Academic literature on the topic 'Gene PARL'
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Journal articles on the topic "Gene PARL"
Merhi, Rawan, Michael Kalyn, Amanda Zhu-Pawlowsky, and Marc Ekker. "Loss of parla Function Results in Inactivity, Olfactory Impairment, and Dopamine Neuron Loss in Zebrafish." Biomedicines 9, no. 2 (February 18, 2021): 205. http://dx.doi.org/10.3390/biomedicines9020205.
Full textLiu, J. F., S. L. Zhang, H. L. Tang, L. Z. Wu, L. J. Dong, L. D. Liu, and W. L. Che. "Overexpression of an Aeluropus littoralis Parl. potassium transporter gene, AlHAK1, in cotton enhances potassium uptake and salt tolerance." Euphytica 203, no. 1 (November 26, 2014): 197–209. http://dx.doi.org/10.1007/s10681-014-1310-2.
Full textIstikharah, Rochmy, Aung Win Tun, Supannee Kaewsutthi, Pratibha Aryal, Bussaraporn Kunhapan, Wanphen Katanyoo, Wanicha Chuenkongkaew, and Patcharee Lertrit. "Identification of the variants in PARL, the nuclear modifier gene, responsible for the expression of LHON patients in Thailand." Experimental Eye Research 116 (November 2013): 55–57. http://dx.doi.org/10.1016/j.exer.2013.08.007.
Full textZhang, A.-Mei, Xiaoyun Jia, Qingjiong Zhang, and Yong-Gang Yao. "No association between the SNPs (rs3749446 and rs1402000) in the PARL gene and LHON in Chinese patients with m.11778G>A." Human Genetics 128, no. 4 (August 14, 2010): 465–68. http://dx.doi.org/10.1007/s00439-010-0875-7.
Full textKo, Kenton, Jeremy Guenther, Nicholas Ostan, and Joshua Powles. "Analysis of the Arabidopsis organellar rhomboid At1g74140 transcript population uncovered splicing patterns different from its close relative At1g74130." F1000Research 8 (November 18, 2019): 1925. http://dx.doi.org/10.12688/f1000research.21219.1.
Full textPowles, Joshua, Katharine Sedivy-Haley, Eric Chapman, and Kenton Ko. "Characterization of three alternative splice variants associated with the Arabidopsis rhomboid protein gene At1g74130." Botany 91, no. 12 (December 2013): 840–49. http://dx.doi.org/10.1139/cjb-2013-0173.
Full textFlores, Andrés, Javier López-Upton, Cristobal D. Rullán-Silva, Adriana E. Olthoff, Ricardo Alía, Cuauhtémoc Sáenz-Romero, and José M. Garcia del Barrio. "Priorities for Conservation and Sustainable Use of Forest Genetic Resources in Four Mexican Pines." Forests 10, no. 8 (August 9, 2019): 675. http://dx.doi.org/10.3390/f10080675.
Full textPowles, Joshua, and Kenton Ko. "Alternative splice variants of rhomboid proteins: In silico analysis of database entries for select model organisms and validation of functional potential." F1000Research 7 (February 1, 2018): 139. http://dx.doi.org/10.12688/f1000research.13383.1.
Full textPowles, Joshua, and Kenton Ko. "Alternative splice variants of rhomboid proteins: Comparative analysis of database entries for select model organisms and validation of functional potential." F1000Research 7 (May 31, 2018): 139. http://dx.doi.org/10.12688/f1000research.13383.2.
Full textSawhney, Shikhar, Sandeep Bansal, Madhur Kalyan, Indu Verma, Ramandeep Singh Virk, and Ashok Kumar Gupta. "Analysis of differential expression of protease-activated receptors in patients with allergic fungal rhinosinusitis." Allergy & Rhinology 9 (January 2018): 215265671876419. http://dx.doi.org/10.1177/2152656718764199.
Full textDissertations / Theses on the topic "Gene PARL"
Semir, Frappart David de. "Reparación de mutaciones en el gent CFTR como estrategia de terapia génica para la fibrosis quística." Doctoral thesis, Universitat Pompeu Fabra, 2005. http://hdl.handle.net/10803/7084.
