Publications by authors named "Ericka Nelly Pompa-Mera"

Patients with 2019 coronavirus disease (COVID-19) exhibit a broad spectrum of clinical presentations. A person's antimicrobial antibody profile, as partially shaped by past infection or vaccination, can reflect the immune system health that is critical to control and resolve the infection. We performed an explorative immunoproteomics study using microbial protein arrays displaying 318 full-length antigens from 77 viruses and 3 bacteria.

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  • This study investigates how specific gene variations (SNPs) affect the development of high triglyceride levels in HIV patients on antiretroviral therapy.
  • A total of 602 patients were genotyped, revealing strong associations between hypertriglyceridemia and certain SNPs (notably rs964184 in APOA5) as well as factors like age and type of medication.
  • The findings suggest that these genetic variations could play a significant role in the side effects experienced by HIV patients undergoing treatment with protease inhibitors.
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Background: Cytomegalovirus (CMV) is able to cause serious and even deadly diseases in immunocompromised patients. It is important to have a sensitive, specific and molecular viral tests for its detection, using as targets, key genes for viral replication. The following genes have been used in the molecular detection of CMV: UL122 (replication) and UL83 (most abundant protein of the tegument).

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Hepatitis C virus (HCV) infection affects an estimated 71 million people worldwide. HCV is classified into eight genotypes and >70 subtypes. Determination of HCV genotype is important for selection of type and duration of antiviral therapy, and genotype is also a predictor of treatment response.

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  • Mexico has a high rate of childhood leukemia, with worse mortality rates compared to other countries, potentially linked to specific gene rearrangements in acute lymphoblastic leukemia (ALL).
  • A study conducted at eight public hospitals from 2010 to 2012 analyzed 282 bone marrow samples to identify the prevalence of four key gene rearrangements: ETV6-RUNX1, TCF3-PBX1, BCR-ABL1, and MLL.
  • Gene rearrangements were found in 17.7% of patients, with a correlation between specific rearrangements and early deaths within the first few months of diagnosis, indicating a possible connection to the aggressive nature of leukemia in these children.
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