ライフサイエンスコーパス: infinitely

1 These cells are believed to divide infinitely and to support spermatogenesis throughout lif

2 al beams and images using interfaces between infinitely anisotropic media are demonstrated.

3 been treated as being either independent or infinitely coupled thermodynamically with regard to thei

4 applications because, in principle, they are infinitely deformable while retaining metallic conductiv

5 These values are used to extrapolate to the infinitely dilute limit.

6 olyparameter linear energy relationships and infinitely dilute solution in n-hexadecane as the refere

7 At the same time, for infinitely dilute solutions the renormalized electric co

8 by V(D)J recombination to produce an almost infinitely diverse repertoire of antigen specificities.

9 of the hairpin) connect the hairpins into an infinitely extended beta-sheet.

10 It is shown that an infinitely extended polyhedron of one sheet composed of

11 de processes that approach the "reversible" (infinitely fast) limit under voltammetric conditions hav

12 ranscytolemmal water exchange is effectively infinitely fast.

13 antities have no limit when particles become infinitely hard, as confirmed numerically.

14 Kd values of the T52A and D128N enzymes were infinitely high and could not be measured, while those o

15 Thr-52 to Ala resulted in an enzyme with an infinitely high Km for both substrates and an 800-fold d

16 VWF propeptide (VWFpp) was elevated with an infinitely high VWFpp to VWF:Ag ratio (VWFpp:Ag) consist

17 Relapse occurred when VWFpp:Ag was again infinitely high, with associated decreased VWFpp but unc

18 the dissociation rate constant (EI-->E+I) is infinitely higher than the isomerization rate constant f

19 a ray catastrophe-in which light rays become infinitely intense.

20 Infinitely iterated rippled noise (IIRN) is generated wh

21 es larger cation (phosphazenium salt) and an infinitely large cation are required to decrease DeltaU(

22 asymptotically approach constant values for infinitely large cations.

23 tically solve all the models in the limit of infinitely large networks and find an excellent agreemen

24 olves a finite number of unlinked loci in an infinitely large population, with a normal distribution

25 itionally studied on homogeneously mixed and infinitely large populations.

26 nce threshold for deterministic dynamics and infinitely large populations.

27 alue the lifetime diverges (that is, becomes infinitely large), marking a change from transient to pe

28 ntally with a disk probe brought near a semi-infinitely long band electrode as a geometrical model fo

29 correction terms or any assumptions such as infinitely long cells.

30 ulk water, in gas phase water chains, and in infinitely long channels).

31 We argue that given even an infinitely long data sequence, it is impossible (with an

32 proximate theories give the same results for infinitely long waves.

33 ing value of 63 mV (vs Ag/AgCl) as n becomes infinitely long.

34 nt nanogap structures, a single, effectively infinitely-long slit passes incident electromagnetic wav

35 entrations of receptor with extrapolation to infinitely low receptor concentration takes ligand deple

36 Third, in diploid models, there are infinitely many combinations of fecundity distributions

37 than the cost of punishment, then there are infinitely many cooperative Nash equilibria and the resp

38 luding nonlinearity, memory, and potentially infinitely many degrees of freedom, which are often diff

39 This results in infinitely many different definitions of relatedness - o

40 ngly, despite the fact that the opponent has infinitely many donation levels from which to choose, a

41 The model of infinitely many neutral sites is posited; the linkage ma

42 de stoichiometric matrix that corresponds to infinitely many possible flux distributions that are per

43 s V1 activity representing a small subset of infinitely many possible solutions to ambiguous stimuli,

44 an generate simulated datasets, assuming the infinitely many sites mutation model, and compute the F

45 ection classes, such as the K-allele models, infinitely-many-alleles models.

46 DNA sequence models, and infinitely-many-sites models, and briefly discuss the di

47 Because no organism is infinitely or ideally plastic, theory suggests that ther

48 B block assembly may continue infinitely or until monomeric peptides are depleted from

49 ription and B lymphocyte transformation into infinitely proliferating lymphoblastoid cells (LCLs).

50 Metals are infinitely recyclable in principle, but in practice, rec

51 nge, delta H degrees(un), extrapolated to an infinitely slow scanning rate, are analyzed considering

52 stant equilibrium, approximating the case of infinitely slow tip motion.

53 (N)2 displacements of this sort in water are infinitely slower than in the gas phase.

54 , time stands still and waves oscillate with infinitely small wavelengths.

55 In the limit of irreversible aggregation, infinitely strong interparticle bonds lead to diffusion-

56 e of the Au92 nanocrystal can be generalized infinitely to construct the bulk two-dimensional SAMs an

57 of surfacing is quantified by considering an infinitely wide body of water of constant depth.

58 ative to the thin film resistivity (i.e., an infinitely wide wire).