Sentence examples for binding studies have shown from inspiring English sources

In vivo binding studies have shown that the Ste50 SAM domain binds to the SAM domain in Ste11 (Posas et al. 1998; Wu et al. 1999; Jansen et al. 2001), while in vitro studies demonstrated that the Ste50 SAM domain can homo-dimerize as well as hetero-dimerize with Ste11 SAM (Bhattacharjya et al. 2004; Grimshaw et al. 2004; Kwan et al. 2004, 2006).

While autoradiographic binding studies have shown no SSTR expression in glioblastomas, immunohistochemistry (IHC) and western blot have detected increased expression of subtypes SSTR1, SSTR2, and SSTR3 [5,6].

Cryo-EM and antibody binding studies have shown that molecules on the C terminus of the MVP are displayed on the outside of the particle at the cap [26].

Coimmunoprecipitation and in vivo binding studies have shown that phosphorylation significantly decreases binding of GluR2 to the PDZ domain of GRIP1/2 but not of PICK1.

Interestingly, preliminary binding studies have shown that 45 n M SR31747A displaced H DTG binding to sigma2 (H Vidal, personal communication).

Suramin can act as a partial agonist at constitutively active P2X2 receptors (Cao et al., 2007), and radioligand binding studies have shown that suramin can competitively displace radioligands from P2X receptors (Michel et al., 1996).

With regard to binding energetics, our equilibrium-binding studies have shown that the ribose interactions are energetically important consistent with previous non-equilibrium studies with hCNTs (Clarke et al., 2006).

Although in vitro DNA-binding studies have shown that many of these factors have a certain degree of flexibility in the sequences to which they bind, defined in terms of a position weight matrix [ 60], our studies show that for any given appearance these sites are actually highly conserved across all species of the Drosophila genus.

In addition to the SH2 and phosphotyrosine-binding (PTB) domains, the two archetype domain families known for pTyr binding, recent studies have shown that at least a handful of additional protein modules are capable of reading out the tyrosine phosphorylation.

Furthermore, these binding and transmission studies have shown that the binding properties of HA can affect virulence, organ tropism and transmission in mammals.

From the protein-binding perspective, previous studies have shown that androgen receptor binding promotes SM breakpoints [ 20].