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This study focused on the investigation microplastics (MPs) with a size of ≤1.0 mm in sand samples from Thanh Phu beach, Ben Tre, Vietnam. MPs in sand from the clam beach (from 39.67 ± 6.67 to 92.00 ± 12.93 items kg-1 dried sand) were higher than those from the bathing beach (from 21.33 ± 8.76 to 51.67 ± 16.11 items kg-1 dried sand), indicating a direct contribution of MPs from coastal aquaculture. For the clam beach, MPs in surface samples (0-4 cm) were lower than in deep samples (4-6 cm). In contrast, MPs in surface samples (0-2 cm) from the bathing beach were higher than deep samples (2-5 cm). A combination of microscopy and Fourier-transform infrared spectroscopy methods confirmed that 62.5% of the representative MPs samples or 18.9% of the suspected MPs samples were plastics. Low-density polyethylene, polypropylene and polyethylene terephthalate were the largest in abundance. Further studies are needed to assess the environmental risk of MPs accumulation.
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http://dx.doi.org/10.1080/09603123.2024.2377306 | DOI Listing |
Neuromuscul Disord
April 2017
Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, UK. Electronic address:
Reports of aberrant distribution for some nuclear envelope proteins in cells expressing a few Emery-Dreifuss muscular dystrophy mutations raised the possibility that such protein redistribution could underlie pathology and/or be diagnostic. However, this disorder is linked to 8 different genes encoding nuclear envelope proteins, raising the question of whether a particular protein is most relevant. Therefore, myoblast/fibroblast cultures from biopsy and tissue sections from a panel of nine Emery-Dreifuss muscular dystrophy patients (4 male, 5 female) including those carrying emerin and FHL1 (X-linked) and several lamin A (autosomal dominant) mutations were stained for the proteins linked to the disorder.
View Article and Find Full Text PDFMol Cell
June 2016
The Wellcome Trust Centre for Cell Biology and Institute of Cell Biology, University of Edinburgh, Edinburgh EH9 3BF, UK. Electronic address:
Whether gene repositioning to the nuclear periphery during differentiation adds another layer of regulation to gene expression remains controversial. Here, we resolve this by manipulating gene positions through targeting the nuclear envelope transmembrane proteins (NETs) that direct their normal repositioning during myogenesis. Combining transcriptomics with high-resolution DamID mapping of nuclear envelope-genome contacts, we show that three muscle-specific NETs, NET39, Tmem38A, and WFS1, direct specific myogenic genes to the nuclear periphery to facilitate their repression.
View Article and Find Full Text PDFNanoscale
February 2016
SKKU Advanced Institute of Nanotechnology, Sungkyunkwan University, Suwon 440-746, Republic of Korea.
WO3/BiVO4 is one of the attractive Type II heterojunctions for photoelectrochemical (PEC) water splitting due to its well-matched band edge positions and visible light harvesting abilities. However, two light absorption components generally suffer from poor charge collection and cannot be efficiently utilized because of non-ideal interfaces. Herein, a triple-deck three-dimensional (3D) architecture was designed through a one-step shaping process with an additional stress relaxation WO3 underlayer.
View Article and Find Full Text PDFNeuromuscul Disord
February 2015
Friedrich-Baur-Institut, Department of Neurology, Ludwig-Maximilians-University of Munich, Munich, Germany. Electronic address:
Emery-Dreifuss muscular dystrophy (EDMD) is a neuromuscular disease characterized by early contractures, slowly progressive muscular weakness and life-threatening cardiac arrhythmia that can develop into cardiomyopathy. In X-linked EDMD (EDMD1), female carriers are usually unaffected. Here we present a clinical description and in vitro characterization of a mildly affected EDMD1 female carrying the heterozygous EMD mutation c.
View Article and Find Full Text PDFAdv Exp Med Biol
September 2014
Wellcome Trust Centre for Cell Biology, University of Edinburgh, Kings Buildings, Michael Swann Building, Edinburgh, EH9 3JR, UK,
There are many ways that the nuclear envelope can influence the cell cycle. In addition to roles of lamins in regulating the master cell cycle regulator pRb and nuclear envelope breakdown in mitosis, many other nuclear envelope proteins influence the cell cycle through regulatory or structural functions. Of particular note among these are the nuclear envelope transmembrane proteins (NETs) that appear to influence cell cycle regulation through multiple separate mechanisms.
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