geenit

name

• geenit

Works about geenit

• A functional genomics approach to the study of alkaloid biosynthesis and metabolism in Nicotiana tabacum and Hyoscyamus muticus cell cultures
• A functional study of the Drosophila host defense
• A ras-like GTP-binding protein regulates post-Golgi vesicle traffic in yeast Saccharomyces cerevisiae
• A study of candidate genes in depression and disturbed sleep
• ADHD voimavarana : missä kohtaa kirjoa olet?
• Adipose tissue metabolism in acquired obesity
• Adult-type hypolactasia : genotype-phenotype correlation
• Aivojen ajatus, kiehtova mieli : ihminen evoluution tuotteena
• Alterations resulting both HSD17B1 enzyme inhibition and the off-target effect on the Naglu gene
• Alternative sigma factors F, E, G, and K in Clostridium botulinum sporulation and stress response
• Alzheimer's disease -related genes and pathways :
• Alzheimer's disease-related genes and pathways : special emphasis on seladin-1, δ-opioid receptor 1 and BACE1
• AMIGO and its friends in developing and adult brain
• AMIGO-Kv2.1 potassium channel complex :
• Amplification and overexpression of ERBB2, uPA, TRPSI, EIF3S3 and MYC genes in prostate cancer
• Analyses of kidney organogenesis through in vitro and in vivo approaches : generation of conditional Wnt4 mouse models and a method for applying inducible Cre-recombination for kidney organ culture
• Analysis of high-dimensional and left-censored data with applications in lipidomics and genomics
• Analysis of quantitative variation and inbreeding depression with marker genes in Arabidopsis thaliana and its outcrossing relatives
• Analysis of somatic mutations in leukemias
• Androgen receptor signaling pathway in prostate cancer
• Androgen receptor-mediated gene activation in prostate cancer cells
• Applications of fluorescence in situ hybridization : from gene hunting to mutation visualization
• Assessment of copy number variations in the nebulin gene and other nemaline myopathy-causing genes
• ATM, ATR and Mre11 complex genes in hereditary susceptibility to breast cancer
• ATM, RAD50 and p53 in breast cancer
• Avain viljeltävien taimen-, harjus- ja siikaemokalastojen geneettiseen tietokantaan Riista- ja kalatalouden tutkimuslaitoksen vesiviljelyssä
• Bayesian multilocus association models for prediction and mapping of genome-wide data
• Behavioral responses in mice selectively bred for high and low levels of open-field thigmotaxis
• Biogeeni : ammatillista biokemiaa ja geenitekniikkaa
• Bioinformatic identification of genomic alterations in breast cancer
• Bioinformatic tools for analysis, mining and modelling large-scale gene expression and drug testing datasets
• Biologia : lukio : Geeni
• Biomaailman säätely - ihmisen ulottuvilla?
• Biotekniikka kauran jalostuksessa : uudet menetelmät laadun parantamiseksi
• Born to be heavy? : determinants of body size from birth to early adulthood in Finnish twins
• Bovine B cells :
• Bovine DNA markers in mapping loci affecting milk production traits
• Brain immune gene network in inbred mouse models of anxiety- and sociability-related neuropsychiatric disorders
• BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer
• Breeding against hip and elbow dysplasia in dogs
• Caenorhabditis elegans as a model for human synucleopathies
• Calculating life : nation, nature and the nativisation of nonhuman genetics
• Candidate gene studies in human anxiety disorders
• Candidate gene studies on cardiovascular traits
• Candidate genes for coronary heart disease in patients with type 2 diabetes : studies on the fatty acid-binding protein 2, [beta][sub 3]-adrenergic receptor, receptor for advanced glycation end products, apolipoprotein A1 and endothelial nitric oxide synthase genes
• Canonical Wnt signaling in hair and mammary gland patterning and development
• Catechol-O-methyltransferase and pain in rodents and humans
• Cationic lipids as antisense oligonucleotide carriers into cells : studies on complexation and transfection
• Cellular physiology and cell-to-cell propagation of tau in neurodegeneration : the impact of late-onset Alzheimer's disease susceptibility genes
• Characterisation of Cladonia rangiferina transcriptome and genome, and the effects of dehydration and rehydration on its gene expression
• Characterisation of the autoimmune regulator (AIRE) protein : autoimmunity on a molecular level
• Characterization and functional studies of PPM1D in breast cancer
• Characterization of bacteria causing outbreaks by using molecular methods in a clinical microbiology laboratory
