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The Global ETD Search service is a free service for researchers
to find electronic theses and dissertations. This service is
provided by the
Networked Digital Library of Theses and Dissertations.
Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
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Showing 501 to 510 of 1404 (0.085 seconds)Spelling suggestions: "subject:"designal transduction"" "subject:"absignal transduction""
| 501 |
Signal Transduction in Diabetic NephropathySimonson, Michael Scott 27 August 2012 (has links)
No description available.
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| 502 |
Na/K ATPase: Signaling Versus PumpingLiang, Man January 2006 (has links)
No description available.
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| 503 |
Na/K-ATPase, A Signaling ReceptorTian, Jiang 14 April 2007 (has links)
No description available.
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| 504 |
Molecular Mechanisms of Synergy Between IL-13 and IL-17A in Severe AsthmaHall, Sara L., M.S. January 2017 (has links)
No description available.
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| 505 |
THE OPIOID RECEPTOR-LIKE RECEPTOR ORL1: SIGNALING AND INTERACTION WITH OPIOID RECEPTORSZHANG, SHENGWEN 27 September 2002 (has links)
No description available.
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| 506 |
Role of Matrix Metalloproteinases in Acrolein-Induced Mucin 5 (Subtype A and C) IncreaseDeshmukh, Hitesh S. 03 April 2006 (has links)
No description available.
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| 507 |
Characterization of the Serine/Threonine Protein Kinase Fused: An Insight into the Mechanism of Hedgehog Signal TransductionAscano, Manuel, Jr. 28 September 2006 (has links)
No description available.
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| 508 |
Characterization of miR-21 and miR-196b in Myeloid Signaling PathwaysStoffers, Sara L. 26 September 2011 (has links)
No description available.
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| 509 |
Using Quantitative Proteomics to Study the Early Events of GravitropismSchenck, Craig A. 26 July 2012 (has links)
No description available.
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| 510 |
MID1IP1 and CCT2 in HIV-1 TransductionErmakova, Marina January 2020 (has links)
HIV-1 completes its life cycle by coopting host proteins. Hundreds of proteins have been identified as potential host factors functioning in viral infection through screens, two of which are MID1IP1 and CCT2. Little is known about MID1IP1, but its localization to microtubules may suggest a cytoskeletal function and a possible role in microtubule transport of HIV-1 viral cores. We use the CRISPR/Cas9 system to create frameshift mutations in MID1IP1 in 293 cells and find that these mutations do not produce effects on HIV-1 transduction in experiments capable of assaying for completion of the life cycle from initial entry into host cells to gene expression. Furthermore, we were unable to find an effect on the staining for markers of microtubule stability using Western blots as a result of the mutations in these cells. CCT2 is a component of the TRiC/CCT protein folding complex whose substrates include actin and tubulin, which also suggests that CCT2 might function in the HIV-1 life cycle in a cytoskeleton-dependent manner. siRNA knockdowns in TE671 cells demonstrate a slight effect on HIV-1 transduction. Our data does not support a role for MID1IP1 in the entry stage of the HIV-1 life cycle, but does suggest CCT2 may be a potential candidate for further study.
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