1,050 research outputs found
Colors 1981
CONTENTS
Untitled, John I. C. Ramirez 2;
Love will fly, Tim Furness 3;
Untitled, Palmer Hoovestal 4;
The wave, Jerome Lightbourne 6;
The land*lord, R. Lea 7;
Song of the newborn, Heidi Muller 8;
Untitled, Mary Ostervold 9;
Good crops, Gina Larson 10;
Come, challenge the sea, Paula Schafer 12;
Untitled, Pat Dooris 14;
Untitled, Eric Peterson 16;
A flight of fancy, Tony Schaan 17;
Ode upon a london tube, Kit Warfield 18;
Sponge, Debbie Court 19;
Untitled, Debbie Court 20;
Untitled, John I. C. Ramirez 21;
Untitled, Joyce Lowry 21;
Untitled, Mary Taft 22;
Thank you, Lord [unidentified author] 23;
From generation to generation, Denise Marsh 24;
Untitled, S. M. 25;
Untitled, M. F. 26;
Brain Cramp, Francine Bergeron 27;
Untitled, Pat Dooris 28;
Untitled, Tom Mertes 30;
Untitled, John I. C. Ramirez 31;
Untitled, Dolores Bock 31;
Untitled, Christopher Perez 32;
Untitled, Pat Dooris 33;
Echoes of Innocence, Kelly Cosgrove 35;
Beloved, M. Bowen 36;
Untitled, Mary Ostervold 36
Lobatostoma kemostoma MacCallum & MacCallum 1913
Lobatostoma kemostoma (MacCallum & MacCallum, 1913) [Syn. Aspidogaster kemostoma MacCallum & MacCallum, 1913] Trachinotus carolinus (Actinopterygii); marine; intestine, pyloric caeca, stomach; NAO and SAO; Brazil, USA, Mexico, Puerto Rico (North and South America) (MaCallum & MacCallum 1913; Skryabin 1952; Dollfus 1958 b; Yamaguti 1963; Fernandes et al. 1985; Bunkley-Williams et al. 1996; Lamothe- Argumedo et al. 1997; Sanchez-Ramirez & Vidal-Martinez 2002; Kohn et al. 2007; Alves et al. 2014). Remark: Type host; sequences of partial 28 S in the GenBank database KF 561238 and KF 561239 (Alves et al. 2014). Trachinotus marginatus (Actinopterygii); marine; intestine; SAO; Brazil (South America) (Pereira Jr et al. 2004). Trachinotus ovatus (Actinopterygii); marine; intestine; SAO; Brazil (South America) (Gomes et al. 1978; Kohn et al. 2007). Trachinotus paitensis (Actinopterygii); marine; intestine; SPO; Peru (South America) (Luque & Oliva 1993; Kohn et al. 2007).Published as part of Alves, Philippe V., Vieira, Fabiano M., Santos, Cláudia P., Scholz, Tomáš & Luque, José L., 2015, A Checklist of the Aspidogastrea (Platyhelminthes: Trematoda) of the World, pp. 339-396 in Zootaxa 3918 (3) on page 352, DOI: 10.11646/zootaxa.3918.3.2, http://zenodo.org/record/24120
A study of the hexose-6-phosphate dehydrogenase gene R453Q and 11 (beta)-hydroxysteroid dehydrogenase type 1 gene 83557 ins a polymorphisms in the polycystic ovary syndrome.
Context: The R453Q variant in the hexose-6-phosphate dehydrogenase gene (H6PD) and 83557insA mutations in 11β-hydroxysteroid dehydrogenase (11βHSD) type 1 gene (HSD11B1) interact, resulting in cortisone reductase deficiency (CRD), a rare disorder characterized by a polycystic ovary syndrome (PCOS)-like phenotype.Objective: The objective was to study these mutations in PCOS.Design: The design was a case-control study.Setting: The study was conducted in an academic hospital.Participants: A total of 116 PCOS patients and 76 nonhyperandrogenic controls participated.Main Outcome Measures: Genotype distributions and influence ofgenotypes on clinical and biochemical variables and, in 28 patients and 12 controls, estimates of 11βHSD oxoreductase activity were the main outcome measures.Conclusions: Digenic triallelic genotypes of the H6PD R453Q variant and HSD11B1 83557insA mutation do not always cause CRD. On the contrary, the H6PD R453Q variant is associated with PCOS and might influence its phenotype by influencing adrenal activity
Biodiversity and biogeography of hydrothermal vent species: thirty years of discovery and investigations
Author Posting. © Oceanography Society, 2007. This article is posted here by permission of Oceanography Society for personal use, not for redistribution. The definitive version was published in Oceanography 20, 1 (2007): 30-41.The discovery of hydrothermal vents and the unique, often endemic
fauna that inhabit them represents one of the most extraordinary
scientific discoveries of the latter twentieth century. Not surprisingly,
after just 30 years of study of these remarkable—and extremely
remote—systems, advances in understanding the animals and microbial
communities living around hydrothermal vents seem to
occur with every fresh expedition to the seafloor. On average, two
new species are described each month—a rate of discovery that has
been sustained over the past 25–30 years. Furthermore, the physical, geological, and
geochemical features of each part of the ridge system and its associated
