Academic literature on the topic 'SinRIP gene'
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Journal articles on the topic "SinRIP gene"
Ivanova, Lidia, Sondra Schlesinger, and Paul D. Olivo. "Regulated Expression of a Sindbis Virus Replicon by Herpesvirus Promoters." Journal of Virology 73, no. 3 (March 1, 1999): 1998–2005. http://dx.doi.org/10.1128/jvi.73.3.1998-2005.1999.
Full textMarketon, Melanie M., Sarah A. Glenn, Anatol Eberhard, and Juan E. González. "Quorum Sensing Controls Exopolysaccharide Production in Sinorhizobium meliloti." Journal of Bacteriology 185, no. 1 (January 1, 2003): 325–31. http://dx.doi.org/10.1128/jb.185.1.325-331.2003.
Full textKÜPELİ, İlke, Ufuk KUYRUKLUYILDIZ, Sara TAŞ, Nigar BİRCAN OCAK, and Ayşin ALAGÖL. "Comparison of the Effects of Regional Anesthesia/Peripheral Nerve Block and General Anesthesia on Preoperative Anxiety." Turkiye Klinikleri Journal of Anesthesiology Reanimation 14, no. 1 (2016): 1–6. http://dx.doi.org/10.5336/anesthe.2015-48041.
Full textBarros, Mércia R., Mateus M. da Costa, Chirles A. de França, Tomoe N. Saukas, Leonildo B. G. da Silva, Vanessa Anny S. Silva, Raíssa V. Cavalcante, and Rinaldo A. Mota. "Perfil de resistência a antimicrobianos de Staphylococcus spp. isolados de frangos de corte e poedeiras comerciais no estado de Pernambuco." Pesquisa Veterinária Brasileira 31, no. 8 (August 2011): 672–76. http://dx.doi.org/10.1590/s0100-736x2011000800007.
Full textGebara, C. M. S., S. R. Wosiacki, F. J. Negrão, D. B. de Oliveira, S. N. E. Beloni, A. A. Alfieri, and A. F. Alfieri. "Detecção do gene da nucleoproteína do vírus da cinomose canina por RT-PCR em urina de cães com sinais clínicos de cinomose." Arquivo Brasileiro de Medicina Veterinária e Zootecnia 56, no. 4 (August 2004): 480–87. http://dx.doi.org/10.1590/s0102-09352004000400009.
Full textSöyler, Nazlı, Mehmet Sedat İpar, and Demet Kocatepe. "Determination of the genetically modified organism (GMO) awareness levels of hospital workers: example of Sinop." Food and Health 7, no. 1 (2021): 1–14. http://dx.doi.org/10.3153/fh21001.
Full textKraut, Anthea. "Female Surrogate Labor and White Corporeal Debt in Singin’ in the Rain." Camera Obscura: Feminism, Culture, and Media Studies 36, no. 2 (September 1, 2021): 1–31. http://dx.doi.org/10.1215/02705346-9052774.
Full textBon, Carlotta, Riccardo Luffarelli, Roberta Russo, Silvia Fortuni, Bianca Pierattini, Chiara Santulli, Cristina Fimiani, et al. "SINEUP non-coding RNAs rescue defective frataxin expression and activity in a cellular model of Friedreich's Ataxia." Nucleic Acids Research 47, no. 20 (October 4, 2019): 10728–43. http://dx.doi.org/10.1093/nar/gkz798.
Full textBasso, Roberta M., José P. Oliveira-Filho, Mariana I. P. Palumbo, Luiza S. Zakia, João P. Araújo Jr, and Alexandre S. Borges. "Ocorrência do SNP c.767G>T no gene DNM1responsável pelo colapso induzido pelo exercício em cães da raça Labrador Retriever no Estado de São Paulo." Pesquisa Veterinária Brasileira 35, no. 5 (May 2015): 486–90. http://dx.doi.org/10.1590/s0100-736x2015000500017.
Full textRosin da Silva, Júlia, Débora Rodrigues Silveira, and Cláudio Dias Timm. "FATORES DE PATOGENICIDADE DE Yersinia enterocolitica." Science and Animal Health 8, no. 3 (July 25, 2022): 220–35. http://dx.doi.org/10.15210/sah.v8i3.20253.
Full textDissertations / Theses on the topic "SinRIP gene"
Schroder, Wayne Ashley, and n/a. "Cloning and Characterisation of the Human SinRIP Proteins." Griffith University. School of Biomolecular and Biomedical Science, 2003. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20030829.140754.
Full textSchroder, Wayne Ashley. "Cloning and Characterisation of the Human SinRIP Proteins." Thesis, Griffith University, 2003. http://hdl.handle.net/10072/366190.
Full textThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Biomolecular and Biomedical Sciences
Faculty of Science
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Rocha, Flávia Riso. "Identificação e análise funcional de genes relacionados à transdução de sinais na cana-de-açúcar." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-18092006-224457/.
