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Journal articles on the topic 'Vesicular'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Riet-Correa, Franklin, Valéria Moojen, Paulo Michel Roehe, and Rudi Weiblen. "Viroses confundíveis com febre aftosa." Ciência Rural 26, no. 2 (August 1996): 323–32. http://dx.doi.org/10.1590/s0103-84781996000200027.

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Revisam-se as doenças que devem ser consideradas no diagnóstico diferencial de febre aftosa. Dentre as doenças vesiculares ou erosivas, descrevem-se os principais aspectos relacionados ao diagnóstico da estomatite vesicular, diarréia viral bovina, febre catarral maligna, infecções por herpesvírus bovino 1 e 5, e uma estomatite ulcerativa associada a parvovírus bovino, que ocorreu no Rio Grande do Sul; língua azul, para a qual tem sido detectados anticorpos em bovinos e ovinos do Rio Grande do Sul; mamilite herpética que ocorre em outros Estados do País;peste bovina, que foi diagnosticada e erradicada no Estado de São Paulo em 1921; estomatite popular; e duas doenças exóticas:exantema vesicular e doença vesicular do suíno.

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2

Tauc, L. "Quantal neurotransmitter release: Vesicular or not vesicular?" Neurophysiology 29, no. 4-5 (July 1997): 219–26. http://dx.doi.org/10.1007/bf02461232.

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3

Krantz, David E. "Vesicular Monogamy?" Neuron 49, no. 1 (January 2006): 1–2. http://dx.doi.org/10.1016/j.neuron.2005.12.013.

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4

Schmitt, Beverly. "Vesicular stomatitis." Veterinary Clinics of North America: Food Animal Practice 18, no. 3 (November 2002): 453–59. http://dx.doi.org/10.1016/s0749-0720(02)00031-2.

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5

Warren, Graham. "Vesicular consumption." Nature 345, no. 6274 (May 1990): 382–83. http://dx.doi.org/10.1038/345382a0.

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6

KOMINE, MAYUMI, KIYOKO NASHIRO, AKIHIKO ASAHINA, TOMOHIKO MATSUYAMA, MASUTAKA FURUE, TETSUYA TSUCHIDA, and YASUMASA ISHIBASHI. "VESICULAR PEMPHIGOID." International Journal of Dermatology 31, no. 12 (December 1992): 868–70. http://dx.doi.org/10.1111/j.1365-4362.1992.tb03546.x.

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7

Dourmishev, Assen L., and Mohamed Moalla. "Vesicular Scabies." International Journal of Dermatology 33, no. 2 (February 1994): 149–50. http://dx.doi.org/10.1111/j.1365-4362.1994.tb01553.x.

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8

Barr, Francis. "Vesicular transport." Essays in Biochemistry 36 (December 1, 2000): 37–46. http://dx.doi.org/10.1042/bse0360037.

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9

Donaldson, A. I., and N. P. Ferris. "Vesicular stomatitis." Equine Veterinary Education 7, no. 4 (August 1995): 205–7. http://dx.doi.org/10.1111/j.2042-3292.1995.tb01226.x.

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10

Donaldson, A. I., and N. P. Ferris. "Vesicular stomatitis." Equine Veterinary Education 8, S2 (June 10, 2010): 44–46. http://dx.doi.org/10.1111/j.2042-3292.1996.tb01856.x.

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11

LETCHWORTH, G. J., L. L. RODRIGUEZ, and J. DEL CBARRERA. "Vesicular Stomatitis." Veterinary Journal 157, no. 3 (May 1999): 239–60. http://dx.doi.org/10.1053/tvjl.1998.0303.

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12

Sylvester, Robert K. "Vesicular Eruption." JAMA 255, no. 3 (January 17, 1986): 385. http://dx.doi.org/10.1001/jama.1986.03370030105038.

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13

Gordon, Rachel. "Vesicular Eruption." JAMA 307, no. 14 (April 11, 2012): 1528. http://dx.doi.org/10.1001/jama.2012.436.

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14

Menger, Fredric M., Jianwei Bian, and Victor A. Seredyuk. "Vesicular Latex." Angewandte Chemie 116, no. 10 (February 27, 2004): 1285–87. http://dx.doi.org/10.1002/ange.200352936.

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15

Menger, Fredric M., Jianwei Bian, and Victor A. Seredyuk. "Vesicular Latex." Angewandte Chemie International Edition 43, no. 10 (February 27, 2004): 1265–67. http://dx.doi.org/10.1002/anie.200352936.

