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1 gonist and can bind only one molecule of the growth hormone receptor.
2 ed to the ligand binding determinants of the growth hormone receptor.
3 ased on an archetypal cytokine receptor, the growth hormone receptor.
4 development in vitro and in vivo, as did the growth hormone receptor, a nonhematopoietic receptor.
5                                   Changes in growth hormone receptor and IGF-I mRNA expression may ac
6                                              Growth hormone receptor and IGF-I mRNA levels were reduc
7 n of human erythropoietin receptor and human growth hormone receptor and is supported by evidence sho
8 ed in signaling pathways found downstream of growth hormone receptor and receptor tyrosine kinases, i
9 re variation in Europeans and for genes with growth hormone receptor and regulation functions.
10 my, or growth hormone replacement on CYP2C6, growth hormone receptor, and growth hormone-binding prot
11 lso uncommon in humans with mutations in the growth hormone receptor, and natural genetic variants in
12 0A4, S100A6, c-Myb, estrogen receptor alpha, growth hormone receptor, and progesterone receptor were
13 e regulator and rodent alpha2-macroglobulin, growth hormone receptors, and insulin-like growth factor
14 a co-chaperone and regulator of androgen and growth hormone receptor (AR, GHR) signalling.
15 ul5-Rbx2 (CRL5(SOCS2)), binds phosphorylated growth hormone receptor as its main substrate.
16 rant nature of the guinea-pig growth hormone-growth hormone receptor axis is due to these replacement
17 r cytokines, the extracellular domain of the growth hormone receptor circulates as a binding protein,
18              Site-directed antibodies to the growth hormone receptor could be potentially useful as g
19 .SIGNIFICANCE STATEMENT People and mice with growth hormone receptor deficiency (GHRD or Laron syndro
20                                              Growth hormone receptor deficiency (GHRD) results in sho
21 y alternative splicing or proteolysis of the growth hormone receptor extracellular domain (ECD).
22 ets KIR apart from the C2-type hematopoietic growth hormone receptor fold.
23 quence were found to lead to upregulation of growth hormone receptor gene (Ghr) expression in transdu
24                                              Growth hormone receptor (GHR) endocytosis is a highly re
25             To clarify the divergence of the growth hormone receptor (GHR) family, we characterized a
26 ce caused by cytokine-induced suppression of growth hormone receptor (GHR) gene expression.
27 an important mechanism for the regulation of growth hormone receptor (GHR) gene expression.
28                                          The growth hormone receptor (GHR) gene in cattle is expresse
29  the muscle, we specifically inactivated the growth hormone receptor (ghr) gene in postnatal mouse sk
30                         A portion of the rat growth hormone receptor (GHR) gene was cloned by PCR.
31 vine riboprobes, expression of the IGF-I and growth hormone receptor (GHR) genes was examined in ovin
32                                          The growth hormone receptor (GHR) is a cell surface receptor
33                                              Growth hormone receptor (GHR) is a cytokine receptor sup
34 elopmental and tissue-specific regulation of growth hormone receptor (GHR) mRNA expression is complex
35                                              Growth hormone receptor (Ghr) signaling is important in
36 rtial hepatectomy by preventing increases in growth hormone receptor (GHR) via ubiquitination, suppre
37                                          The growth hormone receptor (GHR), a cytokine receptor super
38 ted model of tissue-specific deletion of the growth hormone receptor (GHR).
39 n growth hormone (hGH) variants to the human growth hormone receptor (hGHR) and the human prolactin r
40                    Two isoforms of the human growth hormone receptor (hGHR), which differ in the pres
41 ve been previously noted in meningiomas (eg, growth hormone receptor, IGFBP-7, endothelin receptor A,
42 ll set of contacts are crucial for the human growth hormone-receptor interaction.
43                              In both groups, growth hormone receptor mRNA expression was examined by
44 rf mouse models, including Ames, Little, and growth hormone receptor-null mice.
45 utated the extracellular domain of the ovine growth hormone receptor (oGHR) to the corresponding amin
46 es using beads decorated with phosphorylated growth hormone receptor peptides.
47                           The exon 3-deleted growth hormone receptor polymorphism (GHR(d3)) may accou
48 tisera generated using peptides derived from growth hormone receptor sequences failed to recognize th
49             Whereas CHO cells expressing the growth hormone receptor showed marked downregulation of
50 quired for ligand-induced endocytosis of the growth hormone receptor, suggesting that ubiquitin-depen
51 y of epitope-switching between rat and ovine growth hormone receptors to produce rat epitopes in the
52                           In contrast to the growth hormone receptor, we found that the initial endoc
53 arison of the structure to that of the human growth hormone receptor, which belongs to a different cl

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