perinnöllisyys

name

• perinnöllisyys

Works about perinnöllisyys

• A diagnostic view of the genetics of Cadasil
• A molecular genetic study and expression-based analysis of risk factors of Alzheimer's disease : emphasis on Aβ-degrading enzymes, IDE and NEP
• Adipose tissue inflammation, liver fat and insulin resistance in humans
• Aivot : pidä huolta pääomastasi
• Allerginen kansa : allergia kansanterveysongelmana : konsensuskokous 9.-11.11.1998
• AMIGO-Kv2.1 potassium channel complex :
• Arabihevosten näyttelytulosten periytymisasteet ja perinnölliset yhteydet
• Arkiajattelu, tieto ja oikeudenmukaisuus
• Assignment of genetic loci and variants predisposing to migraine with aura and episodic ataxia type 2
• Back function testing and paraspinal muscle magnetic resonance image parameters: their associations and determinants : a study on male, monozygotic twins
• Body-height : determinants and associations with social position and adult health
• Brain dopamine receptors and genetic risk for schizophrenia : a twin study using positron emission tomography
• Brain responses to changes in tone and speech stimuli in infants with and without a risk for familial dyslexia
• Brain white matter structure, body mass index and physical activity in individuals at risk for psychosis :
• BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer
• Breeding against hip and elbow dysplasia in dogs
• Cadasil : molecular studies on the most common hereditary vascular dementing disorder
• Cancer family syndrome : studies on the hereditary nonpolypous colorectal carcinoma syndrome
• Catechol-O-methyltransferase and pain in rodents and humans
• Characterization of Drosophila melanogaster Manf : an evolutionarily conserved neurotrophic factor
• Chromosomal polymorphisms and speciation in the Chrysomelid Galerucella nymphaeae complex
• Chronic atrophic gastritis in first-degree relatives of gastric carcinoma patients
• Classification principles and genetics of chronic gastritis
• Clinical and genetic findings in early-onset primary osteoporosis
• Clinical and genetic risk factors in acute coronary syndromes
• Clinical characteristics and pathophysiological mechanisms of familiar migraine with and without aura
• CLN5 - from mutation to defective protein and clinical phenotype
• Common variants of the leptin, leptin receptor and [beta[sub 3]]-adrenergic receptor genes in human morbid obesity
• Contribution of immunoregulatory genes to genetic susceptibility to type 1 diabetes : association and linkage studies
• Crib-biting in horses : a physiological and genetic study of candidate causative factors
• De skuldlösa mördarna : essäer om biologi : liv i nuet och i det förgångna
• Determinants of clinical course and outcome of Puumala hantavirus-induced nephropathia epidemica
• Determination of HLA polymorphisms by time-resolved fluorometric DNA hybridisation assays
• Dissection of the genetic background of childhood onset progressive myoclonic epilepsies
• Ei yksin geeneistä : matkaopas rodun, normaaliuden ja sikiämisen genomiikkaan
• Elämän kehitys
• Elämänlanka : geenitekniikan tarina
• Emakoiden maitokuumeen (MMA) periytyvyys ja siihen vaikuttavat tekijät
• Emakoiden porsimakertojen lukumäärä ja poistosyyt sekä niihin vaikuttavat tekijät
• Epidemiology and risk markers of autoimmune diseases in Russian Karelia and in Finland
• Evoluutio ja ihmisluonto
• Evoluutiobiologia
• Evoluutioteoria ja sosiobiologia
• Expectations, frames and practices of genetic counselling in different contexts of genetic testing
• Familial factors and diabetic nephropathy in type 1 diabetes
• Familial glioma : a molecular genetic and epidemiological study
• Fibromyalgia :
• Flight metabolic rate and dispersal in the Glanville fritillary butterfly - from genes to populations
• From molecular targets to public health : proceedings of the Symposium on Disease Prevention and Health Promotion, 15 November 2002, Helsinki
• Fyysinen Venus
• Geeneistä yhteiskuntaan
• Geenien tulo yhteiskuntatieteisiin
• Geenit, kokemus ja ihmisenä oleminen
• Geenitestit : oikeudellisia kysymyksiä
• Gen-väg? : genetiska möjligheter, risker och myter
• Gene polymorphism and systemic inflammatory response in chronic periodontitis
• Genes outside the HLA region affecting susceptibility to type 1 diabetes : the role of IDDM2 and IDDM9 in the Finnish population
• Genetic and clinical features of familial Meniere's disease in Northern Ostrobothnia and Kainuu
• Genetic and environmental effects on resting electrocardiography and the association between electrocardiography and physical activity, walking endurance and mortality in older people