Full textDASILIO, A. "Utilidade filogenética de genes nucleares em comparação com gene mitocondrial para Phyllostomidae (Chiroptera)." Universidade Federal do Espírito Santo, 2016. http://repositorio.ufes.br/handle/10/3861.
Full textPhyllostomidae, da subordem Microchiroptera, é uma família com uma grande variedade morfológica e de hábitos alimentares, com mais gêneros do que qualquer outra família de morcegos. Porém um grande desafio tem sido a resolução de suas relações filogenéticas principalmente devido ao paralelismo evolutivo e convergência entre linhagens. Várias tentativas foram feitas para resgatar as relações dentro dessa família, a fim de reconstruir suas transições evolutivas e identificar as relações entre gêneros, desde estudos morfológicos a moleculares. Entretanto, estas pesquisas em sua maioria, tem usado principalmente o DNA mitocondrial, com pouco sucesso com marcadores nucleares. Estudos apresentando incongruências entre filogenias têm se expandido rapidamente, derivadas, principalmente, de dados morfológicos em face de análises moleculares, ou até mesmo entre as árvores baseadas em diferentes subconjuntos de seqüências moleculares. Diante deste cenário, este trabalho teve como objetivo fazer uma investigação filogenética de cinco genes (um mitocondrial e quatro nucleares) a fim de identificar marcadores nucleares que apresentassem os melhores resultados para Phyllostomidae. Isso ainda não havia sido reportado na literatura para filostomideos. Os genes selecionados para o estudo foram: dois éxons de genes nucleares recombination activating protein 2 (RAG2) e o gene for von Willebrand factor (VWF), dois íntrons Beta-Fibrinogênio (Fgb) e o B-spectrin non-erythrocytic 1 (SPTBN1), e um gene mitocondrial cytochrome oxidase subunit 1 (COI). A metodologia de obtenção das sequências nucleotídicas consistiu em extração do DNA total da célula, amplificação da região controle do DNA mitocondrial através da Reação em Cadeia da Polimerase, purificação do produto da PCR e sequenciamento. Sequências disponíveis no GenBank também foram utilizadas. Dentre os marcadores nucleares estudados os resultados das análises indicaram que o Beta-Fibrinogênio é o marcador nuclear mais promissor, estimulando futuros trabalhos moleculares com os morcegos filostomídeos utilizando esse gene. Palavras-chaves: Phyllostomidae, investigação filogenética, marcadores nucleares, DNA mitocondrial.
Wagner, Priscilla Koch. "Uma nova abordagem para identificação da provável origem de genes exclusivos de bactérias." Universidade de São Paulo, 2018. http://www.teses.usp.br/teses/disponiveis/100/100131/tde-24052018-175017/.
Full textComparison of genomes, genes or even non-coding nucleotide sequences is an important task in which bioinformatics can be applied, since it allows the application of phylogenetic analyses. Phylogenetic analysis, in its turn, seeks to analyze the evolutionary relation of each species, considering its genetic characteristics. These processes and the techniques that implement them are based on nucleotide sequences sequenced and stores in databases of public genomes. With phylogenetic analysis it is also possible to identify possible origins of a gene. This task has a great importance, because it allows the identification of the origin of pathogenic genes, which may help to combat or prevent deseases. A potencial problem of these sequences is the possibility of having annotation errors (sequences marking as genes). These errors are little explored by researchers nowadays. Another unexplored topic is the phylogenetic analysis of exclusive genes, which are genes thaht manifest in only one species, considering a group of nearby species. The identification of exclusive genes of a species may serve to correctly identify, for example, a desease, in order to allow the use of a more especific and appropriate treatment. The importance of discovering phylogenies of exclusive genes and the difficulty of guaranteeing the consistency of genetic annotations motivated this work, whose objective was to implement tools to interpret data of genetic comparison, identifying annotation errors in exclusive genes and creating strategies to identify the origin of these genes.The origins of exclusive genes explored in this work involve the possibility of the exclusive genes have derived of other gene families of the organism itself, or, the exclusive genes differed a lot from the ancestral genes. Theses hypotheses, with the hypotesis of the existance of annotation errors, were explored in experiments using the developed tools. The experiments aimed to analyse the applicability of the developed strategy. Genomes of bacteria of the genus Xanthomonas were used, which contains a large group of bacteria that cause diseases in plants. The results show that there is a considerable amount of annotation errors on the genomes, proving the hypothesis that the inconsistency in genomic annotations has a great influence on the difficulty in identifying phylogenies (both exclusive and non-exclusive genes). The results also show that much of exclusive genes possibly originated from other gene families of the genome itself. Furthermore, these genes may have sufferedmodifications in relation to the ancestral genes, but still have certain similarities with nucleotide sequences that don\'t encode genes in other more distant species. Finally, the strategy developed proved useful on phylogenetic analysis of the studied bacteria, which is a strong indication that the same approach can be used for similar problems with other species of living beings
Melo, Vinicius André Morais Rocha. "Construção de ferramentas para estudo da possível interação entre interferon-beta e p53." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-17082009-121304/.