Full textA diversity of processes related to growth, development and adaptation to environmental conditions are regulated by signal transduction pathways. The SUCAST Project (Sugarcane Signal Transduction) (Souza et al., 2001) aims to identify, characterize and associate putative functions to sugarcane signal transduction components using bioinformatic tools and to evaluate their expression profiles using cDNA microarrays. BLAST searches conducted on sequences stored in the SUCEST databank - The Sugar Cane EST Project (Vettore et al., 2003) - revealed more than 3,500 putative genes related to signaling in sugarcane. The protein kinases were anaçyzed for the presence of conserved domains and classified according to a phylogenetic analysis of the predicted catalytic domain. The phylogenetic approach indicated six characteristic groups for protein kinases and four mains groups for receptor-like kinases. The expression patterns of SUCAST components were evaluated in six organs (root, flower, leaf, lateral bud, first and fourth internodes), in response to different stimuli (treatment with the phytohormones abscisic acid and methyljasmonate, drought, endophytic bacteria interaction, attack by Diatraea saccharalis and phosphate deficiency) and in sugarcane cultivars contrasting for sucrose accumulation. The tissue profiling experimenta showed 217 differentially expressed genes in at least one of the six organs analyzed and 153 genes of ubiquitous expression. A total of 179 differentially expressed genes were obtained in response to phytohormones and environmental stimuli, in at least one of the conditions analyzed were obtained. Comparisons between high and low sucrose (brix) cultivars led to the detection of 51 differentially expressed genes in at least one of the samples analyzed (leaves +1 and internodes at different maturing stages). The expression patterns were also analyzed in time-course experiments of phosphate deficiency, drought and phytohormone treatments by Self-Organizing Maps (SOM) clusterization. Quantitative PCR results confirmed 72% of the microarray expression data in sugarcane organs for 25 selected genes and 80.5% of the 36 expression profiles selected in response to phytohormones and environmental stimuli. Additionally, real-time PCR reactions were carried out to evaluate the expression levels of five genes in individuals contrasting for sucrose accumulation and 57% of the results obtained were in agreement with the microarray data. All data generated were integrated and compiled into the SUCAST databank (http://www.sucest-fun.org). The knowledge generated adds to the comprehension of the function of SUCAST components, indicating targets to be explored in the improvement of sugarcane cultivars.
Toledo, Ricardo Acayaba de. "Sinais clínicos em pacientes com espondiloartrites na presença e na ausência do gene HLA-B*27." Faculdade de Medicina de São José do Rio Preto, 2013. http://bdtd.famerp.br/handle/tede/183.
Full textIntroduction: Spondyloarthritis is a group of diseases with clinical, laboratory and image similar. Analysis of clinical manifestations of spondyloarthritis in patients with and without the HLA-B*27 were performed, but the results revealed great heterogeneity. Objectives: The aim of this study was to evaluate the clinical manifestations of spondyloarthritis according to the classification criteria of the European Study Group Spondyloarthropathy (ESSG) in the presence and absence of the HLA-B*27. Patients and methods: From a total of 156 patients with clinical suspicion referred for the investigation of gene HLA-B*27, 73 were diagnosed with spondyloarthritis according to the criteria of ESSG. The HLA-B*27 were identified using commercial kits (Dynal ReliTM SSO HLA-B Typing Kit, Invitrogen). Clinical data were collected from medical records of patients. The results were compared using the chi-square or Fisher exact test. The values of Odds Ratio (OR) and confidence interval of 95% were also calculated. The p-value equal to or less than 0.05 was considered significant. Results: Of the 73 selected patients, 53 (72.6%) were male and 20 (27.4%) were female. The mean age was 49.4 and did not differ between genders (p = 0337). The spondyloarthritis found among the 73 patients were: ankylosing spondylitis (n = 47; 64.4%), psoriatic spondyloarthritis (n = 9; 12.3%), undifferentiated spondyloarthritis (n = 9; 12.3%), spondyloarthritis enteropathica (n = 6; 8.2%) and reactive arthritis (n = 2; 2.7%). The average age of onset was equal to 39.1 (± 11.7) and did not differ between genders (p = 0.9057). Of the total, 35 (47.9%) patients were HLA-B*27 positive and 38 (52.1%) were negative. This gene was positively associated with ankylosing spondylitis (OR: 5.37, 95% CI: 1813-15905, p = 0.003) and negatively with spondyloarthritis enteropathica (OR: 0.07, 95% CI: 0003-1301, p = 0.025). The sacroiliitis was associated with the presence of the gene (OR: 10 552, 95% CI: 1260-88256, p = 0.014) and intestinal injury absence (OR: 0.195, 95% CI: 0038-0978, p = 0.048). Conclusions: The HLA-B * 27 was associated with ankylosing spondylitis, enteropathic but not to spondyloarthritis. The radiological signs of sacroiliitis prevailed in patients positive for HLA-B*27, while intestinal involvement was associated with the absence of this gene. especially in cases of dystrophic scoliosis. In both cases, studies with larger samples are needed to assess whether these trends are evident.
