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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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Relatives with Opposite Chromosome Constitutions, rec 10 dup 10p inv 10 p Recurrent genetiks syndromic spina bifida associated with 3q Rheumatoid arthritis in Poland and Lithuania: Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes. Sign In or Create an Account. Vilniaus universitetas, Medicinos fakultetas,p.

In these studies, we have found and published associations between several diseases and various genetic factors. Research Directions and labs.


Molekulārās ģenētikas zinātniskā laboratorija | RSU

Vilniaus universiteto leidykla,p. Nova Science Publishers,p. The main priority of the group is translational research combining the genetic, pharmacogenomic and functional studies in genetiika to understand the Human biology, disease and drug action mechanisms with emphasis on metabolic and endocrine processes.

Laura Ansone Laboratory assistant Phone: Functional characterization of the ZEB2 regulatory landscape. Vilniaus universiteto leidykla, Highly polymorphic microsatellites IRI3. Ancient human genomes suggest three ancestral populations for present-day Europeans.

PAH gene mutations identified in Lithuania. Clin Genet 91, 73— ABCA4 disease progression and a proposed strategy for gene therapy.

Latvian Biomedical Research and Study Centre – Directions and labs

Oxford University Genetioa is a department of the University of Oxford. San Raffaele, Milano, Italy. Alpha-Mannosidosis presenting with two different clinical phenotypes. Array CGH analysis of a cohort of Russian patients with intellectual disability.

Kučinskas Vaidutis

Balkan Journal of Medical Genetics 19 2 Familial variables as predictors of psychological maladjustment in Lithuanian children with phenylketonuria.

Range of clinical severity and previously not described symptoms.

Two New de novo Interstitial Duplications Covering 2pp Close mobile search navigation Article navigation. COL1A1 mutation analysis in Lithuanian patients with osteogenesis imperfecta.


Genetikos ir genomikos pagrindai. It is further planned to use health care medical information for the research of other multifactorial diseases as well.

Clinical and molecular characterisation of Osteogenesis imperfecta in patients from Lithuania. Genetic services in Lithuania. A new single gene deletion on 2q Investigation of genetiia between multiple determinants influencing response to metformin: Genetic influences on schizophrenia and subcortical brain volumes: Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: Clinical and Molecular Analysis.

It furthers the University’s objective of excellence in research, scholarship, and education by publishing worldwide. Because of that, we have been able to recruit most of the registered pituitary adenoma patients in Latvia.

Monografijos kartu su kitais autoriais: Novel ANO5 mutation c. Ilze ElbereMSc.