Automatic Sequencing
Mostrando 1-12 de 43 artigos, teses e dissertações.
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1. Does the Glyphosate Treatment Interfere Negatively on RNA Integrity in Glyphosate-Resistant and -Sensitive Conyza bonariensis?
RESUMO: A buva (Conyza bonariensis (L.) Cronq.) está entre as plantas daninhas resistentes ao glifosato mais difíceis de serem manejadas em todo o mundo. Na ciência das plantas daninhas, abordagens moleculares, como o sequenciamento de RNA (RNA-Seq) e a reação da transcriptase reversa da polimerase em tempo real (RT-qPCR), têm sido empregadas para estu
Planta daninha. Publicado em: 04/11/2019
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2. Avaliação da heterogeneidade molecular de Cryptosporidium sp. em amostras clínicas / Evaluation of the molecular heterogeneity of Cryptosporidium sp. in clinical specimens
O Cryptosporidium é um parasito coccídeo reconhecido por causar diarréia em humanos e animais em todo o mundo. O gênero compreende pelo menos 20 espécies confirmadas, sendo o C. hominis e C. parvum as principais espécies causadoras de criptosporidiose em humanos. Ferramentas moleculares têm sido desenvolvidas para detectar e diferenciar espécies/gen�
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 29/03/2012
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3. Análise dos genes GHRH e GL12 em pacientes com deficiência de hormônio do crescimento congênita / GHRH and GLI2 genes analysis in patients with congenital growth hormone deficiency
Introduction: Alterations in genes related to GH secretion and pituitary organogenesis have been identified in patients with congenital GH deficiency (GHD). However, in only few cases of GHD the etiology has been established. GH-releasing hormone (GHRH) is an obvious candidate to explain isolated GH deficiency (IGHD). Previous reports in the literature did n
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 14/02/2012
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4. Programação Genética Aplicada à Programação de Controladores Lógico Programáveis / Genetic Programming Applied to Scheduling Programmable Logic Controllers
This research proposes the application of an artificial intelligence technique called genetic programming (GP) to make easier the programming of programmable logical devices (PLC) by the automatic generation of Ladder and Instruction List programs. The system data input can be done by not-specialized people using scenarios composed by time lines. These time
Publicado em: 2009
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5. RelaÃÃes filogenÃticas de abelhas indÃgenas sem ferrÃo do tÃxon Melipona Illiger, 1806 (Apidae: Meliponina) baseadas em seqÃÃncias parciais da regiÃo its1 do DNA ribossÃmico nuclear / FilogenÃticas relations of aboriginal bees without sting of tÃxon Melipona Illiger, 1806 (Apidae: Meliponina) based in partial sequences of the region its1 of the nuclear ribossÃmico DNA
O presente trabalho foi conduzido no perÃodo de abril de 2006 a marÃo de 2008, nos departamentos de Zootecnia e de Biologia, da Universidade Federal do CearÃ. O objetivo desta pesquisa foi investigar, atravÃs de dados moleculares, as relaÃÃes filogenÃticas de algumas abelhas indÃgenas sem ferrÃo do tÃxon Melipona Illiger, 1806, nativas do Brasil. P
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 26/02/2008
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6. p.F508del in a heterogeneous cystic fibrosis population from Minas Gerais, Brazil
Cystic fibrosis (CF) is the most common autosomal recessive disease of the Caucasian population. Among the various CF mutations, p.F508del is the most frequent, accounting for two-thirds of the global CF chromosomes, although showing great variability among populations. We have studied 115 unrelated CF patients from a mixed population of Minas Gerais (Brazil
Brazilian Journal of Medical and Biological Research. Publicado em: 2008-08
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7. Caracterização molecular da fenilcetonuria em pacientes da região de Campinas / Molecular characterization of phenylketonuria in patients of Campinas region
Phenylketonuria (PKU) is an autosomal recessive genetic disorder caused by deficiency of the hepatic phenylalanine-4-hydroxylase (PAH), which catalyzes hydroxylation of phenylalanine to tyrosine. Deficiency of PAH is caused by mutations in the PAH gene, resulting in high serum levels of phenylalanine and mental retardation. Restriction of phenylalanine intak
Publicado em: 2008
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8. Disturbios do desenvolvimento cortical e epilepsia autossomica dominante com auras auditivas : estudos geneticos e moleculares / Malformations of cortical development and autosomal dominant partial epilepsy with auditory features
Temporal Lobe Epilepsy (TLE) and malformations of cortical development (MCD) are two of the most important causes of epilepsy. Extensive molecular genetic studies have resulted in gene discovery for MCD such as periventricular nodular heterotopia (PNH), lisencephaly/ subcortical band heterotopia spectrum (LIS-SBH), schizencephaly, polymicrogyria and for a su
Publicado em: 2008
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9. Análise de Polimorfismos de Nucleotídeos Únicos (SNPs) em pacientes com câncer de cabeça e pescoço.
Head and neck cancer is responsible for a high death rate. Single nucleotide polymorphisms (SNPs) are the most common variation of human genome and can be associated to the molecular basis of cancer. Objectives: To establish the incidence of this disease in the Otorhinolaryngology and Head and Neck Surgery Service of Hospital de Base in São José do Rio Pre
Publicado em: 2008
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10. Mitocondrial DNA sequencing of Biomphalaria tenagophila (Orbigny, 1835) (Mollusca: Gastropoda). / Seqüenciamento do DNA mitocondrial de Biomphalaria tenagophila (Orbigny, 1835) (Mollusca: Gastropoda).
With the advent of the automatic sequencing of nucleotides it has been possible in a short period of time to obtain a great amount of information about genomes of different organisms. The mitochondrial DNA sequencing has been considerably increasing in the last years. Just one species of the genus Biomphalaria Biomphalaria glabrata had its mitochondrial geno
Publicado em: 2007
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11. Characterization of gene expresiion of tumoral cells in patients with sporadic colon adenocarcinoma / Caracterização da expressão genica de celulas tumorais de pacientes com adenocarcinoma esporadico do colon
The molecular mechanisms involved in sporadic colon adenocarcinoma (SCA) are still not completely elucidated. Recently, the serial analysis of gene expression (SAGE) method has allowed the global analysis of genes expressed in diverse cellular types but there are no studies in purified epithelial cells of SCA moderately differenciated. We have characterized
Publicado em: 2007
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12. Caracterização molecular do vírus da hepatite c em indivíduos co-infectados com HIV-1
Human immunodeficiency virus (HIV-1) and Hepatitis C virus (HCV) are considered problems of public health with about 40 millions infected by HIV-1 and 170 millions infected by HCV worldwide. The co-infection HIV-1/HCV is common in individuals exposed to percutaneous pathways and the hepatitis C has been emerging as the main cause of death in HIV-1 positive i
Publicado em: 2007