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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Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. CNV analysis in the Lithuanian population. Secondly, we are performing the studies on pathogenesis of pituitary tumors and identification of molecular biomarkers for prediction of tumor development and therapy efficiency.

Latvijas biomedicīnas pētījumu un studiju centrs – Virzieni un grupas

Linda ZaharenkoDr. BMC Med Genet Investigation of interplay between multiple determinants influencing response to metformin: Sign In or Create an Account. Investigation of interaction of smoked dietary products with gut microbiome. Identification of novel mutations in the COL1A1 gene.

Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients. Familial variables as predictors of psychological maladjustment in Lithuanian children with phenylketonuria. Rihards Saksis Laboratory assistant Phone: Ilona MandrikaMSc. Highly polymorphic microsatellites IRI3.

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Molekulārās ģenētikas zinātniskā laboratorija | RSU

Origin of the most common pah mutation RW in the Lithuanian population. Mathematical model of pharmacokinetics for personalized optimization of metformin therapy. Annals of Human Genetics 79, — Clinical and Molecular Analysis.

High frequency of the c. Human anotocephaly aprosopus, acrania-synotia in the Vilnius anatomical collection. Kuclnskas — Italija, Vokietija, Latvija. 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.

Origins and Divergence of the Roma Gypsies. PCDH18 — A new candidate gene for intellectual disability? Research Directions and labs.

Challenges in exome analysis by LifeScope and its alternative computational pipelines. Array CGH analysis of a cohort of Russian patients with intellectual disability.

A single gene deletion on 4q Novel ANO5 mutation c. 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 of 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.

San Raffaele, Milano, Italy. Mitochondrial lineages in the Roma. Cytogenetic prenatal diagnosis in Lithuanian human genetics centre: PAH gene mutations identified in Lithuania.

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Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies. Schizophrenia risk from complex variation of complement component 4. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: Molecular Basis of Cystic Fibrosis in Lithuania: Following the genetic studies on diabetes, we first engaged the studies of T2D pharmacogenomics and drug action mechanisms, establishing prospective cohort of T2D patients more than patients at this moment and doing several small clinical studies.

Origin of the most common RW mutation. COL1A1 mutation analysis in Lithuanian patients with osteogenesis imperfecta. Alpha-Mannosidosis presenting with two different clinical phenotypes.

Ethically and socially responsible governance of research biobanks in Latvia: The main priority of the group is translational research combining the genetic, pharmacogenomic and functional studies in order to understand the Human biology, disease and drug action mechanisms with emphasis on metabolic and endocrine processes.

Molekulārās ģenētikas zinātniskā laboratorija

Clin Genet 91, 73— Taiwanese Journal of Obstetrics and Gynecology 55, — Duplication of segment 1p21 following paternal insertional translocation, ins 6;1 q25;p European Journal of Human Genetics.

Email alerts New issue alert. Vilnius, Vilniaus universitetas, Valentin Haecker and his examination of the phenotype.