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8 Jan 2014: þXij1. kIU;jkUF;jDj. Yiljþ1. kA;l þ1kA;l þ1 þkIU;l þkUI;l þkUF;lDl. :. ð6Þ. ... determine the derivative in terms of kA,iþ1; weprovide the exact expression in Supplementary Eq.

23 Sep 2018: 3 = ka/k, we could determine the elongation rateconstant to be approximately ⟨k+⟩ = 2.0 1.2 M. ... For the two-state fits, the imposed bounds were ka 0, K̃ 1, and 0 α 1 1018.

2 Jun 2014: The rate kA,i1 isan important quantity because it defines the average speed atwhich codon i is translated.The other relevant rates are those associated with the process. ... and genomic sequences. This information enables reasonableestimates of kA,i1, kFU

4 Oct 2013: 14,15 Besides, the higher affinity of Phe-(Gly)2(Ka,ternary = 2 10. ... contribution for hostguest binding (Ka up to 106M1, ΔH up to 70 kJ mol1).

28 Sep 2021: REVIEW ARTICLE OPEN. The Amyloid-β Pathway in Alzheimer’s DiseaseHarald Hampel 1, John Hardy2, Kaj Blennow3,4, Christopher Chen 5, George Perry 6, Seung Hyun Kim7,Victor L. Villemagne 8,9, Paul Aisen10, Michele Vendruscolo 11, Takeshi Iwatsubo12,

23 Sep 2018: Na DHbb (kcal/mol) –TDSb. c (kcal/mol) DGbd (kcal/mol) Ka (10. 7 M21)e Kd (1029 M)e. ... kona (106 M21 s21) koff. a (1023 s21) Ka (107 M21)b Kd (10.

16 Jul 2013: where Ka is the number of codons encoding for the amino acid a, ns,a(ca) is the number of. ... times a spin s is associated to the codon ca of the amino acid a and Ns,a =Ka.

15 Jan 2012: Dill KA (1985) Theory for the folding and stability of globular proteins.

14 Aug 2012: ka Aggregation of U 5 m3(n1)mol(n1)min1. n Power dependence of aggregation. ... Thus, we speculate. Table 2. Correlating changes in the parameters kf, ka, and n with outputs in the ADPr and ADPr+ models.

4 Oct 2013: doi:10.1074/jbc.M109541200. 4. Weinreb PH, Zhen W, Poon AW, Conway KA, Lansbury PT (1996) NACP, a.