نتایج جستجو برای: pull down

تعداد نتایج: 221618  

2016
Yi Sun Javier Jaldin-Fincati Zhi Liu Philip J. Bilan Amira Klip Patrick J. Brennwald

Insulin promotes glucose uptake into skeletal muscle through recruitment of glucose transporter 4 (GLUT4) to the plasma membrane. Rab GTPases are molecular switches mobilizing intracellular vesicles, and Rab13 is necessary for insulin-regulated GLUT4-vesicle exocytic translocation in muscle cells. We show that Rab13 engages the scaffold protein MICAL-L2 in this process. RNA interference-mediate...

Journal: :Chemical communications 2012
Liqian Gao Mahesh Uttamchandani Shao Q Yao

A library of 176 human phosphotyrosine-containing peptides was used to establish cell lysate binding profiles in a two colour microarray format. The resulting hits led to the pull-down and identification of biomarkers associated with cancer states.

Journal: :Central European journal of sport sciences and medicine 2023

It is believed that a strong core will enable an athlete to effectively transfer forces from the lower extremities through torso upper extremities. Control of shoulder girdle force important for proper function extremities, although stabilising trunk and pelvis are also important. The purpose this study determine association between isometric push-up/pull-down strength abdominal muscles. Using ...

Journal: :Journal of applied physiology 2003
Amy L Hakeman Don D Sheriff

Tolerance to +G(z) stress is reduced by preceding exposure to -G(z) (push-pull effect). The mechanism(s) responsible for this effect are not fully understood, although the arterial baroreceptor reflexes have been implicated. We investigated the integrative response of the autonomic nervous system by studying responses to gravitational stress before and after autonomic function was inhibited by ...

2013
Ka Young Chung Peter W. Day Gisselle Vélez-Ruiz Roger K. Sunahara Brian K. Kobilka

G protein-coupled receptors (GPCRs) have critical roles in various physiological and pathophysiological processes, and more than 40% of marketed drugs target GPCRs. Although the canonical downstream target of an agonist-activated GPCR is a G protein heterotrimer; there is a growing body of evidence suggesting that other signaling molecules interact, directly or indirectly, with GPCRs. However, ...

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