• Characterization of neurotoxin gene location, toxigenesis and cold tolerance in Clostridium botulinum
• Characterization of novel genes predominantly expressed in the epididymis : from genome analyses to genetically modified mice
• Childhood hearing impairment in northern Finland :
• Clinical and genetic findings in early-onset primary osteoporosis
• Clustering of cardiometabolic risk factors, liver enzymes and PNPLA3 polymorphism with special reference to children
• Collagen XVII and pathomechanisms of junctional epidermolysis bullosa and gestational pemphigoid
• Common and rare variants of the renin-angiotensin system and their relation to antihypertensive drug responses
• Complement factor C4 and immunoglobulins in recurrent or chronic mucosal infections
• Computational analysis of microRNAs in biomedicine
• Computational approaches to analyzing gene regulatory processes
• Computational genomics of lactobacilli
• Computational techniques for haplotype inference and for local alignment significance
• Computational tools for a novel transcriptional profiling method
• Consequences of balanced translocations and loss-of-function mutations
• Contribution of immunoregulatory genes to genetic susceptibility to type 1 diabetes : association and linkage studies
• Contribution of the ARLTS1 gene to prostate cancer susceptibility
• Control of nephrogenesis by Wnt4 signaling : mechanisms of gene regulation and targeting of specific lineage cells by tissue engineering tools
• Coordinated functions of the HCpro and VPg proteins of Potato virus A (PVA) with the translation initiation factors eIF4E and eIF(iso)4E
• Cyanobactins : ribosomally synthesized and post-translationally modified peptides produced by cyanobacteria
• De novo purine nucleotide biosynthesis in gram-positive bacteria : regulation of Bacillus subtilis purA encoding adenylosuccinate synthetase
• Deciphering potential factors affecting β-amyloid pathology in idiopathic normal pressure hydrocephalus
• Defects in tricarboxylic acid cycle enzymes fumarate hydratase and succinate dehydrogenase in cancer
• Determinants of clinical course and outcome of Puumala hantavirus-induced nephropathia epidemica
• Development and application of Tobacco rattle virus induced gene silencing in Gerbera hybrida
• Developments in the evolutionary theory of social interactions
• Differentially expressed genes in prostate cancer
• Discovery and characterization of novel genes expressed in the mouse epididymis
• Dissecting genetic susceptibility to gluten sensitivity : HLA-linked risk factors in coeliac disease and dermatitis herpetiformis
• Dissecting genetic variation in European Scots pine (Pinus sylvestris L.) : special emphasis on polygenic adaptation
• Dissecting the pathophysiology of cardiovascular risk factors by means of genetics
• Dissection of the genetic background of childhood onset progressive myoclonic epilepsies
• DNA copy number changes and gene expression profiling in squamous cell lung cancer and malignant mesothelioma
• DNA hypermethylation in prostate cancer
• Doing the decent thing with genes : proceedings from the International Turku Symposium on Genetic Ethics, 9-11 August 1995
• Dystrophia myotonica type 2 (DM2) in Finland : a mutation with extensive clinical implications
• Eettiset aivot
• Effects of chronic hypoxia on myocardial gene expression and function
• Effects of lifestyle and genetic factors on the levels of serum adiponectin, a novel marker of the metabolic syndrome, in Finnish servicemen
• Effects of maternal smoking and aflatoxin B1 on cytochrome P450 enzymes, transporters and other proteins expressed in human placenta
• Ei yksin geeneistä : matkaopas rodun, normaaliuden ja sikiämisen genomiikkaan
• Electroconvulsive therapy : association of genetic polymorphisms with treatment resistant depression and treatment response
• Elämä : lyhyt oppimäärä
• Elämän kehitys
• Elämän tiede : tutkimus lääketieteellisestä teknologiasta, vanhemmuudesta ja perimän hallinnasta
• Elämänlanka : geenitekniikan tarina
• Environment-sensing mechanisms of gene expression and their effects on the dynamics of genetic circuits across cell generations
• Epidemiology and risk markers of autoimmune diseases in Russian Karelia and in Finland
• Establishment and enhancement of Mu in vitro DNA transposition applications : novel procedures and new tools
• Evolutionary genetics of immunity and infection in social insects
• Evoluutio
• Evoluutio : miten lajit kehittyvät?
