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Search Results to Tomi Pastinen

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Pastinen, Tomi

One or more keywords matched the following items that are connected to Pastinen, Tomi

Item Type	Name
Concept	Animals
Concept	Animal Structures
Concept	Animals, Laboratory
Concept	Animals, Wild
Concept	Disease Models, Animal
Concept	Animals, Genetically Modified
Academic Article	No evidence for an association between common nonsynonymous polymorphisms in delta and bristle number variation in natural and laboratory populations of Drosophila melanogaster.
Academic Article	The effect of polymorphisms in the enhancer of split gene complex on bristle number variation in a large wild-caught cohort of Drosophila melanogaster.
Academic Article	A low-cost open-source SNP genotyping platform for association mapping applications.
Academic Article	Mapping cis-acting regulatory variation in recombinant congenic strains.
Academic Article	Patterns of variation in DNA segments upstream of transcription start sites.
Academic Article	An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
Academic Article	Fine mapping of the insulin-induced gene 2 identifies a variant associated with LDL cholesterol and total apolipoprotein B levels.
Academic Article	The study of eQTL variations by RNA-seq: from SNPs to phenotypes.
Academic Article	Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Academic Article	Optimizing ChIP-seq peak detectors using visual labels and supervised machine learning.
Academic Article	Conserved expression of transposon-derived non-coding transcripts in primate stem cells.
Academic Article	Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities.
Academic Article	Pitx1 directly modulates the core limb development program to implement hindlimb identity.
Academic Article	Pioneer factor Pax7 deploys a stable enhancer repertoire for specification of cell fate.
Academic Article	A hidden markov model for identifying differentially methylated sites in bisulfite sequencing data.
Academic Article	H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis.
Academic Article	Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.
Academic Article	X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems.
Academic Article	Adverse Maternal Environments Perturb Hepatic DNA Methylome and Transcriptome Prior to the Adult-Onset Non-Alcoholic Fatty Liver Disease in Mouse Offspring.
Academic Article	Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease.
Academic Article	A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.

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Animals