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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Molekulārās ģenētikas zinātniskā laboratorija | RSU
The high frequency of GJB2 gene mutation c. 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. Rheumatoid arthritis in Poland and Lithuania: Cytogenetic prenatal diagnosis in Jucinskas human genetics centre: Results of Mass Neonatal Screening in Lithuania.
Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. Y chromosome and mitochondrial DNA variation and the origin of Lithuanians. Genetic Structure of Europeans: Ethnic variation in the mitochondrial targeting sequence polymorphism of MnSOD. Genetic services in Lithuania. Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies. GRP75 overexpression rescues frataxin deficiency and mitochondrial phenotypes in Friedreich Ataxia cellular models.
Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1. In these studies, we have found and published associations between several diseases and various genetic factors. It furthers the University’s objective of excellence in research, scholarship, and education by publishing worldwide.
Oxford University Press is a department of the University of Oxford. Few associations of candidate genes with nonsyndromic orofacial clefts in the population lucinskas Lithuania. 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.
Molekulārās ģenētikas zinātniskā laboratorija
Differential diagnosis of low maternal oestriol level. 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.
Acting senior researcher Phone: Familial variables as predictors of psychological maladjustment in Lithuanian children with phenylketonuria.
Nova Science Publishers,p. Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity.
ERBB4 is associated with intellectual disability. BMC Musculoskelet Disord Investigation of interaction of smoked dietary products with gut microbiome.
Terminal deletion of chromosome 18q in apatient with multiple congenital malformations including mental retardation. CNV analysis in the Lithuanian population.
Ilze Izabella DinduneBSc. Duplications in addition to terminal deletions genetikz present in a proportion of ring chromosomes: Genetic diversity within the RW phenylketonuria mutation lineages in Europe. Genetikos ir genomikos pagrindai.
Clinical and Molecular Analysis. Secondly, we are performing the studies on pathogenesis of pituitary tumors and identification of molecular biomarkers for prediction of tumor development and therapy efficiency. Vilniaus universitetas, Medicinos fakultetas,genetiak. Balkan Journal of Medical Genetics 19 2 Genetic counseling in carriers of reciprocal chromosomal translocations involving long arm of chromosome Email alerts New issue alert.