• Evoluutio ja biologinen informaatio
• Evoluutio ja ihmisluonto
• Examination of genetic components affecting human obesity-related quantitative traits
• Experimental and genetic studies on podocyte molecules CD2AP and SHIP2 in diabetic nephropathy
• Exploring genetic susceptibility to autism spectrum disorders
• Exposure-related human cancer : molecular changes in sinonasal cancer and lung cancer with focus on TP53 mutations
• Expression and functions of cystatin C in epileptogenesis and epilepsy
• Expression and regulation of two RFamide peptide genes in the rat
• Expression of collagen, TGF-[beta] and c-fos genes in developing human skeletal tissues
• Expression of nucleoprotein, hsp70-related protein, and calmodulin genes during spermatogenesis
• Expression profiling of novel iron-related genes in mouse models of iron overload
• Familial dyslexia : genetic and neuropsychological findings
• Familial factors and diabetic nephropathy in type 1 diabetes
• Fatty acid metabolism genes LDLR, SOAT1 and DHCR24 and Alzheimer's disease risk
• Filopodia and stromal extracellular matrix as regulators of cancer cell invasion and growth
• Finnish population genetics in a forensic context
• FISH mapping : from chromosomal localization to an ESTablished transcript map
• Fitness effects of receptor genes for arginine vasopressin 1a and oxytocin in the bank vole Myodes glareolus
• Flavonoid metabolomics in Gerbera hybrida and elucidation of complexity in the flavonoid biosynthetic pathway
• Flight metabolic rate and dispersal in the Glanville fritillary butterfly - from genes to populations
• Fumarate hydratase and succinate dehydrogenase in neoplasia
• Function of psoriasis susceptibility gene CCHCR1
• Functional and cellular analysis of autoimmune regulator (AIRE) protein
• Functional characterization of a novel plant viral RNAi suppressor
• Functional characterization of MutL homologue mismatch repair proteins and their variants
• Functional genes and gene array analysis as tools for monitoring hydrocarbon biodegradation
• Functional significance of minor MLH1 germline alterations found in colon cancer patients
• Functions of AHR-1 and CYP-35A subfamily genes in Caenorhabditis elegans
• Geenien tulo yhteiskuntatieteisiin
• Geenikartoitusopas
• Geenin itsekkyys
• Geeniseulontatyöryhmän muistio
• Geenit, kokemus ja ihmisenä oleminen
• Geeniteknologia, arvot ja vastuu
• Geenitieto kuuluu kaikille
• GeeniVarat
• Gen-väg? : genetiska möjligheter, risker och myter
• Gene amplification and overexpression in gastric adenocarcinoma and Barrett adenocarcinoma
• Gene copy number alterations in prostate cancer
• Gene expression and functional studies on psoriatic epidermis
• Gene expression in rat brain : alterations by antipsychotic drugs
• Gene expression profiling in experimental models of cardiac load
• Gene expression profiling of human lipoprotein-loaded macrophages and atherosclerotic lesions with special emphasis on ADAMs
• Gene flow from transgenic plant populations : models and applications for risk assessment
• Gene polymorphism and systemic inflammatory response in chronic periodontitis
• Generation and characterization of knockout mice and analysis of patient material demonstrates a role for tissue inhibitor of metalloproteinases 4 (Timp4) in the cardiovascular system and tumor metastasis
• Genes and genome of Lactobacillus phage LL-H
• Genes regulating insulin secretion and insulin signaling as candidate genes for type 2 diabetes in subjects with impaired glucose tolerance
• Genetic analysis of demography and selection in Lyrate rockcress (Arabidopsis lyrata) populations
• Genetic and clinical features of familial Meniere's disease in Northern Ostrobothnia and Kainuu
• Genetic and environmental influence on asthma and related phenotypes : the effect of profession and inflammatory cytokine genes IL1A, IL1B and IL10
• Genetic and epigenetic mechanisms of tumor predisposition in hereditary non-polyposis colorectal carcinoma and sporadic cancers
• Genetic and expressional studies of Alzheimer's disease candidate genes : emphasis on CYP19, seladin-1 and HSPG2 genes
• Genetic and functional characterisation of Alzheimer's disease-associated genes
• Genetic and functional studies of genes involved in the pathogenesis of Alzheimer's disease
• Genetic and molecular background of ascending aortic aneurysms
• Genetic aspects of alcoholism : proceedings of the satellite symposium "Alcohol and Genetics" held in Sapporo, Japan, June 23-24, 1988, fourth congress of the International Society for Biomedical Research on Alcoholism
• Genetic association of the tenomodulin gene (TNMD) with obesity- and inflammation-related phenotypes
• Genetic background and antenatal risk factors of bronchopulmonary dysplasia
• Genetic background of biopolar disorder and related cognitive impairments
• Genetic background of bipolar disorder and related cognitive impairments
• Genetic backround and phenotype of autosomal dominant polycystic kidney disease in eastern Finland
• Genetic basis of adaptation : bud set date and frost hardiness variation in Scots pine
• Genetic basis of atherosclerosis, ischemic stroke and lipoprotein oxidation :
