Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes.
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RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expressionRapid phenotyping of knockout mice to identify genetic determinants of bone strengthVariants in the interleukin-1 alpha and beta genes, and the risk for periodontal disease in dogs.Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysisGenetic factors affecting drug disposition in Asian cancer patients.Variants at the 9p21 locus and melanoma riskGenotypic and allelic variability in CYP19A1 among populations of African and European ancestryFunctional classification of 15 million SNPs detected from diverse chicken populationsDetection and characterization of small insertion and deletion genetic variants in modern layer chicken genomes.BDNF promoter methylation and genetic variation in late-life depression.No associations between aromatase gene polymorphisms and breast cancer risk in Saudi patients.Human Obesity Associated with an Intronic SNP in the Brain-Derived Neurotrophic Factor Locus.Endothelial Gata5 transcription factor regulates blood pressure.SNPs in FNDC5 (irisin) are associated with obesity and modulation of glucose and lipid metabolism in Saudi subjects.Fluticasone propionate pharmacogenetics: CYP3A4*22 polymorphism and pediatric asthma control.Selected single-nucleotide polymorphisms in FOXE1, SERPINA5, FTO, EVPL, TICAM1 and SCARB1 are associated with papillary and follicular thyroid cancer risk: replication study in a German population.Candidate gene analysis in israeli soldiers with stress fractures.Correlation of Cytochrome P450 Oxidoreductase Expression with the Expression of 10 Isoforms of Cytochrome P450 in Human Liver.Analysis of allele-specific expression in mouse liver by RNA-Seq: a comparison with Cis-eQTL identified using genetic linkage.Association Between Oxytocin Receptor Genotype, Maternal Care, and Eating Disorder Behaviours in a Community Sample of Women.Genetic variation in PPARGC1A may affect the role of diet-associated inflammation in colorectal carcinogenesis.Recent genetic findings in schizophrenia and their therapeutic relevanceCommon single nucleotide variants underlying drug addiction: more than a decade of research.Mechanisms underlying human genetic diversity: consequence for anti-graft antibody responses.Circulating Triglycerides and the Association of Triglycerides with Dietary Intake Are Altered by Alpha-2-Heremans-Schmid Glycoprotein Polymorphisms.Effect of g.9476869G>A myeloperoxidase (MPO) gene polymorphism on the antioxidant activity of milk from Polish Holstein-Friesian cows of the Black-and-White variety (HO).Associations between PTPRC rs10919563 A/G and FCGR2A R131H polymorphisms and responsiveness to TNF blockers in rheumatoid arthritis: a meta-analysis.Brief Report: Common Genetic Variation in Chromosome 10 q22.1 Shows a Strong Sex Bias in Human Embryonic Stem Cell Lines and Directly Controls the Novel Alternative Splicing of Human NODAL which is Associated with XIST Expression in Female Cell LineA Photoreceptor Contributes to the Natural Variation of Diapause Induction in Daphnia magna.Prospective cohort study of the risk factors for stress fractures in Chinese male infantry recruitsWhole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patientsGenetic Variations of Melatonin Receptor Type 1A are Associated with the Clinicopathologic Development of Urothelial Cell Carcinoma.rs10767664 Gene Variant in Brain-Derived Neurotrophic Factor Is Associated with Diabetes Mellitus Type 2 in Caucasian Females with Obesity.Genetic correlates of the development of theta event related oscillations in adolescents and young adults.Associations of High-Dose Melphalan Pharmacokinetics and Outcomes in the Setting of a Randomized Cryotherapy Trial.Genomic variants in the ASS1 gene, involved in the nitric oxide biosynthesis and signaling pathway, predict hydroxyurea treatment efficacy in compound sickle cell disease/β-thalassemia patients.Effects of hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 polymorphisms on fat androstenone level and gene expression in Duroc pigs.Natural variation in genes potentially involved in plant architecture and adaptation in switchgrass (Panicum virgatum L.).A comprehensive overview of FCGR3A gene variability by full-length gene sequencing including the identification of V158F polymorphism
P2860
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P2860
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes.
@en
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes.
@nl
type
label
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes.
@en
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes.
@nl
prefLabel
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes.
@en
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes.
@nl
P2860
P1433
P1476
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes.
@en
P2093
David N Cooper
P2860
P2888
P304
P356
10.1186/1479-7364-4-5-284
P577
2010-06-01T00:00:00Z
P5875
P6179
1028990691