Introdução: Espondiloartrite é um grupo de doenças com características clínicas, laboratoriais e imagenológicas semelhantes. Análises das manifestações clínicas das espondiloartrites em pacientes com e sem o gene HLA-B*27 foram realizadas, mas os resultados revelaram grande heterogeneidade. Objetivos: O objetivo deste trabalho foi avaliar as manifestações clínicas das espondiloartrites utilizadas nos critérios de classificação do European Spondyloarthropathy Study Group (ESSG) na presença e na ausência do gene HLA-B*27. Casuística e método: De um total de 156 pacientes com suspeita clínica, encaminhados para investigação do gene HLA-B*27, 73 tiveram diagnóstico de espondiloartrites confirmado, de acordo com os critérios do ESSG. O gene HLA-B*27 foi identificado com o uso de kits comerciais (Dynal ReliTM SSO HLA-B Typing Kit, Invitrogen). Os dados clínicos foram colhidos dos prontuários médicos dos pacientes. Os resultados foram comparados com o uso dos testes Qui-quadrado ou o teste exato de Fisher. Os valores de Odds Ratio (OR) e intervalo de confiança a 95% também foram calculados. O valor p igual ou menor que 0,05 foi considerado significante. Resultados: Dos 73 pacientes selecionados, 53 (72,6%) eram do sexo masculino e 20 (27,4%), femininos. A média de idade foi igual a 49,4 e não diferiu entre os sexos (p=0.337). As espondiloartrites encontradas entre os 73 pacientes foram: espondilite anquilosante (n=47; 64,4%), espondiloartrite psoriásica (n=9; 12,3%), espondiloartrite indiferenciada (n=9; 12,3%), espondiloartrite enteropática (n=6; 8,2%) e artrite reativa (n=2; 2,7%). A média de idade de início dos sintomas foi igual a 39,1 (±11.7) e não diferiu entre os sexos (p=0,9057). Do total, 35 (47.9%) pacientes eram HLA-B*27 positivo e 38 (52.1%), negativos. Este gene foi associado positivamente à espondilite anquilosante (OR: 5.37; IC 95%: 1.813-15.905; p=0.003) e negativamente à espondiloartrite enteropática (OR: 0.07; IC 95%: 0.003-1.301; p=0.025). A sacroiliíte se associou à presença do gene (OR: 10.552; IC 95%: 1.260-88.256; p=0.014) e o comprometimento intestinal à ausência (OR: 0.195; IC 95%: 0.038-0.978; p=0.048). Conclusões: O gene HLA-B*27 foi associado à espondilite anquilosante, mas não à espondiloartrite enteropática. Os sinais radiológicos de sacroiliíte prevaleceram nos pacientes positivos para o gene HLA-B*27, enquanto o comprometimento intestinal foi associado à ausência deste gene.
Nascimento, Sandra Regina Dantas. "Estudo clinico e sequenciamento direto do gene Twist em individuos com sinais sugestivos da sindrome de Saethre-Chotzen." [s.n.], 2001. http://repositorio.unicamp.br/jspui/handle/REPOSIP/312240.
Full textDissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas
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Resumo: A Síndromede Saethre-Chotzen(SSC,Acrocefalossindactiliatipo 111) é uma heredopatia autossômica dominante, com alta penetrância e expressividade variável, sendo craniossinostose um de seus principais sinais clínicos. Mutações nos genes FGFR1-FGFR3 e Twist são causas conhecidas de craniossinostoses, a primeira por aumento da expressão e a última por haploinsuficiência. O gene Twist foi mapeado na região 7p21 e algumas deleções e translocações balanceadas, bem como mutações no exon 1 deste gene, têm sido descritas nas formas de craniossinostose associadas a SSC. Quatro famílias brasileiras com ACS 111foram avaliadas do ponto de vista dismorfológico e rastreadas para mutações no gene Twist. O protocolo de investigação incluiu exame dismorfológico dirigido, estudo de imagem (radiografia de crânio, tórax, coluna vertebral, tomografia computadorizada de crânio e ultrassonografia abdominal), estudo citogenético com bandamento G e seqüenciamento direto de DNA dos produtos de PCR amplificados para o exon 1 do gene Twist, nos indivíduos que apresentavam ao menos um sinal clínico desta condição. Ao exame, observou-se importante variabilidade de características faciais, incluindo assimetria facial (20/24), braquicefalia (16/24), orelhas com acentuação do ramo da hélice (15/24) e implantação baixa (13/24), hipoplasia malar (13/24), ponte nasal proeminente (13/24), implantação baixa dos cabelos na fronte (12/24), ptose palpebral (12/24).Achados adicionais incluiram sindactilia cutânea parcial dos artelhos (18/24), clinodactilia do 50 dedo (13/24), háluces alargados (13/24). Somente em umafamília observou-se sindactilia cutânea total, entre o 20 e 30 artelhos. Sete indivíduos apresentaram radiografia de crânio com craniossinostose bicoronal, um, craniossinostose unicoronal e dois com forame parietal bilateral. O sinal da prata batida apareceu nos oito casos. A radiografia de tórax em dois indivíduos mostrou fusão parcial dos 10 e 20 arcos costais à esquerda e na radiografia de coluna lombo-sacra dois casos apresentaram espinha bífida lombar. O exame de cariótipo dos propósitos de cada família foi normal e o estudo molecular nãodetectou alterações no exon 1 do gene Twist. Esse estudo reforça a importância da avaliação dismorfológica em SSC e sugere que o emprego de outras técnicas de biologia molecular poderia contribuir para elucidar o papel do gene Twist nos achados clínicos desta casuística. Além disso, os dismorfismos detectados poderiam, ainda, ser decorrentes de outros genes envolvidos na regulação do desenvolvimento craniofacial e de membros
