Academic literature on the topic 'Candia albicans'
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Journal articles on the topic "Candia albicans"
Aliyev, N. N., and F. A. Heydarova. "THE STUDY OF THE ANTIMICROBIAL ACTIVITY OF SOME NEW AZO DERIVATIVES OF PYRIDOXINE AND THEIR ZINC COMPLEXES." Epidemiology and Infectious Diseases 17, no. 2 (April 15, 2012): 60–62. http://dx.doi.org/10.17816/eid40678.
Full textYamada, Tsuyoshi, Shigeo Shindo, Kazuyuki Otani, and Osamu Nakai. "Candia albicans lumbar spondylodiscitis contiguous to infected abdominal aortic aneurysm in an intravenous drug user." BMJ Case Reports 14, no. 4 (April 2021): e241493. http://dx.doi.org/10.1136/bcr-2020-241493.
Full textHarsini, H. "Pengaruh Ekstrak Etanolik Kulit Batang Jambu Mete (Anacardium occidentale Linn) sebagai Bahan Kumur terhadap Daya Perlekatan C. Albicans pada Plat Resin Akrilik." Majalah Kedokteran Gigi Indonesia 19, no. 1 (October 20, 2016): 137. http://dx.doi.org/10.22146/majkedgiind.15398.
Full textMatsushita, Sho, Kumiko Hashimoto, Rie Takagi, and Takehiro Higashi. "Curdlan induces Th17 polarization via Jagged1 activation in human dendritic cells (47.12)." Journal of Immunology 182, no. 1_Supplement (April 1, 2009): 47.12. http://dx.doi.org/10.4049/jimmunol.182.supp.47.12.
Full textHafizah, Yunita, Yuliana Salman, Risnawati Risnawati, and Hajrah Hidriya. "GAMBARAN Candida albicanss PADA URIN REMAJA DI PANTI ASUHAN X BANJARMASIN." Jurnal Kajian Ilmiah Kesehatan dan Teknologi 4, no. 2 (November 1, 2022): 54–60. http://dx.doi.org/10.52674/jkikt.v4i2.76.
Full textAgbedo, E. S., O. R. Osumah, E. P. Woghiren, and I. P. Omusi. "Prevalence of Candida albicans Among Pregnant and Non-Pregnant Women attending a Medical Facility in Oredo, Edo State, Nigeria." Journal of Applied Sciences and Environmental Management 27, no. 1 (January 31, 2023): 101–5. http://dx.doi.org/10.4314/jasem.v27i1.15.
Full textIrawan, Yogie, and Riky Riky. "UJI DAYA HAMBAT ANTIFUNGI Candida Albicans TERHADAP UMBI BAWANG PUTIH (Allium sativum) DAN DAUN SAMBILOTO (Andrographis Paniculata Nees) MENGGUNAKAN METODE CAKRAM KERTAS." Jurnal Borneo Cendekia 2, no. 1 (March 10, 2018): 104–10. http://dx.doi.org/10.54411/jbc.v2i1.111.
Full textSupriyanto, Supriyanto, Kuswiyanto Kuswiyanto, and Etiek Nurhayati. "Efektivitas Air Perasan Daun Lidah Buaya (Aloe Vera) Terhadap Pertumbuhan Jamur Trichophyton Rubrum Dengan Metode Dillution Test." Jurnal Laboratorium Khatulistiwa 1, no. 2 (April 30, 2018): 152. http://dx.doi.org/10.30602/jlk.v1i2.155.
Full textWijaya, C. Hanny, A. Fieki Rachmatillah, and Boy M. Bachtiar. "PENGHAMBATAN CAJUPUTS CANDY TERHADAP VIABILITAS KHAMIR Candida albicans SECARA IN VITRO [Inhibition of Cajuputs Candy Toward the Viability of Candida albicans by using In Vitro Assay]." Jurnal Teknologi dan Industri Pangan 25, no. 2 (December 2014): 158–67. http://dx.doi.org/10.6066/jtip.2014.25.2.158.
