The role of antibodies to complement component C1Q in the pathogenesis of SLE and hypocomplementemic urticarial vasculitis

SIGLEAvailable from British Library Document Supply Centre-DSC:DXN022183 / BLDSC - British Library Document Supply CentreGBUnited Kingdo

Genetic Analysis of the Cardiac Methylome at Single Nucleotide Resolution in a Model of Human Cardiovascular Disease

10.1371/journal.pgen.1004813PLoS Genetics101

Dessecação de plantas daninhas com glyphosate em mistura com ureia ou sulfato de amônio Weed desiccation with glyphosate mixed with urea or ammonium sulfate

O glyphosate é um herbicida não-seletivo, sistêmico, usado para controle de plantas daninhas anuais e perenes em todo o mundo. A absorção da molécula do glyphosate ocorre pelos tecidos fotossinteticamente ativos das plantas, porém alguns fatores podem reduzir sua eficácia, como a morfologia e diversidade de espécies, chuva após aplicação, qualidade da água e misturas em tanque com outros defensivos, entre outros. Objetivou-se com este trabalho avaliar a influência da adição de sulfato de amônio ou ureia em calda na eficácia do herbicida glyphosate para dessecação de plantas daninhas. Dois experimentos foram desenvolvidos em Piracicaba - SP, com aplicações de glyphosate (720 e 1.440 g ha-1) isolado ou combinado com duas doses de sulfato de amônio (7,5 e 15,0 g L-1) ou ureia (2,5 e 5,0 g L-1) sobre as plantas daninhas: apaga-fogo (Alternanthera tenella) e capim-massambará (Sorghum halepense). Para a espécie menos suscetível ao herbicida (capim-massambará), a adição de fontes nitrogenadas à menor dose de glyphosate acelerou a morte das plantas, elevando os níveis de controle em até 7,3% na avaliação de 21 dias após aplicação (DAA) dos tratamentos. Contudo, os efeitos não foram observados nas avaliações de controle, massa fresca e seca, conduzidas aos 28 DAA. A dose recomendada de glyphosate para cada espécie proporcionou controle satisfatório, sem a necessidade de adição de sulfato de amônio ou ureia.<br>Glyphosate is a non-selective systemic herbicide used to control annual and perennial weeds worldwide. Molecule absorption occurs through the plant's photosynthetically-active tissues; however, some factors might reduce its efficacy, such as morphology and specific diversity, rain after application, water quality and tank mixtures with other chemicals. Thus, this work aimed to evaluate the influence of ammonium sulfate or urea addiction to spray tank on glyphosate efficacy for weed desiccation. Two trials were carried out in Piracicaba - SP, with applications of glyphosate (720 and 1440 g ha-1) alone or combined with two rates of ammonium sulfate (7.5 and 15.0 g L-1) or urea (2.5 and 5.0 g L-1), over the weeds Alternanthera tenella and Sorghum halepense. For the least susceptible species (S. halepense), the addition of nitrogen sources to the lower rate of glyphosate accelerated plant death, increasing the control levels up to 7.3%, at 21 days after application (DAA). However, the effects were not observed when control, fresh and dry mass were evaluated at 28 DAA. Glyphosate recommended rate for each species promoted appropriate control, without the need to add ammonium sulfate or urea

Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

© 2022, The Author(s).Alzheimer’s disease (AD), the leading cause of dementia, has an estimated heritability of approximately 70%1. The genetic component of AD has been mainly assessed using genome-wide association studies, which do not capture the risk contributed by rare variants2. Here, we compared the gene-based burden of rare damaging variants in exome sequencing data from 32,558 individuals—16,036 AD cases and 16,522 controls. Next to variants in TREM2, SORL1 and ABCA7, we observed a significant association of rare, predicted damaging variants in ATP8B4 and ABCA1 with AD risk, and a suggestive signal in ADAM10. Additionally, the rare-variant burden in RIN3, CLU, ZCWPW1 and ACE highlighted these genes as potential drivers of respective AD-genome-wide association study loci. Variants associated with the strongest effect on AD risk, in particular loss-of-function variants, are enriched in early-onset AD cases. Our results provide additional evidence for a major role for amyloid-β precursor protein processing, amyloid-β aggregation, lipid metabolism and microglial function in AD

Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

© 2022, The Author(s).Alzheimer’s disease (AD), the leading cause of dementia, has an estimated heritability of approximately 70%1. The genetic component of AD has been mainly assessed using genome-wide association studies, which do not capture the risk contributed by rare variants2. Here, we compared the gene-based burden of rare damaging variants in exome sequencing data from 32,558 individuals—16,036 AD cases and 16,522 controls. Next to variants in TREM2, SORL1 and ABCA7, we observed a significant association of rare, predicted damaging variants in ATP8B4 and ABCA1 with AD risk, and a suggestive signal in ADAM10. Additionally, the rare-variant burden in RIN3, CLU, ZCWPW1 and ACE highlighted these genes as potential drivers of respective AD-genome-wide association study loci. Variants associated with the strongest effect on AD risk, in particular loss-of-function variants, are enriched in early-onset AD cases. Our results provide additional evidence for a major role for amyloid-β precursor protein processing, amyloid-β aggregation, lipid metabolism and microglial function in AD