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perinnöllinen alttius
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http://www.yso.fi/onto/yso/p24980
name
perinnöllinen alttius
Works about perinnöllinen alttius
A study on genetic mutations involving mitochondrial disorders :
Brain responses to speech sounds in infants and children with and without familial risk for dyslexia
BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer
Catechol-O-methyltransferase and pain in rodents and humans
DNA damage response gene mutations and inherited susceptibility to breast cancer
Early adversity, psychosis risk and brain response to faces
Etiological pathways of osteoarthritis
Familial adenomatous polyposis :
Genetic background and antenatal risk factors of bronchopulmonary dysplasia
Genetic background of spontaneous preterm birth and lung diseases in preterm infants : studies of potential susceptibility genes and polymorphisms
Genetic causes and risk factors associated with phenotypes occurring in mitochondrial disorders
Genetic predisposition to breast and ovarian cancer :
Genetic predisposition to spontaneous preterm birth : approaches to identify susceptibility genes
Genetic risk factors for hereditary prostate cancer in Finland : from targeted analysis of susceptibility loci to genome-wide copy number variation study
Genetic risk profiles for coronary heart disease
Genetic studies on susceptibility genes in osteoarthritis
Genetic susceptibility factors for prostate cancer at chromosomal region 11q13.5
Genetic susceptibility to asbestos and tobacco smoke related non-malignant pleuropulmonary changes
Genetic susceptibility to childhood bronchiolitis
Genetic variants predisposing to prognosis in pulmonary sarcoidosis
Genetics of breast and ovarian cancer predisposition with a focus on RAD51C and RAD51D genes
Genetics of multiple sclerosis
Genome-wide associations and computational search for the genetic risk factors for diabetic nephropathy
Germline predisposition to childhood acute lymphoblastic leukemia and bone marrow failure, and mitochondrial DNA variants in leukemia
Hereditary predisposition to breast cancer : with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes
Histological characteristics and gene expression profiling of Dupuytren's disease
Human pluripotent stem cells and CRISPR-Cas9 genome editing to model diabetes
Identification of novel tumor predisposition families and underlying genetic defects
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
Interplay of genetic and environmental triggers in intestinal inflammation : genetics and transcriptomics in celiac disease and inflammatory bowel disease
Iskiasoireyhtymään liittyvät perinnölliset tekijät : perimänlaajuinen tutkimus neljässä suuressa väestöotoksessa
Molecular and functional characterization of ABRAXAS and PALB2 genes in hereditary breast cancer predisposition
New insights into the genetic basis of colorectal cancer
Obesity, physical activity and cardiorespiratory fitness in young adulthood : studies in Finnish twins
On the genetics of intracranial aneurysms and on growth factor induced angiogenesis in the murine brain
PALB2 and RAP80 genes in hereditary breast cancer predisposition
Perinatal factors as predictors of brain damage and neurodevelopmental outcome :
Periytyvän rintasyöpäalttiusmutaation (BRCA1/2) kantajamiesten hypoteettinen perinnöllisyysneuvontamalli
Rare genetic variants and complex diseases : a bayesian approach
Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer
Skeletal and extra-skeletal characteristics of WNT1 osteoporosis
Studies on causes of multiple sclerosis : from genes to transcriptome
Studies on the genetics of heart failure
Systems and mechanistic understanding of genetic predisposition to prostate cancer
Syöpäsolun tarina
The development of immune responses and gut microbiota in children at genetic risk of type 1 diabetes
The search for genetic factors in hand osteoarthritis
The search for susceptibility genes in lumbar disc degeneration : focus on young individuals
Tupakka- ja nikotiiniriippuvuus
Type 1 family history and gad autoantibodies in subjects without diabetes and patients with type 2 diabetes
Variation of the PALB2 and PTEN genes and eIF4E protein expression as prognostic factors in breast cancer
Yksilöllisten alttiustekijöiden merkitys rakennustyöntekijöiden vaikean asbestoosin ja emfyseeman synnyssä :
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