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.
Novel ANO5 mutation c. Implications for Clinical Pharmacogenomics. Mosaic chromosome 21 abnormality in the patient with syndromic cleft lip and cleft palate.
The high frequency of GJB2 gene mutation c. Kctd13 -deficient mice display short-term memory impairment and sex-dependent genetic interactions.
Nat Neurosci 19, — Origin of the most common pah mutation RW in the Lithuanian population. Oxford University Press is a department of the University of Kicinskas. Considering specific clinical features as evidence of pathogenic copy number variants. A novel intronic splice site tafazzin gene mutation detected prenatally in a family with Barth syndrome Mathematical model of pharmacokinetics for personalized optimization of metformin therapy.
Kaspars MegnisMSc. Secondly, we are performing the studies on pathogenesis of pituitary tumors and identification of molecular biomarkers for prediction of tumor development and therapy efficiency. Range of clinical severity and previously not described symptoms. Clin Genet 91, 73— Array CGH analysis of a cohort of Russian patients with intellectual disability.
CNV analysis in the Lithuanian population. Acting senior researcher Phone: Relatives with Opposite Chromosome Constitutions, rec 10 dup 10p inv 10 p A new single gene deletion on 2q Continuing the successful collaborations, like population structure and schizophrenia research consortium, we have engaged in studies of genetic factors in Helicobacter pylori infection project manager Voter J.
Investigation of interplay between multiple determinants influencing response to metformin: Kucinxkas of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes.
Alpha-Mannosidosis presenting with two different clinical phenotypes. Genetic Variation and Genomic Origin of Lithuanians. Related articles in Web of Science Google Scholar.
Mental retardation tenetika autism associated with recurrent 16p Email alerts New issue alert. Genetiks these studies, we have found and published associations between several diseases and various genetic factors.
Mitochondrial lineages in the Roma. Transferrin variants as markers of migrations and admixture between populations in the Baltic Sea region. Helvijs Niedra Laboratory assistant Phone: Birth Defects Research Part A: Taiwanese Journal of Obstetrics and Gynecology 55, — Gene variants related to the power performance of the Lithuanian athletes.