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Search Results to Tomi Pastinen

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

Item TypeName
Concept Carrier Proteins
Concept Contractile Proteins
Concept DNA-Binding Proteins
Concept Egg Proteins
Concept Membrane Proteins
Concept Microfilament Proteins
Concept Microtubule-Associated Proteins
Concept Neoplasm Proteins
Concept Nerve Tissue Proteins
Concept Nuclear Proteins
Concept Proto-Oncogene Proteins
Concept Recombinant Proteins
Concept Repressor Proteins
Concept Ribosomal Proteins
Concept Viral Proteins
Concept Protozoan Proteins
Concept Extracellular Matrix Proteins
Concept Immediate-Early Proteins
Concept Homeodomain Proteins
Concept Bone Morphogenetic Proteins
Concept Monomeric GTP-Binding Proteins
Concept Mitochondrial Proteins
Concept LDL-Receptor Related Proteins
Concept Membrane Transport Proteins
Concept Drosophila Proteins
Concept Mitochondrial Membrane Transport Proteins
Concept Intercellular Signaling Peptides and Proteins
Concept Intracellular Signaling Peptides and Proteins
Concept Phospholipid Transfer Proteins
Concept Proto-Oncogene Proteins c-ets
Concept Wnt Proteins
Concept ELAV Proteins
Concept snRNP Core Proteins
Academic Article Contribution of the CCR5 and MBL genes to susceptibility to HIV type 1 infection in the Finnish population.
Academic Article A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays.
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 Systematic assessment of the human osteoblast transcriptome in resting and induced primary cells.
Academic Article Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.
Academic Article Epigenetic modification of the gene for the vitamin B(12) chaperone MMACHC can result in increased tumorigenicity and methionine dependence.
Academic Article Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations.
Academic Article Common sequence variation in FLNB regulates bone structure in women in the general population and FLNB mRNA expression in osteoblasts in vitro.
Academic Article Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.
Academic Article Fine mapping of the insulin-induced gene 2 identifies a variant associated with LDL cholesterol and total apolipoprotein B levels.
Academic Article RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression.
Academic Article Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines.
Academic Article Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
Academic Article Genome-wide association study of age at menarche in African-American women.
Academic Article Integration of high-resolution methylome and transcriptome analyses to dissect epigenomic changes in childhood acute lymphoblastic leukemia.
Academic Article Global identification of conserved post-transcriptional regulatory programs in trypanosomatids.
Academic Article Genome-wide search for exonic variants affecting translational efficiency.
Academic Article Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR.
Academic Article Genetic implication of a novel thiamine transporter in human hypertension.
Academic Article An epigenome-wide association study of total serum immunoglobulin E concentration.
Academic Article Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts.
Academic Article Global miRNA expression and correlation with mRNA levels in primary human bone cells.
Academic Article High-dose folic acid supplementation alters the human sperm methylome and is influenced by the MTHFR C677T polymorphism.
Academic Article Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Academic Article Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional Activator.
Academic Article Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Academic Article Combining omics data to identify genes associated with allergic rhinitis.
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 Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism.
Academic Article APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.
Academic Article Exploring rare and low-frequency variants in the Saguenay-Lac-Saint-Jean population identified genes associated with asthma and allergy traits.
Academic Article Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate gene.
Academic Article Asthma-associated polymorphisms in 17q12-21 locus modulate methylation and gene expression of GSDMA in na?ve CD4+ T cells.
Academic Article Rare Genetic Variants in Immune Genes and Neonatal Herpes Simplex Viral Infections.
Academic Article Non-CG methylation and multiple histone profiles associate child abuse with immune and small GTPase dysregulation.
Academic Article Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease.
Academic Article Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B12.
Academic Article Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature.
Academic Article IRF7 and UNC93B1 variants in an infant with recurrent herpes simplex virus infection.
Academic Article The cellular and immunological dynamics of early and transitional human milk.
Academic Article Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort.
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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