301) ream regulators have been identified, the molecular recognition of the receptor inte |
302) ontrivial to predict the mechanism of the molecular recognition which progresses via |
303) e of their structures which can model the molecular recognition. |
304) wed reported methodologies for Salmonella molecular serotyping and determined the "s |
305) s represents a considerable challenge for molecular serotyping approaches. |
306) methods have been investigated to develop molecular serotyping schemes. |
307) ehydration-induced inactivation of Cov by molecular sieve powder was found to occur |
308) The dehydration kinetics of Cov by molecular sieve powder were determined by |
309) g in the presence of different amounts of molecular sieve powder. |
310) However, molecular structure modifications arising |
311) Determination of the molecular structure of Aβ fibrils is tech |
312) parameters and provided knowledge of the molecular structure. |
313) Molecular techniques used to differentiate |
314) We used molecular techniques to identify and compa |
315) cted characterization by cell culture and molecular techniques. |
316) Analysis of molecular variance (AMOVA) detected no sig |
317) (TZ, WZ, ND and ZZ) via both hierarchical molecular variance analysis (AMOVA) and pa |
318) Analysis of molecular variance and pairwise FST reveal |
319) We have carried out 25 ns Molecular Dynamics (MD) simulation studies |
320) wn mutant A313T forms, involved QM/MM and Molecular Dynamics (MD) simulations analys |
321) a were analysed to establish an effective molecular approach to differentiate Nemato |
322) ncing could be developed into a promising molecular approach to serotype Salmonella. |
323) Recent behavioral, histochemical and molecular biological studies have shown th |
324) ouse model and a host of histological and molecular biological techniques, we report |
325) Molecular classification of these metastas |
326) phenotype and was a potential biomark for molecular classification in ESCC. |
327) ossil taxa presented here and with recent molecular clock estimates. |
328) ation based on the assumption of a global molecular clock indicated that speciation |
329) Molecular dating supported Niviventer orig |
330) enetic methods, coalescent reasoning, and molecular dating interpreted in conjunctio |
331) rovide a valuable tool to analyse further molecular details of D. |
332) The molecular details of peptidoglycan growth |
333) creased, owing to differences in rates of molecular diffusion and thermal conduction |
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