Zobrazeno 1 - 10
of 66
pro vyhledávání: '"A V, Mikelsaar"'
Autor:
L. Beckman, Astrida Krumina, Vaidutis Kučinskas, A.-V. Mikelsaar, C. Sikström, Gunhild Beckman
Publikováno v:
Human Heredity. 49:52-55
The distribution of α1-antitrypsin (PI) alleles was studied in an attempt to elucidate migrations and admixture between populations in the Baltic Sea region. The frequency of the PI Z allele, a typically Northwesteuropean marker gene, showed a highl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc7f15593305ea5a4a7b48093366fa3c
https://doi.org/10.1159/000022841
https://doi.org/10.1159/000022841
Autor:
Astrida Krumina, Lars Beckman, Vaidutis Kučinskas, A.-V. Mikelsaar, D. Ambrasiene, Gunhild Beckman, C. Sikström
Publikováno v:
Human Heredity. 48:185-191
Transferrin (TF) types were examined by isoelectric focusing in an attempt to elucidate migrations and admixture between populations in the Baltic Sea region. A highly significant heterogeneity between populations was found with respect to TF*C subty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::523e976cfb0997fd090f16f0305172b5
https://doi.org/10.1159/000022800
https://doi.org/10.1159/000022800
Publikováno v:
European Journal of Epidemiology. 16:1107-1109
In previous studies, the highest frequencies (16%) of the CCR5 Δ32 deletion have been found in populations of Finno-Ugric origin. We here report a high CCR5 Δ32 frequency (15%) in another Finno-Ugric populations, the Estonians. The highest frequenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d97a8ef81fa6e4ac10ede78e5f15f41
https://doi.org/10.1023/a:1010829816334
https://doi.org/10.1023/a:1010829816334
Autor:
G, Tasa, J, Kals, K, Muru, E, Juronen, A, Piirsoo, S, Veromann, S, Jänes, A V, Mikelsaar, A, Lang
Publikováno v:
Investigative ophthalmologyvisual science. 42(12)
To identify the genetic defect in the M1S1 gene causing gelatinous droplike corneal dystrophy (GDLD) in an Estonian family.DNA was extracted from members of a GDLD-affected family and control persons. Polymerase chain reaction followed by direct sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6818d02def7e8f7c6186079a2bd2c2e1
https://pubmed.ncbi.nlm.nih.gov/11687514
https://pubmed.ncbi.nlm.nih.gov/11687514
Publikováno v:
European journal of epidemiology. 17(3)
Four hundred and forty two adult individuals of Estonian nationality were examined in different regions of Estonia for the C282Y and H63D HFE mutations to determine the allele and genotype frequencies. The sample consisted only of those people whose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e36d9b920cf49a6ed1e53eb1f30df3fa
https://pubmed.ncbi.nlm.nih.gov/11680538
https://pubmed.ncbi.nlm.nih.gov/11680538
Publikováno v:
European journal of epidemiology. 16(12)
In previous studies, the highest frequencies (16%) of the CCR5 delta32 deletion have been found in populations of Finno-Ugric origin. We here report a high CCR5 delta32 frequency (15%) in another Finno-Ugric populations, the Estonians. The highest fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2da55f6ed44f3a76abe4787d6c7a42f1
https://pubmed.ncbi.nlm.nih.gov/11484798
https://pubmed.ncbi.nlm.nih.gov/11484798
Autor:
E, Juronen, G, Tasa, S, Veromann, L, Parts, A, Tiidla, R, Pulges, A, Panov, L, Soovere, K, Koka, A V, Mikelsaar
Publikováno v:
Investigative ophthalmologyvisual science. 41(8)
To investigate the possible association between glutathione S-transferase GSTM1, GSTM3, GSTT1, and GSTP1 polymorphism and the occurrence of age-related cataracts in Estonian patients.Patients with cortical (155), nuclear (77), posterior subcapsular (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad8ebfac753ae0c601ad9e2cde270e53
https://pubmed.ncbi.nlm.nih.gov/10892871
https://pubmed.ncbi.nlm.nih.gov/10892871
Publikováno v:
Gene geography : a computerized bulletin on human gene frequencies. 10(3)
The distribution of glutathione S-transferase T1 (GSTT1) phenotypes was studied in a total sample of 673 Estonians whose four grandparents were born in Estonia, by an ELISA test able to differentiate between GSTT1 positive and GSTT1 negative phenotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::55d045f24b3c8605e5c9678b6f983f13
https://pubmed.ncbi.nlm.nih.gov/9263772
https://pubmed.ncbi.nlm.nih.gov/9263772
Publikováno v:
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine. 13(4)
A new monoclonal antibody (MAb 9H8, IgM class) reactive with human ovarian carcinoma has been raised after immunizing C57BL/6 mice with bovine sperm. Immunohistological studies indicated that 20/21 serous ovarian adenocarcinomas expressed 9H8-defined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df6f44c09f56760ba8dc261470d87c15
https://pubmed.ncbi.nlm.nih.gov/1384106
https://pubmed.ncbi.nlm.nih.gov/1384106
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