hydrothermal-vent structures appear to dictate which novel
biological species can live where. Only 10 percent of the ridge
system has been explored for hydrothermal activity to date (Baker
and German, 2004), yet we find different diversity patterns in that
small fraction. While it is well known that species composition varies
along discrete segments of the global ridge system, this “biogeographic
puzzle” has more pieces missing than pieces in place.E. Ramirez-Llodra is supported by
the ChEss-Census of Marine Life program
(A.P. Sloan Foundation), which
is kindly acknowledged. C.R. German
also acknowledges support from ChEss-
Census of Marine Life and further support
from the Natural Environment
Research Council (UK) and from the
US National Science Foundation (NSF)
and National Oceanic and Atmospheric
Administration (NOAA). T. Shank
acknowledges support from NSF, the US
National Aeronautic and Space Administration
Astrobiology Program, NOAA-Ocean
Exploration, and the Deep-Ocean
Exploration Institute at the Woods Hole
Oceanographic Institution
Microvesicles from indoxyl sulfate-treated endothelial cells induce vascular calcification in vitro
Vascular calcification (VC), an unpredictable pathophysiological process and critical event in patients with cardiovascular diseases (CVDs), is the leading cause of morbi-mortality and disability in chronic kidney disease (CKD) patients worldwide. Currently, no diagnostic method is available for identifying patients at risk of VC development; the pathology is detected when the process is irreversible. Extracellular vesicles (EVs) from endothelial cells might promote VC. Therefore, their evaluation and characterization could be useful for designing new diagnostic tools. The aim of the present study is to investigate whether microvesicles (MVs) from endothelial cells damaged by uremic toxin and indoxyl sulfate (IS) could induce calcification in human vascular smooth muscle cells (VMSCs). Besides, we have also analyzed the molecular mechanisms by which these endothelial MVs can promote VC development. Endothelial damage has been evaluated according to the percentage of senescence in endothelial cells, differential microRNAs in endothelial cells, and the amount of MVs released per cell. To identify the role of MVs in VC, VSMCs were treated with MVs from IS-treated endothelial cells. Calcium, inflammatory gene expression, and procalcification mediator levels in VSMCs were determined. IS-treated endothelial cells underwent senescence and exhibited modulated microRNA expression and an increase in the release of MVs. VSMCs exposed to these MVs modulated the expression of pro-inflammatory genes and some mediators involved in calcification progression. MVs produced by IS-treated endothelial cells promoted calcification in VSMCs
Lobatostoma ringens Linton 1905
Lobatostoma ringens (Linton, 1905) [Syns. A. ringens Linton, 1905; Cotylogaster chaetodipteri MacCallum, 1921 ] Calamus bajonado (Actinopterygii); marine; intestine; NAO; Bahamas, USA (North America) (Manter 1947; Skryabin 1952; Dollfus 1958 b; Sogandares-Bernal 1959; Yamaguti 1963). Calamus calamus (Actinopterygii); marine; intestine; NAO; USA (North America) (Linton 1910; Manter 1947; Skryabin 1952; Dollfus 1958 b; Yamaguti 1963). Chaetodipterus faber (Actinopterygii); marine; intestine; NAO; USA (North America) (MacCallum 1921; Skryabin 1952; Dollfus 1958 b; Yamaguti 1963). Remark: Described by MacCallum (1921) as C. chaetodipteri. Crassostrea tulipa (Bivalvia); brackish, marine; unspecified site of infection; NAO; Guinea (Africa) (Machkevsky & Gaevskaya 2000). Remark: Dubious parasite identification for Gibson et al. (2005). Cynoscion guatucupa (Actinopterygii); marine; intestine; SAO; Brazil (South America) (Sabas & Luque 2003; Timi et al. 2005). Dactylopterus volitans (Actinopterygii); marine; intestine; SAO; Brazil (South America) (Cordeiro & Luque 2005). Donax roemeri protracta (Bivalvia); marine; unspecified site of unfection; NAO; USA (North America) (Hendrix & Overstreet 1977). Remark: Immature specimens; L. ringens probably requires a vertebrate host to complete its life cycle, as in L. jungwirthi and L. manteri (Rohde 1973; Zylber & Ostrowski de Núñez 1999). Halichoeres radiatus (Actinopterygii); marine; intestine; NAO; British Overseas Territory (North America) (Linton 1907; Skryabin 1952; Dollfus 1958 b). Hyporhamphus roberti roberti (Actinopterygii); marine; intestinal caeca, intestine; NAO; Mexico (North America) (Caballero & Bravo-Hollis 1965; Lamothe-Argumedo 1997). Menticirrhus americanus (Actinopterygii); marine; intestine; NAO; USA (North