Abstract: Saethre-Chotzensyndrome(acrocephalosyndactyly type 111)is an autosomal dominant craniosynostosis condition, with high penetrance and variable expressivity. Mutations in the Fgfr1-Fgfr3 and Twist genes are known to cause craniosynostosis, the former by constitutive activation and the latter by haploinsufficiency. The Twist gene maps to 7p21 and mutations in the gene have been reported in the SCS form of craniosynostosis. The aims of this study were characterize the dysmorphological variability and mutations in exon 1 of Twist gene using direct sequencing in four Brazilian famílies presenting SCS. Twenty-four patients were included in our study, diagnosed as having features of Saethre-Chotzen syndrome. The phenotypic characteristics of ali patients were inventoried. Also, a DNA test had been performed and their genotype was noted. Facial features, present were facial asymmetry (20/24), brachycephaly (16/24), small ear with prominent crura (15/24), maxillary hypoplasia (13/24), lowset ears (13/24), and ptosis of the eyelids (12/24), lowset frontal hairline (12/24), ocular hypertelorism (11/24). Additional findings included partial hands and feet cutaneous syndactyly (18/24), clinodactyly (13/24), and broad great toes (13/24); in one family was observed total cutaneous syndactyly in feet. Skull X-rays were abnormal in 8 patients in which it was performed;partiaI fusionof 1st and 2ndribs wasdetectedin 2 individuaisand 2 had lumbar spina bifida. Chromossomal analysis on GTG-banding were normal. The analysis was carried out by direct DNA sequencing of PCR amplified products for exon 1 in the proband of each family. No Twist mutations were found. In conclusion, this four SCS famílies may have mutations in other genes of the same developmental pathway. This study reinforces the importance of the dysmorphological evaluation in patients with craniosynostosis, as well as ali their famílies, especially ACS 111,in which inter and intrafamilial variability make the diagnosis more difficult
Mestrado
Genetica Medica
Mestre em Ciências Médicas
Santos, Juliana da Silva. "Identificação de fatores de transcrição e sinais celulares que regulam a expressão do gene cspC em Caulobacter crescentus." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/42/42132/tde-25052012-091050/.
Full textThe cold shock proteins belong to a family of proteins presenting a highly conserved domain, called cold shock domain (CSD). They are involved in various cellular processes, including adaptation to low temperature, nutritional stress, cell growth and stationary phase. In C. crescentus, a non-pathogenic α-proteobacteria, the cold shock proteins CspC and CspD have two CSDs and they are induced during stationary phase. This study aims to determine the transcription factors and cellular signals involved in cspC gene regulation in C. crescentus. In the present study we scanned a library of 4000 mutant clones with the Tn5 transposon, from which seven mutants were identified presenting reduced expression of cspC: CCNA03569 (hypothetical protein); CCNA02510 (polysaccharide deacetylase); CCNA01594 (ribosomal protein L11 methyltransferase); CCNA02186 (acetolactate synthase 3 regulatory subunit); CCNA00084 (bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase); CCNA03616 (sulfite reductase (NADPH)) e CCNA01448 (fructose 1,6-bisphosphatase II). Expression assays in the presence of a conditioned medium, showed that cspC and cspD are apparently not induced in response to increased cell density. The phenotype of the mutant cspC was evaluated as to oxidative stress resistance in the stationary phase. The results showed that the DcspC strain is highly sensitive to hydrogen peroxide and superoxide but is not sensitive to organic hydroperoxide. The absence of cspC probably is compensated by dps, since the expression of this gene is increased in DcspC strain. In contrast, the transcritpion of katG is decreased, but the activities of KatG and SodB are not affected in the cspC mutant. Under conditions of stress caused by hydrogen peroxide, sucrose or salt, cspC expression is not affected. The sigma factors sigmas SigT and SigU and transcription regulator Fur are not involved in the regulation of cspC, but cspC expression is increased in DsigJ and decreased in DoxyR strains, respectively. It was also determined that cspC shows a positive autoregulation, which may occur via stabilization of its own mRNA.