• Genetic basis of familial lymphoma predisposition
• Genetic causes and risk factors associated with phenotypes occurring in mitochondrial disorders
• Genetic components of late-onset Alzheimer's disease with special emphasis on ApoE, IL-6, CYP46, SERPINA3 and PPARγ
• Genetic consequences of directional selection in Arabidopsis lyrata
• Genetic defects of calcium and potassium signaling in inherited ventricular arrhythmias
• Genetic differences between species and their implications for speciation and adaptation in ants
• Genetic diversity in the wild : cyclic population dynamics and population isolation
• Genetic effects on mobility, obesity and their association in older female twins
• Genetic factors in schizophrenia :
• Genetic factors in the regulation of striatal and extrastriatal dopamine D2 receptor expression
• Genetic heterogeneity in autism spectrum disorders in a population isolate
• Genetic mapping of traits important in barley breeding
• Genetic mechanisms of stress response and sporulation in Clostridium botulinum
• Genetic polymorphism of human HLA-linked complement C4 genes
• Genetic predisposition to breast and ovarian cancer : BRCA 1/2-negative families
• Genetic regulation of energy homeostasis and obesity : studies on genes encoding sirtuin 1, melanocortin receptors 3 and 4 and melanin-concentrating hormone receptor 1
• Genetic regulatory networks in avian B cells
• Genetic risk factors for lumbar intervertebral disc disease characterized by sciatica
• Genetic structure in Finland and Sweden : aspects of population history and gene mapping
• Genetic studies of the human complement C4 region in MHC class III
• Genetic studies of tissue-specific mitochondrial DNA segregation in mammals
• Genetic studies on Finnish lupus erythematosus patients with cutaneous manifestations
• Genetic studies on primary immunodeficiency diseases
• Genetic studies on susceptibility genes in osteoarthritis
• Genetic susceptibility to celiac disease - HLA-unlinked candidate genes
• Genetic susceptibility to childhood bronchiolitis
• Genetic variants predisposing to cardiac arrhythmia disorders and sudden cardiac death
• Genetic variation : effect on the risk of cancers of lung and oropharynx
• Genetic variation and structure of ribosomal DNA (rDNA) in Scots pine and Norway spruce
• Genetic variation in premature adrenarche : association studies on candidate genes in a case-control cohort
• Genetic variation in the LDL receptor-related protein 5 (LRP5) gene : association with bone health and metabolic parameters
• Genetic variation of barley [beta]-amylase gene expressed in grain
• Genetic, epidemiological and cell culture studies on human resistin
• Genetic, prenatal and postnatal determinants of weight gain and obesity in young children : the STEPS study
• Genetically determined hypometabolism in Alzheimer's disease and midlife risk factors for cognitive impairment
• Genetics and family aspects of coeliac disease
• Genetics behind mood disorders : candidate gene studies of bipolar and major depressive disorders
• Genetics of cardiovascular disease : a candidate gene study of USF1
• Genetics of children's bone growth
• Genetics of inherited small vessel diseases : in search of a novel small vessel disease and mofifiers of the clinical course of CADASIL
• Genetics of local adaptation in the three-spined stickleback
• Genetics of monosymptomatic hereditary optic neuropathies
• Genetics of multiple sclerosis
• Genetics of Müllerian aplasia
• Genetics of obesity : abstracts
• Genetics of Parkinson's disease in the Finnish population
• Genetics of schizophrenia : the 1q42 locus in Finnish families
• Genetics of skeletal muscle characteristics and maximal walking speed among older female twins
• Genetics of sleep : sleep and comorbidities : connection at the genetic level
• Genetiikkaa sukututkijoille ja väestöjen juurtenetsijöille
• Genome-based natural product biosynthetic gene cluster discovery : from sequencing to mining
• Genome-wide analysis of androgen receptor function in prostate cancer
• Genome-wide characterization of genetic aberrations in pancreatic cancer
• Genome-wide regulation of glucocorticoid signaling by SUMO modifications
• Genomic approach to organ-specific growth control
• Genomic evolution and diversity in Artiodactyla
• Genomic microarrays in chromosomal analysis of leukemia
• Genomic profiling of gastric cancer
• Genomics approaches to study music perception and performance
• Globaalit ongelmat : evolutiivisten juurten etsintää
• GPRA and the asthma locus on chromosome 7p14-p15
• Harjoittele tehokkaammin, voi paremmin, elä pitempään
• HER-2 positive breast cancer : molecular and epidemiological studies
• Hereditary predisposition to breast cancer : evaluation of candidate genes
• Hereditary predisposition to breast cancer : with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes
• Hereditary prostate cancer in Finland : from genetic linkage to susceptibility genes
• Heterogeneity in genetic susceptibility to prostate cancer
• Homogeneous assays for simplified screening of HLA-conferred genetic disease risk
• Hormonal regulation of endocrine-resistant breast cancer