Full textFormation of tumors it must to combinations of factors. The p53 pathway has an essential role in proliferation control and apoptosis. The interferon-beta (IFNb) is important in modulation of the immunologic response, in the antitumoral effect and in the apoptotic impact in tumor cells. According to literature, IFNb activate the p53 transcription and components of IFN system effect its function to p53/p14arf pathway. In this project, a series of tools was constructed to explore interactions between p53 and IFNb. The first tool, a cellular lineage derivative of B16 with expression of p53 reduced by miRNA. We also construct plasmidial and adenoviral vectors carriers of cDNAs for eGFP, Luciferase, p53 or IFNb. The vectors are used to introduce these factors, alone or agreed, in the target cell. Even confirming the activity of p53 or IFNb alone, an additive effect of these factors combined was not observed with this type of assay. Future studies of the possible interactions between p53 and IFNb pathways will have the benefit of the tools constructed in this project.
Fernandes, Jussara Gonçalves. "Análise comparativa dos processos inflamatórios agudo e crônico no tecido subcutâneo e exsudato em camundongos selecionados para máxima ou mínima inflamação." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/42/42133/tde-30012013-092920/.
Full textAIRmax and AIRmin mouse lines differ in terms of acute inflammatory response after Biogel injection. The distinct AIR in these lines is well established, however, differences in late or chronic inflammatory response to Biogel were not described yet. Thus, we decided to check if the genetic selection that modified the acute inflammatory response in these lines, also affected the development of a chronic inflammatory response. We found that AIRmax mice had higher cellular influx in the inflammatory exudate than AIRmin mice in both analyzed periods (48h and 30d) and that after 48 hours of Biogel injection, AIRmax mice showed higher cytokine levels in inflammatory exudates. This line also showed higher number of up regulated genes in AIRmax than in AIRmin mice involved with inflammatory response, immune response and signal transduction. Some acute inflammatory response genes also showed differences on day 30. Our results indicate that the genetic selection for acute inflammatory response may also have affected the chronic inflammatory response to Biogel.
Jaskowiak, Pablo Andretta. "Estudo de coeficientes de correlação para medidas de proximidade em dados de expressão gênica." Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/55/55134/tde-05052011-143134/.
Full textThe development of microarray technology made possible the expression level measurement of hundreds or even thousands of genes simultaneously for various experimental conditions. The huge amount of available data generated the need for computational methods that allow its analysis in an effcient and automated way. In many of the computational methods employed during gene expression data analysis the choice of a proximity measure is necessary. Among the proximity measures available, correlation coefficients have been widely employed because of their ability to capture similarity trends among the compared numeric sequences (genes or samples). The present work has as objective to compare different correlation measures for the three major tasks involved in the analysis of gene expression data: clustering, feature selection and classification. To this extent, in this dissertation an overview of gene expression data analysis and the different correlation measures considered for this comparison are presented. In the present work are also presented empirical results obtained from the comparison of correlation coefficients for gene clustering, sample clustering, gene selection for sample classification and sample classification
Araujo, Tânia Kawasaki de 1985. "Utilização da técnica de Open Array para investigação de genes associados a fendas labiopalatais em amostra da população brasileira." [s.n.], 2015. http://repositorio.unicamp.br/jspui/handle/REPOSIP/313118.