Costa, Karen Regina Carim da. "Aspectos fenotípicos e moleculares da adesão e atividade enzimática de Candida sp isoladas de pacientes com sinais clínicos de candidíase oral." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/60/60135/tde-03122010-093837/.
Full textThe wide spectrum of candidiasis and its clinical importance encourage the research with the purpose of clarifying the mecanisms of pathogenicity and identification of virulence factors of Candida sp. Therefore, the aim of this study was to verify through phenotypic and molecular assays the adhesion, enzymatic activity e genetic variability of clinical C. albicans and C. tropicalis isolates. The adhesion ability to the extracellular matrix glycoproteins laminin and fibronectin was evaluated using the ELISA technique (Enzyme-linked imunosorbent assay). The research of proteases was carried out in agar plate containing bovine albumin and through a quantitative method in buffer solution containing hemoglobin. The presence of ALS2, ALS3, SAP1, SAP3 and PLB1 was verified using polimerase chain reaction (PCR) and intra and interespecies polimorphisms through Random Amplified Polymorphic DNA (RAPD) technique. All C. albicans and C. tropicalis isolates binded to immobilized laminin and fibronectin. Ca33 and Ct13 isolates had relative adhesion index significantly higher than the other isolates for both glycoproteins (p < 0,001). Protease activity was observed in all isolates of C. albicans using either the semi-quantitative or quantitative assay. The protease activity of C. tropicalis was better detected through the quantitative assay. The amplification of genes related to adhesion (ALS2 and ALS3), proteases (SAP1 and SAP3) and phospholipase (PLB1) activity using PCR was observed in all C. albicans strains. PCR amplification products were not observed in C. tropicalis isolates for the researched genes. The genetic variability by RAPD revealed an heterogeneous population in both species. Nevertheless, C. tropicalis presented higher genetic variability than C. albicans strains.
Lopes, Leticya Lerner. "Detecção do vírus da cinomose em cães naturalmente infectados no Mato Grosso." Universidade Federal de Mato Grosso, 2014. http://ri.ufmt.br/handle/1/535.
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CAPES
O vírus da cinomose canina (VCC) é um vírus RNA, que pertence ao gênero Morbillivírus e família Paramyxoviridae. A capacidade de resposta imune, assim como sua virulência são fatores críticos para a invasão viral dos tecidos epiteliais e do sistema nervoso central (SNC). O VCC é o maior responsável pelas encefalites em cães, acometendo diversas idades. O objetivo desse estudo foi detectar o VCC nos cães com sinais neurológicos encaminhados para necropsia no Laboratório de Patologia Veterinária da Universidade Federal de Mato Grosso (LPV-UFMT). Durante um período de um ano, 85% (68/80) dos cães necropsiados tinham lesões microscópicas compatíveis com encefalomielite causada pelo VCC. Desses, 67.6% (46/68) foram confirmadas positivas através da imuno-histoquímica (IHQ). Microscopicamente, as lesões do SNC foram classificadas em encefalite desmielinizante aguda em 15.2% (7/46) dos cães, em subaguda em 73.9% (34/46) e crônica em 10.8% (5/46) dos cães. O cerebelo foi principal órgão a apresentar marcação positiva na IHQ (97.8%). O VCC é responsável pelos sinais neurológicos em cães principalmente abaixo de um ano de idade. A cinomose demonstrou sua relevância dentro da população canina de Cuiabá, sendo necessário ao nosso entendimento, caracterizar a estirpe viral relacionada à região.
Canine distemper virus (CDV) is a RNA virus classified under the genus Morbillivirus within the family of Paramyxoviridae. The time of onset of the immune response and, likely, also the virulence of the virus are critical factors in the extent of viral invasion of epithelial tissues and of the central nervous system. The CDV is the most responsible of encephalitis in dogs from different ages. In this study, the aim was to detected CDV in dogs with neurologicals signs referred for necropsy at the Laboratory of Veterinary Pathology, Federal University of Mato Grosso (LPV-UFMT).Over a period of 1 year, 85% (68/80) of the dogs necropsied had microscopic lesions compatible encephalomyelitis by CDV. Which 67.6% (46/68) were confirmed by immunohistochemistry (IHC). Microscopically, the CNS lesions were classified demyelinating encephalitis in 15.2% (7/46) to acute, 73.9% (34/46) in subacute and 10.8% (5/46) to chronic. The cerebellum (97.8%) was the main target organ to verify positivity in the IHC. Canine distemper virus is a pathogen responsible for neurological clinical signs in dogs mainly under one year of age. Distemper demonstrated its relevance within the canine population of Cuiabá, being necessary to our understanding, characterizing the viral strain related to the region.
Paulo, Katia Cristina Silva. "Identificação de padrões de sinais acústicos com base em classificação paraconsistente." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/18/18153/tde-16112016-160217/.
Full textBy using a new concept, which is based on Paraconsistent Logic (LPA) and has not yet been applied for classification, this work aims at constructing an intelligent system for Music Genre Classification (MGC). This topic, that is emergent in the literature, has received an increasing attention from the scientific community due to its applicability, emphazising both a commercial potential to commercialize multimedia content on the Internet and data mining tasks involving music signals. By adopting a database formed by samples of songs, which represent different styles of music, such as jazz, bolero, bossa nova, forró, salsa and sertanejo, and a discriminative paraconsistent classifier, a supervised procedure is used to solve the problem. The system is divided in two modules. The first extracts features from the music files, based on the concepts of time-frequency analysis and crictical bands of the human ear. On the other hand, the second implements the proposed classifier, which allows an efficient treatment of contradictions in such a way that is more similar to the human brain. The results obtained, when compared with existing approaches used to MGC, demonstrate how LPA is suitable for this purpose. Additionally, this is the original contribution to the state-of-the-art: the use of LPA for MGC, an inexistent approach up to date.
Nascimento, Marcus Vinícius Batista. "Interpretação da língua brasileira de sinais a partir do gênero jornalístico televisivo: elementos verbo-visuais na produção de sentidos." Pontifícia Universidade Católica de São Paulo, 2011. https://tede2.pucsp.br/handle/handle/13551.
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This research aims to conduct a descriptive analysis of the performance of LIBRAS (Brazilian Sign Language) / Portuguese translator interpreter (TILSP), in the journalism genre and in the sphere of television activity, from the work experience of the author of this research as an interpreter in this kind of discourse. For this, we chose as corpus a public domain television journalistic production, consisting of an edition cut of Programa Sentidos with the libras interpretation during it. The show is broadcasted by a cable television channel and then is available on the internet. We question which verbal-visual elements contribute and / or interfere with the libras interpretation of the journalistic genre, in the television sphere; how these elements affect the translations choices and lexical and syntactic construction in the libras interpretation from this genre, and which sense effects are produced from the interference of these elements in the process of Portuguese-LIBRAS interpretation. In this sense, The Circle of Bakhtin will serve as theoretical foundations of our research, and the comprehension of the Bakhtinian concepts of exotopy, chronotope, speech genres, enunciation, concrete utterance, text, discourse, authorship and extraverbal situation are the guidelines for the corpus analysis, which was transcribed and described from an exotopic movement shift, from the analyzed subject to the researcher, in a way that the researcher could look at himself taking into consideration the linguistic and extralinguistic elements of the target language in the act of translation/interpretation. The target language, LIBRAS, was transcribed using the Sign Language transcription system ELAN (EUDICO Language Annotator), developed by Max Planck Institute for Psycholinguistics and used on the research group Estudos da Comunidade Surda: Língua, Cultura e História (Deaf Community Studies: Language, Culture and History) in the University of São Paulo and in the course de Letras/Libras (Language Studies/Libras) of the Federal University of Santa Catarina.The analysis showed that the verbal-visual elements and images of all the reports are factors of libras linguistic marks modification, as look and body direction, and that these images are crucial for the negotiation of discursive meanings from this sphere at the time of interpretation. The incorporation of shapes and outlines of the images during signaling TILSP showed us that the whole verbal-visual component of that sphere, not only interferes with the interpretation of sign language, but also contributes to the realization of TILSP interpretive strategies aiming the transmission of senses brought by the enunciators discursive project in this genre. From the analysis we propose a theoretical and methodological possibility of referral to TILSP training and working from an enunciative-discursive perspective, adopting the analysis of Programa Sentidos as an orientation for this proposal. To this end, we used as guidelines some television journalistic productions, taking into account the possibility of future insertions of TILSP in this sphere of discourse production and realization of interpretative practices in the journalistic genre, suggesting the expansion of its operations in other genres circulating in this sphere
