KUCINSKAS GENETIKA PDF

Genetika citogenetika. (B). Klinikinė genetika (B). Medicinos. Žmogaus ir . Po-Ru Loh, Bhatia G, Gusev A, Kucinskas V, Kucinskiene ZA et al. Kučinskas V. Genetika. Šviesa, , p. ISBN 3. Langlois S, Brock JA, Wilson RD, Audibert F,. Brock JA, Carroll J, Cartier L, Gagnon A. Abstract. The chemokine receptor CCR5 is encoded by the CMKBR5 gene located on the p region of human chromosome 3, and constitutes the major.

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It furthers the University’s objective of excellence in research, scholarship, and education by publishing worldwide. Investigation of interaction of smoked dietary products with gut microbiome.

Results of Mass Neonatal Screening in Lithuania. Taking advantages of Biobank developments and established collaborations with hospitals and medical doctors we aim to perform omics based research on number of proprietary directions involving identification genetikaa new disease and therapy related biomarkers and drug targets as well as their characterisation using cell and animal model systems followed by possible clinical validation and development of diagnostics and therapies.

Physiological Genomics 48, — Recurrent fetal syndromic spina bifida associated with 3q Molecular genetic study of autosomal dominant retinitis pigmentosa kucinskad Lithuanian patients. Valentin Haecker and his examination of the phenotype.

In previous years, we have done several candidate gene and replication research projects, in purpose to study genetic predisposition of such multifactorial diseases, like diabetes, cardiovascular and endocrine diseases as well as various metabolic parameters.

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Mental retardation and autism associated geneika recurrent 16p Besides that, we are obtaining and studying pituitary adenoma stem-like cell cultures, in order to analyse their origin and differentiation as well as to create pituitary adenoma cell model, in which we could independently evaluate drug effectiveness and molecular maker dynamics.

Mitochondrial lineages in the Roma. With these resources, we are performing complex epigenetics, expression and other biomarkers studies, such as the host and mikrobioma interaction in order to explore the factors that modify drug exposure. Population genetics of Lithuanians. Alpha-Mannosidosis presenting with two different clinical phenotypes.

Genetic Structure of Europeans: Mosaic chromosome 21 abnormality in the patient with syndromic cleft lip and cleft palate. Linda ZaharenkoDr. Genetic Variation and Genomic Origin of Lithuanians.

Highly polymorphic microsatellites IRI3. CNV analysis in the Lithuanian population. Close mobile search navigation Article navigation.

Molekulārās ģenētikas zinātniskā laboratorija | RSU

New DNA polymorphisms define ethnically distinct haplotypes in the human transferrin receptor gene. Researches are based on cohort more than patients at kucisnkas momentthat has been deliberately collected since yearinvolving major medical institutions in Latvia – Pauls Stradins Clinical University Hospital and Riga East Clinical University Hospital.

Origin of the most common pah mutation RW in the Lithuanian population. Clinical and molecular characterization of a second case of 7p Clinical and molecular characterisation of Osteogenesis imperfecta in patients from Lithuania.

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Finally we are interested in elaboration the mechanisms of metabolic regulation and its interplay with inflammatory processes of adipose tissue as well as patient stem cell derived models of diabetes including the characterisation of existing and new drugs.

Management and results of mass neonatal screening in Lithuania Hong Kong: Y chromosome and mitochondrial DNA variation and the origin of Lithuanians. Ancient human genomes suggest three ancestral populations for present-day Europeans. Ilze Izabella DinduneBSc.

Implications for Clinical Pharmacogenomics. These alleles were found respectively in only 2 or 1.

Kučinskas Vaidutis

Citing articles via Web of Science Clinical, cytogenetic and molecular study of a case of ring chromosome CF identified by whole genome sequencing in a big family with atypical gnathodiaphyseal dysplasia. Origin of the most common RW mutation. European Journal of Medical Genetics 60— Nat Genet 47, — Ethnic variation in the mitochondrial targeting sequence polymorphism of MnSOD.

COL1A1 mutation analysis in Lithuanian patients with osteogenesis imperfecta. Duplication of segment 1p21 following paternal insertional translocation, ins 6;1 q25;p Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients.