ライフサイエンスコーパス: be exchanged for

1 ing groove of CD1 during assembly until they are exchanged for a glycolipid Ag(s) within the recyclin

2 This proximal imidazole can be exchanged for a variety of exogenous ligands.

3 omplexes in D2O, the phenolic proton of Y(Z) is exchanged for a deuterium in less than 2 min as oppos

4 ible betaGlcN(1-->6)GlcN backbone of Lipid A is exchanged for a rigid trehalose-like alphaGlcN(1<-->1

5 cardium to re-enter the right heart where it is exchanged for a suture.

6 nts were recently modified such that a (13)C was exchanged for a (15)N.

7 T-hook peptide was exchanged for a corresponding length peptide in the

8 0-nt-long segment inside the amplicon region was exchanged for a new segment of similar GC content an

9 The medium was exchanged for a serum-free defined medium containing

10 Higher resolution can be exchanged for acceleration of the analyses by up to ~

11 Whereas ACP2 and ACP4 of DEBS could be exchanged for ACP3, ACP6 was a substantially poorer p

12 nthetic cation exchange reaction in which Pb is exchanged for Ag.

13 s in which residues His-186 and Asn-189 have been exchanged for alanine residues.

14 The alpha,omega-alkanedisulfonates were exchanged for alpha,omega-alkanedicarboxylates, lea

15 ubiquitin mutants where the lysine residues were exchanged for asparagine one at a time.

16 s (e.g., chicken for red meat), but they may be exchanged for carbohydrate-rich foods varying in qual

17 rt mechanism, in which extracellular protons are exchanged for cytoplasmic cations.

18 in the catalytic properties when Glu and Gln were exchanged for each other in QFR and SQR.

19 ysteine residues 100 and 108 or 104 and 115, was exchanged for endogenous RLC in rabbit skeletal musc

20 The resulting diols were exchanged for ethyl ester groups by base-catalyzed

21 ted a chimeric APP in which the Abeta domain is exchanged for its homologous domain from the amyloid

22 me and a calcineurin mutant in which Met 406 was exchanged for Leu.

23 PCh in EPCR could be exchanged for lysophosphatidylcholine (lysoPCh) and p

24 d within the first 14 positions within fimY, were exchanged for major arginine codons.

25 associated counteranions and that these can be exchanged for other anionic guests.

26 omyelin synthesis, suggesting that 25OH must be exchanged for PI-4P to be concentrated at contact sit

27 ples were plastic chips, some of which could be exchanged for prizes.

28 rified that 40-60% of endogenous LC17a could be exchanged for recombinant LC17a or LC17b.

29 ulatory domain of CaM KII (residues 281-315) was exchanged for residues 781-813 of smMLCK, MK(CK281-3

30 hat, with their partner's cooperation, could be exchanged for rewards.

31 ved in all Atox1 homologues, Thr11 and Lys60 are exchanged for Ser and Tyr in bacteria.

32 served aspartic acid residue (HePTP-D/A) had been exchanged for serine and alanine, respectively.

33 nge in colloidal CsPbBr3 NCs, whereby Pb(2+) is exchanged for several isovalent cations, resulting in

34 and PI(4)P as an alternate ligand that could be exchanged for sterol in the Golgi apparatus.

35 rs, in which a capsid protein from one virus is exchanged for that of another.

36 When the C-tail of CXCR4 was exchanged for that of CCR5, the resulting CXCR4-CCR5

37 When the Ca(1)a(2)X motif of Ggamma5, CSFL, was exchanged for that of Ggamma2, CAIL, Ggamma5 was com

38 n which the carboxyl-terminal part of mBE II was exchanged for that of mBE I at a BspHI restriction s

39 e residues at these positions in rabbit FMO1 are exchanged for the corresponding residues of pig FMO1

40 , in which the peptide binding domain of Ssb is exchanged for the analogous domain of the more "class

41 Labeled RLC (termed Cys108-5 or Cys108-6) was exchanged for the endogenous RLC in single, skinned

42 irected mutants in which amino acids in CNF1 were exchanged for the amino acids in CNF2 between amino

43 hich potential surface-exposed loops in DDR2 were exchanged for the corresponding loops of functional

44 ct parental FCV strains (CFI, KCD, and NADC) were exchanged for the equivalent sequences in an FCV Ur

45 Prostheses were exchanged for the following reasons - fractures (5

46 , the residues that confer anion selectivity are exchanged for those that specify cation selectivity.

47 the gC glycoprotein of herpes simplex virus were exchanged for those encoding the analogous regions

48 ther Loop 1+Loop 2 or Loop 2 of alpha-myosin were exchanged for those of beta-myosin were expressed i

49 1 gene such that the PB1 packaging sequences were exchanged for those of the neuraminidase (NA) gene

50 These drugs are exchanged for two protons despite the apparent inabi