Este trabalho tem por objetivo realizar uma análise descritiva da atuação do tradutor intérprete de libras/português (TILSP) no gênero jornalístico e na esfera de atividade televisiva a partir da experiência de atuação do autor desta pesquisa como intérprete nesse gênero do discurso. Para isso escolhemos como corpus uma produção telejornalística, de domínio público, constituída por um recorte de uma edição do Programa Sentidos, veiculado por meio de um canal de TV a cabo, disponibilizado na internet posteriormente, com interpretação para a libras durante a exibição. Questionamos que elementos verbo-visuais colaboram e/ou interferem na interpretação da libras no gênero jornalístico, esfera televisiva; como esses elementos afetam as escolhas tradutórias e a construção lexical e sintática na interpretação da libras a partir desse gênero; e quais efeitos de sentidos são produzidos a partir da interferência desses elementos no processo de interpretação do português para a libras. Nesse sentido, fundamentamos a pesquisa na teoria do Círculo de Bakhtin compreendendo os conceitos de exotopia, cronotopo, gêneros do discurso, enunciação, enunciado concreto, texto, discurso, autoria e situação extraverbal como fios condutores da análise do corpus que foi transcrito e descrito, a partir de um movimento exotópico de deslocamento de sujeito analisado para o de pesquisador, de forma que o pesquisador olhe a si mesmo, considerando os elementos linguísticos e extralinguísticos da língua alvo no ato tradutório/interpretativo, a libras, por meio do sistema de transcrição de língua de sinais ELAN (EUDICO Language Annotator) desenvolvido pelo Max Planck Institute for Psycholinguistics e utilizado no grupo Estudos da Comunidade Surda: Língua, Cultura e História na Universidade de São Paulo e no curso de Letras/Libras da Universidade Federal de Santa Catarina. A análise mostrou que os elementos verbo-visuais e a totalidade das imagens das reportagens são fatores de modificação das marcas linguísticas da libras como direção do olhar e do corpo e que essas imagens são decisivas para a negociação de sentidos discursivos provenientes dessa esfera no momento da interpretação. A incorporação das formas e delineios das imagens durante a sinalização do TILSP nos mostraram que a totalidade verbo-visual, constituinte dessa esfera, não só interfere na interpretação da língua de sinais, mas também colabora para que o TILSP realize estratégias interpretativas objetivando a transmissão dos sentidos instaurados pelo projeto discursivo dos enunciadores desse gênero. A partir da análise propomos uma possibilidade de encaminhamento teórico metodológico para a formação e atuação do TILSP a partir de uma perspectiva enunciativo-discursiva, adotando a análise do Programa Sentidos como norteador desta proposta. Para tanto, utilizamos como fio condutor algumas produções telejornalísticas considerando a possibilidade de futuras inserções dos TILSP nessa esfera de produção do discurso e a realização de práticas interpretativas a partir do gênero jornalístico, sugerindo a expansão de sua atuação em outros gêneros circulantes nessa esfera
Books on the topic "SinRIP gene"
Polla, Franco La. Stanley Donen, Gene Kelly: Cantando sotto la pioggia. Torino: Lindau, 1997.
Find full textFogarty, Mary. Gene Kelly. Edited by Melissa Blanco Borelli. Oxford University Press, 2014. http://dx.doi.org/10.1093/oxfordhb/9780199897827.013.008.
Full textCohan, Steven. Self-Reflexive Hollywood. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780190865788.003.0002.
Full textPropst, Andy. They Made Us Happy. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780190630935.001.0001.
Full textCoimbra, João. Torre de Babel e Monte Sinai: modelos de exegese do Antigo Testamento. Brazil Publishing, 2022. http://dx.doi.org/10.31012/978-65-5861-755-6.
Full textBook chapters on the topic "SinRIP gene"
Arnoldi, Michele, Giulia Zarantonello, Stefano Espinoza, Stefano Gustincich, Francesca Di Leva, and Marta Biagioli. "Design and Delivery of SINEUP: A New Modular Tool to Increase Protein Translation." In Methods in Molecular Biology, 63–87. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2010-6_4.
Full textBuchman, Andrew. "Developing the Screenplay for Singin’ in the Rain (1952)." In The Oxford Handbook of the Hollywood Musical, 307—C13.N58. Oxford University Press, 2022. http://dx.doi.org/10.1093/oxfordhb/9780197503423.013.19.
Full textJayasuriya, Katy. "“An Inescapable Failure”." In The Oxford Handbook of the Hollywood Musical, 482—C21.N59. Oxford University Press, 2022. http://dx.doi.org/10.1093/oxfordhb/9780197503423.013.27.
Full textLewis, Hannah. "The Virtuosic Camera." In The Oxford Handbook of the Hollywood Musical, 567—C25.N44. Oxford University Press, 2022. http://dx.doi.org/10.1093/oxfordhb/9780197503423.013.32.
Full textAdair Almeida Oliveira, Mayke, Gabriela Mendes Souza Mascarenhas, Annie Alves de Sousa Lima, Vinícius Mendes Souza Carneiro, Carlos Danilo Cardoso Matos Silva, and Marcus Vinícius Cardoso Matos Silva. "CORRELAÇÃO DOS FATORES GENÉTICOS DOS VÍRUS HPV 16/ 18 E O CÂNCER DE COLO DE ÚTERO." In Estudos Interdisciplinares em Ciências da Saúde, 124–48. Editora Acadêmica Periodicojs, 2022. http://dx.doi.org/10.51249/easn03.2022.696.
