Planar structures dramatically increase the surface‐area‐to‐volume ratio, which is critically important for multicellular organisms. In this study, we utilize naturally occurring phenotypic variation among three
Progress is needed before explicit photodynamic therapy (PDT) dosimetry can treat peritoneal carcinomatosis and yet spare all healthy tissue. A report by Cengel et al. in this issue of
- Award ID(s):
- 1856765
- NSF-PAR ID:
- 10375778
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- Photochemistry and Photobiology
- Volume:
- 96
- Issue:
- 2
- ISSN:
- 0031-8655
- Page Range / eLocation ID:
- p. 437-439
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Sansivieria species (Asperagaceae) to investigate leaf margin expression patterns that are associated with mediolateral and adaxial/abaxial development. We identified differentially expressed genes (DEGs) between center and margin leaf tissues in two planar‐leaf speciesSansevieria subspicata and and compared these with expression patterns within the cylindrically leavedSansevieria trifasciata . TwoSansevieria cylindrica YABBY family genes, homologs ofFILAMENTOUS FLOWER andDROOPING LEAF , are overexpressed in the center leaf tissue in the planar‐leaf species and in the tissue of the cylindrical leaves. As mesophyll structure does not indicate adaxial versus abaxial differentiation, increased leaf thickness results in more water‐storage tissue and enhances resistance to aridity. This suggests that the cylindrical‐leaf in is analogous to the central leaf tissue in the planar‐leaf species. Furthermore, the congruence of the expression patterns of theseS. cylindrica YABBY genes inSansevieria with expression patterns found in other unifacial monocot species suggests that patterns of parallel evolution may be the result of similar solutions derived from a limited developmental toolbox. -
Abstract Birds are known to act as potential vectors for the exogenous dispersal of bryophyte diaspores. Given the totipotency of vegetative tissue of many bryophytes, birds could also contribute to endozoochorous bryophyte dispersal. Research has shown that fecal samples of the upland goose (
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Abstract Fusion to form a chimera has been documented in many marine invertebrate taxa, including poriferans, cnidarians, bryozoans, and colonial ascidians. Allogenic interactions in chimeric ascidian colonies vary widely across taxonomic groups but are poorly characterized in the invasive colonial ascidian
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Abstract Benthic primary producers are recognised for their important role in contributing to ecosystem productivity and nutrient cycling in lake and stream ecosystems, particularly in polar environments. In Arctic lakes, benthic producers often comprise mats or colonies of cyanobacteria capable of producing cyanotoxins. However, the extent to which benthic communities contribute cyanotoxins in polar regions remains poorly described.
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CYP2C19 andSTAT6 associate with PPI plasma concentration and magnitude of inflammatory response, respectively. Our objective was to determine if genetic variation in the genes forCYP2C19 andSTAT6 influence differentiation between PPI responsive esophageal eosinophilia versus PPI nonresponsive EoE (PPI‐REE, PPI‐nonresponsive EoE).Methods: Genomic DNA was isolated from 92 esophageal tissue biopsies collected from participants of a prospective clinical trial of high‐dose PPI therapy for esophageal eosinophilia in children.
Results: Of the 92 patients examined, 57 (62%) were PPI‐REE and 35 (38%) were PPI‐nonresponsive EoE. Forty‐six of the 92 patients were further characterized by pH probe monitoring; there was no association between reflux index and carriage of
CYP2C19 * 17 (P = 0.35). In children who received a PPI dose between ≥1.54 and ⩽2.05 mg/kg/day, binary logistic regression modeling showed that carriage ofCYP2C19 * 17 associated with PPI‐nonresponsive EoE (odds ratio (OR) [95% confidence interval (CI)] = 7.71 [1.21, 49.11],P = 0.031). Carriage ofSTAT6 allelic variant rs1059513 predicts PPI‐REE (OR [95% CI] = 6.16 [1.44, 26.4],P = 0.028), whereas carriage ofSTAT6 rs324011 synergizes withCYP2C19 * 17 to predict PPI‐nonresponsive EoE (rs324011 OR [95% CI] = 5.56 [1.33, 20.72],P = 0.022;CYP2C19 * 17 OR [95% CI] = 8.19[1.42, 50.57],P = 0.023).Conclusions: Common variants in
CYP2C19 andSTAT6 associate with a PPI‐nonresponsive EoE outcome of PPI therapy for esophageal eosinophilia suggesting that response rates may be improved by adopting a genotype‐guided approach to PPI dosing.