Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR039189-09
Application #
2079439
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1988-02-01
Project End
1998-06-30
Budget Start
1996-07-01
Budget End
1998-06-30
Support Year
9
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Kansas
Department
Biochemistry
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Shimokawa, Ken-Ichi; Nagase, Hideaki (2010) Purification of MMPs and TIMPs. Methods Mol Biol 622:123-55
Thummel, Ryan; Ju, Mila; Sarras Jr, Michael P et al. (2007) Both Hoxc13 orthologs are functionally important for zebrafish tail fin regeneration. Dev Genes Evol 217:413-20
Lauer-Fields, Janelle L; Minond, Dmitriy; Sritharan, Thilaka et al. (2007) Substrate conformation modulates aggrecanase (ADAMTS-4) affinity and sequence specificity. Suggestion of a common topological specificity for functionally diverse proteases. J Biol Chem 282:142-50
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Minond, Dmitriy; Lauer-Fields, Janelle L; Nagase, Hideaki et al. (2004) Matrix metalloproteinase triple-helical peptidase activities are differentially regulated by substrate stability. Biochemistry 43:11474-81
Lauer-Fields, Janelle L; Kele, Peter; Sui, Guodong et al. (2003) Analysis of matrix metalloproteinase triple-helical peptidase activity with substrates incorporating fluorogenic L- or D-amino acids. Anal Biochem 321:105-15
Zhang, Jinsong; Bai, Shan; Tanase, Carmen et al. (2003) The expression of tissue inhibitor of metalloproteinase 2 (TIMP-2) is required for normal development of zebrafish embryos. Dev Genes Evol 213:382-9
Zhang, Jinsong; Bai, Shan; Zhang, Xiaoming et al. (2003) The expression of novel membrane-type matrix metalloproteinase isoforms is required for normal development of zebrafish embryos. Matrix Biol 22:279-93

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