Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Amela, Sehić"'
Publikováno v:
Collegium antropologicum. 28
Deletions of two of four DAZ (Deleted in AZoospermia) gene copies located on the Y chromosome were associated with spermatogenic failure, but the information on DAZ copy number is still very scarce. The aim of this study was to determine the frequenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::825ab1ba292a9fa232dd704395d850c0
https://pubmed.ncbi.nlm.nih.gov/15571102
https://pubmed.ncbi.nlm.nih.gov/15571102
Publikováno v:
Collegium antropologicum. 27(2)
Angiotensin II is the major effector molecule of renin-angiotensin system; its production can be conveniently interrupted by angiotensin-converting enzyme (ACE). Typical plasma levels of ACE accompany the I/D polymorphism; however, a controversy exis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8bc8819b3a771c8b663fb775ad212ab7
https://pubmed.ncbi.nlm.nih.gov/14746140
https://pubmed.ncbi.nlm.nih.gov/14746140
Autor:
Rifet, Terzić, Emir, Tupković, Natasa, Logar, Amela, Sehić, Emira, Duricić, Osman, Sinanović, Borut, Peterlin
Publikováno v:
Medicinski arhiv. 56(4)
Huntington's disease is the most prominent basal ganglion disease. Huntington's gene, IT15, in chromosome 4p16.3, has 67 axons with 10,366 bp coding space and unstable CAG sequence that codes glutamine on 5' terminal. The molecular-genetic analysis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::799d1519614960b0fc016d0702299a17
https://pubmed.ncbi.nlm.nih.gov/12518531
https://pubmed.ncbi.nlm.nih.gov/12518531