Full textTese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas
Made available in DSpace on 2018-08-27T00:02:24Z (GMT). No. of bitstreams: 1 Araujo_TaniaKawasakide_D.pdf: 3447671 bytes, checksum: 97911848c6334882843e4b270b9c6771 (MD5) Previous issue date: 2015
Resumo: A fenda de labiopalatal (FLP) isolada é o defeito craniofacial mais comum em humanos. O objetivo deste estudo foi avaliar associações entre 39 genes e a etiologia de FLP isolada em uma amostra da população brasileira. Este estudo de associação do tipo caso-controle foi desenhado com um poder estatístico de 81,29% por meio de regressão logística. O grupo de casos foi composto por 182 pacientes com FLP isolada registrados na Base Brasileira de Dados Clínicos e Familiais de Fendas Orofaciais Típicas. O grupo controle foi formado por 355 indivíduos saudáveis, sem história de fendas orais em três gerações. Toda a amostra foi genotipada por meio do sistema OpenArray®TaqManTM para 253 polimorfismos de nucleotídeo único (SNPs) em 39 genes, incluindo dois genes que, recentemente, haviam sido descritos por este grupo de pesquisa. A seleção de SNPs foi feita com o programa SNPbrowser 4.0 (Applied Biosystems) para verificar o número e a localização dos SNPs apropriados para explorar a associação de cada gene com FLP isolada. A análise de associação foi realizada por meio de regressão logística e regressão stepwise. Os resultados foram corrigidos para múltiplos testes (correção de Bonferroni). Vinte e quatro SNPs em 16 genes foram significativamente associados com a etiologia da FLP isolada, incluindo MSX1, SPRY1, MSX2, PRSS35, TFAP2A, SHH, VAX1, TBX10, WNT11, PAX9, BMP4, JAG2, AXIN2, DVL2, KIF7 e TCBE3. A análise de regressão stepwise revelou que 11 genes contribuiram em 15,5% do fenótipo de FLP isolada nessa amostra. Este é o primeiro estudo a associar os genes KIF7 e TCEB3 à FLP isolada
Abstract: Nonsyndromic cleft lip and palate (NSCLP) is the most common craniofacial birth defect. The aim of this study was to evaluate associations between 39 genes and the etiology of NSCLP in a Brazilian population. This case-control association study was designed with 81.29% statistical power according to logistic regression. The case group was composed of 182 patients with NSCLP enrolled in the Brazilian Database on Orofacial Clefts. The controls included 355 healthy individuals with no history of oral clefting in the past three generations. All samples were genotyped by TaqMan®OpenArrayTM system for 253 single nucleotide polymorphisms (SNPs) in 39 genes, including two that had recently been associated with this process. The SNPs selection was made by SNPbrowser 4.0 (Applied Biosystems) in order to establish the best SNPs to explor the association between each gene and NSCLP. The association analysis was performed using logistic regression and stepwise regression. The results were corrected for multiple testing (Bonferroni correction). Twenty-four SNPs in 16 genes were significantly associated with the etiology of NSCLP, including MSX1, SPRY1, MSX2, PRSS35, TFAP2A, SHH, VAX1, TBX10, WNT11, PAX9, BMP4, JAG2, AXIN2, DVL2, KIF7 and TCBE3. Stepwise regression analysis revealed that 11 genes contributed to 15.5% of the phenotype of NSCLP in the sample. This is the first study to associate KIF7 and TCEB3 with NSCLP
Doutorado
Ciencias Biomedicas
Doutora em Ciências Médicas
Pereira, Joana Filipa de Sousa. "Estudo do gene FOXE1 e identificação de novos genes de susceptibilidade para o cancro da tiróide familiar." Master's thesis, Faculdade de Ciências e Tecnologia, 2012. http://hdl.handle.net/10362/9925.
