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Daniel Kirchhofer

Showing results (51-60 of 91) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 21, 2007
Utilizing the activation mechanism of serine proteases to engineer hepatocyte growth factor into a Met antagonistDaniel Kirchhofer, Michael T Lipari, Lydia Santell, et al.
The Journal of Biological Chemistry|February 25, 2012
Inhibiting alternative pathway complement activation by targeting the factor D exositeKenneth J Katschke, Ping Wu, Rajkumar Ganesan, et al.
The Journal of Biological Chemistry|June 26, 2004
Structural and functional basis of the serine protease-like hepatocyte growth factor beta-chain in Met binding and signalingDaniel Kirchhofer, Xiaoyi Yao, Mark Peek, et al.
The Journal of Biological Chemistry|March 1, 2013
Mutational tail loss is an evolutionary mechanism for liberating marapsins and other type I serine proteases from transmembrane anchorsKavita Raman, Neil N Trivedi, Wilfred W Raymond, et al.
Blood|February 10, 2011
Mechanisms of enhanced thrombus formation in cerebral microvessels of mice expressing hemoglobin-SFelicity N E Gavins, Janice Russell, Elena L Senchenkova, et al.
Journal of Molecular Biology|June 9, 2026
Novel macrocyclic peptides as potent and selective inhibitors of human neutrophil serine protease 4Wanjian Tang, Mark Ultsch, Emel Adaligil, et al.
Nature Communications|May 22, 2024
Cystine-knot peptide inhibitors of HTRA1 bind to a cryptic pocket within the active site regionYanjie Li, Yuehua Wei, Mark Ultsch, et al.
The Journal of Biological Chemistry|June 17, 2010
Proteolysis-induced N-terminal ectodomain shedding of the integral membrane glycoprotein CUB domain-containing protein 1 (CDCP1) is accompanied by tyrosine phosphorylation of its C-terminal domain and recruitment of Src and PKCdeltaYaowu He, Andreas Wortmann, Les J Burke, et al.
Structure (London, England : 1993)|May 15, 2012
Structural and functional analysis of HtrA1 and its subdomainsCharles Eigenbrot, Mark Ultsch, Michael T Lipari, et al.
ACS Chemical Biology|January 22, 2020
Design of Organo-Peptides As Bipartite PCSK9 AntagonistsDaniel J Burdick, Nicholas J Skelton, Mark Ultsch, et al.
Pageof 10

Showing results (51-60 of 91) with videos related to

Sort By:
Pageof 10
Proceedings of the National Academy of Sciences of the United States of America|March 21, 2007
Utilizing the activation mechanism of serine proteases to engineer hepatocyte growth factor into a Met antagonistDaniel Kirchhofer, Michael T Lipari, Lydia Santell, et al.
The Journal of Biological Chemistry|February 25, 2012
Inhibiting alternative pathway complement activation by targeting the factor D exositeKenneth J Katschke, Ping Wu, Rajkumar Ganesan, et al.
The Journal of Biological Chemistry|June 26, 2004
Structural and functional basis of the serine protease-like hepatocyte growth factor beta-chain in Met binding and signalingDaniel Kirchhofer, Xiaoyi Yao, Mark Peek, et al.
The Journal of Biological Chemistry|March 1, 2013
Mutational tail loss is an evolutionary mechanism for liberating marapsins and other type I serine proteases from transmembrane anchorsKavita Raman, Neil N Trivedi, Wilfred W Raymond, et al.
Blood|February 10, 2011
Mechanisms of enhanced thrombus formation in cerebral microvessels of mice expressing hemoglobin-SFelicity N E Gavins, Janice Russell, Elena L Senchenkova, et al.
Journal of Molecular Biology|June 9, 2026
Novel macrocyclic peptides as potent and selective inhibitors of human neutrophil serine protease 4Wanjian Tang, Mark Ultsch, Emel Adaligil, et al.
Nature Communications|May 22, 2024
Cystine-knot peptide inhibitors of HTRA1 bind to a cryptic pocket within the active site regionYanjie Li, Yuehua Wei, Mark Ultsch, et al.
The Journal of Biological Chemistry|June 17, 2010
Proteolysis-induced N-terminal ectodomain shedding of the integral membrane glycoprotein CUB domain-containing protein 1 (CDCP1) is accompanied by tyrosine phosphorylation of its C-terminal domain and recruitment of Src and PKCdeltaYaowu He, Andreas Wortmann, Les J Burke, et al.
Structure (London, England : 1993)|May 15, 2012
Structural and functional analysis of HtrA1 and its subdomainsCharles Eigenbrot, Mark Ultsch, Michael T Lipari, et al.
ACS Chemical Biology|January 22, 2020
Design of Organo-Peptides As Bipartite PCSK9 AntagonistsDaniel J Burdick, Nicholas J Skelton, Mark Ultsch, et al.
Pageof 10