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Home
:: The Persistent Entity
Search:
Link Phylogeny for FOXO1
FOXO1
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Nutrigenomics
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FOX proteins
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Genomics
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FOXP2 (forkhead box P2)
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Linguistics
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SIRT1
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Apoptosis
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Immunology
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Galectins
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Lectinology
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Adhesins
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Cadherins
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Carbohydrates as Biological Markers
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Galactose
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Integrins
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Lectins
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Selectins
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Anoikia
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Galectin 3, hGal-3
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Thomsen-Friedenreich (T-Tn) antigen
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Histone deacetylases (HDAC)
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DNA
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Base pair
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Chromosome
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Gene
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Genetic architecture
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RNA
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Transcription (DNA transcription)
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Transcription factors
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Translation (RNA translation)
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CpG sites
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DNA methyltransferase
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Epigenetics
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Canalisation
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Conrad Hal Waddington
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Jean-Baptiste de Lamarck (Lamarckism)
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Quantitative trait locus analysis
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Eukaryote
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Allele
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Mutation
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Histone
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Chromatin
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Deoxyribonucleic acid (DNA)
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Genetic linkage
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Genotype
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Locus
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Phenotype
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RNA (ribonucleic acid)
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Gene conservation
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Histone methyltransferases (HMT)
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Maternal effect
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Methylation
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Biochemistry
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Methylenetetrahydrofolate reductase (MTHFR) polymorphism
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Polymorphism
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Thymidylate synthase (TS) polymorphism
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Nucleotide
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Single nucleotide polymorphisms (SNPs)
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Purine
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Guanine
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Adenine
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Thymine
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Cytosine
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Uracil
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Phenotypic plasticity
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5,10-methylenetetrahydrofolate reductase (MTHFR)
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p53
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Wild type
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Amorph
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P glycoprotein and MDR polymorphism
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P glycoprotein and ABO blood group
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Inhibition of P-glycoprotein by natural products
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Pharmacology
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Glycoside
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Flavonoid glycosides
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Resveratrol
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Phase II metabolism
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Physiology
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Phase I metabolism
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Drug metabolism
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Cytochrome P450 oxidase
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Acetylator phenotype
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Glucuronic acid
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Xenobiotics
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PDK4 pyruvate dehydrogenase kinase, isozyme 4 polymorphism
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Fatty acid binding protein 2 (FABP-2) polymorphism
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Fatty acid binding protein 2 (FABP-2) polymorphism, obesity and insulin resistance
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References
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Polymorphisms in the fatty acid-binding protein 2 and apolipoprotein C-III genes,metabolic syndrome and dyslipidemia
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The role of FABP2 gene polymorphism in alcoholic cirrhosis
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Paraoxonase 2 (PON2) polymorphism
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Trp64Arg polymorphism of the beta3-adrenergic receptor gene
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Mitochondria
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Mitochondrial DNA
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Inheritance
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