publications
CYP gene expressions in obesity-associated metabolic syndrome
The contribution of cytochrome P450 (CYP) gene expressions in metabolic syndrome (MetS) has not been elucidated, and was the aim of this study. …
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Publications
Human Neuropsychiatric Disease Modeling Using Conditional Deletion Reveals Synaptic Transmission Defects Caused By Heterozygous Mutations in NRXN1
Heterozygous mutations of the NRXN1 gene, which encodes the presynaptic cell-adhesion molecule neurexin-1, were repeatedly associated with autism and schizophrenia. …