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  2. Yeast deletion project - Wikipedia

    en.wikipedia.org/wiki/Yeast_deletion_project

    The yeast deletion project, formally the Saccharomyces Genome Deletion Project, is a project to create data for a near-complete collection of gene-deletion mutants of the yeast Saccharomyces cerevisiae. Each strain carries a precise deletion of one of the genes in the genome. This allows researchers to determine what each gene does by comparing ...

  3. Synthetic genetic array - Wikipedia

    en.wikipedia.org/wiki/Synthetic_genetic_array

    Synthetic genetic array analysis is generally conducted using colony arrays on petriplates at standard densities (96, 384, 768, 1536). To perform a SGA analysis in S.cerevisiae, the query gene deletion is crossed systematically with a deletion mutant array (DMA) containing every viable knockout ORF of the yeast genome (currently 4786 strains). [9]

  4. CSM1 - Wikipedia

    en.wikipedia.org/wiki/CSM1

    Print/export Download as PDF; Printable version; ... "Heterozygous yeast deletion collection screens reveal essential targets of Hsp90". PLOS ONE. 6 (11): e28211.

  5. BCK2 - Wikipedia

    en.wikipedia.org/wiki/BCK2

    An mpk1 deletion strain was transformed with a library of plasmid vectors containing parts of the entire yeast genome. One of the cells that grew out harbored BCK2 on its plasmid, whose overexpression rescued the mpk1 deletion phenotype. In the same publication, Bck2 was found to rescue a pck1 deletion phenotype as well. [citation needed]

  6. Gene knockout - Wikipedia

    en.wikipedia.org/wiki/Gene_knockout

    This technique can be used in a variety of organisms, including bacteria, yeast, plants, and animals, and it allows scientists to study the function of specific genes by observing the effects of their absence. CRISPR-based gene knockout is a powerful tool for understanding the genetic basis of disease and for developing new therapies.

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  8. Delitto perfetto - Wikipedia

    en.wikipedia.org/wiki/Delitto_perfetto

    Delitto perfetto (Italian: [deˈlitto perˈfɛtto]) is a genetic technique for in vivo site-directed mutagenesis in yeast. This name is the Italian term for "perfect murder", and it refers to the ability of the technique to create desired genetic changes without leaving any foreign DNA in the genome.

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