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1 synaptotagmin-1, proprotein convertase, and secretogranins).
2 pling identified extracellular peptides from secretogranin-1, ProSAAS, pro-opiomelanocortin (POMC), a
4 protein levels of SCLC NE markers INSM1 and Secretogranin-3 and of driver transcription factors ASCL
5 s ER stress response genes, decreases INSM1, Secretogranin-3, and NEUROD1 and inhibits proliferation
7 bombyxin-type, starfish myorelaxant peptide, secretogranin 7B2-like, Ap15a-like, and ApNp35) and Dele
10 Yet, large dense-core vesicles marked by secretogranin attach to plasma membranes at foci contain
11 ciation between a regulatory polymorphism in Secretogranin II (SCG2) and hypertension in African-Amer
14 achykinin (PPT), preproenkephalin (PPE), and secretogranin II (SGII) mRNA levels in the striatum with
15 IV CD, as well as Syt IV depletion, reduces secretogranin II (SgII) processing by prohormone convert
17 ermore, lack of change in chromogranin B and secretogranin II cleavage after diminution of PCl sugges
19 (PC2) autocatalytic cleavage, processing of secretogranin II to its product p18, and the correlation
20 e GH4C1 secretes granins (chromogranin B and secretogranin II) and prolactin by the regulated secreto
22 me, including multiple peptides derived from secretogranin II, cocaine and amphetamine regulated tran
24 nkephalin, promelanin-concentrating hormone, secretogranin II, pituitary adenylate cyclase-activating
25 etworks that are responsive to the conserved secretogranin II-derived neuropeptide secretoneurin A (S
29 ated IOP: interleukin-6, preprotachykinin-1, secretogranin-II, cathepsin-L, stromelysin-1, thymosin-b
34 ecretogranin II, members of the chromogranin/secretogranin secretory protein family, are overexpresse
35 enesis is dependent on the secretory protein secretogranin (Sg) II, a member of the granin family of
37 experiences (ACEs) and neonatal DNAm in the secretogranin V gene (SCG5), which is important in neuro
38 E peptide blocked discharge of (35)S-labeled secretogranin with the same structural selectivity and p