America) (Hendrix & Overstreet 1977). Micropogonias furnieri (Actinopterygii); marine; intestine; NAO and SAO; Argentina, Brazil, Jamaica, Uruguay (North and South America) (Sardella et al. 1995, Nahhas & Cable 1964; Suriano 1966; Alves & Luque 2000, 2001a, 2001 b; Kohn et al. 2007; Luque et al. 2010). Micropogonias undulatus (Actinopterygii); marine; intestine; NAO; USA (North America) (Linton 1905; Manter 1931; Skryabin 1952; Dollfus 1958 b; Yamaguti 1963; Diaz & Johnson 1974; Hendrix & Overstreet 1977; Halton & Hendrix 1978; Thoney 1991; Baker et al. 2007). Remark: Linton (1905) described L. ringens from M. undulatus and Trachinotus carolinus. Oncopterus darwinii (Actinopterygii); marine; intestine; SAO; Argentina (South America) (Szidat 1961; Suriano & Martorelli 1983; Kohn et al. 2007). Pomatomus saltatrix (Actinopterygii); marine; intestine; NAO; British Overseas Territory (North America) (Hanson 1950). Remark: Probably this host (Hanson 1950). Stenotomus chrysops (Actinopterygii); marine; intestine; NAO; British Overseas Territory (North America) (Rees 1970). Trachinotus carolinus (Actinopterygii); marine; intestine; NAO; USA, Mexico (North America) (Linton 1905; MacCallum & MacCallum 1913; Skryabin 1952; Dollfus 1958 b; Sparks 1958; Caballero & Bravo-Hollis 1965; Hendrix & Overstreet 1977; Peréz-Ponce de Léon et al. 1996; Lamothe-Argumedo 1997; Sanchez-Ramirez & Vidal-Martinez 2002). Trachinotus falcatus (Actinopterygii); marine; intestine; NAO; USA (North America) (Hendrix & Overstreet 1977). Trachinotus maxillosus (Actinopterygii); marine; intestine; NAO; Guine (Africa) (Machkevsky 1997). Trachinotus ovatus (Actinopterygii); marine; intestine; NAO; Mexico (North America) (Lamothe- Argumedo 1997). Umbrina coroides (Actinopterygii); marine; intestine; NAO; Venezuela (South America) (Chinchilla & Mago 2005). Micropogonias sp. (Actinopterygii); marine; intestine; SAO; Brazil (South America) (Gomes & Fábio 1976).Published as part of Alves, Philippe V., Vieira, Fabiano M., Santos, Cláudia P., Scholz, Tomáš & Luque, José L., 2015, A Checklist of the Aspidogastrea (Platyhelminthes: Trematoda) of the World, pp. 339-396 in Zootaxa 3918 (3) on page 353, DOI: 10.11646/zootaxa.3918.3.2, http://zenodo.org/record/24120
Lucena desagraviada. Disertacion apologetica sobre el verdadero autor de la prision del Rey Chico de Granada. Añadida una breve apologia del verdadero autor del poema Lagrimas de Angelica, que elogia Cervantes. Por D. Fernando Ramirez de Luque...
Fecha de impr. probableDedicatoria fechada en 1782Antep.El autor de Las lágrimas de Angélica es Luis Barahona de SotoEnc. HolandesaSign.: [ ]4, B-L4, M
Silicon photonics: advanced metamaterials and sensors
Photonics North, PN (2022. Niagara Falls, Canada)We acknowledge funding from Consejería de Economía, Conocimiento, Empresas y Universidad, Junta de Andalucía (P18-RT-793, CV20-91577), Universidad de Málaga (UMA18-FEDERJA-219; UMA20-FEDERJA-158), and Ministerio de Ciencia, Innovación y Universidades (PID2019-106747RBI00, FPU19/02408, FPU19/03330).Halir, R., Leuermann, J., Fernandez-Gavela, A., Stirling, C.J., Manuel Luque-Gonzalez, J., Ginel-Moreno, P., Torres-Cubillo, A., Sanchez-Ramirez, A., Pereira-Martin, D., Sanchez-Postigo, A., Perez-Armenta, C., Hadij-Elhouati, A., De-Oliva-Rubio, J., Schmid, J.H., Ortega-Monux, A., Nedeljkovic, M., Wanguemert Perez, J.G., Cheben, P., Molina-Fernandez, I
More than just a Green Façade: Vertical Gardens as Active Air Conditioning Units
AbstractThis paper explores the potential of a vertical garden to function as an active evaporative cooling air conditioning unit. It builds on previous work by Davis, Ramirez and Vallejo [1]. This study shows the results of a full scale, building incorporated vertical garden that measured 1.5 m wide by 2.8 m high. Air flowed behind the garden substrate, where it was cooled and humidified as it flowed down the back of the garden through its contact with the humid surface. The experimental results were compared to the mathematical model developed by Davis and Hirmer [2]. Overall, it was suspected that variations in ambient temperatures during the measurements taking process had a major influence on the results. In taking the data considered most reliable into account however, the results of the mathematical model end experimental data were within 0.44°C. The results indicate that such gardens show great promise for building climate control, but where further research is needed in order to mitigate the influence of fluctuations in ambient temperatures
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