• Genetic and environmental influence on asthma and related phenotypes : the effect of profession and inflammatory cytokine genes IL1A, IL1B and IL10
• Genetic and immunological risk factors and carotid artery atherosclerosis
• 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 background of spontaneous preterm birth and lung diseases in preterm infants : studies of potential susceptibility genes and polymorphisms
• Genetic basis of familial lymphoma predisposition
• Genetic basis of hereditary colorectal cancers : hereditary nonpolyposis colorectal cancer and familial adenomatous polyposis
• Genetic biomarkers for lung cancer susceptibility : the role of polymorphisms in xenobiotic metabolism and DNA repair
• Genetic causes of mitochondrial complex I deficiency in children
• Genetic diversity of enteroviruses
• Genetic epidemiology of hereditary prostate cancer in Finland
• Genetic heterogeneity in autism spectrum disorders in a population isolate
• Genetic modulation of age-associated brain pathology : a population-based molecular genetic study on Finns aged 85 years or over
• Genetic polymorphism of human HLA-linked complement C4 genes
• Genetic polymorphisms in collectins and Toll-like receptor 4 as factors influencing susceptibility to severe RSV infections and otitis media
• Genetic predisposition to breast and ovarian cancer :
• Genetic predisposition to breast and ovarian cancer in Eastern Finnish population
• Genetic risk factors for hereditary prostate cancer in Finland :
• Genetic studies on Finnish lupus erythematosus patients with cutaneous manifestations
• 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 clinical manifestations in inflammatory bowel disease
• Genetically determined hypometabolism in Alzheimer's disease and midlife risk factors for cognitive impairment
• Genetics behind mood disorders : candidate gene studies of bipolar and major depressive disorders
• Genetics of children's bone growth
• Genetics of condition and sexual selection
• Genetics of inherited small vessel diseases :
• Genetics of neurodegeneration :
• 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
• Genome-wide characterization of genetic aberrations in pancreatic cancer
• Haasteena harvinaiset harmit : Väestöliiton perinnöllisyysklinikka 20 vuotta
• Hereditary predisposition to breast cancer : evaluation of candidate genes
• Hereditary prostate cancer in Finland : from genetic linkage to susceptibility genes
• Heritability and genetic risk factors in Finnish families with childhood otitis media
• Heritability of type 2 diabetes and related traits
• Heterogeneity in genetic susceptibility to prostate cancer
• Hevosen värit
• Human genetic variation in the Baltic Sea region : features of population history and natural selection
• Identification of genetic susceptibility loci for migraine
• Identification of new genetic syndromes with epilepsy by whole-exome sequencing
• Identification of novel tumor predisposition families and underlying genetic defects
• Idiopathic pulmonary fibrosis : from epidemiology to gene mapping
• 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
• Infantile haemangioma and venous malformations :
• Inherited DNA repair capacity and individual responses to carcinogens
• Kaksoset : geenit, ympäristö ja identiteetin arvoitus
• Kaksostutkimuksia reumataudeissa
• Karitsojen painojen ja kasvujen perinnölliset ja fenotyyppiset tunnusluvut suomenlampaalla
• Karjujen jälkeläisten kantakoe- ja tilatestituloksiin perustuvien jalostusarvostelujen vastaavuus
• Kettujen luonteen periytyvyys ja yhteys hedelmällisyysominaisuuksiin
• Kodin terveyskirjasto : Miten terveyttäsi tutkitaan
• Kulttuurieläin : ihmistutkimuksen biologiaa
• Kuulovikojen genetiikkaa, kuulo ja vanheneminen, apuvälinekuntoutuksen saatavuus ja laatu : XXVII valtakunnalliset audiologian päivät Oulussa 6.-7.4.2006
• Lamarckin haamu : biologisen yhtenäisteorian hahmottelua
• Lapsia valitessa : geenit, vammaisuus ja suunnittelu
• Leisure-time physical activity in a Finnish twin study : genetic and environmental influences as determinants and motives as correlates
• Lemmikkieläinten jalostus
• Liharotuisten nautojen painojen perinnölliset tunnusluvut
• Lypsylehmien rakenneominaisuuksien perinnölliset tunnusluvut
• Lypsylehmien rakenneominaisuuksien perinnölliset tunnusluvut
• Lypsyrotuisten vasikoiden syntymäpainon perinnölliset tunnusluvut ja yhteydet muihin ominaisuuksiin
• Lääketieteellinen genetiikka
• Maidon juoksettumis- ja tuotanto-ominaisuuksien perinnölliset tunnusluvut
• Mapping of susceptibility genes for systemic lupus erythematosus (SLE)
• Me ja ne : rotuopeista sukulaisuuteen
• Microtia
• Mihin geenitietoa käytetään?
