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C Poulos

Showing results (31-40 of 70) with videos related to

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Oncotarget|September 11, 2015
The search for cis-regulatory driver mutations in cancer genomesRebecca C Poulos, Mathew A Sloane, Luke B Hesson, et al.
Insect Biochemistry and Molecular Biology|July 19, 2000
Mathematical modelling of insect neuropeptide potencies. Are quantitatively predictive models possible?M J Lee, S de Jong, G Gäde, et al.
Proteomics|September 10, 2022
Opportunities for pharmacoproteomics in biomarker discoveryRebecca C Poulos, Zhaoxiang Cai, Phillip J Robinson, et al.
International Journal of Peptide and Protein Research|December 1, 1991
Application of 2-chlorotrityl resin in solid phase synthesis of (Leu15)-gastrin I and unsulfated cholecystokinin octapeptide. Selective O-deprotection of tyrosineK Barlos, D Gatos, S Kapolos, et al.
Neuropeptides|February 1, 1995
GR 73,632 and [Glu(OBzl)11]substance P are selective agonists for the septide-sensitive tachykinin NK1 receptor in the rat urinary bladderS Meini, R Patacchini, A Lecci, et al.
International Journal of Peptide and Protein Research|April 1, 1993
Synthesis of potent antagonists of substance P by modifying the methionyl and glutaminyl residues of its C-terminal hexapeptide and without using D-amino acidsA Manolopoulou, K Karagiannis, G Stavropoulos, et al.
International Journal of Peptide and Protein Research|September 1, 1992
Application of carboxylic-phospholanic mixed anhydrides to fragment coupling in peptide synthesisC Poulos, C P Ashton, J Green, et al.
Plos Genetics|November 10, 2018
Analysis of 7,815 cancer exomes reveals associations between mutational processes and somatic driver mutationsRebecca C Poulos, Yuen T Wong, Regina Ryan, et al.
Journal of Medicinal Chemistry|November 1, 1982
Structure-activity studies on the C-terminal amide of substance PE Escher, R Couture, C Poulos, et al.
International Journal of Peptide and Protein Research|October 1, 1991
Synthesis of a potent agonist of substance P by modifying the methionyl and glutaminyl residues of the C-terminal hexapeptide of substance P. Structure-activity relationshipsK Karagiannis, A Manolopoulou, G Stavropoulos, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Oncotarget|September 11, 2015
The search for cis-regulatory driver mutations in cancer genomesRebecca C Poulos, Mathew A Sloane, Luke B Hesson, et al.
Insect Biochemistry and Molecular Biology|July 19, 2000
Mathematical modelling of insect neuropeptide potencies. Are quantitatively predictive models possible?M J Lee, S de Jong, G Gäde, et al.
Proteomics|September 10, 2022
Opportunities for pharmacoproteomics in biomarker discoveryRebecca C Poulos, Zhaoxiang Cai, Phillip J Robinson, et al.
International Journal of Peptide and Protein Research|December 1, 1991
Application of 2-chlorotrityl resin in solid phase synthesis of (Leu15)-gastrin I and unsulfated cholecystokinin octapeptide. Selective O-deprotection of tyrosineK Barlos, D Gatos, S Kapolos, et al.
Neuropeptides|February 1, 1995
GR 73,632 and [Glu(OBzl)11]substance P are selective agonists for the septide-sensitive tachykinin NK1 receptor in the rat urinary bladderS Meini, R Patacchini, A Lecci, et al.
International Journal of Peptide and Protein Research|April 1, 1993
Synthesis of potent antagonists of substance P by modifying the methionyl and glutaminyl residues of its C-terminal hexapeptide and without using D-amino acidsA Manolopoulou, K Karagiannis, G Stavropoulos, et al.
International Journal of Peptide and Protein Research|September 1, 1992
Application of carboxylic-phospholanic mixed anhydrides to fragment coupling in peptide synthesisC Poulos, C P Ashton, J Green, et al.
Plos Genetics|November 10, 2018
Analysis of 7,815 cancer exomes reveals associations between mutational processes and somatic driver mutationsRebecca C Poulos, Yuen T Wong, Regina Ryan, et al.
Journal of Medicinal Chemistry|November 1, 1982
Structure-activity studies on the C-terminal amide of substance PE Escher, R Couture, C Poulos, et al.
International Journal of Peptide and Protein Research|October 1, 1991
Synthesis of a potent agonist of substance P by modifying the methionyl and glutaminyl residues of the C-terminal hexapeptide of substance P. Structure-activity relationshipsK Karagiannis, A Manolopoulou, G Stavropoulos, et al.
Pageof 7