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1 of ghrelin, a secreted metabolism-regulating peptide hormone.
2 n large part by the N-terminal domain of the peptide hormone.
3 g receptor selectivity in this fast evolving peptide hormone.
4 his region for full agonist activity of this peptide hormone.
5 idates including Neuromedin U, a circulating peptide hormone.
6 e the regulated release of neuropeptides and peptide hormones.
7 the knowledgebase of this critical class of peptide hormones.
8 citonin, and other therapeutically important peptide hormones.
9 ase 1 in response to many growth factors and peptide hormones.
10 endogenously stimulated by moderately large peptide hormones.
11 receptors has been implicated in binding to peptide hormones.
12 AM) catalyzes the COOH-terminal amidation of peptide hormones.
13 nity/protection, sperm-binding proteins, and peptide hormones.
14 ectables and can likely be extended to other peptide hormones.
15 domain, and their signalling is regulated by peptide hormones.
16 py loss-of-function states for the indicated peptide hormones.
17 for developing stabilized analogues of other peptide hormones.
19 metabolic products of neurotransmitters and peptide hormones, a novel consequence of the phenomenon
20 coupled receptor that, when activated by the peptide hormone ACTH, stimulates cAMP production and adr
24 ialized endocrine cells secrete a variety of peptide hormones all along the gastrointestinal (GI) tra
28 ence of HID-1 results in specific defects in peptide hormone and monoamine storage and regulated secr
30 This enzyme is able to activate/inactivate peptide hormones and could be involved in a cascade of e
31 of G protein-coupled receptors (GPCRs) bind peptide hormones and have causal roles in many diseases,
34 that most proteins participate in producing peptide hormones and neurotransmitters, enzymes, and the
35 en the importance of insulin and its related peptide hormones and previous studies of glycosylated in
38 ing a TIR domain-containing protein, a plant peptide hormone, and many OLIGO PEPTIDE TRANSPORTER gene
39 in catecholamine neurotransmitters, amidated peptide hormones, and collagen biosynthetic pathways.
40 a rich source of bioactive molecules such as peptides, hormones, and neurotransmitters, but relativel
43 ), cytokinin (CK), brassinosteroids (BR) and peptide hormones are also implicated in plant defence si
51 he previously held paradigm that steroid and peptide hormones are the primary regulators of mammary g
53 -related increases in circulating ghrelin, a peptide hormone, are necessary and sufficient for stress
54 processing of proglucagon yields three major peptide hormones as follows: glucagon in the alpha cells
55 polypeptide (IAPP or amylin) is a 37-residue peptide hormone associated with glucose metabolism that
56 levels of brain natriuretic peptide (BNP, a peptide hormone associated with left ventricular systoli
58 , they do not differentiate to express their peptide hormone battery, nor do they project an axon via
60 6 amino acids with two functional domains, a peptide hormone-binding domain and a G-protein-coupled r
61 re all members of the insulin superfamily of peptide hormones but bind to several distinct classes of
62 way, allows for high-affinity sensing of the peptide hormone by binding to an Arg-His-Asn motif in ID
65 olysis-resistant variants of other important peptide hormones can also be found using this strategy t
66 rids (phybrids) comprising covalently linked peptide hormones can leverage independent biological pat
69 ation of islet amyloid polypeptide (IAPP), a peptide hormone co-synthesized and co-stored with insuli
71 and the complicated topology of this 51-mer peptide hormone consisting of two chains and three disul
72 ike peptide 5 (INSL5) is a complex two-chain peptide hormone constrained by three disulfide bonds in
75 ssue by determining the mechanism by which a peptide hormone, crustacean cardioactive peptide (CCAP),
76 ting to the VTA were suppressed by leptin, a peptide hormone derived from adipocytes that signals per
77 that parathyroid hormone-related peptide, a peptide hormone derived from normal and tumor cells that
78 hytosulfokines (PSKs) are secreted, sulfated peptide hormones derived from larger prepropeptide precu
79 r, they provide evidence that the endogenous peptide hormone does not function as an activator per se
80 r numbers of known bioactive peptides (e.g., peptide hormones) during the analysis of gut samples, su
81 rine cells, including those that secrete the peptide hormones (e.g., ghrelin and glucagon-like peptid
82 mplex actions and interactions among several peptide hormones: ecdysis triggering hormone (ETH), eclo
83 he ECD scaffold and the helical structure of peptide hormones emphasizes this hot dog model as a gene
84 inducible and ABA/sugar-repressible putative peptide hormone encoded by GASA6 was severely repressed
86 cades of research have demonstrated that the peptide hormone endothelin-1 (ET-1) plays multiple, comp
87 interaction, with the amino terminus of the peptide hormone extended toward the transmembrane helix
89 The corticotropin-releasing factor (CRF) peptide hormone family members coordinate endocrine, beh
92 ription 3 (Stat3) transduces signals of many peptide hormones from the cell surface to the nucleus an
103 n octanoyl group to the appetite-stimulating peptide hormone ghrelin, potentially preventing obesity.
107 mor-homing peptides, antimicrobial peptides, peptide hormones, growth factors and matrix metalloprote
113 PCRs), cell-surface proteins that respond to peptide hormones, has been restricted to the amino-termi
114 herapeutic properties of recombinant relaxin peptide hormone have been investigated in several diseas
118 A major focus is on the regulation of the peptide hormone hepcidin during the inflammatory respons
128 emic iron balance is controlled by the liver peptide hormone hepcidin, which is transcriptionally reg
134 ADM), and amylin belong to a unique group of peptide hormones important for homeostasis in diverse ti
136 urther support the concept of C-peptide as a peptide hormone in its own right and suggest a potential
137 ly conserved sequences, we predicted another peptide hormone in pro-somatostatin and named it neurono
140 ction of ACTH, beta-endorphin, and alpha-MSH peptide hormones in the regulated secretory pathway.
141 mice that have defects in the production of peptide hormones, in the function of cell membrane recep
142 ropin releasing factor (CRF)/urocortin (Ucn) peptide hormones include four structurally similar pepti
146 embers of the oxytocin/vasopressin family of peptide hormones induce in Hirudo verbana a sequence of
148 ptide binding in which the C terminus of the peptide hormone interacts almost exclusively with the N-
149 served that a major portion of both of these peptide hormones interacts with the phospholipid head gr
152 rs (GPCRs) respond to paracrine or endocrine peptide hormones involved in control of bone homeostasis
153 nt techniques to determine specific forms of peptide hormones involved in physiologic processes; inve
155 in the concentration of functionally related peptide hormones is critical to understanding the etiolo
156 However, the remodelling capacity of these peptide hormones is difficult to study in chronic settin
160 s system cells but does not co-localize with peptide hormones known to elicit molting behavior, sugge
161 isting variation in a subfamily of plant CLE peptide hormones leads to a synthetic bifunctional pepti
162 on of the receptor for the adipocyte-derived peptide hormone leptin (OB-R) is a characteristic featur
169 tegrated to obtain a structural model of the peptide hormone neuropeptide Y (NPY) bound to its human
170 sults support the hypothesis that packing of peptide hormones/neuropeptides in dense-core vesicles do
171 quence of OCN predicts that, like many other peptide hormones, OCN is first synthesized as a prohormo
172 stimulating factor (G-CSF) is an endogenous peptide hormone of the hematopoietic system that has bee
173 stimulating factor (G-CSF) is an endogenous peptide hormone of the hematopoietic system that has ent
174 7) [Ang-(1-7)] is an endogenous 7-amino acid peptide hormone of the renin-angiotensin system that has
178 zes recent progress on the identification of peptide hormones participating in the pathophysiology of
179 eoblasts that inactivates an uncharacterized peptide hormone, phosphatonin, which suppresses bone min
182 es involved in the proteolytic maturation of peptide hormone precursors and are implicated in a varie
188 mation requires hepcidin, an iron regulatory peptide hormone produced in the liver, but the inflammat
192 ology and mass spectrometry, we identified a peptide hormone product of the gastrin gene (glycine-ext
194 evolutionary lineage of the neurohypophysial peptide hormone receptor family of G-protein coupled rec
196 search for small-molecule drugs that act at peptide hormone receptors has resulted in the identifica
197 iverse plant peptides, suggesting that plant peptide hormone receptors may share a common ligand bind
198 anistic link between increased expression of peptide hormone receptors, such as GRP-R, and proangioge
200 n agonist at three key metabolically-related peptide hormone receptors: glucagon-like peptide-1 (GLP-
202 Parathyroid hormone (PTH) is an important peptide hormone regulator of bone formation and osteobla
205 recombinant form of the naturally occurring peptide hormone relaxin-2, is a pleiotropic vasodilating
207 eyond the widely accepted role of regulating peptide hormone release from enteroendocrine cells in th
211 d (acoustic) extraction of insulin and other peptide hormones released from freshly prepared islets,
212 edullin (Adm, gene; AM, protein)-a mitogenic peptide hormone required for normal cardiovascular devel
214 at subtle changes in the native structure of peptide hormone(s) could alter its conformational dynami
217 lin is a 28 amino acid, appetite-stimulating peptide hormone secreted by the food-deprived stomach.
