ライフサイエンスコーパス: neuromedin B

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1 eristic of the GRPr: bombesin > or = GRP > > neuromedin B.

2 esin(5-14) which has the sequence [Gln3,Arg6]neuromedin B.

3 ignificant upregulation of 1080 genes (e.g., neuromedin B), and a significant downregulation of 518 g

4 r 15 (GDF15), angiopoietin-like 6 (Angptl6), neuromedin B, and nesfatin, linked to energy expenditure

5 dization, we show here that a single marker, Neuromedin B mRNA (Nmb), identifies RTN neurons in roden

6 dentified with a single and specific marker, Neuromedin B mRNA (Nmb).

7 ptides, including gastrin-releasing peptide, neuromedin B, neurotensin, gastrin, cholecystokinin and

8 ors for the mammalian bombesin-like peptides neuromedin B (NMB) and gastrin-releasing peptide.

9 o uncover the expression of the neuropeptide neuromedin B (NMB) in the trigeminal ganglia of mice.

10 Neuromedin B (NMB) is a mammalian member of the bombesin

11 opeptides gastrin-releasing peptide (GRP) or neuromedin B (NMB) produced a large membrane depolarizat

12 he gastrin-releasing peptide (GRP) receptor, neuromedin B (NMB) receptor, or BLP receptor subtype 3]

13 Neuromedin B (NMB) receptor-null and bombesin receptor s

14 gastrin-releasing peptide (GRP) receptor and neuromedin B (NMB) receptor.

15 Neuromedin B (NMB), a mammalian bombesin related peptide

16 eptides [gastrin-releasing peptide (GRP) and neuromedin B (NMB)] are important in numerous biological

17 chymase (CMA1), tryptase (TPS1) and mastin, neuromedin-B (NMB), nerve growth factor (NGF), and leuko

18 of mRNA for the three BLP receptor subtypes (neuromedin B [NMB]) receptor, gastrin-releasing peptide

19 omedin B to Rat-1 cells transfected with the neuromedin B preferring receptor also activated p42(mapk

20 eptor number and receptor type (i.e., GRP or neuromedin B preferring).

21 y conserved G-protein-coupled receptors: the neuromedin B-preferring, the gastrin-releasing peptide-p

22 pecifically to GRP-R (0.8 nmol/L) and to the neuromedin B receptor (NMB-R) (0.9 nmol/L), with no affi

23 hares high homology with bombesin receptors (neuromedin B receptor (NMB-R) and gastrin-releasing pept

24 gastrin-releasing peptide receptor (GRP-R), neuromedin B receptor (NMB-R), and bombesin receptor sub

25 trin-releasing peptide receptor (GRP-R), the neuromedin B receptor (NMB-R), and bombesin receptor sub

26 trin-releasing peptide receptor (GRP-R), the neuromedin B receptor (NMB-R), bombesin receptor subtype

27 , functions through a distinct receptor, the neuromedin B receptor (NMB-R), of which little is known

28 -releasing peptide receptor (GRP-R, or bb2), neuromedin B receptor (NMB-R, or bb1), and the bombesin

29 PD168368 was found to be a potent selective neuromedin B receptor (NMBR) antagonist.

30 electivity for GRPR over the closely related neuromedin B receptor (NMBR).

31 ma cells which possess native NMB-Rs and rat neuromedin B receptor (rNMR-R) transfected BALB 3T3 cell

32 gastrin-releasing peptide receptor (GRP-R), neuromedin B receptor, and bombesin receptor subtype 3.

33 NAs encoding bombesin receptor subtype 3 and neuromedin-B receptor (NMB-R), but not gastrin-releasing

34 or subtype (BRS)-1 (GRP receptor) and BRS-2 (neuromedin-B receptor), but the mRNA for GRP ligand was

35 hat antagonists of gastrin-releasing peptide/neuromedin B receptors (BB/BB) PD168368 [(S)-a-methyl-a-

36 Furthermore, addition of neuromedin B to Rat-1 cells transfected with the neurome

37 ily, including gastrin-releasing peptide and neuromedin B, which are found in axons in the mediobasal

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