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  • 1
    Publication Date: 2019
    Description: The Valsequillo reservoir is a Ramsar wetland due to its importance as a point of convergence of migratory waterfowl. It is located in Central Mexico and is currently endangered by the constant spill of municipal and industrial discharges from Puebla city. On this context, we evaluated thirteen potential toxic metals (PTMs) in water, Water hyacinth (E. crassipes) plants and sediments at this site. A combined number of 31 samples were collected from the study area. The degree/extent of metal contamination in sediments was assessed through different geochemical indexes, namely: Geoaccumulation index (Igeo), Enrichment Factor (EF) and Potential Ecological Risk Index (PERI). The ability of Water hyacinth plants residues as a phytodepurator in the Ramsar site was tested in terms of the bioaccumulation factor (BF) and the translocation factor (TF). The results concerning sediments showed that Pb, Cu and Hg pose a threat to the aquatic environment since Igeo and EF indicate sediments ranging from moderately contaminated to contaminated. Moreover, PERI pointed out Hg as the main contributor to the ecological risk in sediments, especially in the part of the reservoir covered by E. crassipes. Water hyacinth plants displayed good capacity to absorb PTMs from the water, since the content of Co, Zn, As, Ni, Cu, Pb, Ti, Cr, Ba, Mo and V in the total plant was (all values in mg/kg of dry weight) 21 ± 9, 408 ± 300, 12 ± 6, 93 ± 21, 93 ± 69, 53 ± 29, 1067 ± 643, 78 ± 55, 362 ± 39, 14 ± 0.6 and 96 ± 35, respectively. Metal content in sediments resembles to that of E. crassipes; especially in the roots, suggesting a constant deposition of plants at the bottom of the reservoir, which contributes to the eutrophication of the water. The present work encourages the need for a sustainable management of Water hyacinth plants in the Ramsar site, since they represent a plague and a natural phyto-depurator at the same time.
    Electronic ISSN: 2073-4441
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Published by MDPI
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  • 2
    Publication Date: 2016-01-02
    Description: CRISPR/Cas9-mediated genome editing holds clinical potential for treating genetic diseases, such as Duchenne muscular dystrophy (DMD), which is caused by mutations in the dystrophin gene. To correct DMD by skipping mutant dystrophin exons in postnatal muscle tissue in vivo, we used adeno-associated virus-9 (AAV9) to deliver gene-editing components to postnatal mdx mice, a model of DMD. Different modes of AAV9 delivery were systematically tested, including intraperitoneal at postnatal day 1 (P1), intramuscular at P12, and retro-orbital at P18. Each of these methods restored dystrophin protein expression in cardiac and skeletal muscle to varying degrees, and expression increased from 3 to 12 weeks after injection. Postnatal gene editing also enhanced skeletal muscle function, as measured by grip strength tests 4 weeks after injection. This method provides a potential means of correcting mutations responsible for DMD and other monogenic disorders after birth.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760628/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760628/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Long, Chengzu -- Amoasii, Leonela -- Mireault, Alex A -- McAnally, John R -- Li, Hui -- Sanchez-Ortiz, Efrain -- Bhattacharyya, Samadrita -- Shelton, John M -- Bassel-Duby, Rhonda -- Olson, Eric N -- DK-099653/DK/NIDDK NIH HHS/ -- HL-077439/HL/NHLBI NIH HHS/ -- HL-093039/HL/NHLBI NIH HHS/ -- HL-111665/HL/NHLBI NIH HHS/ -- R01 DK099653/DK/NIDDK NIH HHS/ -- R01 HL077439/HL/NHLBI NIH HHS/ -- R01 HL093039/HL/NHLBI NIH HHS/ -- R01 HL111665/HL/NHLBI NIH HHS/ -- U01 HL100401/HL/NHLBI NIH HHS/ -- U01-HL-100401/HL/NHLBI NIH HHS/ -- U54 HD 087351/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2016 Jan 22;351(6271):400-3. doi: 10.1126/science.aad5725. Epub 2015 Dec 31.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Hamon Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Sen. Paul D. Wellstone Muscular Dystrophy Cooperative Research Center, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. ; Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. ; Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Hamon Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Sen. Paul D. Wellstone Muscular Dystrophy Cooperative Research Center, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. eric.olson@utsouthwestern.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26721683" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *CRISPR-Cas Systems ; Dependovirus ; Disease Models, Animal ; Dystrophin/*genetics ; Exons/genetics ; Female ; Forelimb/physiopathology ; Genetic Therapy/*methods ; Genome/genetics ; Hand Strength ; Male ; Mice ; Mice, Inbred mdx ; Muscle, Skeletal/metabolism ; Muscular Dystrophy, Duchenne/genetics/*therapy ; Myocardium/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2018-10-05