223 gulates the expression of genes encoding the peptide hormones secreted by each cell type, including t
225 rantee continuous availability and function, peptide hormone secretion must be tightly coupled to its
226 ein expressed in cells with stimulus-coupled peptide hormone secretion, including pancreatic beta cel
229 been implicated as a downstream effector of peptide hormone signaling during urogenital ridge develo
230 aling pathways, multiple growth factors, and peptide hormone signaling systems, and genes involved in
231 The endocrine system mediates long-range peptide hormone signaling to broadcast changes in metabo
232 egation and fibril reversibility of a cyclic peptide hormone somatostatin (SST)-14 using various tech
236 PC2), an enzyme involved in the synthesis of peptide hormones, such as glucagon and proopiomelanocort
237 mammals, the production of insulin and other peptide hormones, such as the islet amyloid polypeptide
239 tropin-releasing hormone (GnRH) is a trophic peptide hormone synthesized by hypothalamic neurons and
240 have decreased urinary levels of hepcidin, a peptide hormone that binds to the cellular iron exporter
241 -Fc(mIgG)-Leptin, a bifunctional therapeutic peptide hormone that combines the glucagon-like peptide
242 e peptide 1 (GLP-1) is a 30 or 31 amino acid peptide hormone that contributes to the physiological re
246 al peptide (Hamp) is a hepatic defensin-like peptide hormone that inhibits duodenal iron absorption a
248 ation factor 1 (AtRALF1) is a small secreted peptide hormone that inhibits root growth by repressing
252 l natriuretic peptide (ANP) is an endogenous peptide hormone that is synthesized and secreted by the
253 Fibroblast growth factor 21 (FGF21) is a peptide hormone that is synthesized by several organs an
255 tropin-releasing hormone (GnRH) is a trophic peptide hormone that modulates reproductive function and
261 e intestine secrete cholecystokinin (CCK), a peptide hormone that stimulates digestion of fat and pro
263 n of this strategy to oxyntomodulin (OXM), a peptide hormone that stimulates insulin secretion from i
264 ich is processed to ghrelin, an octanoylated peptide hormone that stimulates release of growth hormon
268 o proteolytically process a diverse suite of peptide hormones that coordinate larval and pupal growth
269 ve successfully identified other steroid and peptide hormones that impact on mammary gland developmen
270 thesis coupling for glucagon, one of several peptide hormones that increase blood glucose levels.
271 This variation is mediated by steroid and peptide hormones that influence ion currents through cha
272 quences homologous to other classes of plant peptide hormones that may be utilized by these pests.
273 is that AMON acts to proteolytically process peptide hormones that regulate hatching, larval growth,
276 cardioactive peptide (CCAP) neurons and the peptide hormones they secrete are critical for ecdysis;
277 ue role as the sole blood glucose-decreasing peptide hormone, this coupling is considered an exceptio
278 the first to report DOPA cross-linking of a peptide hormone to a GPCR and the first to identify a re
279 nd imipramine pamoate (Tofranil-PM); and the peptide hormones triptorelin pamoate (Trelstar) and octr
284 chanism that accounts for the ability of the peptide hormone vasopressin to regulate water excretion
286 ocrine tissues secrete neurotransmitters and peptide hormones via large dense-core vesicles (LDCVs).
287 aracterize conformational changes induced by peptide hormones, we investigated interactions of the cl
288 interactions at the N-terminal domain of the peptide hormone were manifested by suppressed cAMP gener
293 recombinant human relaxin-2, is a vasoactive peptide hormone with many biological and haemodynamic ef
298 vous system, equipped with neuropeptides and peptide hormones with potent antimicrobial properties, m
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