نتایج جستجو برای: direct mutagenesis

تعداد نتایج: 451037  

Journal: :Comparative and Functional Genomics 2004
Louisa Matthew

A major challenge in the post-genome era of plant biology is to determine the functions of all the genes in the plant genome. A straightforward approach to this problem is to reduce or knock out expression of a gene with the hope of seeing a phenotype that is suggestive of its function. Insertional mutagenesis is a useful tool for this type of study, but it is limited by gene redundancy, lethal...

2012
Rachel J. Bergerson Lara S. Collier Aaron L. Sarver Raha A. Been Sanne Lugthart Miechaleen D. Diers Johannes Zuber Amy R. Rappaport Molly J. Nixon Kevin A. T. Silverstein Danhua Fan Anne-Francoise J. Lamblin Linda Wolff John H. Kersey Ruud Delwel Scott W. Lowe M. Gerard O’Sullivan Scott C. Kogan David J. Adams David A. Largaespada

1Department of Genetics, Cell Biology and Development and Department of Pediatrics, Masonic Cancer Center, University of Minnesota Twin Cities, Minneapolis, MN; 2Division of Pharmaceutical Sciences, School of Pharmacy, University of Wisconsin-Madison, Madison, WI; 3Biostatistics and Bioinformatics, Masonic Cancer Center, University of Minnesota Twin Cities, Minneapolis, MN; 4Department of Hemat...

2017
Ying Wang Ying Wáng Qi Tan Ying Nv Gao Yan Li Da Peng Bao

High-throughput technologies of functional genomics such as T-DNA insertional mutagenesis and microarray expression profiling have been employed to identify genes related to pathogenicity in Magnaporthe oryzae. However, validation of the functions of individual genes identified by these high-throughput approaches is laborious. In this study, we compared two published lists of genes putatively r...

2013
Orquídea Ribeiro Frederico Magalhães Tatiana Q Aguiar Marilyn G Wiebe Merja Penttilä Lucília Domingues

To improve the general secretion ability of the biotechnologically relevant fungus Ashbya gossypii, random mutagenesis with ethyl methane sulfonate (EMS) was performed. The selection and screening strategy followed revealed mutants with improved secretion of heterologous Trichoderma reesei endoglucanase I (EGI), native α-amylase and/or native β-glucosidase. One mutant, S436, presented 1.4- to 2...

2017
Shan Zhang Zhengzhong Zou Jens Kreth Justin Merritt

Studies of the dental caries pathogen Streptococcus mutans have benefitted tremendously from its sophisticated genetic system. As part of our own efforts to further improve upon the S. mutans genetic toolbox, we previously reported the development of the first cloning-independent markerless mutagenesis (CIMM) system for S. mutans and illustrated how this approach could be adapted for use in man...

Journal: :ACS Chemical Neuroscience 2021

Post-translational modifications of proteins are ubiquitous in living organisms, as they enable an accurate control the interactions these macromolecules. For mechanistic studies, it would be highly advantageous to able produce vitro post-translationally modified with site-specificity. Here, we demonstrate one facile way achieve this goal through use post-translational chemical mutagenesis. We ...

Journal: :Infection and immunity 2001
S A Coleman M F Minnick

The invasion-associated locus A and B genes (ialAB) of Bartonella bacilliformis were previously shown to confer an erythrocyte-invasive phenotype upon Escherichia coli, indirectly implicating their role in virulence. We report the first direct demonstration of a role for ialB as a virulence factor in B. bacilliformis. The presence of a secretory signal sequence and amino acid sequence similarit...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1992
G C Rice D V Goeddel G Cachianes J Woronicz E Y Chen S R Williams D W Leung

We have developed a general method for screening randomly mutagenized expression libraries in mammalian cells by using fluorescence-activated cell sorting (FACS). The cDNA sequence of a secreted protein is randomly mutagenized by PCR under conditions of reduced Taq polymerase fidelity. The mutated DNA is inserted into an expression vector encoding the membrane glycophospholipid anchor sequence ...

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