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1 yntaxin, SNAP-25, and N-cadherin, as well as chromogranin B.
2 y was confined to heavy fractions containing chromogranin B, a marker of large dense core vesicles.
3 tory pathway; furthermore, lack of change in chromogranin B and secretogranin II cleavage after dimin
5 pituitary cell line GH4C1 secretes granins (chromogranin B and secretogranin II) and prolactin by th
9 olytic fragments of chromogranin A (CgA) and chromogranin B (CgB) represent the major proteins of the
10 at neonatal and adult cardiomyocytes express chromogranin B (CGB), a Ca(2+) binding protein that modu
12 uroendocrine cells, chromogranin A (CGA) and chromogranin B (CGB), have been shown to undergo pH- and
13 tidylinositol-4-phosphate kinase (PIPKI) and chromogranin B (CGB), proteins acting synergistically to
14 the granin proteins chromogranin A (CgA) and chromogranin B (CgB); CgA- and CgB-derived peptides regu
16 curring genetic variation in the promoter of chromogranin B (CHGB), a major constituent of catecholam
17 zophrenia patient-derived neurons, including chromogranin B (CHGB), neurotensin, and natriuretic pept
18 om chromogranin A (CHGA), and other CHGA- or chromogranin B (CHGB)-related peptides, in 545 US and 12
22 ce, which enhances accumulation of CD40L and chromogranin B granules at the human TFH cell synapse an
23 se findings are consistent with reports that chromogranin B levels are reduced in the cerebrospinal f
24 phenylethanolamine N-methyl transferase and chromogranin B mRNA was similar in TH-null and wild-type
25 ptides identified decreased transcription of chromogranin B, PCSK6, NPR1, and NFAT genes in cPC2-KOs.
26 cells contain dense-core granules marked by chromogranin B, which are normally found in neuronal pre
27 i significantly predicted vascular response: chromogranin B, which encodes a protein that catalyzes c
28 aq was stimulated show only two transcripts, chromogranin B, which is involved in secretory function,