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Studium genetické příbuznosti asijských zástupců rodu Orbea pomocí molekulárních markerůDoubková, Ivona January 2011 (has links)
No description available.
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852 |
Studium evolučního vývoje v rámci rodu CarexVeselá, Petra January 2011 (has links)
No description available.
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853 |
Aplikace metod založených na amplifikaci DNA při studiu genomu rodu PrunusRaddová, Jana January 2004 (has links)
Angl. resumé
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854 |
Variabilita DNA genů MYF6, IGF2 a ACSL4 u prasatVykoukalová, Zuzana January 2005 (has links)
Angl. resumé
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855 |
Detekce pekařské jakosti pšenice s využitím DNA markerůLišková, Danuše January 2004 (has links)
Angl. resumé
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856 |
Vyhodnocení genetické variability siky japonského ve vybraných oblastech ČRKřížová, Alena January 2008 (has links)
No description available.
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857 |
Ověření autenticity hovězího masa v rámci systému zpětné dohledatelnostiPáralová, Viktorie January 2012 (has links)
No description available.
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858 |
Morfologická a genetická variabilita sírovce žlutooranžového (Laetiporus sulphureus)Byrtusová, Zuzana January 2012 (has links)
No description available.
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859 |
Evolutionary biology of the Western rattlesnake, (Serpentes: Viperidae: Crotalus viridis) : phylogeny, morphology, and venom evolutionPook, Catharine Emma January 2001 (has links)
A multidisciplinary hypothesis testing approach is adopted to investigate the intraspecific relationships, and venom evolution within the polytypic species, Crotalus viridis, in western North America. A molecular phylogeny is reconstructed from mitochondrial cytochrome b (678 bp) and NADH dehydrogenase subunit 4 (ND4; 669 bp) DNA sequence information. The phylogeny is not concordant with the conventional subspecies categories, but shows strong geographical structuring corresponding to the major geographic regions of the western U. S. The basal split gives rise to two lineages (5.1-6.4% sequence divergence) corresponding to haplotypes east and west of the Rocky Mountains. Within the western lineage, Crotalus viridis cerberus forms a sister group to the other western haplotypes, and appears to have a long, independent evolutionary history. Multivariate morphometric analysis also reveals regional structuring. Clear eastern and western forms are apparent, although these populations are not totally reproductively isolated. North-south clinal variation in morphology is found among populations east of the Rocky Mountains between Montana and Arizona. Among the western forms, there is clearly a zone of intergradation between the Great Basin and Pacific Coast forms, represented by a morphological cline in Idaho. Clinal variation was also found between the northern and southern Pacific Coast forms. Venom evolution is of interest in C. viridis, since C. v. concolor is the only subspecies of C. viridis to secrete a high toxicity PLA2 phospholipase (Concolor toxin) in its venom in adulthood. Isoelectric focusing of venom proteins revealed 14 variable bands, of which only one was unique (pI 8.52) to C. v. concolor. Principal coordinates analysis revealed three main venom types, corresponding to the Pacific Coast, C. v. concolor, and the remaining populations respectively. However, C. v. concolor tends to cluster with the latter group when the unique venom band is excluded from the analysis. 1 Phylogeny, rather than ecology, appears to be an important cause of geographic variation in both morphology and venom, as revealed by partial Mantel tests. Many characters are influenced by both phylogeny and ecology, however, probably because many causes of variation are intercorrelated. It is suggested that selection on venom composition probably varies according to the function of individual components. The systematics of Crotalus viridis complex is reviewed according the criteria of the general lineage concept of species. Combined evidence from the molecular phylogeny and morphology (and to a lesser extent venom) suggests the existence of three species, to be named Crotalus viridis, Crotalus cerberus, and Crotalus oreganus (including the subspecies C. o. oreganus, C. o. lutosus and C. o. concolor).
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860 |
The origins and spread of the Neolithic in the Old World using ancient genomesGallego Llorente, Marcos January 2018 (has links)
One of the biggest innovations in human prehistory was the advent of food production, consisting of the ability to grow crops and domesticate animals for consumption. This wide-scale transition from hunting and gathering to food production led to more permanent settlements, and set in motion major societal changes. In western Eurasia, this revolution spread from the Near East into Europe, Africa and diverse regions of Asia. Agriculture was brought into Europe by the descendants of early Anatolian farmers starting approximately 8,000 years ago. But little was known of the people who developed agriculture in the Fertile Crescent: where they all closely related to the early Anatolian farmers, or were there multiple ethnic groups who developed agriculture in parallel? In the first data chapter, I use the first genome from a Neolithic woman from Ganj Dareh, in the Zagros Mountains (Iran), a site with evidence of early goat domestication 10,000 years ago. I showed that Western Iran wan inhabited by populations mostly similar to Hunter- gatherer populations from the Caucasus, but remarkably, very distinct from the Anatolian farmers who spread the Neolithic package into Europe. While a degree of cultural diffusion between Anatolia, Mesopotamia and the Zagros highlands likely happened, genetic dissimilarity supports a model in which Neolithic societies of that area were distinct. The second chapter deals with how Africa was affected by population movements, originating in the Near East, during the Neolithic times. Characterising genetic diversity in Africa is a crucial step for analyses reconstructing human evolution. Using Mota, an ancient genome from a male from the Ethiopian highlands, I showed a backflow into Africa by populations closely related to the Anatolian Neolithic farmers. The third chapter deals with some common problems and themes in the analysis of ancient DNA, such as merging capture datasets with diverse number of ascertained SNPs, combining capture and shotgun data in the same analysis, and the effect of UDG treatment in ancient samples. I describe the most common problems and their effect in summary statistics, and propose a guide on how to work with ancient DNA to avoid data compatibility problems.
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