Full textBastian, Firna Nuha, Maria Ulva, and Rossa Veronneca. "Utilization of Carbohydrates in Bamboo Shoots (Dendrocalamus asper) As an Alternative Media for the Growth of Candida albicans fungus." Sainmatika: Jurnal Ilmiah Matematika dan Ilmu Pengetahuan Alam 20, no. 1 (June 30, 2023): 1–7. http://dx.doi.org/10.31851/sainmatika.v20i1.11303.
Full textDissertations / Theses on the topic "Candia albicans"
Sousa, Diana Sofia Ortiga de. "Mistranslation in Candida albicans." Master's thesis, Universidade de Aveiro, 2011. http://hdl.handle.net/10773/8156.
Full textThe genetic code establishes the rules that determine the transfer of genetic information from nucleic acids to proteins. The importance of the genetic code in genome decoding and its high conservation suggests that its evolution is highly restricted or even frozen. Despite this, various prokaryotic and eukaryotic genetic code alterations have been found, showing that the code is surprisingly flexible. For instance, the human pathogen Candida albicans contains an ambiguous tRNACAG that decodes a CUG codon as Ser (97%) and as Leu (3%). To further study ambiguity in other amino acid codons, we have engineered 8 mutant tRNASer that misincorporate Ser at 8 different codons belonging to distinct amino acids families (Glu, Arg, Asn, Cys, Phe, Gln, His and Pro) in Candida albicans. The wild-type tRNA was subjected to site-directed mutagenesis in order to change its anticodon to CUC, CCU, GUU, GCA, GAA, CUG, GUG and GGG. The tRNA stability, the cellular changes and the stress response of the resulting mistranslating strains were evaluated through northern blot analysis, cell transformation efficiency, growth rate and expression of a HSP104-GFP reporter system. A phenotypic screening probing various environmental stress conditions was performed in order to further characterize these strains. Experimental data suggest that these genetic code ambiguities affect fitness negatively in standard growth conditions and introduce growth advantages in presence of stress conditions. Thus, stress response triggered by codon ambiguity increase adaptation potential.
O código genético estabelece regras que determinam a transferência de informação genética a partir dos ácidos nucleicos para proteínas. A importância do código genético na descodificação do genoma e sua alta conservação sugere que a sua evolução é altamente restrita. Apesar disso, várias alterações no código genético dos procariotas e eucariotas têm sido encontradas, mostrando que o código é surpreendentemente flexível. Por exemplo, o patogénico humano Candida albicans contém um tRNACAG ambíguo que descodifica o codão CUG como Ser (97%) e como Leu (3%). Para continuar o estudo da ambiguidade noutros codões, induzimos 8 tRNASer mutantes, que incorporam incorretamente o aminoácido serina a 8 codões diferentes, pertencentes a distintas famílias de aminoácidos (Glu, Arg, Asn, Cys, Phe, Gln, His e Pro), em Candida albicans. O tRNA não mutado foi submetido a mutagénese dirigida, a fim de modificar o seu anticodão UGA para CUC, CCU, GUU, GCA, GAA, CUG, GUG e GGG. A estabilidade do tRNA, as alterações celulares e resposta ao stress das estirpes mutantes resultantes foram avaliadas através da análise de Northern blot, da eficiência de transformação das células, da taxa de crescimento e da expressão do sistema repórter HSP104-GFP. Além disso, a caracterização fenotípica em determinadas condições de stress foi realizada com o intuito de caracterizar melhor essas estirpes. Os dados experimentais sugerem que essas ambiguidades ao código genético afetam negativamente a aptidão das células em condições de crescimento normais e introduzem vantagens no crescimento na presença de condições de stress. Assim, a resposta ao stress provocada pela ambiguidade dos codões pode aumentar o potencial de adaptação.
Bockmühl, Dirk Paul Helmut. "Regulation der Morphogenese des humanpathogenen Pilzes Candida albicans durch Komponenten eines cAMP-abhängigen Signalweges." [S.l. : s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=96232227X.
Full textMartchenko, Mikhail. "Postgenomic studies of Candida albicans." Thesis, McGill University, 2007. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=103029.
Full textO'Donnell, Raymond William. "Chitinolytic enzymes of Candida albicans." Thesis, University of Aberdeen, 1991. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=158392.
Full textJackson, Deborah Jane. "Chitinase activities from Candida albicans." Thesis, Liverpool John Moores University, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337857.
Full textPeters, D. W. "RNA synthesis in Candida albicans." Thesis, University of Warwick, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373051.
Full textClark, Fiona S. "Multidrug resistance in Candida albicans." Thesis, University of Aberdeen, 1994. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU073141.
Full textKlippel, Nina. "Interaktionen des humanpathogenen Hefepilzes Candida albicans mit Phagozyten." Tönning Lübeck Marburg Der Andere Verl, 2009. http://d-nb.info/994297548/04.
Full textFerreira, Maria Aurea Feitosa. "Eficacia de limpadores quimicos a base de peroxidos e hipoclorito na remoção de Candida spp. em rembasadores resilientes." [s.n.], 2008. http://repositorio.unicamp.br/jspui/handle/REPOSIP/288157.
Full textTese (doutorado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba
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Resumo: Candida albicans está associada com a etiologia da estomatite protética, patologia que acomete entre 11 a 67% dos usuários de próteses removíveis. Entretanto, mais recentemente, a Candida glabrata tem se destacado por apresentar hidrofobicidade e adesão à superfície de resina acrílica superior à da Candida albicans. Em acréscimo, características de superfície dos materiais como rugosidade (Ra) e energia livre de superfície (ELS) podem contribuir para a adesão de microrganismos. Desse modo, o objetivo desta pesquisa foi avaliar a rugosidade e energia livre de superfície dos rembasadores de próteses à base de poli - metilmetacrilato (Coe Soft e Kooliner) e silicone (Ufi Gel P) antes da contaminação com C. albicans ATCC 90028 e C. glabrata ATCC 2001, bem como verificar a eficácia dos limpadores químicos à base de peróxidos (Polident 3 minutes e Efferdent) e Hipoclorito de sódio a 0,5% na remoção desses microrganismos.Assim, para cada material rembasador foram confeccionadas 64 bases de resina acrílica Onda CryI (25 x 12 x 1mm), preparadas conforme as instruções do fabricante e, reembasadas constituindo dessa forma os corj'i>osde prova. Estes tiveram a rugosidade e energia de superfície determinadas. A seguir, foram separadas aleatoriamente em 2 grupos constituídos de 32 amostras cada, conforme o tipo de Candida. Em seguida, estes foram subdivididos em 4 grupos de 8 de acordo com os tratamentos: G1 - Água destilada (Controle); G2 - Polident ; 3 minutes; G3 - Efferdent; G4 - Hipoclorito de sódio 0,5%. Todas as amostras foram imersas em saliva humana durante'30 minutos para a formação da película adquirida. Posteriormente, foram submetidas ao teste de adesão durante período de 2 horas com uma das candidas, e então submetidos aos tratamentos nos tempos de: G1 - 15 minutos; G2 - 3 minutos; G3 -15 minutos e G4 -10 minutos. A contagem das células remanesce.ntes após o tratamento foi realizada em microscópio de luz (400x). Os dados foram submetidos à análise de variância e teste de Tukey (rugosidade de superfície e aderência fúngica) e ANOVA on Ranks para ELS, com nível de significância de 5%. O rembasador à base de silicone (Ufi Gel P) apresentou os menores valores de rugosidade comparados aos rembasadores à base de poli-imetil metacrilato (Coe 50ft e Kooliner), p<0,05. Entretanto, todos os materiais diferiram entre si para a energia de superfície (p<0,05), sendo que o Coe 50ft e o Ufi Gel P apresentaram os maiores e menores valores, respectivamente. Candida glabrata apresentou o maior número de células remanescentes aderidas, independente do rembasador utilizado (p<0,01). Dentre os limpadores, apenas o hipoclorito de sódio 0,5% diferiu do controle (p=0.001), apresentando um menor número de células remanescentes aderidas. Condui-se que o hipoclorito de sódio a 0,5% foi eficaz na remoção das células aderidas dos rembasadores, independente da espécie de Candida
Abstract: Candida albicans is associated with denture stomatitis etiology, pathology which affect about 11 to 67% of removable prostheses users. However, more recently, the Candida glabrata has been highlighted for presenting superior hydrophobicity and resin acrylic surface adherence when compared to the C. albicans. In addition, surface characteristics' materiais such roughness (Ra) and surface free energy (EL8) may contribute to the microorganisms' adhesion. Thus, the purpose of this study was to evaluate the surface roughness and surface free energy of methyl methacylate liners materiais (Coe 80ft and Kooliner) and silicone (Ufi Gel P) before contamination with C. albicans (ATCC 90028) and C. glabrata (ATCC2001), as well to verify the peroxide chemical denture cleansers efficacy (Polident 3 minutos and Efferdent) and 0.5% sodium hypochlorite - NaOCl, in the miaoorganisms' removing. Thus, 64 rectangular bases measuring 25 x 12 x 1 mm using microwave-polymerized acryli~ resins, following manufacturers' recommendations, to each material were made, then were relined and after surface roughness and surface free energy were measured. Next, the samples were randomly separated by lottery into two groups of 32 each, according to the fungus and these were subdivided into four groups of eight as the treatments: G1 - Distilled water (Control); G2 - Polident 3 min. utes; G3 - Efferdent; G4 - 0,5% NaOCI. Ali the samples rested in human whole saliva for 30 minutes to form an acquired pellicle. After, they were submitted to the adherence assay with one of the fungus for two hours, and then, treated, following these times: G1 - Distilled water (15 minutes); 2 - Polident 3 minutes (3 minutes); 3 - Efferdent (15 minutes); 4 - 0,5% sodium hypochlorite (10 minutes). The adhered cells were counted using a light microscope (Axiostar 2 Plus, Carl Zeiss, Jena, Germany) at 400 x magnification. The data were submitted to the analysis of variance and Tukey test (roughness and fungus adherence) and ANOVA on Ranks for EL8, with significance levei of 5%. The silicone-based liner (Ufi Gel P) showed lower values of roughness compared to the methyl methacrilate-based liners (Coe 80ft and Kooliner), (p<0.05). However, ali these materiais were different among them for surface free energy (p<0.05), where the Coe 80ft and Ufi Gel P showed the highest and lowest values, respectively. Candida glabrata showed the highest number of adhered cells for ali materiais (p<0.01). Among evaluated cleansers, only 0.5% sodium hypochlorite differed from the control (p=0.001), showing the lowest number of remaining cells adhered. The conclusion is that the 0.5% sodium hypochlorite was the only one chemical cleanser efficient in the adhered cells removing in ali denture liners independent of the Candida specie
Doutorado
Protese Dental
Doutor em Clínica Odontológica
Vieira, Ana Paula Coelho. "Eficácia de limpadores químicos na remoção e re-colonização de biofilmes de Candida spp. formados na superfície de material reembasador." [s.n.], 2010. http://repositorio.unicamp.br/jspui/handle/REPOSIP/288379.
Full textDissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba
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Resumo: Os reembasadores para base de prótese, após a exposição à cavidade bucal, apresentam alterações de superfície facilitando a adesão e a colonização por micro-organismos. Para a limpeza de superfície desses materiais são indicados os limpadores químicos para evitar os danos mecânicos que podem ser provocados pelas cerdas das escovas dentais. Assim, o objetivo nesta pesquisa foi avaliar a eficácia de limpadores químicos na remoção de biofilme de Candida spp. desenvolvido sobre a superfície de um reembasador classificado como permanente à base de poli-metilmetacrilato e na prevenção da re-colonização dessa superfície, especialmente a Candida spp., comumente associada ao desenvolvimento da candidíase. Espécimes (10 mm diâmetro X 3 mm altura) de resina acrílica reembasada com um reembasador mais representativo disponível comercialmente teve sua rugosidade de superfície mensurada antes (baseline) e biofilme de C. albicans ATCC 90028 ou C. glabrata ATCC 2001 foi desenvolvido sobre os mesmos. Após a formação dos biofilmes os espécimes foram aleatorizados e submetidos aos tratamentos (n=16): AD - Água destilada (Controle), 15 min; POL - Polident 3 minutos, 3 min; EFF - Efferdent, 15 min; HPS - Hipoclorito de sódio a 0,5%, 10 minutos. Metade destes espécimes (n=8) foi utilizada para determinação da eficácia dos limpadores, utilizando contagem de células viáveis, enquanto os espécimes remanescentes (n=8), após os tratamentos, foram novamente colocados em meio de cultura estéril e incubados por mais 48 h a fim de determinar o efeito dos limpadores na prevenção da recolonização. Após os tratamentos os espécimes tiveram a rugosidade de superfície determinada, considerada pós-tratamento. Alguns espécimes de cada uma das espécies de Candida tiveram a superfície analisada após os tratamentos, por microscopia eletrônica de varredura (MEV). Os dados foram submetidos à análise de variância e teste de Tukey HSD em nível de significância de 5%. A rugosidade de superfície foi significantemente maior após os tratamentos (P<0,05). Quantos aos tratamentos, o HPS mostrou-se efetivo tanto para a desinfecção quanto na recolonização de ambas as espécies de Candida, pois houve ausência total de crescimento. Na avaliação da desinfecção, imediatamente após os tratamentos, quando C. albicans foi considerada, não houve diferença significativa entre os peróxidos alcalinos (p>0,05) e ambos diminuíram o número de células fúngicas (p<0,05) comparado ao tratamento com AD. Entretanto, para C. glabrata, os tratamentos com ADD e peróxidos alcalinos não se diferenciaram entre si (p>0,05). Na análise dos resultados para a recolonização foi observada que houve inversão no comportamento, pois enquanto, para C. albicans, os tratamentos com AD e peróxidos alcalinos não diferiram entre si (p>0,05), para C. glabrata os tratamentos com peróxidos alcalinos apresentaram valores similares e menores (p>0,05),quando comparados com o tratamento com AD (p<0,05). Na comparação entre as espécies de Candida observou-se que C. glabrata apresentou os maiores níveis de células viáveis quando os dados foram avaliados na situação de imediatamente após os tratamentos com os peróxidos alcalinos e foi diferente de C albicans (p<0,05). Entretanto não houve diferença para a recolonização (p>0,05). Os resultados sugerem que os limpadores a base de peróxidos alcalinos não foram efetivos na remoção total dos micro-organismos e também não impediram a recolonização por Candida spp
Abstract: The denture liners exhibits surface changes in oral environment by constant loss of its constituent elements, which facilitate microorganisms adherence that leads to biofilm formation. Denture liners surface can be cleaned by brushing or using denture cleaners, which are recommended, in order to avoid mechanic injuries to denture liners by brushing it. Therefore, the aim of this study was to evaluate the long term efficacy of denture cleansers on Candida spp. biofilm recolonization on liner surface. Specimens of poly (methylmethacrilate) were lined according to manufacturer instructions (10 mm diameter X 3.0 mm thickness). Surface roughness was measured at baseline and after the treatments. Next, biofilms of C. albicans ATCC 90028 and C. glabrata ATCC 2001 were allowed to develop on liner surface for 48 h. Subsequently, the specimens were randomly assigned for the cleaning treatments (n=16): distilled water (DW - control), 15 min; Polident 3 minutes (POL) - 3min; Efferdent (EFF)-15 min; sodium hypochlorite (HYP) - 10 min. After the treatments, specimens (n=8) were sonicated for biofilm disruption and the viable cells were counted (cell/mL). To determine the long term effectiveness of the cleaning process, a set of cleaned specimens (n=8) were submitted to new biofilm growth conditions. After 48 h, biofilm were disrupted by sonication and cell number estimated. Scanning electron microscopy was performed to analyze the specimen topography after denture cleanser treatment. Data were analyzed by ANOVA and Tukey's HSD test was used as post-ANOVA employing a significance level fixed at 5%. The liner surface was rougher after the treatments (P<0.05). Results showed significant differences in cleanliness among the treatments (p<0.05), however for Candida species (p<0.05) no significant difference was observed in the recolonization condition (p>0.05). Alkaline denture cleansers showed similar cleaning performance and both showed lower cells counts compared with the control (p<0.05). Hypochlorite was the only effective treatment as no viable cells were detected even after the recolonization test. Within the limits of this study, it can be concluded that alkaline denture cleansers were not effective on biofilm removal, once denture liner surface by Candida spp biofilm recolonization was not prevented
Mestrado
Protese Dental
Mestre em Clínica Odontológica
Books on the topic "Candia albicans"
Cihlar, Ronald L., and Richard A. Calderone, eds. Candida albicans. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6.