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16

Timoney, Peter. "Vesicular stomatitis." Veterinary Record 179, no. 5 (July 28, 2016): 119–20. http://dx.doi.org/10.1136/vr.i4075.

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17

Benning, Christoph, Changcheng Xu, and Koichiro Awai. "Non-vesicular and vesicular lipid trafficking involving plastids." Current Opinion in Plant Biology 9, no. 3 (June 2006): 241–47. http://dx.doi.org/10.1016/j.pbi.2006.03.012.

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18

de Winter, Niels J., Johan Vellekoop, Robin Vorsselmans, Asefeh Golreihan, Jeroen Soete, Sierra V. Petersen, Kyle W. Meyer, Silvio Casadio, Robert P. Speijer, and Philippe Claeys. "An assessment of latest Cretaceous <i>Pycnodonte vesicularis</i> (Lamarck, 1806) shells as records for palaeoseasonality: a multi-proxy investigation." Climate of the Past 14, no. 6 (June 8, 2018): 725–49. http://dx.doi.org/10.5194/cp-14-725-2018.

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Abstract. In order to assess the potential of the honeycomb oyster Pycnodonte vesicularis for the reconstruction of palaeoseasonality, several specimens recovered from late Maastrichtian strata in the Neuquén Basin (Argentina) were subject to a multi-proxy investigation, involving scanning techniques and trace element and isotopic analysis. Combined CT scanning and light microscopy reveals two calcite microstructures in P. vesicularis shells (vesicular and foliated calcite). Micro-XRF analysis and cathodoluminescence microscopy show that reducing pore fluids were able to migrate through the vesicular portions of the shells (aided by bore holes) and cause recrystallization of the vesicular calcite. This renders the vesicular portions not suitable for palaeoenvironmental reconstruction. In contrast, stable isotope and trace element compositions show that the original chemical composition of the foliated calcite is well-preserved and can be used for the reconstruction of palaeoenvironmental conditions. Stable oxygen and clumped isotope thermometry on carbonate from the dense hinge of the shell yield sea water temperatures of 11°C, while previous TEX86H palaeothermometry yielded much higher temperatures. The difference is ascribed to seasonal bias in the growth of P. vesicularis, causing warm seasons to be underrepresented from the record, while TEX86H palaeothermometry seems to be biased towards warmer surface water temperatures. The multi-proxy approach employed here enables us to differentiate between well-preserved and diagenetically altered portions of the shells and provides an improved methodology for reconstructing palaeoenvironmental conditions in deep time. While establishing a chronology for these shells was complicated by growth cessations and diagenesis, cyclicity in trace elements and stable isotopes allowed for a tentative interpretation of the seasonal cycle in late Maastrichtian palaeoenvironment of the Neuquén Basin. Attempts to independently verify the seasonality in sea water temperature by Mg ∕ Ca ratios of shell calcite are hampered by significant uncertainty due to the lack of proper transfer functions for pycnodontein oysters. Future studies of fossil ostreid bivalves should target dense, foliated calcite rather than sampling bulk or vesicular calcite. Successful application of clumped isotope thermometry on fossil bivalve calcite in this study indicates that temperature seasonality in fossil ostreid bivalves may be constrained by the sequential analysis of well-preserved foliated calcite samples using this method.

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19

Navarro López, Roberto, Lauro Velázquez Salinas, Susana Arellano Chávez, Irene López González, César Luis Villarreal Chávez, and Juan Antonio Montaño Hirose. "Caracterización epidemiológica de las áreas endémicas de estomatitis vesicular en México (1981-2012)." Revista Mexicana de Ciencias Pecuarias 6, no. 3 (September 22, 2015): 277. http://dx.doi.org/10.22319/rmcp.v6i3.4091.

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El presente estudio se diseñó para mejorar el sistema de vigilancia de las enfermedades vesiculares en México, bajo el sistema de planeación estratégica, identificando las zonas endémicas a través de la estabilidad de linajes virales del serotipo Nueva Jersey, y analizando epidemiológicamente la información generada en 32 años de vigilancia e investigación. Se presentan los resultados que permitieron caracterizar epidemiológicamente las áreas donde se mantiene el virus de estomatitis vesicular de manera secular en México, y con ello, los componentes necesarios para la construcción de la Matriz de Indicadores para Resultados (MIR) para el programa de vigilancia de las enfermedades vesiculares en México, que pueden también servir para otros países afectados por esta enfermedad. Adicionalmente se aportan elementos para la prevención de la enfermedad, así como mejorar el comercio internacional de animales de países endémicos de estomatitis vesicular.