Full textAs formas familiares de carcinomas não-medulares da tiróide (FNMTC) representam 5% das neoplasias da tiróide. Foram já mapeados 8 loci de susceptibilidade para o FNMTC, no entanto, até à data, apenas o gene DICER1 foi identificado. O envolvimento de diferentes loci sugere a existência de heterogeneidade genética para o FNMTC, contudo, a sua base molecular, é essencialmente desconhecida. Os factores de transcrição NKX2-1, FOXE1, PAX8 e HHEX estão envolvidos na morfogénese e diferenciação da tiróide. Estudos recentes levaram à identificação de mutações germinais no gene NKX2-1 em famílas com FNMTC. No entanto, continua por esclarecer o papel destes factores de transcrição na etiologia do FNMTC. A nova tecnologia de sequenciação global do exoma (WES) tem facilitado a identificação de genes de susceptibilidade para diferentes doenças hereditárias. Este projecto teve como objectivos o estudo do papel do gene FOXE1 em FNMTC e a identificação de novos genes de susceptibilidade para esta doença, utilizando a WES. Desenvolveram-se estudos funcionais para a variante p.A248G do gene FOXE1, identificada numa família com FNMTC, usando como modelos células de tiróide normal (PCCL3) e uma linha celular de carcinoma papilar da tiróide (TPC-1). Nestes ensaios, observou-se que a variante p.A248G promovia a proliferação e migração celular, sugerindo que esta variante poderá contribuir para a tumorigénese na tiróide. Por WES, identificou-se uma nova variante (p.T22I) no gene C8orf48. Esta variante segregava com a doença na família. O gene C8orf48 interage com proteínas da via de sinalização WNT. Em estudos preliminares de expressão génica, identificaram-se alguns genes-alvo desta via (CCND1 e MYC) que apresentavam sobre-expressão no tumor da tiróide relativamente à tiróide normal no probando. Estudos funcionais poderão esclarecer o papel desta variante na tumorigénese. Neste trabalho, foram identificadas variantes genéticas, potencialmente patogénicas nos genes FOXE1 e C8orf48, que constituem a primeira evidência do seu envolvimento em FNMTC.
Carvalho, Anna Carolina Pereira Vieira de. "Construção e caracterização de um vírus Adeno-associado com expressão direcionada para células em divisão." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-18062010-125910/.
Full textThe utilization of recombinant adeno-associated virus (AAVr) as a gene transfer vector in tumor cells is increasing. In this work, the promoter of the E2F-1 gene, active during cell division, was inserted in an AAVr vector and used to drive the expression of HSV-tk or luciferase and, simultaneously, eGFP with the intent of limiting viral expression to proliferating cells. Also, vectors with the constitutive CMV promoter were constructed to be used as controls. The E2F-1 promoter was not efficient in driving the expression of the transgenes in the HT1080 cell line, while the CMV promoter shows high level expression of the reporter and the therapeutic genes. The low efficiency of E2F promoter has not yet been explored, though this problem could be related to the intrinsic performance of this promoter, the biology of the vector AAV and cell-specific factors. However, the performance of the AAVr containing the CMV promoter creates the possibility of performing new gene transfer protocols for the treatment and visualization of tumor cells.
Leal, Dora Yovana Barrios. "História Demográfica e Estrutura de Populações para a Espécie Cactófila Drosophila meridionalis." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/17/17135/tde-12062013-150608/.
Full textDrosophila meridionalis is an endemic species of South America, being widely distributed in the Atlantic Coast of Brazil. Aiming to develop a phylogeographic hypothesis for this species, sequences of mitochondrial COI and nuclear period genes were obtained. The diversity indexes, AMOVA, neutrality tests, Mismatch Distribution, Bayesan Skyline Plot and NCPA were calculated. We obtained three networks for the COI gene, denominated A (inland populations), B (south coast populations) and C (eastern and southeastern coast populations) and a single network obtained for the period gene, this network divides the population into two groups, being the first congruent with the network A of the COI gene and the second comprising the networks B and C of the COI gene. The AMOVA results, showed a high and significant structuring among inland and coastal populations, for both genes (ct=0,72 COI gene; ct=0,70 period gene), that can be explained by the presence of geographical barriers, such as Serra do Mar. Population expansion events and restricted gene flow with isolation by distance events were detected in coastal and inland populations respectively. The expansion of the area of occurrence of D. meridionalis probably was initiated with the populations of the coast of Rio Grande do Sul, towards the coast of Santa Catarina with subsequent long-distance colonization of the states of São Paulo, Rio de Janeiro and Bahia. Asynchronic migrations of individuals from coastal populations of São Paulo and Santa Catarina probably colonized the inland of São Paulo, and from these populations, a population expansion towards the south through the inland was initiated, colonizing the states of Paraná and Rio Grande do Sul. The bayesian analysis (MCCT) indicated that the time of the most recent common ancestor (TMRCA) for all haplotypes of D. meridionalis is from 81,700 years ago, a date that marks the separation of inland and coastal populations approximately at the end of the Pleistocene. Similar events have been suggested to explain the geographic distribution of species of the cluster D. buzzatii, occurring in sympatry largely with populations of D. meridionalis. This species, as the cluster D. buzzatii species, presented indicatives of demographic fluctuations, which can be associated with the expansion and contraction of the distribution of xerophytic vegetation, during the paleoclimatic fluctuations of the Pleistocene.