Full textPrasad, Rajendra, ed. Candida Albicans. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-75253-7.
Full textCandida albicans. Montréal: Hippocampe - ÉdiForma, 1995.
Find full textTerrass, Stephen. Candidiasis: (candida albicans). Madrid: Tutor, 1996.
Find full textL, Cihlar Ronald, and Calderone Richard A. 1942-, eds. Candida albicans: Methods and protocols. Totowa, N.J: Humana Press, 2009.
Find full textCandida albicans et candidose généralisée. Sherbrooke, Québec: Éditions du IIIe millénaire, 1990.
Find full textPeters, David William. RNA synthesis in 'Candida albicans'. [s.l.]: typescript, 1985.
Find full textL, Cihlar Ronald, and Calderone Richard A. 1942-, eds. Candida albicans: Methods and protocols. Totowa, N.J: Humana Press, 2009.
Find full textCandida albicans: The pathogenic fungus. New York: Hemisphere Pub. Corp., 1989.
Find full textPrasad, Rajendra, ed. Candida albicans: Cellular and Molecular Biology. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-50409-4.
Full textBook chapters on the topic "Candia albicans"
Sreevalsan, T. "Isolation of Dendritic Cells from Human Blood for In Vitro Interaction Studies with Fungal Antigens." In Candida albicans, 1–8. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_1.
Full textCalderone, Richard A. "In Vitro and Ex Vivo Assays of Virulence in Candida albicans." In Candida albicans, 85–93. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_10.
Full textPolonelli, Luciano, and Stefania Conti. "Biotyping of Candida albicans and Other Fungi by Yeast Killer Toxins Sensitivity." In Candida albicans, 97–115. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_11.
Full textPujol, Claude, and David R. Soll. "DNA Fingerprinting Candida Species." In Candida albicans, 117–29. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_12.
Full textBlackwell, Chris, and Jeremy D. Brown. "The Application of Tandem-Affinity Purification to Candida albicans." In Candida albicans, 133–48. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_13.
Full textChauhan, Neeraj. "Preparation of Samples for Proteomic Analysis of the Candida albicans Cell Wall." In Candida albicans, 149–55. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_14.
Full textSturtevant, Joy. "Reporter Gene Assays in Candida albicans." In Candida albicans, 157–67. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_15.
Full textRamon, Ana M., and William A. Fonzi. "Genetic Transformation of Candida albicans." In Candida albicans, 169–74. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_16.
Full textNobile, Clarissa J., and Aaron P. Mitchell. "Large-Scale Gene Disruption Using the UAU1 Cassette." In Candida albicans, 175–94. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_17.
Full textChauhan, Neeraj, and Michael D. Kruppa. "Standard Growth Media and Common Techniques for Use with Candida albicans." In Candida albicans, 197–201. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_18.
Full textConference papers on the topic "Candia albicans"
Kristanto, Yanuar, Willy Sandhika, and Agung Dwi Wahyu Widodo. "Differences in Caspase-3 Expressions of Liver Organs and Spleen in Animals Model Rattus Norvegicus Infected with Candida Albicans and Candida Non Albican Fungus." In 2nd International Conference Postgraduate School. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0007541102630268.
Full textLins, Nathalia Alexandre Eloy, Maria Carolina Oliveira Lins, Renan Lennon Silva Henrique, Pettely Thaíse De Souza Santos Palmeira, Maria Helena Chaves de Vasconcelos Catão, Sérgio de Lemos Campello, Anderson Stevens Leônidas Gomes, Patrícia Lins Azevedo do Nascimento, and Cláudia Cristina Brainer de Oliveira Mota. "Analysis of biofilm growth over bulk fill composite resins through optical coherence tomography." In Latin America Optics and Photonics Conference. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/laop.2022.tu1b.4.
