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1  failure is often attributed to dysregulated somatotropin action, however marked genetic and phenotyp
2  for quantitative analysis using insulin and somatotropin as model systems.
3  Strains of E. coli which overproduce bovine somatotropin (BST) have a significant fraction of the BS
4 f bovine growth hormone also known as bovine somatotropin (bST) shows that the proposed biosensor can
5 olonged review of the veterinary drug bovine somatotropin (bST), or bovine growth hormone, during the
6 olding was evident for some epitopes, bovine somatotropin cannot refold to the native state following
7 eneficial then the controlled enhancement of somatotropin expression.
8 n chorionic gonadotropin and human chorionic somatotropin hormone (CSH) produced by the placental tro
9 d CXC chemokine protein families, as well as somatotropin hormones, serpins, and various kringle-cont
10 lasts can express a secretory protein, human somatotropin, in a soluble, biologically active, disulfi
11                        The plastid-expressed somatotropin is nearly devoid of complex post-translatio
12                   The degree to which bovine somatotropin is stabilized by disulfide bonds was examin
13 ting that the two disulfide bonds within the somatotropin molecule impart some degree of global stabi
14 ronmental impact of using recombinant bovine somatotropin (rbST) in dairy production was examined on
15 or sensitive detection of recombinant bovine somatotropin (rbST) was developed.
16 We found that the neuropeptide somatostatin [somatotropin release inhibiting factor (SRIF)] also inhi
17  associated with a reduction in hypothalamic somatotropin release inhibiting factor (Srif; somatostat
18  growth hormone from the anterior pituitary (somatotropin release inhibitory factor, SRIF).
19                    The peptide somatostatin [somatotropin release-inhibiting factor (SRIF)] is widely
20 mander retina of one of the somatostatin [or somatotropin release-inhibiting factor (SRIF)] receptors
21 ropin-releasing hormone, beta-endorphin, and somatotropin release-inhibiting factor.
22 r trafficking of (125)I-Tyr1-somatostatin-14 somatotropin-release inhibiting factor (SRIF) and 2 of i
23   These proteins include recombinant porcine somatotropin (rpSt), recombinant human granulocyte-macro
24 e antibodies allowed the stability of bovine somatotropin to be "dissected" based on individual struc
25                        The ability of bovine somatotropin to refold after reducing or nonreducing the
26                                       Bovine somatotropin was studied with respect to thermal stabili
27      We also describe approaches to obtain a somatotropin with a non-methionine N terminus, similar t