• Host-microbe interactions in bovine mastitis Staphylococcus epidermidis, Staphylococcus simulans and Streptococcus uberis
• Human genetic variation in the Baltic Sea region : features of population history and natural selection
• Human pathogenic mutations in protein domains
• Identification and characterization of genes and proteins involved in the development and progression of melanomas
• Identification and validation of novel prostate cancer biomarkers
• Identification of biomarkers for type 2 diabetes
• Identification of loci for migraine with aura
• Identification of new genetic syndromes with epilepsy by whole-exome sequencing
• Identification of novel genes involved in the pathophysiology of adrenocortical tumorigenesis
• Identification of novel regulators for tumor progression in breast cancer
• Identifying genetic risk factors in canine autoimmune disorders
• Identifying the contribution of specific genes
• Idiopathic normal pressure hydrocephalus :
• Ihme nimeltä ihminen
• Immune system genes and multiple sclerosis : a case-control study in a Finnish population
• Immunopathogenesis of asthma and atopic diseases : the specific role of a selected panel of genes in human T helper cell differentiation
• In quest of genetic susceptibility to disorders manifesting in fractures : assessing the significance of genetic factors in femoral neck stress fractures and childhood non-OI primary osteoporosis
• In search of high-penetrant hereditary prostate cancer susceptibility genes in Finland
• In silico genomics of fungal oxidoreductase genes
• Individual differences in response to psychological challenge : a study of the effects of EGF A61G and ApoE genetic polymorphisms and temperamental characteristics
• Influences of genetic factors and regular exercise on bone in middle-aged men
• Inherited developmental diseases related to reproductive failures in cattle
• Insights into cancer-related effects of electromagnetic fields
• Insights into the molecular genetics of celiac disease : applying family- and population-based strategies
• Insulin-sensitizing genes and risk of type 2 diabetes : studies on the PGC-1α, PPARγ, adiponectin, leptin receptor and hepatic lipase genes
• Integration of Eda signaling with other signaling pathways in oral ectodermal organogenesis
• Investigating the genetic susceptibility to rare and common manifestations
• Involvement of a genetic variation in the human [alpha] [sub 2B]-adrenoceptor in acute coronary events and hypertension
• Ion channel gene variants predisposing to severe human ventricular arrhythmias
• Itämeren lohen levinneisyyshistoria
• Johdatus geneettiseen sukututkimukseen
• Juuresi näkyvät : geneettisen sukututkimuksen ABC
• Kauniit turkiseläimemme - ja niiden värityyppigenetiikka
• Kelpoisimman valmistus : DNA ja evoluution kiistattomat todisteet
• Kiehtovat geenit : mihin geenitietoa käytetään?
• Kissan genetiikka : Kurssi 1
• Kissankasvattajan kissan genetiikka ja jalostus
• Kodin terveyskirjasto : Terve ruokavalio
• Konsilienssi
• Kuhakantojen geneettinen kartoitus : kuinka suuret ovat kuhakantojemme väliset perinnölliset erot?
• Kärpänen, hiiri ja ihminen
• Käyttäytymisgenetiikka : geeneistä yhteiskuntaan
• Lactobacillus crispatus and Propionibacterium freudenreichii :
• Lapsia valitessa : geenit, vammaisuus ja suunnittelu
• Leaf traits associated with drought adaptation in faba bean (Vicia faba L.)
• Leisure activities and obesity in adolescence : a follow up study among twins
• Lemmikkieläinten jalostus
• Liposome nanoparticles for targeted drug delivery, gene delivery and magnetic imaging
• Liver insulin resistance and hyperglycemia : genetic determinants and association with cardiovascular risk factors
• Loputtomat kauniit muodot : evodevon uusi tiede
• Loss of heterozygosity and tumour suppressor gene alterations in human cancer : studies on FHIT and NF2 genes in lung cancer, malignant mesothelioma and gastrointestinal stromal tumours
• Lyhyt selitys pienille ja isoille asioille molekyyleistä mustiin aukkoihin
• Lääketieteellinen genetiikka
• Maidon juoksettumattomuuteen liittyvien geenien kartoitus
• Major histocompatibility complex genes : method of analysis, association with acute coronary syndromes and effect on immune reactions
• Me ja ne : rotuopeista sukulaisuuteen
• MED12 : a novel player in uterine leiomyomas
• MED29 possesses a complex role in pancreatic cancer
• Membranous core domain of complex I and mitochondrial disease modeling
• Metabolic and genetic determinants of HDL in families with low HDL cholesterol and premature coronary heart disease
• Methods for mining data from genome wide high-throughput technologies
• Metsäpuiden erikoismuotoja : kultakuusesta luutakoivuun
• Microarray study : gene expression in endothelial cell cultures and intracranial aneurysms
• Microarrays in molecular profiling of cancer : focus on head and neck squamous cell carcinoma
• Microarrays in molecular profiling of Ewing sarcoma family of tumors and CDKN2A aberrations
• Miksi Kiina lähtee lentoon ja Kongo ei? : yhteiskuntien älykkyyserot ja niiden huomiointi kehityksessä
• Mistä suomalaiset ovat tulleet?