Full textHasan, Ziaul, Asimul Islam, and Luqman Ahmad Khan. "Signature Garlic Phytochemical as a Potential Anti-Candidal Candidate Targeting Virulence Factors in Candida albicans." In International Electronic Conference on Biomedicines. Basel Switzerland: MDPI, 2023. http://dx.doi.org/10.3390/ecb2023-14080.
Full textBatista, Renata Duarte, and CIBELE LOPES. "CANDIDA ALBICANS: AGENTE ETIOLÓGICO DA ENDOCARDITE INFECCIOSA FÚNGICA." In II Congresso Brasileiro de Estudos Patológicos On-line. Revista Multidisciplinar em Saúde, 2023. http://dx.doi.org/10.51161/ii-conbesp/13416.
Full text"Prevalence and clonality of Non Albicans Candida species." In 3rd INTERNATIONAL CONFERENCE ON BIOLOGICAL RESEARCH AND APPLIED SCIENCE. Jinnah University for Women, Karachi,Pakistan, 2023. http://dx.doi.org/10.37962/ibras/2023/179-180.
Full textApolinário, Joelma Maria dos Santos da Silva, and Lorrane De Sousa Barbosa. "DISTÚRBIOS MUCOCUTÂNEOS CRÔNICOS CAUSADOS POR INFECÇÕES FÚNGICAS CORRELACIONADAS A CANDIDA ALBICANS E CANDIDA SPP." In I Congresso Brasileiro de Doenças Infectocontagiosas On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/2247.
Full textSantos, Emmanuely dos, Janaina Sardi, Pedro Rosalen, Joice Graciani, Mayara Garcia, Josy Lazarini, and Luís Regasini. "Bioprospecting of chalcones against mixed biofilm of Candida albicans and Candida tropicalis." In Congresso de Iniciação Científica UNICAMP. Universidade Estadual de Campinas, 2019. http://dx.doi.org/10.20396/revpibic2720192598.
Full textNegri, M., T. Lorenço, S. Silva, M. Henriques, J. Azeredo, and R. Oliveira. "Effect of antifungal agents on non-Candida albicans Candida species enzymatic activity." In Proceedings of the International Conference on Antimicrobial Research (ICAR2010). WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814354868_0061.
Full textPawlat, Joanna, Michal Kwiatkowski, Piotr Terebun, Barbara Chudzik, and Mariusz Gagos. "Candida albicans inactivation with DBD He/O2 plasma jet." In 2017 International Conference on Electromagnetic Devices and Processes in Environment Protection with Seminar Applications of Superconductors (ELMECO & AoS). IEEE, 2017. http://dx.doi.org/10.1109/elmeco.2017.8267745.
Full textMASUI, S., T. MAJIMA, S. ITO-KUWA, K. NAKAMURA, and S. AOKI. "VISUALIZATION OF SUPEROXIDE GENERATED FROM COLONIES OF CANDIDA ALBICANS." In Proceedings of the 13th International Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702203_0073.
Full textReports on the topic "Candia albicans"
Maheshwari, E. Uma, and G. Jyothilakshmi. A STUDY OF ANTIFUNGAL SUSCEPTIBILITY TESTING AMONG NON ALBICANS CANDIDA IN PATIENTS OF VULVO VAGINAL CANDIDIASIS AT TERTIARY CARE CENTER. World Wide Journals, February 2023. http://dx.doi.org/10.36106/ijar/9605846.
Full textCastro, Ricardo Dias de. Chemical and antifungal analysis of essential oils and phytochemicals against Candida albicans. Science Repository OÜ, March 2019. http://dx.doi.org/10.31487/j.cmr.2018.01.005.
Full textTasso, Camilla Olga, Analú Barros de Oliveira, Túlio Morandin Ferrisse, and Janaina Habib Jorge Jorge. Association between Candida Albicans and Squamous Cell Carcinoma: A Systematic Literature Review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, March 2021. http://dx.doi.org/10.37766/inplasy2021.3.0005.
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