Publications by authors named "Artur Luiz da Costa Silva"

Article Synopsis
  • Understanding the molecular aspects of oocyte and embryo competence is vital for improving reproductive technologies, with RNA-seq providing important transcriptomic data for computational analysis.
  • This study analyzed the transcriptomic profiles of matured oocytes and blastocysts from buffalo crossbreds, revealing insights into gene expression and molecular quality indicators.
  • Analyzing gene co-expression showed strong preservation of modules related to key biological processes, while some modules exhibited weak preservation, suggesting differences between buffalo and bovine embryo development.
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Microsatellites, also known as SSRs or STRs, are polymorphic DNA regions with tandem repetitions of a nucleotide motif of size 1-6 base pairs with a broad range of applications in many fields, such as comparative genomics, molecular biology, and forensics. However, the majority of researchers do not have computational training and struggle while running command-line tools or very limited web tools for their SSR research, spending a considerable amount of time learning how to execute the software and conducting the post-processing data tabulation in other tools or manually-time that could be used directly in data analysis. We present EasySSR, a user-friendly web tool with command-line full functionality, designed for practical use in batch identifying and comparing SSRs in sequences, draft, or complete genomes, not requiring previous bioinformatic skills to run.

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  • * Four treatment levels of PKC (0%, 0.25%, 0.5%, and 1% of body weight) were tested, finding that PKC increased supplement consumption while reducing forage and non-fibrous carb intake.
  • * Although PKC supplementation did not change the dry matter degradability of Marandu grass, it improved fermentation kinetics, suggesting that feeding buffaloes with up to 1% PKC of their body weight is advantageous without negatively impacting their overall performance.
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The use of palm kernel cake as an alternative to conventional ingredients, due to the presence of residual fat, can also reduce methane emissions. The objective of the study was to evaluate, in two different experiments, the effects of palm kernel cake supplementation on feed intake, enteric methane production and estimates, and the ingestive behavior of buffaloes in the Amazon biome. In experiment 1, to evaluate feed intake, methane production, and feed efficiency, 20 crossbred females, dry and empty, with a mean age of 34 months and an initial body weight of 514 ± 69 kg, were supplemented with palm kernel cake for 60 days.

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is the causative bacterial agent of the zoonotic disease known as caseous lymphadenitis, and it presents several mechanisms of response to host defenses, including the presence of virulence factors (VFs). The genomes of these bacteria have several polymorphic markers known as microsatellites, or simple sequence repeats (SSRs), that can be used to characterize the genome, to study possible polymorphisms existing among strains, and to verify the effects of such polymorphic markers in coding regions and regions associated with VFs. In this study, several SSRs were identified within coding regions throughout the 54 genomes of this species, revealing possible polymorphisms associated with coding regions that could be used as strain-specific or serotype-specific identifiers of .

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Background: Ameloblastoma (AMB) is a benign odontogenic tumour, with an aggressive local behaviour and a high rate of recurrence. Previous studies have demonstrated that hypoxia-induced factor alpha 1 (HIF-1) and activated caspase-3 contribute to tumour invasiveness and cytogenesis in ameloblastoma. Hypoxia increases HIF-1 levels, which triggers a number of signalling pathways.

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  • Fluoropyrimidines are commonly used cancer drugs but have significant toxicity, and this study examined genetic variations in patients treated with these drugs in the Brazilian Amazon.
  • The research involved 216 patients with gastrointestinal cancers, analyzing 33 gene polymorphisms and using advanced genotyping technology to assess ancestry and potential toxicity risks.
  • Four specific genetic polymorphisms (in the ABCC4, FPGS, SLC29A1, and MTHFR genes) were identified as significant predictors of toxicity, highlighting the importance of personalized medicine in this unique population.
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  • Acute Lymphoblastic Leukemia (ALL) is the most common cancer in children, and this study looks into genetic variations affecting the microRNAs related to its development in a Brazilian population.
  • The study analyzed 10 genetic polymorphisms in 100 pediatric ALL patients and 180 healthy controls, finding that specific genotypes significantly increased the risk of developing ALL, particularly the rs3746444 and rs3805500 polymorphisms.
  • Results indicate that certain genetic variations can indicate susceptibility to ALL, highlighting their potential use in risk assessment and facilitating a better understanding of the disease's complex causes.
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  • - Acute Lymphoblastic Leukemia (ALL) is the most common childhood cancer, but treatment outcomes vary among different ethnic groups, particularly showing lower success rates in children with high Native American ancestry.
  • - A study analyzed 27 genetic markers related to ALL treatment in Amerindian populations from the Brazilian Amazon and compared these to data from five continents, revealing significant differences in marker frequencies.
  • - The unique genetic profile of the indigenous Amazonian population suggests they may require tailored treatment strategies for ALL due to their distinct pharmacogenomic variants.
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The variation in the allelic frequencies of polymorphic pharmacogenes among different ethnic groups may be responsible for severe adverse reactions to or altered efficacy of a wide variety of drugs. Amazonian Amerindian populations have a unique genetic profile that may have a fundamental on the efficacy and safety of certain drugs. The genetic characteristics of these populations are poorly known, which can negatively impact the systematic application of treatments guided by pharmacogenomic guidelines.

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Introduction: This study confirmed the absence of natural infection with Xenotropic murine leukemia virus-related virus (XMRV) or XMRV-related disease in human populations of the Brazilian Amazon basin. We demonstrated that 803 individuals of both sexes, who were residents of Belem in the Brazilian State of Pará, were not infected with XMRV.

Methods: Individuals were divided into 4 subgroups: healthy individuals, individuals infected with human immunodeficiency virus, type 1 (HIV-1), individuals infected with human T-lymphotrophic virus, types 1 or 2 (HTLV-1/2), and individuals with prostate cancer.

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Corynebacterium ulcerans is a bacterial species with high importance because it causes infections in animals and, rarely, in humans. Its virulence mechanisms remain unclear. The current study describes the draft genome of C.

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Multiple Displacement Amplification (MDA) of DNA using φ29 (phi29) DNA polymerase amplifies DNA several billion-fold, which has proved to be potentially very useful for evaluating genome information in a culture-independent manner. Whole genome sequencing using DNA from a single prokaryotic genome copy amplified by MDA has not yet been achieved due to the formation of chimeras and skewed amplification of genomic regions during the MDA step, which then precludes genome assembly. We have hereby addressed the issue by using 10 ng of genomic Vibrio cholerae DNA extracted within an agarose plug to ensure circularity as a starting point for MDA and then sequencing the amplified yield using the SOLiD platform.

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We proposed a modification the procedure of genotyping based in labeled universal primer and tailed primer. In the standard protocol, three primers are used in the same PCR reaction, a forward primer with tail added at the 5' end of the identical sequence to labeled universal primer with dye-fluorescent and a reverse primer. Unfortunately, the choice of a labeled primer characterized by a large number of complementary sequences in target genomes (which is more probable in larger genomes) result in unspecific amplifications (false positive) can cause absence or decrease amplification of the locus of interest and also false interpretation of the analysis.

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