نتایج جستجو برای: 10 protein

تعداد نتایج: 2125364  

Journal: :WormBook : the online review of C. elegans biology 2006
Patricia M Berninsone

The C. elegans genome contains sequences similar to a large number of mammalian genes implicated in the assembly, processing, and modification of glycans. In recent years, spectacular progress has been made in developing and refining tools to obtain structural information with small amounts of material, increasing our understanding of glycan structural complexity in this organism. These approac...

2016
Anthony L. Luz John P. Rooney Laura L. Kubik Claudia P. Gonzalez Dong Hoon Song Joel N. Meyer

[This corrects the article DOI: 10.1371/journal.pone.0130940.].

Journal: :Science 2000
A J Walhout R Sordella X Lu J L Hartley G F Temple M A Brasch N Thierry-Mieg M Vidal

Protein interaction mapping using large-scale two-hybrid analysis has been proposed as a way to functionally annotate large numbers of uncharacterized proteins predicted by complete genome sequences. This approach was examined in Caenorhabditis elegans, starting with 27 proteins involved in vulval development. The resulting map reveals both known and new potential interactions and provides a fu...

Journal: :acta medica iranica 0
n. abbasi s. khaghani a. sharif-tabrizi b. farzami s. vardasbi m. bahar

to determine the importance of q 10 h 2 as an antioxidant in cancer, we measured the activity of lipoamide dehydrogenase (q 10 h 2 recycling enzyme) in hl-60 and normal lymphocyte. the cultured cells of hl-60 and human normal lymphocytes were assayed in cell lysate of given number of both hl-60 and normal lymphocyte. the activity of lipoamide dehydrogenase and the protein concentration were det...

2013
Ukrae Cho Stephanie M. Zimmerman Ling-chun Chen Elliot Owen Jesse V. Kim Stuart K. Kim Thomas J. Wandless

Destabilizing domains are conditionally unstable protein domains that can be fused to a protein of interest resulting in degradation of the fusion protein in the absence of stabilizing ligand. These engineered protein domains enable rapid, reversible and dose-dependent control of protein expression levels in cultured cells and in vivo. To broaden the scope of this technology, we have engineered...

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