Full textFRATE, ADA ROSA, ASHLEY SARINNY FERREIRA SILVA, GABRIELA HUDSON CARNEIRO, JAQUELINE GISELLE FARIAS FERNANDES, LETÍCIA TANNOUS DE PAULA LEÃO, THAÍS CAROLLINE DE JESUS SOUZA, NATÁLIA NUNES BUENO, and RAISSA CAMELO VALLETTA. "A IMPORTÂNCIA DA FONIATRIA PARA AMENIZAR OS IMPACTOS DOS DISTÚRBIOS DE APRENDIZAGEM NO DESENVOLVIMENTO INFANTIL." In Science Of Health. EDITORA HEALTH, 2023. http://dx.doi.org/10.29327/5164660.1-15.
Full textConference papers on the topic "SinRIP gene"
Ayoub, Dibe Balardini. "BASES ORIGINÁRIAS DAS NEOPLASIAS HEMATOLÓGICAS." In II Congresso Brasileiro de Hematologia Clínico-laboratorial On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/hematoclil/37.
Full textPAIVA, RAFAEL DA SILVA, ALINE MEDEIROS LIMA, ADRYANA TRABASSOS DOS SANTOS, and ELIZA DE JESUS BARROS DOS SANTOS. "IDENTIFICAÇÃO E CARACTERIZAÇÃO GENÔMICA DE GENES DA GLUTATIONA PEROXIDASE EM (MANIHOT ESCULENTA) CRANTZ." In III Congresso Brasileiro de Ciências Biologicas. Revista Multidisciplinar de Educação e Meio Ambiente, 2022. http://dx.doi.org/10.51189/iii-conbracib/6187.
Full textDiniz, Ornella Moreira. "NUTRIGENÔMICA NA OBESIDADE E NO DIABETES MELLITUS TIPO (DM) II." In I SIMPÓSIO MARANHENSE DE GENÉTICA E GENÔMICA EM SAÚDE. Doity - Plataforma de Eventos, 2022. http://dx.doi.org/10.55664/simaggens2022.018.
Full textStuchi, Amanda Maria, Leonardo Paroche de Matos, Allan Luis Barboza Atum, and José Antônio Silva Júnior. "EXPOSIÇÃO PRÉ-NATAL AO ÁLCOOL E A EXPRESSÃO DE GENES RELACIONADOS À HIPERTROFIA CARDÍACA EM CAMUNDONGOS." In Congresso Médico Acadêmico da Universidade Nove de Julho. Universidade Nove de Julho, 2022. http://dx.doi.org/10.5585/comamedvg.2022.9.
Full textIsepon, Marielly, ALESSANDRO ZORZI, VICTOR MONTALLI, FRANCISCO NOCITTI, and ANA MONDADORI DOS SANTOS. "AMELOGÊNESE IMPERFEITA ASSOCIADA AO TAURODONTISMO." In I Congresso Nacional de Pesquisas e Estudos Genéticos On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/geneticon/8153.
Full textBrito, Klairton De Lima, and Zanoni Dias. "Ordenação de Permutações com Sinais por Reversões e Transposições." In XXXII Concurso de Teses e Dissertações da SBC. Sociedade Brasileira de Computação - SBC, 2019. http://dx.doi.org/10.5753/ctd.2019.6337.
Full textda Silva Barros, Daniel Higor, Vitória Maria Xavier Silva, Lucas de Souza Gorjão, and Ericka Bemfica Benavides. "Doença de Wolfram: características clínicas e genéticas." In Semana Online Acadêmica de Medicina. Congresse.me, 2022. http://dx.doi.org/10.54265/alpp2005.
Full textJesus, Anderson Avelino de, Samuel Santana Moura, Rebeca Santos Da Silva, Raqueline Pastor De Santana E. Santana, and Irlandia Oliveira Almeida. "LEUCEMIA MIELÓIDE CRÔNICA: O CROMOSSOMO PHILADELPHIA E O GENE BCR-ABL." In I Congresso Nacional Multidisciplinar de Oncologia On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1529.
Full textMagadan, Eduarda Druck, Eduarda Kotlinsky Weber, Esthela Rodegheri Trevisan, Luiza Fernandes Xavier, and Virgínia Tafas Da Nóbrega. "TROMBOFILIA EM CRIANÇA PORTADORA DE SÍNDROME DE DOWN: UM RELATO DE CASO." In II Congresso Brasileiro de Hematologia Clínico-laboratorial On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/hematoclil/127.
Full textHunka, Anna Luiza Konig, Milena Mello V. A. de Melo, Rodrigo H. M. V. A. de Melo, Victor L. M. V. A. de Melo, Lohana M. A. C. de Lima, and Ricardo E. V. A. de Melo. "NEUROFIBROMATOSE DO TIPO I: ASPECTOS CLÍNICOS E TRATAMENTOS." In I SIMPÓSIO MARANHENSE DE GENÉTICA E GENÔMICA EM SAÚDE. Doity - Plataforma de Eventos, 2022. http://dx.doi.org/10.55664/simaggens2022.001.
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