• Molecular analysis of the interaction between white rot pathogen (Rigidoporus microporus) and rubber tree (Hevea brasiliensis)
• Molecular and clinical characteristics of pituitary adenoma predisposition (PAP)
• Molecular background of three lethal fetal syndromes
• Molecular basis of colorectal cancer predisposition
• Molecular characterization of sediment bacterial communities affected by fish farming
• Molecular classification of familial colorectal and endometrial carcinoma
• Molecular control of the yearly growth cycle in wild strawberry
• Molecular factors and genetic differences defining symbiotic phenotypes of Galega spp. and Neorhizobium galegae strains
• Molecular genetic background of tumours in hereditary leiomyomatosis and renal cell cancer syndrome
• Molecular genetic mechanisms of pulmonary arterial hypertension
• Molecular genetic studies of melanocortin receptors in morbid obesity
• Molecular genetics of early-onset Alzheimer's disease and frontotemporal lobar degeneration
• Molecular genetics of hypercholesterolemia : the Finnish type of low density lipoprotein receptor mutation and DNA polymorphism of the apolipoprotein B gene
• Molecular genetics of Kallmann syndrome and constitutional delay of growth and puberty in Finland
• Molecular genetics of primary open angle glaucoma and exfoliation syndrome
• Molecular genetics of psoriasis
• Molecular genetics of schizophrenia and related intermediate phenotypes in a founder population
• Molecular genetics of Usher syndrome -inherited deafness and blindness
• Molecular mechanisms of cancer predisposition in HNPCC/Lynch syndrome
• Molecular mechanisms of sleep and mood
• Molecular pathogenesis in hereditary non-polyposis colorectal cancer (HNPCC) syndrome
• Molecular patterns behind immunological and metabolic alterations in lysinuric protein intolerance
• Molecular profiling of epileptogenesis :
• Moraalin ja kulttuurin biologiaa
• Multidimensional bioethics : a pluralistic approach to the ethics of modern human biotechnology
• Multiple mechanisms of mutant SOD1 toxicity in ALS models
• Multiple sclerosis in twins : a Finnish twin cohort study on genetic and environmental factors
• Mutations of mitochondrial DNA polymerase gamma : an important cause of neurological disorders
• myc Genes in human lung cancer : regulation and amplification
• Nasopharyngeal colonization by pathogenic bacteria : effect of polymorphisms in innate immune genes of young children
• Ne geenit! Ne geenit!
• Nephrin-associated molecules in human glomerular diseases
• Neurobiology of Parkinson's disease gene pink1 in Danio rerio (Zebrafish)
• Neuron navigator 3 (NAV3) gene aberrations in human cancer : copy number variations and target genes
• Neuronal ceroid lipofuscinosis CLN8 : from gene to protein
• Novel approaches for pluripotent reprogramming
• Novel mechanisms involved in human T helper 1 cell differentiation
• Novel multiple sclerosis predisposing genetic variants outside the HLA region
• Novel regulators of pancreatic cancer cell growth and mobility
• Nucleotide variation of birch (Betula L.) species : population structure and phylogenetic relationships
• Obesity, low-grade inflammation and cardiovascular diseases :
• Ohran RFLP-kartoitus
• Oikeus geenivaroihin
• On the environmental genetics of depressive symptoms : focus on two serotonergic genes
• On the superior power of likelihood-based linkage disequilibrium mapping in large multiplex families compared to population based case-control designs
• PALB2 and RAP80 genes in hereditary breast cancer predisposition
• Pathobiology of Heterobasidion-conifer tree interaction :
• Pathogen-induced defense signaling and signal crosstalk in Arabidopsis
• Pathophysiology and genetics of impaired insulin secretion and insulin resistance
• Pattern discovery from biosequences
• Paviaaneja, punaviiniä ja puutarhanhoitoa : esseitä ihmisen biologiasta
• Perimä : ihmisen historia 23 kappaleessa
• Perinnöllisyyden ja jalostuksen perusteet
• Perinnöllisyyslääketiede
• Pertussis : infection, vaccination and gene polymorphisms
• Pharmacogenetics of SLCO1B1 : population genetics and effect on statins
• Phylogeography and conservation genetics of the lesser white-fronted goose (Anser erythropus)
• Physical activity, genetic variation, and type 2 diabetes
• PIAS1 in androgen-regulated gene programs in prostate and breast cancer cells
• Placental angiogenesis and angiogenesis related risk factors in severe pre-eclampsia
• Plant development and evolution : the dynamic control of flowering, the mitochondrial genome and organellar protein targeting
• Plasmids and aromatic degradation in Sphingomonas for bioremediation : aromatic ring cleavage genes in soil and rhizosphere
• Pleiotropy of vitamin D-mediated gene regulation
• Polygenic risk scores, transcriptomics, and molecular mechanisms of Alzheimer's disease-related risk genes
• Polymorphic low penetrance genes and breast cancer : the role of genes involved in metabolism of xenobiotics, estrogens and reactive oxygen species
• Polymorphisms in genes associated with androgen biosynthesis and metabolism as risk factors for human prostate cancer
• Positional cloning and pathway analysis of the asthma susceptibility gene, NPSR1
• Positional cloning of Mulibrey Nanism gene (MUL)
• Progesterone target genes in breast cancer cells
• Promoting healthy lifestyles with personalized, APOE genotype based health information :
• Prostatic gene expression : probasin, human prostatic acid phosphatase and macrophage inhibitory cytokine-1 as model genes
• Proto-oncogenes in rheumatic diseases
• Rare genomic deletions underlying schizophrenia and related neurodevelopmental disorders
• Rare genomic deletions underlying shizophrenia and related neurodevelopmental disorders
• Receptor tyrosine kinase gene copy numbers and protein expression in astrocytic brain tumors : with special reference to KIT, PDGFRA, VEGFR2 and EGFR
• Regulation and clinical relevance of cancerous inhibitor of protein phosphatase 2A (CIP2A) in human cancers
• Regulation of alternative splicing in obesity and weight loss
• Regulation of androgen receptor signaling by SUMO modifications in prostate cancer cells
• Regulation of B cell gene expression and function by Ikaros, Helios and Bcl6
• Regulation of flowering and canopy structure in timothy (Phleum pratense L.)
