molekyyligenetiikka

name

• molekyyligenetiikka

Works about molekyyligenetiikka

• Applications of fluorescence in situ hybridization : from gene hunting to mutation visualization
• Biotekniikka 2005
• Complementation of cytochrome c oxidase deficiency by transgenic expression of the alternative oxidase in Drosophila
• Cytogenetic and molecular genetic changes in childhood acute leukaemias
• Development of amplification-based technologies for enrichment of nucleic acids with difficult sequences or low-abundance point mutations
• Frontotemporal lobar degeneration in Finland : molecular genetics and clinical aspects
• Genetic diversity of endemic fish in Lake Malawi and Lake Tanganyika
• Genetics and genomics of musical abilities
• Genomics approaches to study music perception and performance
• Hemophilia A : molecular studies in Finnish families
• Identification of new genetic syndromes with epilepsy by whole-exome sequencing
• Käyttäytymisgenetiikka : geeneistä yhteiskuntaan
• Loputtomat kauniit muodot : evodevon uusi tiede
• Me ja ne : rotuopeista sukulaisuuteen
• MED12 :
• Molecular evolution of metazoan hypoxia-inducible factors
• Molecular genetic background of tumours in hereditary leiomyomatosis and renal cell cancer syndrome
• Molecular genetic characterization of some key peptidases from Lactobacillus strains used in the dairy industry
• Molecular genetic mechanisms of pulmonary arterial hypertension
• Molecular genetic studies on nemaline myopathy and related disorders
• Molecular genetics of acute intermittent porphyria in Finland
• Molecular genetics of Alzheimer's disease : with special emphasis on presenilin, amyloid beta precursor protein and apolipoprotein E genes
• Molecular genetics of autism spectrum disorders in the Finnish population
• Molecular genetics of chicken egg quality
• Molecular genetics of Cohen syndrome
• Molecular genetics of early-onset Alzheimer's disease and frontotemporal lobar degeneration
• Molecular genetics of human type II collagen : expression in cultured chondrocytes, cDNA cloning, characterization of polymorphic sites and linkage analysis
• Molecular genetics of lactase persistence
• Molecular genetics of lysinuric protein intolerance (LPI)
• Molecular genetics of Meckel syndrome
• Molecular genetics of Meckel syndrome : ciliary genes are defective in MKS
• Molecular genetics of primary open angle glaucoma and exfoliation syndrome
• Molecular genetics of rare puberty disorders in Finland and Denmark
• Molecular genetics of selective intestinal malabsorption of vitamin B12 : the Gräsbeck-Imerslund disease (megaloblastic anemia 1)
• Molecular genetics of severe ventricular arrhythmias
• Molecular genetics of severe ventricular arrhytmias
• Molecular genetics of the GRACILE syndrome (growth retardation, aminoaciduria, cholestasis, iron overload, lactacidosis and early death)
• Molecular genetics of the immotile short tail sperm defect
• Molecular genetics of variegate porphyria in Finland
• Ne geenit! Ne geenit!
• Neuronal ceroid lipofuscinosis CLN8 : from gene to protein
• Prostate cancer : from molecular genetics to prognostic markers
• Roles of demography and natural selection in molecular evolution of trees, focus on Pinus sylvestris
• Search for genetic variants underlying musical aptitude and related traits
• Selvitys molekyylilääketieteen, -genetiikan ja -epidemiologian tutkimuslaitoksen perustamistarpeesta ja toteuttamisvaihtoehdoista
• Solu- ja molekyylibiologia
• Structure and expression of the manXYZ operon of Escherichia coli
• Studies of the human transcriptome
• The molecular background of severe mitochondrial respiratory chain deficiencies in children and adults, with special emphasis on mitochondrial cardiomyopathies
• Vesiviljelyn kalakantojen monimuotoisuuden merkitys istutushoidossa : Riista- ja kalatalouden tutkimuslaitoksen XXIII vesiviljelypäivät