Year |
Citation |
Score |
2020 |
Babinska A, Clement CC, Li Y, Wzorek J, Przygodzki T, Talar M, Braun M, Swiatkowska M, Ehrlich YH, Kornecki E, Watala C, Salifu MO. data: treatment with the F11R/JAM-A peptide 4D decreases mortality and reduces the generation of atherosclerotic plaques in ApoE-deficient mice. Data in Brief. 30: 105516. PMID 32395574 DOI: 10.1016/J.Dib.2020.105516 |
0.395 |
|
2019 |
Babinska A, Clement CC, Przygodzki T, Talar M, Li Y, Braun M, Wzorek J, Swiatkowska M, Ehrlich YH, Kornecki E, Watala C, Salifu MO. A peptide antagonist of F11R/JAM-A reduces plaque formation and prolongs survival in an animal model of atherosclerosis. Atherosclerosis. 284: 92-101. PMID 30877938 DOI: 10.1016/J.Atherosclerosis.2019.02.014 |
0.348 |
|
2018 |
Cheng SY, Vargas A, Lee JY, Clement CC, Champeil E. Involvement of Akt in Mitomycin C and Its Analog Triggered Cytotoxicity in MCF-7 and K562 cancer cells. Chemical Biology & Drug Design. PMID 30091208 DOI: 10.1111/Cbdd.13374 |
0.392 |
|
2018 |
Clement CC, Gonzalez J, Babinska A, Ewul EL, Timpo E, Salifu MO, Monika D. Development of a label‒free nanolc/ms/ms assay for monitoring the changes in the proteomic landscape of thrombin‒activated human platelets Moj Proteomics & Bioinformatics. 7. DOI: 10.15406/Mojpb.2018.07.00242 |
0.554 |
|
2014 |
Babinska A, Clement CC, Swiatkowska M, Szymanski J, Shon A, Ehrlich YH, Kornecki E, Salifu MO. Development of new antiatherosclerotic and antithrombotic drugs utilizing F11 receptor (F11R/JAM-A) peptides. Biopolymers. 101: 322-34. PMID 24801754 DOI: 10.1002/Bip.22503 |
0.565 |
|
2012 |
Figueiredo AC, Clement CC, Zakia S, Gingold J, Philipp M, Pereira PJ. Rational design and characterization of D-Phe-Pro-D-Arg-derived direct thrombin inhibitors. Plos One. 7: e34354. PMID 22457833 DOI: 10.1371/Journal.Pone.0034354 |
0.531 |
|
2011 |
Carvalho Figueiredo A, Clement CC, Philipp M, Barbosa Pereira PJ. Crystallization and preliminary crystallographic characterization of three peptidic inhibitors in complex with α-thrombin. Acta Crystallographica. Section F, Structural Biology and Crystallization Communications. 67: 54-8. PMID 21206024 DOI: 10.1107/S1744309110043472 |
0.658 |
|
2011 |
Pereira PJB, Figueiredo AC, Macedo-Ribeiro S, Philipp M, Clement CC. Structural characterization ofD-Phe-Pro-D-Arg-derived thrombin inhibitors Acta Crystallographica Section a Foundations of Crystallography. 67: C311-C312. DOI: 10.1107/S010876731109218X |
0.524 |
|
2009 |
Clement CC, Babinska A, Kornecki E, Philipp M. Isothermal titration calorimetry and inhibition of platelets aggregation by [D-Phe/(transcinnamoyl)-Pro-D-Arg-P1'-CONH2] peptides inhibitors of thrombin. Advances in Experimental Medicine and Biology. 611: 579-80. PMID 19400322 DOI: 10.1007/978-0-387-73657-0_255 |
0.659 |
|
2001 |
Subramaniam G, Paz MM, Suresh Kumar G, Das A, Palom Y, Clement CC, Patel DJ, Tomasz M. Solution structure of a guanine-N7-linked complex of the mitomycin C metabolite 2,7-diaminomitosene and DNA. Basis of sequence selectivity. Biochemistry. 40: 10473-84. PMID 11523988 DOI: 10.1021/Bi015147X |
0.311 |
|
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