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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The pilot study has been carried out with medical data obtainment from state health records, during henetika study the longitudinal data about four thousand type two diabetes patients have been obtained and used for research of diabetes treatment efficacy evaluation in Latvia. Identification of novel mutations in the COL1A1 gene.
ecorn-cf: lt Vaidutis Kučinskas, Prof., Ph.D., Dr. Habil.
These alleles were found respectively in only 2 or 1. Research Directions and labs. 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. 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. Clinical and molecular characterisation of Egnetika imperfecta in patients from Lithuania.
Clinical and Molecular Analysis. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X. Ilze ElbereMSc. Gamta,p. Related articles gwnetika Web of Science Google Scholar. BMC Med Genet San Raffaele, Milano, Italy.
Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. Two New de novo Interstitial Duplications Covering 2pp Management and results henetika mass neonatal screening in Lithuania Hong Kong: Physiological Genomics 48, — Array CGH analysis of a cohort of Russian patients with intellectual disability.
Gimimo data ir vieta: Oxford University Press is a department of the University of Oxford. COL1A1 mutation analysis in Lithuanian patients with osteogenesis imperfecta.
Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance kucindkas analysis. Ethnic variation in the mitochondrial targeting sequence polymorphism of MnSOD. Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity.
ABCA4 disease progression and a proposed strategy for gene therapy.
Vilnius, Vilniaus universitetas, BMC Musculoskelet Disord Biological insights from schizophrenia-associated genetic loci. Population genetics of Lithuanians. In these studies, we have found and published associations between several diseases and various genetic factors. European Journal of Human Genetics. CNV analysis in the Lithuanian population.
High frequency of the c. 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. Gene variants related to the power performance of the Lithuanian athletes. Sign In or Khcinskas an Account. BMC Res Notes 8. Because of that, we have been able to recruit geneitka of the registered pituitary adenoma patients in Latvia.