    Description: Mutations in the gene encoding dystrophin, a protein that maintains muscle integrity and function, cause Duchenne muscular dystrophy (DMD). The deltaE50-MD dog model of DMD harbors a mutation corresponding to a mutational "hotspot" in the human DMD gene. We used adeno-associated viruses to deliver CRISPR gene editing components to four dogs and examined dystrophin protein expression 6 weeks after intramuscular delivery ( n = 2) or 8 weeks after systemic delivery ( n = 2). After systemic delivery in skeletal muscle, dystrophin was restored to levels ranging from 3 to 90% of normal, depending on muscle type. In cardiac muscle, dystrophin levels in the dog receiving the highest dose reached 92% of normal. The treated dogs also showed improved muscle histology. These large-animal data support the concept that, with further development, gene editing approaches may prove clinically useful for the treatment of DMD.
    Keywords: Medicine, Diseases, Molecular Biology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2017-04-21
    Description: Skeletal muscle formation occurs through fusion of myoblasts to form multinucleated myofibers. From a genome-wide clustered regularly interspaced short palindromic repeats (CRISPR) loss-of-function screen for genes required for myoblast fusion and myogenesis, we discovered an 84–amino acid muscle-specific peptide that we call Myomixer. Myomixer expression coincides with myoblast differentiation and is essential for fusion and skeletal muscle formation during embryogenesis. Myomixer localizes to the plasma membrane, where it promotes myoblast fusion and associates with Myomaker, a fusogenic membrane protein. Myomixer together with Myomaker can also induce fibroblast-fibroblast fusion and fibroblast-myoblast fusion. We conclude that the Myomixer-Myomaker pair controls the critical step in myofiber formation during muscle development.
    Keywords: Development
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2019-06-14
    Description: The Valsequillo reservoir is a Ramsar wetland due to its importance as a point of convergence of migratory waterfowl. It is located in Central Mexico and is currently endangered by the constant spill of municipal and industrial discharges from Puebla city. On this context, we evaluated thirteen potential toxic metals (PTMs) in water, Water hyacinth (E. crassipes) plants and sediments at this site. A combined number of 31 samples were collected from the study area. The degree/extent of metal contamination in sediments was assessed through different geochemical indexes, namely: Geoaccumulation index (Igeo), Enrichment Factor (EF) and Potential Ecological Risk Index (PERI). The ability of Water hyacinth plants residues as a phytodepurator in the Ramsar site was tested in terms of the bioaccumulation factor (BF) and the translocation factor (TF). The results concerning sediments showed that Pb, Cu and Hg pose a threat to the aquatic environment since Igeo and EF indicate sediments ranging from moderately contaminated to contaminated. Moreover, PERI pointed out Hg as the main contributor to the ecological risk in sediments, especially in the part of the reservoir covered by E. crassipes. Water hyacinth plants displayed good capacity to absorb PTMs from the water, since the content of Co, Zn, As, Ni, Cu, Pb, Ti, Cr, Ba, Mo and V in the total plant was (all values in mg/kg of dry weight) 21 ± 9, 408 ± 300, 12 ± 6, 93 ± 21, 93 ± 69, 53 ± 29, 1067 ± 643, 78 ± 55, 362 ± 39, 14 ± 0.6 and 96 ± 35, respectively. Metal content in sediments resembles to that of E. crassipes; especially in the roots, suggesting a constant deposition of plants at the bottom of the reservoir, which contributes to the eutrophication of the water. The present work encourages the need for a sustainable management of Water hyacinth plants in the Ramsar site, since they represent a plague and a natural phyto-depurator at the same time.
    Electronic ISSN: 2073-4441
    Topics: Energy, Environment Protection, Nuclear Power Engineering
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  • 6
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