Page last updated: 2024-08-25

glycine amide and asparagine

glycine amide has been researched along with asparagine in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Dal Pan, G; Gazis, D; Roy, J; Roy, U; Schwartz, IL	1
Davidson, JS; Davies, P; Elario, R; Flanagan, CA; McArdle, CA; Millar, RP	1

Other Studies

2 other study(ies) available for glycine amide and asparagine

Article	Year
Role of the carboxamide groups of the asparagine and glycinamide residues of oxytocin. Syntheses and biological properties of [5-beta-cyanoalanine] oxytocin and [9-alpha-aminoacetonitrile] oxytocin. International journal of peptide and protein research, 1983, Volume: 22, Issue:5 Topics: Animals; Asparagine; Biological Assay; Diuresis; Female; Glycine; Indicators and Reagents; Oxytocin; Rats; Structure-Activity Relationship; Uterine Contraction	1983
Asn102 of the gonadotropin-releasing hormone receptor is a critical determinant of potency for agonists containing C-terminal glycinamide. The Journal of biological chemistry, 1996, Jun-28, Volume: 271, Issue:26 Topics: Amino Acid Sequence; Asparagine; Binding Sites; Glycine; Gonadotropin-Releasing Hormone; Humans; Inositol Phosphates; Ligands; Molecular Sequence Data; Mutagenesis, Site-Directed; Oligodeoxyribonucleotides; Protein Binding; Protein Structure, Tertiary; Receptors, LHRH; Signal Transduction; Structure-Activity Relationship	1996

Article

Year

Role of the carboxamide groups of the asparagine and glycinamide residues of oxytocin. Syntheses and biological properties of [5-beta-cyanoalanine] oxytocin and [9-alpha-aminoacetonitrile] oxytocin.

International journal of peptide and protein research, 1983, Volume: 22, Issue:5

Topics: Animals; Asparagine; Biological Assay; Diuresis; Female; Glycine; Indicators and Reagents; Oxytocin; Rats; Structure-Activity Relationship; Uterine Contraction

1983

Asn102 of the gonadotropin-releasing hormone receptor is a critical determinant of potency for agonists containing C-terminal glycinamide.

The Journal of biological chemistry, 1996, Jun-28, Volume: 271, Issue:26

Topics: Amino Acid Sequence; Asparagine; Binding Sites; Glycine; Gonadotropin-Releasing Hormone; Humans; Inositol Phosphates; Ligands; Molecular Sequence Data; Mutagenesis, Site-Directed; Oligodeoxyribonucleotides; Protein Binding; Protein Structure, Tertiary; Receptors, LHRH; Signal Transduction; Structure-Activity Relationship

1996