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	Provedor de dados Genet. Mol. Biol. (2) BABT (1) Autor Hajjari,Mohammadreza (3) Saffar,Behnaz (2) Aminzadeh,Majid (1) Golchin,Neda (1) Khoshnevisan,Atefeh (1) Malamiri,Reza Azizi (1) Mohammadi-asl,Javad (1) Mais... Palavra-chave ARSA gene (1) Amplification primer (1) Arylsulfatase A (1) Bioinformatics (1) Codon usage bias (1) Correlation (1) Efficiency (1) Metachromatic leukodystrophy disorder (1) Mutation (1) Polymerase (1) Single step assembly PCR (1) Translational selection (1) Mais... Tipo do documento Info:eu-repo/semantics/article (3) Ano 2017 (1) 2011 (1) 2010 (1) País Brazil (3) Idioma Inglês (3)		Ordenar por:  Relevância Autor Título Ano Registros recuperados: 3 Primeira ... 1 ... Última Translational selection on SHH genes Genet. Mol. Biol. Hajjari,Mohammadreza; Saffar,Behnaz; Khoshnevisan,Atefeh. Codon usage bias has been observed in various organisms. In this study, the correlation between SHH genes expression in some tissues and codon usage features was analyzed by bioinformatics. We found that translational selection may act on compositional features of this set of genes. Tipo: Info:eu-repo/semantics/article Palavras-chave: Bioinformatics; Codon usage bias; Correlation; Translational selection. Ano: 2010 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000200033 Identification of a novel mutation in ARSA gene in three patients of an Iranian family with metachromatic leukodystrophy disorder Genet. Mol. Biol. Golchin,Neda; Hajjari,Mohammadreza; Malamiri,Reza Azizi; Aminzadeh,Majid; Mohammadi-asl,Javad. Abstract Metachromatic leukodystrophy disorder (MLD) is an autosomal recessive and lysosomal storage disease. The disease is caused by the deficiency of the enzyme arylsulfatase A (ARSA) which is encoded by the ARSA gene. Different mutations have been reported in different populations. The present study was aimed to detect the mutation type of the ARSA gene in three relative Iranian patients. We found a novel homozygous missense mutation c.1070 G > T (p.Gly357Val) in exon 6 of these patients. The mutation was found to be reported for the first time in MLD patients. The data can update the mutation profile and contribute toward improved clinical management and counseling of MLD patients. Tipo: Info:eu-repo/semantics/article Palavras-chave: Metachromatic leukodystrophy disorder; ARSA gene; Mutation; Arylsulfatase A. Ano: 2017 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572017000500759 The construction of a short gene by a very fast, modified, and simplified gene synthesis and the analysis of various effects on this synthesis BABT Hajjari,Mohammadreza; Saffar,Behnaz. We have constructed a short gene with a single step assembly PCR without any additional amplification primers with Taq and Pfu polymerases. Since the Taq polymerase is a common and conventional enzyme for PCR reactions, we have analyzed various effects on its efficiency. Eventually, we have been able to synthesize the gene in less than 40 minutes by Taq polymerase. Tipo: Info:eu-repo/semantics/article Palavras-chave: Single step assembly PCR; Efficiency; Amplification primer; Polymerase. Ano: 2011 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132011000100007 Registros recuperados: 3 Primeira ... 1 ... Última

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