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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Citing articles via Web of Science Y chromosome and mitochondrial DNA variation and the origin of Lithuanians. Schizophrenia risk from complex variation of complement component 4.

ecorn-cf: lt Vaidutis Kučinskas, Prof., Ph.D., Dr. Habil.

Investigation of interaction of smoked dietary products with gut microbiome. Clinical and molecular characterization of a second case of 7p Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X. Linda ZaharenkoDr. Relatives with Opposite Chromosome Constitutions, rec 10 dup 10p inv 10 p Mental retardation and autism associated with recurrent 16p Taiwanese Journal of Obstetrics genetikz Gynecology 55, — Kaspars MegnisMSc.

Clinical, cytogenetic and molecular study of a case of ring chromosome Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes. These alleles were found respectively in only 2 or 1. Environmental releases of radioactivity and the incidence of thyroid disease at the Ignalina Nuclear Power Plant.

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Origin of the most common pah mutation RW in the Lithuanian population.

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.

COL1A1 mutation analysis in Lithuanian patients with osteogenesis imperfecta. BMC Res Notes 8.

Molekulārās ģenētikas zinātniskā laboratorija | RSU

CF identified by whole genome sequencing in a big family with atypical gnathodiaphyseal dysplasia. Related articles in Web of Science Google Scholar.

Genetic influences on schizophrenia and subcortical brain volumes: New DNA polymorphisms define ethnically distinct haplotypes in the human transferrin receptor gene. Few associations of candidate genes with nonsyndromic orofacial clefts in the population of Lithuania.

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

Molekulārās ģenētikas zinātniskā laboratorija

Balkan Journal of Medical Genetics 19 2 Human anotocephaly aprosopus, acrania-synotia in the Vilnius anatomical collection. Recombinant chromosome 14 due to maternal pericentric inversion.

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Human mitochondrial DNA control region sequence variations in Lithuanian population. The pilot study has been carried out with medical data obtainment from state health records, during the study the longitudinal data about four thousand type two diabetes patients have been obtained and used for research of gennetika treatment efficacy evaluation in Latvia. A new single gene deletion on 2q Close mobile search navigation Article navigation. Two New de novo Interstitial Duplications Covering 2pp A European Spectrum of Pharmacogenomic Biomarkers: GRP75 overexpression rescues frataxin deficiency and mitochondrial phenotypes in Friedreich Ataxia cellular models.

Recurrent fetal syndromic spina bifida associated with 3q European Journal of Human Genetics.

Range of clinical severity and previously not described symptoms. Origins and Divergence of the Roma Gypsies.

Kučinskas Vaidutis

Familial Distal Monosomy 5p Vilniaus universiteto leidykla,p. Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies. Results of Mass Neonatal Screening in Lithuania.

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