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1  decarboxylase (PvlArgDC) formed by the self-cleavage of a proenzyme into a 5-kDa subunit and a 12-kD
2 hrome c, activation of caspase-9 and -3, and cleavage of Bcl-2 into a shortened 22-kDa fragment.
3                                  Heterolytic cleavage of dihydrogen into a proton and a hydride ion i
4  and P), have been developed for heterolytic cleavage of H2 into a proton and a hydride, akin to frus
5                       The hydroxide-mediated cleavage of ketones into alkanes and carboxylic acids ha
6 poptosis is characterized by endonucleolytic cleavage of chromosomal DNA into an oligonucleosomal lad
7                                        After cleavage of the protoplast into aplanospores, a vacuole
8                            TNF induced rapid cleavage of DNA into approximately 50-kb fragments in DF
9 L3 is necessary for Ca2+- and Mg2+-dependent cleavage of DNA into both oligonucleosomal and high mole
10  of various alpha-keto acids, as well as the cleavage of glycine into CO(2) and NH(3), with concomita
11 e current study was designed to test whether cleavage of CPAF into CPAFn and CPAFc is a physiological
12             Our data show that the extent of cleavage of p67 into different fragments is higher in th
13  We will argue that in meningococcal sepsis, cleavage of albumin into fragments by protease(s) occurs
14  U(L)28, U(L)32, and U(L)33, is required for cleavage of concatameric DNA into genomic lengths and fo
15 g2p and Dug3p were required together for the cleavage of glutathione into glutamate and Cys-Gly.
16  and are independent of the proper enzymatic cleavage of gp140 into gp120 and gp41.
17                                              Cleavage of cellular DNA into high molecular weight (pre
18  cofactors, which promoted factor I-mediated cleavage of C3b into iC3b as well as decay-accelerating
19 nd the shed ClfA fragment increased factor I cleavage of C3b into inactive C3b.
20 ity, resulting in specific factor I-mediated cleavage of C3b into inactive iC3b.
21                  This further suggested that cleavage of the holoreceptor into its two-subunit struct
22 teine protease, apopain, as was indicated by cleavage of the proenzyme into its proteolytically activ
23                                  Proteolytic cleavage of zonulin into its alpha(2)- and beta-subunits
24  of SATB1 by disrupting its dimerization and cleavage of genomic DNA into loop domains to ensure rapi
25 rom the incubation with CMP, indicating that cleavage of pro-FD into mature FD by MASP-1 occurred on
26  of the polyprotein allows for the selective cleavage of MBP3 into MBP and MBP2.
27 required for DNA repair, and no irreversible cleavage of S-adenosylmethionine into methionine and 5'-
28 d enhanced activation of caspase-3 activity, cleavage of PARP into Mr 89,000 and 28,000 fragments, an
29 eaves C3b into iC3b, PAM-bound hPm catalyzes cleavage of iC3b into multiple smaller peptides.
30 iruses by inducing nuclear lysis followed by cleavage of host cells into numerous anucleate vesicles
31 ant biochemical hallmark of apoptosis is the cleavage of chromatin into oligonucleosomal fragments.
32 n appears to cause apoptosis as evidenced by cleavage of DNA into oligonucleosomal-sized fragments, f
33 enzyme A (CoA)-dependent and MgATP-dependent cleavage of citrate into oxaloacetate and acetyl-CoA, re
34 oduction of insulin from proinsulin involves cleavage of intact proinsulin into proinsulin conversion
35                                              Cleavage of triphosphate into pyrophosphate and orthopho
36 hese findings indicate that the differential cleavage of Notch into S2 and S3 products regulated by A
37                It is accomplished by trypsin cleavage of cell proteins into small peptide species, th
38 d Metalloprotease with ThromboSpondin motif) cleavage of ULVWF into smaller, less active forms.
39 r H acts as a cofactor for factor I-mediated cleavage of C3b into the inactive form iC3b and thus pre
40 asmic reticulum into the Golgi apparatus, in cleavage of gPrEnv into the two envelope subunits (the s
41                                  Proteolytic cleavage of Htt into toxic N-terminal fragments is belie
42                                              Cleavage of LON-2 into two parts at the conserved furin
43 otein precursor, is responsible for the self-cleavage of the precursor into two mature products, P150
44 not restrict viral gene expression; however, cleavage of viral DNA into unit-length genomes as well a

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