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20

Hao, Mingming, Sharron X. Lin, Ola J. Karylowski, Daniel Wüstner, Timothy E. McGraw, and Frederick R. Maxfield. "Vesicular and Non-vesicular Sterol Transport in Living Cells." Journal of Biological Chemistry 277, no. 1 (October 26, 2001): 609–17. http://dx.doi.org/10.1074/jbc.m108861200.

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21

Hölttä-Vuori, M., and E. Ikonen. "Endosomal cholesterol traffic: vesicular and non-vesicular mechanisms meet." Biochemical Society Transactions 34, no. 3 (May 22, 2006): 392–94. http://dx.doi.org/10.1042/bst0340392.

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The endoplasmic reticulum is traditionally perceived as the key compartment for regulating intracellular cholesterol metabolism. Increasing evidence suggests that the endocytic pathway provides an additional regulatory level governing intracellular cholesterol trafficking and homoeostasis. Sterols can enter, and apparently also exit, endosomal compartments via both vesicular and non-vesicular mechanisms. A number of studies have focused on endosomal sterol removal as its defects lead to cholesterol storage diseases. So far, the bulk of evidence on endosomal sterol egress describes the involvement of membrane trafficking machineries. Interestingly, two late endosomal sterol-binding proteins were recently shown to regulate the movement of late endosomes along cytoskeletal tracks. These studies provide the first indications of how non-vesicular and vesicular mechanisms may co-operate in endosomal sterol trafficking.

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22

Atamari-Anahui, Noé, and Sendy Solórzano-Gutiérrez. "Incontinentia pigmenti (Síndrome de Bloch- Sulzberger) en un paciente varón. Reporte de un caso." Revista Medica Herediana 26, no. 4 (January 20, 2016): 238. http://dx.doi.org/10.20453/rmh.v26i4.2701.

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Incontinentia pigmenti es una rara genodermatosis ligada al cromosoma X caracterizada por lesiones ampollares distribuidas sobre las líneas de Blaschko. Esta se presenta en cuatro estadios: vesicular, verrugoso, hiperpigmentado y atrófico. Es más frecuente en mujeres por su letalidad en varones, aunque hay casos de sobrevivencia en ellos. Se presenta el caso de un varón de 30 días de nacido que presentó lesiones vesiculo-ampollares de distribución lineal siguiendo las líneas de Blaschko. Se le realizó una biopsia cutánea cuya conclusión fue incontinentia pigmenti en estadio vesicular. Este es el primer caso varón reportado en la literatura peruana.

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23

Stensrud, M. J., F. A. Chaudhry, T. B. Leergaard, J. G. Bjaalie, and V. Gundersen. "Vesicular glutamate transporter-3 in the rodent brain: Vesicular colocalization with vesicular γ-aminobutyric acid transporter." Journal of Comparative Neurology 521, no. 13 (July 17, 2013): 3042–56. http://dx.doi.org/10.1002/cne.23331.

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24

Giedlin, Martin A., David N. Cook, and Thomas W. Dubensky. "Vesicular stomatitis virus." Cancer Cell 4, no. 4 (October 2003): 241–43. http://dx.doi.org/10.1016/s1535-6108(03)00251-4.

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25

Jassal, Sundeep, and Justin Stowens. "Painful vesicular rash." Visual Journal of Emergency Medicine 15 (April 2019): 100546. http://dx.doi.org/10.1016/j.visj.2018.12.008.

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26

Goldberg, Neil S. "Vesicular Erythema Migrans." Archives of Dermatology 128, no. 11 (November 1, 1992): 1495. http://dx.doi.org/10.1001/archderm.1992.01680210073010.

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27

Momtahen, Shabnam, Gerard J. Nuovo, and Cynthia M. Magro. "Vesicular Mycosis Fungoides." American Journal of Dermatopathology 37, no. 9 (September 2015): 724–29. http://dx.doi.org/10.1097/dad.0000000000000242.

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28

Meadows, Kappa P., and Conleth A. Egan. "Vesicular carcinoma erysipelatodes." Journal of the American Academy of Dermatology 40, no. 5 (May 1999): 805–7. http://dx.doi.org/10.1053/jd.1999.v40.a95643.

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29

Olazabal Zudaire, A., and E. Balliu Collgros. "Litiasis vesicular múltiple." FMC - Formación Médica Continuada en Atención Primaria 10, no. 1 (January 2003): 35. http://dx.doi.org/10.1016/s1134-2072(03)75659-x.

