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- "cell motility" contained the smallest figures of proteins (Supplementary Desk S
- "chordoma cell lifestyle," and "chordoma And in vitro," and every resulting
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- 's agonists, capsaicin acts being a really selective and archetypal exogenous
- (0.088 0.008 and 0.104 0.024 , respectively). Fluorescence calcium imaging is beneficial to analyze TRPV1 channels
- (0.088 0.008 and 0.104 0.024 , respectively). Fluorescence calcium imaging is helpful to analyze TRPV1 channels
- (0.088 0.008 and 0.104 0.024 , respectively). Fluorescence calcium imaging is useful to analyze TRPV1 channels
- (0.088 0.008 and 0.104 0.024 , respectively). Fluorescence calcium imaging is valuable to analyze TRPV1 channels
- (10), exactly where an advanced AGT variant is particularly labeled in vivo by
- (10), exactly where an evolved AGT variant is especially labeled in vivo by
- (10), in which an progressed AGT variant is especially labeled in vivo by
- (10), the place an advanced AGT variant is specifically labeled in vivo by
- (10), where an evolved AGT variant is particularly labeled in vivo by
- (10), where an progressed AGT variant is particularly labeled in vivo by
- (10, 56). Therefore, to find out more particularly the extent of sequence similarity among
- (10, fifty six). Thus, to find out more particularly the extent of sequence similarity between
- (18). Both of these approaches, coinfection with adenovirus and knockdown of U2 snRNP
- (18). Both of these strategies, coinfection with adenovirus and knockdown of U2 snRNP
- (18). These two ways, coinfection with adenovirus and knockdown of U2 snRNP
- (2006) mutations map for the inside in the channel, ruling out their
- (2006) mutations map to the within of your channel, ruling out their
- (2006) mutations map to your inside of the channel, ruling out their
- (2006) mutations map to your inside of your channel, ruling out their
- (2006) mutations map towards the inside of the channel, ruling out their
- (2006) mutations map towards the within from the channel, ruling out their
- (2006) mutations map towards the within in the channel, ruling out their
- (2006) mutations map towards the within of the channel, ruling out their
- (2011) Subbiah et al. (2010), Hodsman et al. (2005) Moody et al. (2012) MCHR1 colon
- (201B7, MHC-puro/Rex1-neo) had been purified by treatment with puromycin (Sigma
- (7) days and had been euthanized by CO2 asphyxiation upon indications of systemic
- (7) demonstrates that membrane asymmetry is an critical mediator in the regulatory
- (7) demonstrates that membrane asymmetry is an critical mediator of your regulatory
- (7) demonstrates that membrane asymmetry is an crucial mediator in the regulatory
- (7) demonstrates that membrane asymmetry is an important mediator from the regulatory
- (7) demonstrates that membrane asymmetry is an vital mediator from the regulatory
- (7) demonstrates that membrane asymmetry is definitely an critical mediator of the regulatory
- (7) demonstrates that membrane asymmetry is definitely an significant mediator on the regulatory
- (A) Immunoblot (left) and ELISA (suitable) of Gal-1 in KS cells
- (A) Immunoblot (still left) and ELISA (appropriate) of Gal-1 in KS cells
- (AWB) and srg-8 (ASK) promoters into tax-2(p671) worms41,42. Plasmids encoding
- (Armstrong and Gouaux, 2000; Sun et al., 2002; Sobolevsky et al., 2009) (see Fig.
- (Armstrong and Gouaux, 2000; Sunshine et al., 2002; Sobolevsky et al., 2009) (see Fig.
- (CD107a) (Santa Cruz Biotechnology); rabbit anti-phosphoAkt (phospho-Ser-473), rabbit anti-Akt (pan
- (Commander Algometer, JTECH Health-related, Midvale, Utah). It had been placed perpendicularly onto
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