• Mikrosatelliitti-DNA:n käyttö koirien yksilöntunnistuksessa ja populaatiorakenteen tarkastelussa
• Mitochondrial DNA sequence variation in patients with sensorineural hearing impairment and in the Finnish population
• Mitochondrial DNA variation in extremely selected traits : longevity and elite athletic performance
• Modelling long QT syndrome in patient-specific cardiomyocytes
• Molecular and clinical characteristics of pituitary adenoma predisposition (PAP)
• Molecular and clinical characteristics of tricarboxylic acid cycle-associated tumors
• Molecular and functional characterization of ABRAXAS and PALB2 genes in hereditary breast cancer predisposition
• Molecular basis of colorectal cancer predisposition
• Molecular biology methods in assessing radiation-induced hereditary risks in humans
• Molecular biology of progressive myoclonus epilepsy of Unverricht-Lundborg type (EPM1)
• Molecular diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC)
• Molecular genetics of bipolar disorder and related traits
• Molecular genetics of early-onset Alzheimer's disease and frontotemporal lobar degeneration
• Molecular mechanisms of ectodermal dysplasia syndromes
• Multiple sclerosis in twins : a Finnish twin cohort study on genetic and environmental factors
• Munantuotanto-ominaisuuksien QTL-kartoitus kanan kromosomista 8
• Natural history of celiac disease-associated antibodies and progression to overt disease in children at increased genetic risk
• Neuronal ceroid lipofuscinosis CLN8 : from gene to protein
• Neuropeptide Y in the development of diabetes and vascular diseases : with special reference to genetic risk associated with the Leu7Pro polymorphism in the preproNPY
• Novel insights into the molecular genetic background of colorectal tumors
• Offspring of mothers with psychotic disorder : childhood development and adulthood psychiatric morbidity
• Options for selecting dairy cattle for milk coagulation ability
• PALB2 and RAP80 genes in hereditary breast cancer predisposition
• PCSK9 and berberine as modulators of lipoprotein receptors and neuronal cell death
• Perheen alkoholinkäyttö lapsen kannalta : 'lapsi alkoholistiperheessä' tutkimusten valossa
• Perinnöllinen paksusuolisyöpä
• Perinnölliset sairaudet ja perinnöllisyysneuvonta : luentomoniste : terveydenhuollon, sairaanhoidon ja sosiaalihuollon opiskelijoille
• Perinnöllisyyslääketiede
• Periytyvän rintasyöpäalttiusmutaation (BRCA1/2) kantajamiesten hypoteettinen perinnöllisyysneuvontamalli
• Personality traits in the blue tit
• Phenotypic and genetic variance and covariance in life-history traits in pre-industrial human populations
• Poikimavaikeuksien ja vasikkakuolleisuuden sekä syntymäpainojen perinnölliset tunnusluvut suomalaisessa lihakarjapopulaatiossa
• Polymorphic low penetrance genes and breast cancer : the role of genes involved in metabolism of xenobiotics, estrogens and reactive oxygen species
• Polymorphism of the antioxidative enzyme paraoxonase-1 in the development of atherosclerosis : clinical and autopsy studies
• Population cytogenetics of folate sensitive fragile sites with special reference to mental retardation
• Porsastuotanto- ja lihantuotanto-ominaisuuksien geneettiset ja fenotyyppiset tunnusluvut
• Postural balance and susceptibility to falls in older women : genetic and environmental influences in single and dual task situations
• Predictors, development and outcome
• Quantitative genetics approach
• Rare genomic deletions underlying schizophrenia and related neurodevelopmental disorders