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30

Perez, Caroline, and Sharon E. Jacob. "Localized Vesicular Eruption." Journal of the Dermatology Nurses’ Association 9, no. 1 (2017): 39–40. http://dx.doi.org/10.1097/jdn.0000000000000277.

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31

Sidey, Kirk A., Melissa S. J. Willis, and Karolyn A. Wanat. "Diffuse Vesicular Eruption." JAMA Dermatology 153, no. 2 (February 1, 2017): 219. http://dx.doi.org/10.1001/jamadermatol.2016.3751.

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32

Sobering, Geraldine, and Cheryl Dika. "Vesicular hand dermatitis." Nurse Practitioner 43, no. 11 (November 2018): 33–37. http://dx.doi.org/10.1097/01.npr.0000546445.09474.01.

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33

Mcbride, Dahl, Slater, and Sviland. "Vesicular mycosis fungoides." British Journal of Dermatology 138, no. 1 (January 1998): 141–44. http://dx.doi.org/10.1046/j.1365-2133.1998.02041.x.

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34

Schu, P. "Vesicular protein transport." Pharmacogenomics Journal 1, no. 4 (April 2001): 262–71. http://dx.doi.org/10.1038/sj.tpj.6500055.

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35

Smith, A. J., and B. Schwappach. "Think Vesicular Chloride." Science 328, no. 5984 (June 10, 2010): 1364–65. http://dx.doi.org/10.1126/science.1191529.

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36

Varoqui, Hélène, and Jeffrey D. Erickson. "Vesicular neurotransmitter transporters." Molecular Neurobiology 15, no. 2 (October 1997): 165–91. http://dx.doi.org/10.1007/bf02740633.

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37

Sher, Sarah, and John Browning. "Neonatal vesicular eruption." Journal of the American Academy of Dermatology 64, no. 4 (April 2011): e41. http://dx.doi.org/10.1016/j.jaad.2010.02.044.

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38

Jackson, Hilary A. "Vesicular Cutaneous Lupus." Veterinary Clinics of North America: Small Animal Practice 36, no. 1 (January 2006): 251–55. http://dx.doi.org/10.1016/j.cvsm.2005.09.005.

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39

Jayavardhana, A., A. M. Vijayalakshmi, and Nirmala. "Erythematous vesicular lesions." Indian Pediatrics 49, no. 12 (December 2012): 1015–16. http://dx.doi.org/10.1007/s13312-012-0242-y.

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40

Lee, Yun-Geun, Bob McKay, Kang-Il Kim, Dong-Kyun Kim, and Nguyen Xuan Hoai. "Investigating vesicular selection." Applied Soft Computing 11, no. 8 (December 2011): 5528–50. http://dx.doi.org/10.1016/j.asoc.2011.05.006.

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41

Goldberg, N. S. "Vesicular erythema migrans." Archives of Dermatology 128, no. 11 (November 1, 1992): 1495–98. http://dx.doi.org/10.1001/archderm.128.11.1495.

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42

El Mestikawy, Salah, Åsa Wallén-Mackenzie, Guillaume M. Fortin, Laurent Descarries, and Louis-Eric Trudeau. "From glutamate co-release to vesicular synergy: vesicular glutamate transporters." Nature Reviews Neuroscience 12, no. 4 (March 18, 2011): 204–16. http://dx.doi.org/10.1038/nrn2969.

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43

Moya Sánchez, E., V. Medina Salas, and C. Diéguez Castillo. "Gallbladder duplication and acute cholecystitis." Cirugía Andaluza 30, no. 4 (November 8, 2019): 535–36. http://dx.doi.org/10.37351/2019304.18.

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Resumen La duplicación vesicular es una malformación congénita poco frecuente. Las anomalías morfológicas vesiculares y las variantes anatómicas en su posición se asocian con un aumento del riesgo de complicaciones tras la cirugía. Las técnicas de imagen realizadas de forma preoperatoria ayudan a confirmar el diagnóstico.

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44

McCluskey, Brian J., and Elizabeth L. Mumford. "Vesicular Stomatitis and Other Vesicular, Erosive, and Ulcerative Diseases of Horses." Veterinary Clinics of North America: Equine Practice 16, no. 3 (December 2000): 457–69. http://dx.doi.org/10.1016/s0749-0739(17)30089-5.

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45

El Mestikawy, Salah, Åsa Wallén-Mackenzie, Guillaume M. Fortin, Laurent Descarries, and Louis-Eric Trudeau. "Erratum: From glutamate co-release to vesicular synergy: vesicular glutamate transporters." Nature Reviews Neuroscience 12, no. 7 (May 19, 2011): 425. http://dx.doi.org/10.1038/nrn3054.

