These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
127 related articles for article (PubMed ID: 10632726)
1. Biochemical characterization of the murine S100A9 (MRP14) protein suggests that it is functionally equivalent to its human counterpart despite its low degree of sequence homology. Nacken W; Sopalla C; Pröpper C; Sorg C; Kerkhoff C Eur J Biochem; 2000 Jan; 267(2):560-5. PubMed ID: 10632726 [TBL] [Abstract][Full Text] [Related]
2. Molecular analysis of the mouse S100A9 gene and evidence that the myeloid specific transcription factor C/EBPepsilon is not required for the regulation of the S100A9/A8 gene expression in neutrophils. Nacken W; Lekstrom-Himes JA; Sorg C; Manitz MP J Cell Biochem; 2001; 80(4):606-16. PubMed ID: 11169745 [TBL] [Abstract][Full Text] [Related]
3. Analysis of the MRP8-MRP14 protein-protein interaction by the two-hybrid system suggests a prominent role of the C-terminal domain of S100 proteins in dimer formation. Pröpper C; Huang X; Roth J; Sorg C; Nacken W J Biol Chem; 1999 Jan; 274(1):183-8. PubMed ID: 9867828 [TBL] [Abstract][Full Text] [Related]
4. S100A12 is expressed exclusively by granulocytes and acts independently from MRP8 and MRP14. Vogl T; Pröpper C; Hartmann M; Strey A; Strupat K; van den Bos C; Sorg C; Roth J J Biol Chem; 1999 Sep; 274(36):25291-6. PubMed ID: 10464253 [TBL] [Abstract][Full Text] [Related]
5. S100A8, S100A9 and the S100A8/A9 heterodimer complex specifically bind to human endothelial cells: identification and characterization of ligands for the myeloid-related proteins S100A9 and S100A8/A9 on human dermal microvascular endothelial cell line-1 cells. Eue I; König S; Pior J; Sorg C Int Immunol; 2002 Mar; 14(3):287-97. PubMed ID: 11867565 [TBL] [Abstract][Full Text] [Related]
6. A comparison of human S100A12 with MRP-14 (S100A9). Robinson MJ; Hogg N Biochem Biophys Res Commun; 2000 Sep; 275(3):865-70. PubMed ID: 10973813 [TBL] [Abstract][Full Text] [Related]
7. Novel insights into structure and function of MRP8 (S100A8) and MRP14 (S100A9). Kerkhoff C; Klempt M; Sorg C Biochim Biophys Acta; 1998 Dec; 1448(2):200-11. PubMed ID: 9920411 [TBL] [Abstract][Full Text] [Related]
8. The two calcium-binding proteins, S100A8 and S100A9, are involved in the metabolism of arachidonic acid in human neutrophils. Kerkhoff C; Klempt M; Kaever V; Sorg C J Biol Chem; 1999 Nov; 274(46):32672-9. PubMed ID: 10551823 [TBL] [Abstract][Full Text] [Related]
9. The regulatory role of MRP8 (S100A8) and MRP14 (S100A9) in the transendothelial migration of human leukocytes. Kerkhoff C; Eue I; Sorg C Pathobiology; 1999; 67(5-6):230-2. PubMed ID: 10725790 [TBL] [Abstract][Full Text] [Related]
10. The fatty acid-binding heterocomplex FA-p34 formed by S100A8 and S100A9 is the major fatty acid carrier in neutrophils and translocates from the cytosol to the membrane upon stimulation. Roulin K; Hagens G; Hotz R; Saurat JH; Veerkamp JH; Siegenthaler G Exp Cell Res; 1999 Mar; 247(2):410-21. PubMed ID: 10066369 [TBL] [Abstract][Full Text] [Related]
11. The Ca2+-binding proteins S100A8 and S100A9 are encoded by novel injury-regulated genes. Thorey IS; Roth J; Regenbogen J; Halle JP; Bittner M; Vogl T; Kaesler S; Bugnon P; Reitmaier B; Durka S; Graf A; Wöckner M; Rieger N; Konstantinow A; Wolf E; Goppelt A; Werner S J Biol Chem; 2001 Sep; 276(38):35818-25. PubMed ID: 11463791 [TBL] [Abstract][Full Text] [Related]
12. S100A8 and S100A9 in inflammatory diseases. Roth J; Goebeler M; Sorg C Lancet; 2001 Mar; 357(9261):1041. PubMed ID: 11293617 [No Abstract] [Full Text] [Related]
14. Two proteins modulating transendothelial migration of leukocytes recognize novel carboxylated glycans on endothelial cells. Srikrishna G; Panneerselvam K; Westphal V; Abraham V; Varki A; Freeze HH J Immunol; 2001 Apr; 166(7):4678-88. PubMed ID: 11254728 [TBL] [Abstract][Full Text] [Related]
15. The S100A8/A9 protein as a partner for the cytosolic factors of NADPH oxidase activation in neutrophils. Doussiere J; Bouzidi F; Vignais PV Eur J Biochem; 2002 Jul; 269(13):3246-55. PubMed ID: 12084065 [TBL] [Abstract][Full Text] [Related]
16. Isolation of the murine S100 protein MRP14 (14 kDa migration-inhibitory-factor-related protein) from activated spleen cells: characterization of post-translational modifications and zinc binding. Raftery MJ; Harrison CA; Alewood P; Jones A; Geczy CL Biochem J; 1996 May; 316 ( Pt 1)(Pt 1):285-93. PubMed ID: 8645219 [TBL] [Abstract][Full Text] [Related]
17. Calcium-induced noncovalently linked tetramers of MRP8 and MRP14 are confirmed by electrospray ionization-mass analysis. Strupat K; Rogniaux H; Van Dorsselaer A; Roth J; Vogl T J Am Soc Mass Spectrom; 2000 Sep; 11(9):780-8. PubMed ID: 10976885 [TBL] [Abstract][Full Text] [Related]
18. Overexpression, oxidative refolding, and zinc binding of recombinant forms of the murine S100 protein MRP14 (S100A9). Raftery MJ; Collinson L; Geczy CL Protein Expr Purif; 1999 Mar; 15(2):228-35. PubMed ID: 10049680 [TBL] [Abstract][Full Text] [Related]
19. Myeloid-related proteins 8 and 14 are specifically secreted during interaction of phagocytes and activated endothelium and are useful markers for monitoring disease activity in pauciarticular-onset juvenile rheumatoid arthritis. Frosch M; Strey A; Vogl T; Wulffraat NM; Kuis W; Sunderkötter C; Harms E; Sorg C; Roth J Arthritis Rheum; 2000 Mar; 43(3):628-37. PubMed ID: 10728757 [TBL] [Abstract][Full Text] [Related]
20. Calgranulins S100A8 and S100A9 are negatively regulated by glucocorticoids in a c-Fos-dependent manner and overexpressed throughout skin carcinogenesis. Gebhardt C; Breitenbach U; Tuckermann JP; Dittrich BT; Richter KH; Angel P Oncogene; 2002 Jun; 21(27):4266-76. PubMed ID: 12082614 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]