Publications by authors named "Cynthia Popalis"

Article Synopsis
  • A study on pediatric Crohn disease (CD) patients treated with adalimumab (ADA) showed that 82% achieved clinical remission over 24.8 months, though 15% discontinued due to loss of response (LOR).
  • Factors like being anti-TNF naïve and having inflammatory behavior positively impacted the likelihood of achieving and maintaining remission.
  • Maintaining a trough concentration (TC) above 7.5 ug/mL was linked to durable clinical remission, with higher levels promoting better biomarker and endoscopic outcomes.
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Objectives: To determine time to diagnosis in a paediatric inflammatory bowel disease (IBD) cohort and the relative contribution of the component intervals, and to identify factors associated with diagnostic delay.

Design: Prospective cohort study SETTING: Single-centre study including children with incident IBD at the Hospital for Sick Children diagnosed between December 2013 and December 2015.

Interventions: Time to diagnosis and its subintervals were determined and patient, disease and institutional factors were tested for associations.

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Human kallikreins are a cluster of 15 serine protease genes located in the chromosomal band 19q13.4, a non-randomly rearranged region in many solid tumors, including pancreatic cancer. We utilized the SAGE and EST databases of the Cancer Genome Anatomy Project to perform in-silico analysis of kallikrein gene expression in normal and cancerous pancreatic and colon tissues and cell lines using virtual Northern blotting (VNB), digital differential display (DDD) and X-profiler.

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Recent evidence suggests that many members of the human kallikrein (KLK) gene family are differentially regulated in ovarian cancer and have potential as diagnostic and/or prognostic markers. We used the serial analysis of gene expression and expressed sequence tag databases of the Cancer Genome Anatomy Project to perform in silico analyses of the expression pattern of the 15 human KLK genes in normal and cancerous ovarian tissues and cell lines. We found that seven KLK genes (KLK5, KLK6, KLK7, KLK8, KLK10, KLK11, and KLK14) are up-regulated in ovarian cancer.

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