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46

Mejía Alvarez, Christian Richard, Karina Mayta, Maite Matlin Cárdenas Carranza, Araseli Verastegui-Díaz, Dante M. Quiñones-Laveriano, Julio Maravi Coronado, Eduardo Monge, and Claudia Alejandra Vera Chacchi. "Factores de riesgo para la malignidad de los pólipos vesiculares en dos hospitales públicos de Perú." Revista Colombiana de Gastroenterología 35, no. 4 (December 21, 2020): 414–20. http://dx.doi.org/10.22516/25007440.478.

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Introducción: los pólipos de vesícula biliar, benignos y malignos, en la mayoría de pacientes tienen un diagnóstico generalmente incidental; a través de estudios de imágenes, que no se pueden distinguir con precisión según su grado de malignidad. Objetivo: determinar los factores de riesgo para la malignidad de los pólipos vesiculares en dos hospitales públicos peruanos. Metodología: estudio de cohorte retrospectiva, de datos secundarios, en colecistectomizados del 2004 al 2012 en un hospital de Lima y otro de Callao. Se definió como pólipo maligno según el tipo histopatológico de adenocarcinoma. Se obtuvieron los riesgos relativos y sus intervalos de confianza del 95 % (IC 95 %). Además, mediante curvas ROC (característica operativa del receptor), se obtuvieron la sensibilidad y especificidad según el tamaño de pólipo. Resultados: de las 368 biopsias, 26 (7 %) fueron adenocarcinomas. La mediana del tamaño de los pólipos fue de 4 mm (rango: 1-65 mm), 176 (51 %) tuvieron múltiples pólipos y 85 (23 %) tuvieron litiasis biliar asociada. En el análisis multivariado, se incrementó el riesgo de malignidad por cada milímetro del tamaño del pólipo en 26 % (IC 95 %: 14 %-40 %, valor p < 0,001) y del tamaño de la pared vesicular en 182 % (IC 95 %:46 %-445 %, valor p: 0,002), ajustados por la edad del paciente, la litiasis y el tamaño vesicular. Para un tamaño de 6 mm se tuvo una sensibilidad de 81 % y especificidad del 85 %. Conclusión: se concluye que el tamaño del pólipo y el grosor de la pared vesicular estuvieron asociados con la malignidad de pólipos vesiculares.

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47

Palekar-Shanbhag, Pradnya, Supriya Lande, Riya Chandra, and Drushti Rane. "Bilosomes: Superior Vesicular Carriers." Current Drug Therapy 15, no. 4 (November 30, 2020): 312–20. http://dx.doi.org/10.2174/1574885514666190917145510.

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: In the current era, many formulations have been designed in the form of vesicular carriers like liposomes and niosomes which have been proved to be one of the potential candidates for drug delivery by the oral route but due to the gastrointestinal environment i.e. pH, presence of enzymes, and bile salts, their use is limited. Because of these difficulties, research is being done to increase the stability and efficacy of the drug. Thus bilosomes have been developed as a potential vesicular carrier system for oral vaccine delivery, transdermal and parenteral targeted drug delivery. The present article covers various aspects related to the novel vesicular system that is based on bile salts called bilosomes, for targetted drug delivery systems. It includes information related to bilosome composition, formulation techniques, characterization methods, applications in oral immunization as vaccine delivery approach and advantages over conventional nanocarriers such as liposomes and niosomes. It also focuses on the stability and applications of bilosomes along with scalability and potentiality in biomedical field of oral immunization against various dreadful diseases.

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48

Murphy, C., S. Wang, D. Kestler, F. Klein, A. Stewart, D. Weiss, and A. Solomon. "Vesicular senile systemic amyloidosis." Amyloid 18, sup1 (June 2011): 178–79. http://dx.doi.org/10.3109/13506129.2011.574354066.

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49

Baluska, Frantisek, Markus Schlicht, Dieter Volkmann, and Stefano Mancuso. "Vesicular secretion of auxin." Plant Signaling & Behavior 3, no. 4 (April 2008): 254–56. http://dx.doi.org/10.4161/psb.3.4.5183.

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50

Rodrigues, Gonçalo, Haiying Zhang, and David Lyden. "Tumour vesicular micromachinery uncovered." Nature Cell Biology 21, no. 7 (June 24, 2019): 795–97. http://dx.doi.org/10.1038/s41556-019-0351-0.

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