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S McMurray

Showing results (31-40 of 121) with videos related to

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Bioorganic & Medicinal Chemistry Letters|March 18, 2003
Identification of a high-affinity phosphopeptide inhibitor of Stat3Zhiyong Ren, Larry A Cabell, Timothy S Schaefer, et al.
Bioconjugate Chemistry|May 19, 2005
Probing for integrin alpha v beta3 binding of RGD peptides using fluorescence polarizationWei Wang, Qingping Wu, Marites Pasuelo, et al.
Biochimica Et Biophysica Acta|April 5, 1995
Use of synthetic peptides and copolymers to study the substrate specificity and inhibition of the protein tyrosine kinase pp60c-srcR J Budde, N U Obeyesekere, S Ke, et al.
Biopolymers|May 29, 2001
The synthesis of phosphopeptidesJ S McMurray, D R Coleman, W Wang, et al.
Archives of Biochemistry and Biophysics|February 1, 1996
A synthetic peptidic substrate of minimal size and semioptimal sequence for the protein tyrosine kinase pp60c-srcL Ramdas, N U Obeyesekere, J S McMurray, et al.
Anticancer Research|January 1, 1992
Influence of acidic residues on substrate specificity of oncogene products pp60v-src and p56lck in vitroD A Tinker, J L Cartron, J S McMurray, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|March 1, 1996
Comparison of measured and predicted creatinine excretion is an unreliable index of compliance in PD patientsP G Blake, E Spanner, S McMurray, et al.
Biopolymers|June 8, 2001
Structural basis for the activity of pp60(c-src) protein tyrosine kinase inhibitorsN V Prabhu, S A Siddiqui, J S McMurray, et al.
Journal of Medicinal Chemistry|September 5, 2009
Structure-affinity relationships of glutamine mimics incorporated into phosphopeptides targeted to the SH2 domain of signal transducer and activator of transcription 3Pijus K Mandal, Zhiyong Ren, Xiaomin Chen, et al.
Cancer Biotherapy & Radiopharmaceuticals|October 27, 2005
Convenient solid-phase synthesis of diethylenetriaminepenta-acetic acid (DTPA)- conjugated cyclic RGD peptide analoguesWei Wang, John S McMurray, Qingping Wu, et al.
Pageof 13

Showing results (31-40 of 121) with videos related to

Sort By:
Pageof 13
Bioorganic & Medicinal Chemistry Letters|March 18, 2003
Identification of a high-affinity phosphopeptide inhibitor of Stat3Zhiyong Ren, Larry A Cabell, Timothy S Schaefer, et al.
Bioconjugate Chemistry|May 19, 2005
Probing for integrin alpha v beta3 binding of RGD peptides using fluorescence polarizationWei Wang, Qingping Wu, Marites Pasuelo, et al.
Biochimica Et Biophysica Acta|April 5, 1995
Use of synthetic peptides and copolymers to study the substrate specificity and inhibition of the protein tyrosine kinase pp60c-srcR J Budde, N U Obeyesekere, S Ke, et al.
Biopolymers|May 29, 2001
The synthesis of phosphopeptidesJ S McMurray, D R Coleman, W Wang, et al.
Archives of Biochemistry and Biophysics|February 1, 1996
A synthetic peptidic substrate of minimal size and semioptimal sequence for the protein tyrosine kinase pp60c-srcL Ramdas, N U Obeyesekere, J S McMurray, et al.
Anticancer Research|January 1, 1992
Influence of acidic residues on substrate specificity of oncogene products pp60v-src and p56lck in vitroD A Tinker, J L Cartron, J S McMurray, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|March 1, 1996
Comparison of measured and predicted creatinine excretion is an unreliable index of compliance in PD patientsP G Blake, E Spanner, S McMurray, et al.
Biopolymers|June 8, 2001
Structural basis for the activity of pp60(c-src) protein tyrosine kinase inhibitorsN V Prabhu, S A Siddiqui, J S McMurray, et al.
Journal of Medicinal Chemistry|September 5, 2009
Structure-affinity relationships of glutamine mimics incorporated into phosphopeptides targeted to the SH2 domain of signal transducer and activator of transcription 3Pijus K Mandal, Zhiyong Ren, Xiaomin Chen, et al.
Cancer Biotherapy & Radiopharmaceuticals|October 27, 2005
Convenient solid-phase synthesis of diethylenetriaminepenta-acetic acid (DTPA)- conjugated cyclic RGD peptide analoguesWei Wang, John S McMurray, Qingping Wu, et al.
Pageof 13