Zobrazeno 1 - 10 of 23 pro vyhledávání: '"S Jack Lin"'
2
Akademický článek
Design of a Selective Substrate and Activity Based Probe for Human Neutrophil Serine Protease 4.
Autor: Paulina Kasperkiewicz, Marcin Poreba, Scott J Snipas, S Jack Lin, Daniel Kirchhofer, Guy S Salvesen, Marcin Drag
Publikováno v: PLoS ONE, Vol 10, Iss 7, p e0132818 (2015)
Human neutrophil serine protease 4 (NSP4), also known as PRSS57, is a recently discovered fourth member of the neutrophil serine proteases family. Although its biological function is not precisely defined, it is suggested to regulate neutrophil respo
Externí odkaz: https://doaj.org/article/9a6893e6b5384d4eb3d6fddaa651dc61
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3
Akademický článek
Novel staphylococcal glycosyltransferases SdgA and SdgB mediate immunogenicity and protection of virulence-associated cell wall proteins.
Autor: Wouter L W Hazenbos, Kimberly K Kajihara, Richard Vandlen, J Hiroshi Morisaki, Sophie M Lehar, Mark J Kwakkenbos, Tim Beaumont, Arjen Q Bakker, Qui Phung, Lee R Swem, Satish Ramakrishnan, Janice Kim, Min Xu, Ishita M Shah, Binh An Diep, Tao Sai, Andrew Sebrell, Yana Khalfin, Angela Oh, Chris Koth, S Jack Lin, Byoung-Chul Lee, Magnus Strandh, Klaus Koefoed, Peter S Andersen, Hergen Spits, Eric J Brown, Man-Wah Tan, Sanjeev Mariathasan
Publikováno v: PLoS Pathogens, Vol 9, Iss 10, p e1003653 (2013)
Infection of host tissues by Staphylococcus aureus and S. epidermidis requires an unusual family of staphylococcal adhesive proteins that contain long stretches of serine-aspartate dipeptide-repeats (SDR). The prototype member of this family is clump
Externí odkaz: https://doaj.org/article/9ab686e914474260984f11e6595e12d4
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4
Akademický článek
Phylogenomic analyses reveal the evolutionary origin of the inhibin alpha-subunit, a unique TGFbeta superfamily antagonist.
Autor: Jie Zhu, Edward L Braun, Satomi Kohno, Monica Antenos, Eugene Y Xu, Robert W Cook, S Jack Lin, Brandon C Moore, Louis J Guillette, Theodore S Jardetzky, Teresa K Woodruff
Publikováno v: PLoS ONE, Vol 5, Iss 3, p e9457 (2010)
Transforming growth factor-beta (TGFbeta) homologues form a diverse superfamily that arose early in animal evolution and control cellular function through membrane-spanning, conserved serine-threonine kinases (RII and RI receptors). Activin and inhib
Externí odkaz: https://doaj.org/article/f0670ba69dc94e9c92be3ba9b0b9b9bd
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5
Data from Proteolytic Activation of Pro-Macrophage-Stimulating Protein by Hepsin
Autor: Daniel Kirchhofer, Amitabha Chaudhuri, Robert A. Lazarus, Thomas D. Wu, Lydia Santell, Ming-Hong Xie, S. Jack Lin, Ganesh A. Kolumam, Rajkumar Ganesan
Macrophage-stimulating protein (MSP) is a plasminogen-related growth factor and ligand for the receptor tyrosine kinase RON. The MSP/RON system promotes wound healing and invasive tumor growth and suppresses proinflammatory immune response. MSP bindi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab92bcdb36a8748185ea7692af62458f
https://doi.org/10.1158/1541-7786.c.6542076
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7
Abstract 5070: Anti-tumor activity of HPN328, a DLL3-targeting tri-specific, half-life extended T cell engager, is enhanced by combining with an anti-PD-L1 antibody in an immunocompetent mouse model
Autor: Laura B. Valenzuela, Chi-Heng Wu, Wade Aaron, Raphalea R. Banzon, Mabel Bush, S. Jack Lin, Sony S. Rocha, Subramanian Thothathri, Holger Wesche, Mary Ellen Molloy, Banmeet S. Anand
Publikováno v: Cancer Research. 83:5070-5070
TriTAC® is a T cell engager platform comprised of three binding domains: a target binder for tumor cell engagement, an albumin binder for half-life extension, and a CD3 binder for T cell engagement. HPN328 is a Delta-like ligand 3 (DLL3)-targeting T
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0105608c031459aafbf4ca3c05c93279
https://doi.org/10.1158/1538-7445.am2023-5070
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10
An ancient mechanism of arginine-specific substrate cleavage: What's ‘up’ with NSP4?
Autor: Andrew P. AhYoung, Stefan Gerhardy, Menno van Lookeren Campagne, Daniel Kirchhofer, S. Jack Lin
Publikováno v: Biochimie. 166:19-26
The recently discovered neutrophil serine protease 4 (NSP4) is the fourth member of the NSP family, which includes the well-studied neutrophil elastase, proteinase 3 and cathepsin G. Like the other three NSP members, NSP4 is synthesized by myeloid pr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c0c9fc30800dc52a110981a1d568784
https://doi.org/10.1016/j.biochi.2019.03.020
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