286) This is consistent with the findings that molecular features measured at the transcr |
287) bsence of t(14;18) by FISH or PCR and the molecular features of the mutations strong |
288) otypes often display robust regulation of molecular features that modify biological |
289) eractions occur at circuitry, cellular or molecular levels remains unsolved. |
290) , at the morphological, histological, and molecular levels. |
291) brate central nervous system on different molecular levels. |
292) This study provides a method of molecular marker identification to identif |
293) e promising for using MHC class IIβ as a molecular marker in breeding rainbow trout |
294) rganisms, and has been used as a powerful molecular marker in various evolutionary s |
295) Molecular medicine is the domain of intere |
296) their coverage of scientific evidence of molecular medicine. |
297) framing scientific evidence and risks of molecular medicine. |
298) c structure of molecule, highest occupied molecular orbital (HOMO) and lowest unoccu |
299) The predicted frontier molecular orbital energies at DFT/B3LYP/6- |
300) x potentials is obtained via quantitative molecular orbital theory, and via the deco |
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 |
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