Sökning: "pigmentation"
Visar resultat 1 - 5 av 44 avhandlingar innehållade ordet pigmentation.
1. Dissecting Phenotypic Variation in Pigmentation using Forward and Reverse Genetics
Sammanfattning : Coat color and patterning phenotypes have been extensively studied as a model for advancing our understanding of the relationship between genetic and phenotypic variation. In this thesis, genes of relevance for pigment cell biology were investigated. The dissertation is divided in two parts. LÄS MER
2. The Genetics of Speciation and Colouration in Carrion and Hooded Crows
Sammanfattning : A fundamental goal in biological research is to gain an understanding of the evolutionary processes and genetic elements that drive speciation. Genes responsible for reproductive isolation in young divergent lineages are particularly poorly known. In this thesis, the speciation genetics of carrion (Corvus (corone) corone) and hooded (C. LÄS MER
3. Vitiligo and Piebaldism : Treatmant of Leucoderma by Transplantation of autologous melanocytes
Sammanfattning : Background: Vitiligo and piebaldism are disorders in which the affected skin lack epidermal melanocytes. Vitiligo is acquired and can clinically be subgrouped, but the aetiology is still not fully understood. The most common type, generalized vitiligo (vitiligo vulgaris) has autoimmune involvement and affects about 1. LÄS MER
4. Effects of enhanced ultraviolet-B radiation on subarctic ecosystems
Sammanfattning : Biologically harmful ultraviolet-B radiation (UV-B, 280-320 nm) is increasing at the Earth´s surface owing to stratospheric ozone depletion. This is of global concern due to potential impacts of enhanced UV-B radiation on the biosphere. LÄS MER
5. Monogenic Traits Associated with Structural Variants in Chicken and Horse : Allelic and Phenotypic Diversity of Visually Appealing Traits
Sammanfattning : Domestic animals have rich phenotypic diversity that can be explored to advance our understanding of the relationship between molecular genetics and phenotypic variation. Since the advent of second generation sequencing, it has become easier to identify structural variants and associate them with phenotypic outcomes. LÄS MER