Books on the topic "Gene PARL"
Taman Nasional Gunung Gede Pangrango (Indonesia). Mt. Gede Pangrango National Park. 3rd ed. Cipanas, Cianjur: Indonesian Ministry of Forestry, Directorate General Forest Protection and Nature Conservation, Gunung Gede Pangrango National Park, 2011.
Find full textTaman Nasional Gunung Gede Pangrango (Indonesia), ed. Mt. Gede Pangrango National Park. [Cipanas, Cianjur]: Mt. Gede Pangrango National Park, 1996.
Find full textMerryanto, Yohanes. Genetic variation and gene flow of hard coral population in Savu Sea Marine National Park, East Nusa Tenggara, Indonesia: Final report international research collaborative and publication (first year). Kupang]: Universitas Kristen Artha Wacana, 2010.
Find full textJ, Lamb Christopher, Beachy Roger N, and UCLA Symposium on Plant Gene Transfer (1989 : Park City, Utah), eds. Plant gene transfer: Proceedings of a UCLA symposium held at Park City, Utah, April 1-7, 1989. New York: Wiley-Liss, 1990.
Find full textBarlas, Nami. Para borçlarının ifasında borçlunun temerrüdü ve bu temerrüt açısından düzenlenen genel sonuçlar. İstanbul: Kazancı Kitap Ticaret, 1992.
Find full textGordon, Ringold, and University of California, Los Angeles., eds. Steroid hormone action: Proceedings of a UCLA symposium, held in Park City, Utah, January 17-23, 1987. New York: Liss, 1988.
Find full textSigue tu pasión: Consejos para un nuevo tipo de emprendedor. Argentina: Empresa Activa, 2012.
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 textFranke, Barbara, and Jan K. Buitelaar. Gene–environment interactions. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198739258.003.0005.
Full text(Editor), Detlev Ganten, Klaus Ruckpaul (Editor), and Josef Köhrle (Editor), eds. Molekularmedizinische Grundlagen von para- und autokrinen Regulationsstörungen (Molekulare Medizin). Springer, 2006.
Find full textBook chapters on the topic "Gene PARL"
Tanaka, Motoyoshi, and H. Barton Grossman. "Tumor Suppressor Genes of Bladder Cancer and Potential for Gene Therapy." In Bladder Disease, Part A, 185–91. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4419-8889-8_14.
Full textLandau, Alejandra, Franco Lencina, María Elizabeth Petterson, María Gabriela Pacheco, Susana Costoya, Vanina Brizuela, and Alberto Prina. "The barley chloroplast mutator (cpm) mutant, an extraordinary source of plastome variability." In Mutation breeding, genetic diversity and crop adaptation to climate change, 271–79. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789249095.0027.
Full textJoosten, M. H. A. J., G. Honée, J. A. A. Van Kan, and P. J. G. M. De Wit. "The Gene-for-Gene Concept in Plant-Pathogen Interactions: Tomato-Cladosporium fulvum." In Plant Relationships Part B, 3–16. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-60647-2_1.
Full textGuo, Hui-jun, Yong-dun Xie, Lin-shu Zhao, Hong-chun Xiong, Jia-yu Gu, Shi-rong Zhao, and Lu-xiang Liu. "Progress of mutant resource development and tilling on starch biosynthesis in wheat." In Mutation breeding, genetic diversity and crop adaptation to climate change, 280–84. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789249095.0028.
Full textArdelt, Peter, Ingo Kausch, and Andreas Böhle. "Gene and Antisense Therapy of Bladder Cancer." In Bladder Disease, Part A, 155–83. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4419-8889-8_13.