• Regulation of gene expression by c-Ha-ras and neu oncoproteins
• Regulation of normal and neoplastic steroidogenic cell differentiation in the adrenal gland and ovary
• Relationship of physical activity, unacylated ghrelin and gene variation with changes in cardiovascular risk factors during military service
• Riista- ja kalatalouden tutkimuslaitoksen harjuksen emokalastojen geneettinen monimuotoisuus mikrosatelliittianalyysien perusteella
• Role of CYBA gene polymorphisms in atherosclerosis
• Role of Fto in the gene and microRNA expression of mouse adipose tissues in response to high-fat diet
• Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer
• Role of Wnt11 in kidney ontogenesis and development of renal organoid based models to identify candidate oncogenes
• Role of Wnt4 signaling in mammalian sex determination, ovariogenesis and female sex duct differentiation
• Sata vuotta maataloustutkimusta : mihin tutkimus ohjaa tuotantoa? : esitelmät : maatalouden tutkimus- ja tuotantopäivät Jokioinen 12.-13.8.1998 = Hundred years of agricultural research : where does research lead production? : symposium on agricultural production and research
• Search for genetic variants conferring susceptibility to obesity and related metabolic traits
• Search for genetic variants influencing human height
• Search for metal-responsive genes in plants : putative roles in metal tolerance or accumulation
• Search for molecular mechanisms related to Zn accumulation and tolerance in Thlaspi caerulescens
• Search for susceptibility genes in osteoarthritis
• Search for susceptibility genes in schizophrenia
• Searching for genes predisposing to common dyslipidemias
• Secondary metabolites in Gerbera hybrida
• Selected genetic polymorphisms of epidermal growth factor, dopamine-2 receptor, neuregulin-1 and inflammatory cytokines in schizophrenia
• Selection and genetic diversity in the major histocompatibility complex genes of wolves and dogs
• Signaling in cancer : pim-1 kinase and its partners
• Simulation techniques for disease gene localization in isolated populations
• Single nucleotide polymorphisms in the peroxisome proliferator-activated receptor genes and insulin sensitivity
• Siniketun tuotanto-ominaisuuksiin vaikuttavien kromosomialueiden kartoitus
• Sinu geenid, minu geenid : geneetikaalane info noorpaaridele
• Sinun geenit ja minun : perinnöllisyystietoa perhettä suunnitteleville
• Small RNA-mediated gene regulation in Caenorhabditis elegans
• Sokea kelloseppä
• Stroke-associated carotid atherosclerosis : a role for FABP4 in atheroma vulnerability and cardiometabolic risk
• Structure and expression of the manXYZ operon of Escherichia coli
• Structure of the gene for the [alpha]1 chain of human type IV collagen
• Studies of the genetic epidemiology of cardiovascular disease : focus on inflammatory candidate genes
• Studies of the human transcriptome
• Studies of the plasticity of transcription in Escherichia coli using single-molecule, in vivo detection techniques
• Studies on causes of multiple sclerosis : from genes to transcriptome
• Studies on genetic regulation of basal metabolic rate in obese subjects
• Studies on genomic instability induced by radiation and chemicals
• Studies on retina-specific gene expression
• Studies on selected human obesity candidate genes : genetic variation and adipose tissue expression
• Studies on the molecular pathogenesis of psoriasis
• Studying the functional relevance of lung cancer genetic drivers in their physiological niche
• Suomalaisen ayrshirekarjan geenikartoitus kromosomista 19
• Suomalaisten juuret
• Suomen arvokkaat geenivarat
• Suomen kansa - mistä ja mikä?
