Publications by authors named "Sergio G Munoz-Jimenez"

A new method using a magnetic nanoparticle-based colorimetric biosensing assay (NCBA) was compared with sputum smear microscopy (SSM) for the detection of pulmonary tuberculosis (PTB) in sputum samples. Studies were made to compare the NCBA against SSM using sputum samples collected from PTB patients prior to receiving treatment. Experiments were also conducted to determine the appropriate concentration of glycan-functionalized magnetic nanoparticles (GMNP) used in the NCBA and to evaluate the optimal digestion/decontamination solution to increase the extraction, concentration and detection of acid-fast bacilli (AFB).

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Article Synopsis
  • Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common congenital defect and recent research has identified new genetic factors linked to its occurrence, expanding the understanding of its genetic basis.
  • A study was conducted on a Mesoamerican population to analyze the contribution of 12 genetic loci to NSCL/P risk using a case-control approach.
  • The results indicated significant associations at four loci, suggesting that the genetic risks identified in other populations also apply to the Mesoamerican group, supporting the idea that these regions are crucial for NSCL/P susceptibility.
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Non-syndromic cleft lip with or without cleft palate (NSCL/P) is one of the most common of all congenital malformations and has a multifactorial etiology. Findings in mice suggest that the v-ski sarcoma viral oncogene homolog (SKI) gene is a candidate gene for orofacial clefting. In humans, a significant association between rs2843159 within SKI and NSCL/P has been reported in patients from the Philippines and South America.

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Introduction: Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is one of the most common of all birth defects. NSCL/P has a multifactorial etiology that includes both genetic and environmental factors. The IRF6 gene and three further susceptibility loci at 8q24, 10q25, and 17q22, which were identified by a recent genome-wide association scan (GWAS), are confirmed genetic risk factors for NSCL/P in patients of European descent.

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