Full textKral, Stefan, Markus Triska, and Christoph W. Ueberhuber. "Compiler Technology for Blue Gene Systems." In Euro-Par 2006 Parallel Processing, 279–88. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/11823285_29.
Full textKaragiannaki, Ioulia, Yannis Pantazis, Ekaterini Chatzaki, and Ioannis Tsamardinos. "Pathway Activity Score Learning for Dimensionality Reduction of Gene Expression Data." In Discovery Science, 246–61. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-61527-7_17.
Full textTrapnell, Bruce C., and Michael N. Pensiero. "Development of Viral Vectors for Human Gene Therapy: Retrovirus and Adenovirus (Part I)." In Gene Transfer in the Cardiovascular System, 3–24. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-6277-1_1.
Full textMoreira, José. "The Evolution of the Blue Gene/L Supercomputer." In Euro-Par 2005 Parallel Processing, 13. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/11549468_2.
Full textOulhen, Nathalie, Stephany Foster, Greg Wray, and Gary Wessel. "Identifying gene expression from single cells to single genes." In Echinoderms, Part B, 127–58. Elsevier, 2019. http://dx.doi.org/10.1016/bs.mcb.2018.11.018.
Full textConference papers on the topic "Gene PARL"
Da Silva, Carla Fernandes, Kuruvilla Joseph Abraham, and Evandro Eduardo Seron Ruiz. "Correlacionando genes e doenças através de caminhos metabólicos." In XVII Simpósio Brasileiro de Computação Aplicada à Saúde. Sociedade Brasileira de Computação - SBC, 2017. http://dx.doi.org/10.5753/sbcas.2017.3725.
Full textPrates, Pedro Emílio Gomes. "AVALIAÇÃO DA TERAPIA GÊNICA DO SUICÍDIO COM USO DE GENES SUICIDAS PARA O COMBATE AO CÂNCER: REVISÃO INTEGRATIVA." In II Congresso Brasileiro de Biologia Molecular On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/2334.
Full textHuber, P., J. Dalmon, M. Laurent, G. Courtois, D. Thevenon, and G. Marguerie. "CHARACTERIZATION OFTHE 5’FLANKING REGION FOR THE HUMAN FIBRINOGEN β GENE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642889.
Full textEdenbrandt, C.-M., S. Gershagen, P. Femlund, R. Wydro, J. Stenflo, and Å. Lundwall. "GENE STRUCTURE OF VITAMIN K-DEPENDENT PROTEIN S; A REGION HOMOLOGOUS TO SEX HORMONE BINDING GLOBULIN (SHBG) REPLACES THE SERINE PROTEASE REGION OF FACTORS IX, X AND PROTEIN C." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644640.
Full textDantas, Joao Victor Jose de Barros, PAULO ROBERTO ELEUTÉRIO DE SOUZA, and NARA SUZY AGUIAR FREITAS. "VARIAÇÃO E PADRÕES DE CONSERVAÇÃO ENTRE DIFERENTES CEPAS DE CAMPYLOBACTER JEJUNI PARA O GENE GYRA." In I Congresso Nacional de Pesquisas e Estudos Genéticos On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/geneticon/8298.
Full textNeves, Dyenifer Sara Lopes, Augusto Borges Matos, Rafaella Moniza Bento Palmeira Figueiredo, Letícia de Castro Ottoni, and Letícia Ariane Tanure. "RELAÇÃO CAUSAL ENTRE A SÍNDROME MIELODISPLÁSICA E LEUCEMIA MIELÓIDE AGUDA." In I Congresso Brasileiro de Hematologia Clínico-laboratorial On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/636.
Full textPloos van Amstel, J. K., A. L. van der Zanden, P. H. Reitsma, and R. M. Bertina. "RESTRICTION ANALYSIS AND SOUTHERN BLOTTING OF TOTAL HUMAN DNA REVEALS THE EXISTENCE OF MORE THAN ONE GENE HOMOLOGOUS WITH PROTEIN S cDNA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644639.