• Suomen luonnon geneettinen monimuotoisuus : valtakunnallinen hankekartoitus
• Susceptibility genes and neurodevelopmental mechanisms in dyslexia
• Susceptibility genes for diabetic nephropathy in type 1 diabetes : studies of five genes involved in glucose metabolism, glomerular structure, and blood pressure regulation
• Susceptibility genes of diabetes and endothelial dysfunction in preeclampsia
• Susceptibility to respiratory tract infections in young men : the role of inflammation, mannose-binding lectin, interleukin-6 and their genetic polymorphisms
• Suurivaikutteisten geenien jakauma jalostusvalinnan kohteena olleessa populaatiossa
• Synergism of low-molecular weight polyethylenimines and other cationic carriers in gene delivery in vitro
• Syö itsesi suomalaiseksi
• Säregna former av skogsträd från guldgran till kvastbjörk
• Teknologian arviointeja
• Teknologian arviointeja : 1, Esiselvitys kasvigeenitekniikasta
• Teknologian arviointeja : kasvigeenitekniikka ravinnontuotannossa : 3, Loppuraportti kasvigeenitekniikasta
• Temperature dependence of the transcription dynamics of synthetic genes in Escherichia coli
• The age of the mutations in the Finnish disease heritage : a genealogical and linkage disequilibrium study
• The DISC1 pathway in the genetic etiology of schizophrenia
• The effect of genes and diet on Alzheimer's disease-related molecular mechanisms : influence of ubiquilin-1 and dietary lipids
• The function and regulation of the Insulin-like 3 (Insl3) gene
• The genetics of pubertal growth and timing
• The Gerbera cDNA microarray : a tool for large-scale identification of genes involved in flower development
• The grey zone between type 1 and type 2 diabetes : genetic aspects of diabetes in adults
• The hERG1 (Kv11.1) potassium channel :
• The mechanisms of hedgehog signal transduction
• The molecular mechanisms and evolutionary significance of plumage colour variation in pied flycatchers (Ficedula hypoleuca)
• The regulation of inflammatory cytokines by vitamin D
• The relationships between environment, diet, transcriptome and atopic dermatitis in dogs
• The relevance of donor-specific HLA antibodies in renal transplantation
• The role of 8q amplification and microRNAs in prostate cancer
• The role of adiposity, growth and inflammation related gene variants in physical performance and body composition
• The role of an oncoprotein CIP2A in breast cancer
• The role of BACH1, BARD1 and TOPBP1 genes in familial breast cancer
• The role of Dkk1 and Wnt5a in mammalian kidney development and disease
• The role of genes on chromosome locus 4q12 in human central nervous system tumors
• The role of interleukin 18 gene polymorphism in the development of atherosclerosis
• The role of MADS and TCP transcription factors in Gerbera hybrida flower development
• The role of nuclear factor kappa-B in models of adult and neonatal cerebral ischemia : the effects of pyrrolidine dithiocarbamate
• The role of Snorc, a novel cartilage transmembrane proteoglycan, in skeletal tissue homeostasis
• The role of weight reduction sensitive genes in adipose tissue biology and adipocyte function : special emphasis on the expression of MFAP5 and CPPED1
• The roles of cyclooxygenase-2 and 15-hydroxyprostaglandin dehydrogenase in gastric carcinogenesis
• The roles of WOL and APL in phloem development in Arabidopsis thaliana roots
• The roots of European men : a study on Y-chromosome DNA
• The search for genes predisposing to obesity
• The search for genes predisposing to preeclampsia
• The search for susceptibility genes in lumbar disc degeneration : focus on young individuals
• The search for susceptibility genes in osteoarthritis
• The spectrum of the phenotypes in the C9ORF72 expansion carriers :
• The stress responses of probiotic lactobacilli and a Bifidobacterium with special emphasis on Clp family proteins
• The study of gene regulation and protein targeting in plant cells using gene fusion techniques
• The twenty-second Signe and Ane Gyllenberg Symposium, Hanasaari Congress Center, September 24-26, 2009
• Tiede ja elämä : tieteen päivät 2001
• Tiede ja kansojen älykkyys
• TIM family molecules in hematopoiesis
• Timing is everything : photoperiodicity shaping life-history traits and gene expression
• Toll-like receptor 4 and interleukin 6 gene polymorphisms in Helicobacter pylori related diseases
• TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility
• Transactivation of vitamin D receptor target genes by natural and synthetic ligands
• Transcription factor Nrf2 mediated gene regulation and signaling in the endothelium
• Transcription factors as candidate genes for type 2 diabetes : studies on peroxisome proliferator-activated receptors, hepatic nuclear factor 4α and PPARγ coactivator 1α
• Transcriptional analysis of persistent Chlamydia pneumoniae infection in vitro
• Transcriptional control in the murine adrenal cortex and testis
• Transcriptional regulation of endothelial cell-specific Tie1 and Vegfr3 genes
• Transforming growth factor β1 genotype, p16 expression, and treatment outcome in head and neck squamous cell carcinoma
• Tumor microenvironment in invasion of fibrosarcoma and melanoma cells
• Tuotanto- ja kestävyysominaisuuksien geenikartoitus lypsykarjalla
• Tutkijoiden erikoisimmat välineet
• Tutkimuksen etulinjassa : Tieteen päivät 1995
• Uusin tieto sydämesi toiminnasta ja terveydestä
• Variable expressions of Adam family genes in tissues and cancer cells
• Variation in Connexin37, methylenetetrahydrofolate reductase and upstream transcription factor 1 genes in relation to early atherosclerotic vascular changes in young adults : the cardiovascular risk in young Finns study
• Variation of phytosterols and steryl ferulates in wheat grains and fractions
• Variation of the PALB2 and PTEN genes and eIF4E protein expression as prognostic factors in breast cancer
• Veriryhmät O, A, B, AB ja M, N, MN Suomessa ja asutuksen leviäminen
• Viesti miljardien vuosien takaa
• Virulence of soft-rot Enterobacteria affecting potato