• Rare genomic deletions underlying shizophrenia and related neurodevelopmental disorders
• Ratsuhevosten rakenneominaisuuksien perinnölliset tunnusluvut
• Ravihevosten kinner- ja vuohisnivelten irtopalojen periytyvyys ja yhteydet kilpailutuloksiin
• Recognizing Lynch syndrome by DNA mismatch repair deficiency
• Resting state brain networks in young people with familial risk for psychosis
• Retiniitikon opas : tietoa perinnöllisistä silmänpohjan rappeumasairauksista
• Risk factors for sudden cardiac death from an acute ischemic event in general population : a case-control study
• Role of gabaergic and monoaminergic mechanisms in rat lines developed for differential sensitivity to ethanol-induced motor impairment
• Roles of demography and natural selection in molecular evolution of trees, focus on Pinus sylvestris
• Schooling, family background, and adoption : is it nature or is it nurture?
• Search for genetic variants influencing human height
• Search for susceptibility genes in osteoarthritis
• Search for susceptibility genes in schizophrenia
• Serotonin and dopamine gene polymorphisms and alcohol consumption
• Sikojen lihakkuuden, luun murtolujuuden ja osteokondroosin perinnölliset tunnusluvut
• Sinu geenid, minu geenid : geneetikaalane info noorpaaridele
• Sinun geenit ja minun : perinnöllisyystietoa perhettä suunnitteleville
• Studies on genetic regulation of basal metabolic rate in obese subjects
• Suomalainen lääkärikeskus : 5
• Suomenhevosten ja lämminveristen ravihevosten varsanäyttelytulosten perinnölliset tunnusluvut
• Suomenkarjan risteytysyhdistelmät ja maidontuotanto-ominaisuuksien perinnölliset tunnusluvut
• Suomenpystykorvan epilepsian perinnöllisyys ja vastustaminen jalostuksen avulla
• Suomi-neidon geenit : tautiperinnön takana juurillemme johtamassa
• Surveillance in hereditary nonpolyposis colorectal cancer syndrome
• 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 in hereditary breast cancer
• Suurivaikutteisten geenien jakauma jalostusvalinnan kohteena olleessa populaatiossa
• Suvussa esiintyvän lukemisvaikeusriskin yhteys motoriseen ja kielelliseen kehitykseen : tallaako lapsi kielensä päälle?
• Terveet sukujuuret : miten menneisyys voi parantaa nykyisyyden?
• The heritability and morphology of lumbar Modic changes and their association with pain
• The innocent assassins : biological essays on life in the present and distant past
• The role of BACH1, BARD1 and TOPBP1 genes in familial breast cancer
• The search for genes predisposing to obesity
• The search for susceptibility genes in osteoarthritis
• The spectrum of the phenotypes in the C9ORF72 expansion carriers :
• The transcription regulation of retrotransposon BARE
• The transcriptional regulation of retrotransposon BARE
• TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility
• Transcription factors as candidate genes for type 2 diabetes : studies on peroxisome proliferator-activated receptors, hepatic nuclear factor 4α and PPARγ coactivator 1α
• Tulevaisuuden seksielämä : viettien vallankumouksia
• Tunne itsesi, suomalainen
• Tuotanto- ja kestävyysominaisuuksien geenikartoitus lypsykarjalla
• Twin-singleton differences among esl students : a study of affective and cognitive factors at the age of 12
• Use of inbreeding to increase the response to selection
• 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
• Viattomat tappajat : esseitä biologiasta : elämää nykyisyydessä ja menneisyydessä
• XXI valtakunnalliset audiologian päivät Helsingissä 30.-31.03.2000
• Älykkyys : valoa ja varjoja
• Älykäs eläin