Full textShaposhnikov, A. I., N. A. Vishnevskaya, V. Yu Shakhnazarova, D. S. Syrova, E. V. Borodina, O. N. Kovaleva, and O. K. Strunnikova. "Activation of protective reactions in barley plants during colonization of roots with the phytopathogenic fungus Fusarium culmorum in the presence of Pseudomonas fluorescens 2137." In CURRENT STATE, PROBLEMS AND PROSPECTS OF THE DEVELOPMENT OF AGRARIAN SCIENCE. Federal State Budget Scientific Institution “Research Institute of Agriculture of Crimea”, 2020. http://dx.doi.org/10.33952/2542-0720-2020-5-9-10-118.
Full textMartins, Amanda Pezzini. "A IMPORTÂNCIA DOS MÉTODOS DE EDIÇÃO GÊNICA NA DIMINUIÇÃO DOS CASOS DE CÂNCER DECORRENTES DA MUTAÇÃO DO GENE TP53: UMA REVISÃO." In I Congresso Nacional de Pesquisas e Estudos Genéticos On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/geneticon/7330.
Full textOliveira, Letícia Eduarda de, Mariana Souza Bezerra Cavalcanti, Maria Eduarda de Albuquerque Borborema, and Jaqueline de Azevêdo Silva. "POLIMORFISMO NO GENE GNB3 E O DESENVOLVIMENTO DA DIABETES MELLITUS TIPO II: UMA REVISÃO DE LITERATURA." In XXVII Semana de Biomedicina Inovação e Ciência. Editora IME, 2021. http://dx.doi.org/10.51161/9786588884119/9.
Full textReports on the topic "Gene PARL"
Pichersky, Eran, Alexander Vainstein, and Natalia Dudareva. Scent biosynthesis in petunia flowers under normal and adverse environmental conditions. United States Department of Agriculture, January 2014. http://dx.doi.org/10.32747/2014.7699859.bard.
Full textReisch, Bruce, Avichai Perl, Julie Kikkert, Ruth Ben-Arie, and Rachel Gollop. Use of Anti-Fungal Gene Synergisms for Improved Foliar and Fruit Disease Tolerance in Transgenic Grapes. United States Department of Agriculture, August 2002. http://dx.doi.org/10.32747/2002.7575292.bard.
Full textFriedman, Haya, Julia Vrebalov, James Giovannoni, and Edna Pesis. Unravelling the Mode of Action of Ripening-Specific MADS-box Genes for Development of Tools to Improve Banana Fruit Shelf-life and Quality. United States Department of Agriculture, January 2010. http://dx.doi.org/10.32747/2010.7592116.bard.
Full textSessa, Guido, and Gregory Martin. Role of GRAS Transcription Factors in Tomato Disease Resistance and Basal Defense. United States Department of Agriculture, 2005. http://dx.doi.org/10.32747/2005.7696520.bard.
Full textHeifetz, Yael, and Michael Bender. Success and failure in insect fertilization and reproduction - the role of the female accessory glands. United States Department of Agriculture, December 2006. http://dx.doi.org/10.32747/2006.7695586.bard.
Full textOhad, Nir, and Robert Fischer. Regulation of plant development by polycomb group proteins. United States Department of Agriculture, January 2008. http://dx.doi.org/10.32747/2008.7695858.bard.
Full textStern, David, and Gadi Schuster. Manipulation of Gene Expression in the Chloroplast. United States Department of Agriculture, September 2000. http://dx.doi.org/10.32747/2000.7575289.bard.
Full textLichter, Amnon, Gopi K. Podila, and Maria R. Davis. Identification of Genetic Determinants that Facilitate Development of B. cinerea at Low Temperature and its Postharvest Pathogenicity. United States Department of Agriculture, March 2011. http://dx.doi.org/10.32747/2011.7592641.bard.
Full textPrusky, Dov, Nancy P. Keller, and Amir Sherman. global regulation of mycotoxin accumulation during pathogenicity of Penicillium expansum in postharvest fruits. United States Department of Agriculture, January 2014. http://dx.doi.org/10.32747/2014.7600012.bard.
Full textFluhr, Robert, and Volker Brendel. Harnessing the genetic diversity engendered by alternative gene splicing. United States Department of Agriculture, December 2005. http://dx.doi.org/10.32747/2005.7696517.bard.
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