49 research outputs found
About Bianchi I with VSL
In this paper we study how to attack, through different techniques, a perfect
fluid Bianchi I model with variable G,c and Lambda, but taking into account the
effects of a -variable into the curvature tensor. We study the model under
the assumption,div(T)=0. These tactics are: Lie groups method (LM), imposing a
particular symmetry, self-similarity (SS), matter collineations (MC) and
kinematical self-similarity (KSS). We compare both tactics since they are quite
similar (symmetry principles). We arrive to the conclusion that the LM is too
restrictive and brings us to get only the flat FRW solution. The SS, MC and KSS
approaches bring us to obtain all the quantities depending on \int c(t)dt.
Therefore, in order to study their behavior we impose some physical
restrictions like for example the condition q<0 (accelerating universe). In
this way we find that is a growing time function and Lambda is a decreasing
time function whose sing depends on the equation of state, w, while the
exponents of the scale factor must satisfy the conditions
and
, i.e. for all equation of state relaxing in this way the
Kasner conditions. The behavior of depends on two parameters, the equation
of state and a parameter that controls the behavior of
therefore may be growing or decreasing.We also show that through
the Lie method, there is no difference between to study the field equations
under the assumption of a var affecting to the curvature tensor which the
other one where it is not considered such effects.Nevertheless, it is essential
to consider such effects in the cases studied under the SS, MC, and KSS
hypotheses.Comment: 29 pages, Revtex4, Accepted for publication in Astrophysics & Space
Scienc
Atividade respiratĂłria, produção de etileno e vida Ăștil de repolho (Brassica oleracea, var. capitata) minimamente processado em atmosfera controlada
New insights into the genetic etiology of Alzheimer's disease and related dementias.
Characterization of the genetic landscape of Alzheimer's disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We performed a two-stage genome-wide association study totaling 111,326 clinically diagnosed/'proxy' AD cases and 677,663 controls. We found 75 risk loci, of which 42 were new at the time of analysis. Pathway enrichment analyses confirmed the involvement of amyloid/tau pathways and highlighted microglia implication. Gene prioritization in the new loci identified 31 genes that were suggestive of new genetically associated processes, including the tumor necrosis factor alpha pathway through the linear ubiquitin chain assembly complex. We also built a new genetic risk score associated with the risk of future AD/dementia or progression from mild cognitive impairment to AD/dementia. The improvement in prediction led to a 1.6- to 1.9-fold increase in AD risk from the lowest to the highest decile, in addition to effects of age and the APOE Δ4 allele
New insights into the genetic etiology of Alzheimer's disease and related dementias
Characterization of the genetic landscape of Alzheimer's disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We performed a two-stage genome-wide association study totaling 111,326 clinically diagnosed/'proxy' AD cases and 677,663 controls. We found 75 risk loci, of which 42 were new at the time of analysis. Pathway enrichment analyses confirmed the involvement of amyloid/tau pathways and highlighted microglia implication. Gene prioritization in the new loci identified 31 genes that were suggestive of new genetically associated processes, including the tumor necrosis factor alpha pathway through the linear ubiquitin chain assembly complex. We also built a new genetic risk score associated with the risk of future AD/dementia or progression from mild cognitive impairment to AD/dementia. The improvement in prediction led to a 1.6- to 1.9-fold increase in AD risk from the lowest to the highest decile, in addition to effects of age and the APOE Δ4 allele