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1 han to either murine angiogenin or to murine pancreatic ribonuclease.
2 a class of chemotherapeutic agents based on pancreatic ribonucleases.
3 ages of the oxidative folding of both bovine pancreatic ribonuclease A (RNase A) and a 58-72 fragment
6 is method to the oxidative folding of bovine pancreatic ribonuclease A (RNase A) and show that des[40
10 athway of a three-disulfide mutant of bovine pancreatic ribonuclease A (RNase A) from the fully reduc
14 he major oxidative folding pathway of bovine pancreatic ribonuclease A (RNase A) has been examined at
15 0A, C95A] and [C65S, C72S] mutants of bovine pancreatic ribonuclease A (RNase A) have been studied.
16 nts (P42A, P93A, P114A, and P117A) of bovine pancreatic ribonuclease A (RNase A) in which each mutant
20 ays of two three-disulfide mutants of bovine pancreatic ribonuclease A (RNase A) missing the 65-72 di
21 step in the oxidative regeneration of bovine pancreatic ribonuclease A (RNase A) proceeds through des
23 ase (ONC), an amphibian member of the bovine pancreatic ribonuclease A (RNase A) superfamily, is in p
24 c regions of the polypeptide chain of bovine pancreatic ribonuclease A (RNase A) that are critical fo
26 ent molecular dynamics simulations of bovine pancreatic ribonuclease A (RNase A) up to its melting te
27 adenosine 3'-phosphate (pTppAp) with bovine pancreatic ribonuclease A (RNase A) was characterized by
28 ous crystals (space group P3(2)21) of bovine pancreatic ribonuclease A (RNase A) were prepared at a p
30 nfolding of its structural homologue, bovine pancreatic ribonuclease A (RNase A), has been isolated a
31 uman angiogenin (Ang), a homologue of bovine pancreatic ribonuclease A (RNase A), is a potent inducer
39 n peroxidase (LiP) was examined using bovine pancreatic ribonuclease A (RNase) as a polymeric lignin
41 asured for the nonspecific binding of bovine pancreatic ribonuclease A and Escherichia coli lac repre
42 e major oxidative folding pathways of bovine pancreatic ribonuclease A at pH 8.0 and 25 degrees C inv
43 efolding kinetics of disulfide-intact bovine pancreatic ribonuclease A by fluorescence-detected stopp
45 ded species (Uvf) of disulfide-intact bovine pancreatic ribonuclease A has been monitored by circular
47 ental, variable-pressure NMR data for bovine pancreatic ribonuclease A in 2H2O at pH 2.0 and 295 K yi
48 um unfolded state of disulfide-intact bovine pancreatic ribonuclease A is a heterogeneous mixture of
49 he unfolded state of disulfide-intact bovine pancreatic ribonuclease A is a heterogeneous mixture of
50 slow fluorescence unfolding phase of bovine pancreatic ribonuclease A is studied by stopped-flow kin
51 ing and unfolding of disulfide-intact bovine pancreatic ribonuclease A is used as an example to illus
53 2 to G, A, or L in the model protein, bovine pancreatic ribonuclease A, and through analysis of tempe
54 cturally well-characterized proteins (bovine pancreatic ribonuclease A, bovine pancreatic trypsin inh
55 inct, member of the angiogenin sub-family of pancreatic ribonucleases, and is referred to as angiogen
58 ity between two structural homologues of the pancreatic ribonuclease family: RNase A and eosinophil c
59 to address these questions in a study of the pancreatic ribonuclease gene (RNASE1) and its duplicate
60 d in an assay of a mutated form of the human pancreatic ribonuclease gene inserted into the plasmid p
61 onclude that the His...Asp catalytic dyad in pancreatic ribonucleases has two significant roles: (1)
63 , a highly conserved residue among mammalian pancreatic ribonucleases, lies atop the (40-95) disulfid
69 rate random mutations in the genes of bovine pancreatic ribonuclease (RNase A) and human angiogenin,
71 protein (RI) binds to members of the bovine pancreatic ribonuclease (RNase A) superfamily with an af
72 an angiogenin (ANG) is a homologue of bovine pancreatic ribonuclease (RNase A) that induces neovascul
73 of fluorescein-labeled model protein, bovine pancreatic ribonuclease (RNase A), decreases upon bindin
76 st this notion, glycosylated forms of bovine pancreatic ribonuclease (RNase) were translated in the p
79 bonucleases into five distinct lineages--the pancreatic ribonucleases (RNases 1), the eosinophil-asso
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