996 resultados para Polymorphism for ancestry-admixture mapping
Resumo:
Resource Mapping tool from the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Resource Mapping resources shared during the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Intraspecific genetic variation for morphological traits is observed in many organisms. In Arabidopsis thaliana, alleles responsible for intraspecific morphological variation are increasingly being identified. However, the fitness consequences remain unclear in most cases. Here, the fitness effects of alleles of the BRX gene are investigated. A brx loss-of-function allele, which was found in a natural accession, results in a highly branched but poorly elongated root system. Comparison between the control accession Sav-0 and an introgression of brx into this background (brxS) indicated that, surprisingly, brx loss of function did not negatively affect fitness in pure stands. However, in mixed, well-watered stands brxS performance and reproductive output decreased significantly, as the proportion of Sav-0 neighbors increased. Additional comparisons between brxS and a brxS line that was complemented by a BRX transgene confirmed a direct effect of the loss-of-function allele on plant performance, as indicated by restored competitive ability of the transgenic genotype. Further, because plant height was very similar across genotypes and because the experimental setup largely excluded shading effects, the impaired competitiveness of the brx loss-of-function genotype likely reflects below-ground competition. In summary, these data reveal conditional fitness effects of a single gene polymorphism in response to intraspecific competition in Arabidopsis.
Resumo:
Infantile spasms (IS) is the most severe and common form of epilepsy occurring in the first year of life. At least half of IS cases are idiopathic in origin, with others presumed to arise because of brain insult or malformation. Here, we identify a locus for IS by high-resolution mapping of 7q11.23-q21.1 interstitial deletions in patients. The breakpoints delineate a 500 kb interval within the MAGI2 gene (1.4 Mb in size) that is hemizygously disrupted in 15 of 16 participants with IS or childhood epilepsy, but remains intact in 11 of 12 participants with no seizure history. MAGI2 encodes the synaptic scaffolding protein membrane-associated guanylate kinase inverted-2 that interacts with Stargazin, a protein also associated with epilepsy in the stargazer mouse.
Resumo:
Business survey tool from the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Content outline used during the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Activities used during the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Announcement of the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Information shared at the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Youth survey tool from the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Service provider survey tool from the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Community organizations survey tool from the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Parents survey tool from the Improving Transition Outcomes Resource Mapping Workshops
Resumo:
Community members survey tool from the Improving Transition Outcomes Resource Mapping Workshops