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dihydrosomatostatin

Known as: somatostatin (15-28) 
 
National Institutes of Health

Papers overview

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1985
1985
High plasma concentrations of C-terminal immunoreactive glucagon (IRG) have been found during early life in several mammalian… Expand
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1981
1981
To exemplify the usefulness of the S‐tert‐butylthio group for a reversible blocking of the cysteine thiol function in peptide… Expand
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1981
1981
Comparative studies of the activity of somatostatin and of several of its analogues in releasing histamine from rat mast cells… Expand
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1980
1980
Experimental details for the "Fmoc solid phase peptide synthesis" of somatostatin are described. The 9-fluorenylmethyloxycarbonyl… Expand
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1980
1980
Experimental details for practical syntheses of somatostatin and D-Trp8-somatostatin are described. The peptides were assembled… Expand
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Highly Cited
1978
Highly Cited
1978
N alpha-9-Fluorenylmethyloxycarbonyl (Fmoc) amino acids will be of advantage in solid phase peptide synthesis. The Fmoc-group is… Expand
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1977
1977
 
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1976
1976
Somatostatin and dihydrosomatostatin (H2somatostatin) are equipotent in inhibiting insulin and glucagon release induced by… Expand
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1975
1975
An in vitro system which uses perifused pieces from the antrum of rat stomach has been used to study the effect of… Expand
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1974
1974
Abstract Dihydrosomatostatin (0.001–1.0 ug/ml) inhibited both insulin and glucagon secretion by monolayer cell cultures of… Expand
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