# | title |
1 | Molecular characterization, heterologous expression and kinetic analysis of recombinant Plasmodium falciparum thymidylate kinase |
2 | Molecular characterization, heterologous expression and kinetic analysis of recombinant Plasmodium falciparum thymidylate kinase |
3 | Bioinformatics, enzymologic properties, and comprehensive tracking of Plasmodium falciparum nucleoside diphosphate kinase. |
4 | Bioinformatics, enzymologic properties, and comprehensive tracking of Plasmodium falciparum nucleoside diphosphate kinase. |
5 | Bioinformatics, enzymologic properties, and comprehensive tracking of Plasmodium falciparum nucleoside diphosphate kinase. |
6 | Bioinformatics, enzymologic properties, and comprehensive tracking of Plasmodium falciparum nucleoside diphosphate kinase. |
7 | The Protective Effects of Nigella sativa Oil and Allium sativum Extract on Amikn cm-induced Nephrotoxicity. |
8 | The Protective Effects of Nigella sativa Oil and Allium sativum Extract on Amikn cm-induced Nephrotoxicity. |
9 | The exceptional properties of Plasmodium deoxyguanylate pathways as a potential area for metabolic and drug discovery studies |
10 | The exceptional properties of Plasmodium deoxyguanylate pathways as a potential area for metabolic and drug discovery studies |
11 | The exceptional properties of Plasmodium deoxyguanylate pathways as a potential area for metabolic and drug discovery studies |
12 | Substrate specificity and nucleotides binding properties of NM23H2/nucleoside diphosphate kinase homolog from Plasmodium falciparum |
13 | Substrate specificity and nucleotides binding properties of NM23H2/nucleoside diphosphate kinase homolog from Plasmodium falciparum |
14 | The substrate binding preferences of Plasmodium thymidylate kinase |
15 | The substrate binding preferences of Plasmodium thymidylate kinase |
16 | Binding dynamics and energetic insight into the molecular forces driving nucleotide binding by guanylate kinase |
17 | Binding dynamics and energetic insight into the molecular forces driving nucleotide binding by guanylate kinase |
18 | Thymidylate kinase: the lost chemotherapeutic target |
19 | Thymidylate kinase: the lost chemotherapeutic target |
20 | Thymidylate kinase: the lost chemotherapeutic target |
21 | Thymidylate kinase: the lost chemotherapeutic target |
22 | Nephrotoxicity and oxidative stress of single large dose or two divided doses of gentamicin in rats. |
23 | Nephrotoxicity and oxidative stress of single large dose or two divided doses of gentamicin in rats. |
24 | Nephrotoxicity and oxidative stress of single large dose or two divided doses of gentamicin in rats. |
25 | Nephrotoxicity and oxidative stress of single large dose or two divided doses of gentamicin in rats. |
26 | Nephrotoxicity and oxidative stress of single large dose or two divided doses of gentamicin in rats. |
27 | Macromolecular interactions of spectinomycin with Bovine serum albumin |
28 | Macromolecular interactions of spectinomycin with Bovine serum albumin |
29 | Macromolecular interactions of spectinomycin with Bovine serum albumin |
30 | Analysis of the molecular interactions and complexation of chloroquine with bovine serum albumin |
31 | Analysis of the molecular interactions and complexation of chloroquine with bovine serum albumin |
32 | Carbocyclic thymidine derivatives efficiently inhibit< i> Plasmodium falciparum thymidylate kinase (< i> Pf TMK) |
33 | Carbocyclic thymidine derivatives efficiently inhibit< i> Plasmodium falciparum thymidylate kinase (< i> Pf TMK) |
34 | Carbocyclic thymidine derivatives efficiently inhibit< i> Plasmodium falciparum thymidylate kinase (< i> Pf TMK) |
35 | Carbocyclic thymidine derivatives efficiently inhibit< i> Plasmodium falciparum thymidylate kinase (< i> Pf TMK) |
36 | Carbocyclic thymidine derivatives efficiently inhibit< i> Plasmodium falciparum thymidylate kinase (< i> Pf TMK) |
37 | Synthesis and biological properties of chemically modified siRNAs bearing 1-deoxy-d-ribofuranose in their 3?-overhang region |
38 | Synthesis and biological properties of chemically modified siRNAs bearing 1-deoxy-d-ribofuranose in their 3?-overhang region |
39 | Synthesis and biological properties of chemically modified siRNAs bearing 1-deoxy-d-ribofuranose in their 3?-overhang region |
40 | Synthesis and biological properties of chemically modified siRNAs bearing 1-deoxy-d-ribofuranose in their 3?-overhang region |
41 | Synthesis and biological properties of chemically modified siRNAs bearing 1-deoxy-d-ribofuranose in their 3?-overhang region |
42 | Computational analysis of siRNA recognition by the Ago2 PAZ domain and identification of the determinants of RNA-induced gene silencing |
43 | Computational analysis of siRNA recognition by the Ago2 PAZ domain and identification of the determinants of RNA-induced gene silencing |
44 | In silico molecular docking analysis of the human Argonaute 2 PAZ domain reveals insights into RNA interference |
45 | In silico molecular docking analysis of the human Argonaute 2 PAZ domain reveals insights into RNA interference |
46 | Thermodynamics and molecular bases of the interaction of ampicillin and streptomycin at their binding sites of bovine serum albumin |
47 | Thermodynamics and molecular bases of the interaction of ampicillin and streptomycin at their binding sites of bovine serum albumin |
48 | Thermodynamics and molecular bases of the interaction of ampicillin and streptomycin at their binding sites of bovine serum albumin |
49 | Thermodynamics and molecular bases of the interaction of ampicillin and streptomycin at their binding sites of bovine serum albumin |
50 | Thermodynamics and molecular bases of the interaction of ampicillin and streptomycin at their binding sites of bovine serum albumin |
51 | Thermodynamics and molecular bases of the interaction of ampicillin and streptomycin at their binding sites of bovine serum albumin |
52 | Efficacy of amprolium and toltrazuril in chicken with subclinical infection of cecal coccidiosis |
53 | Current and future asthma therapies. |
54 | Current and future asthma therapies. |
55 | Current and future asthma therapies. |
56 | Current and future asthma therapies. |
57 | Effect of Amlodipine and Trimetazidine on Gentamicin-Induced Nephrotoxicity in Rats |
58 | Effect of Amlodipine and Trimetazidine on Gentamicin-Induced Nephrotoxicity in Rats |
59 | Chelating efficiency and mechanisms of interaction of some toxic and biologically important cations with EDTA by isothermal titration calorimetry |
60 | Chelating efficiency and mechanisms of interaction of some toxic and biologically important cations with EDTA by isothermal titration calorimetry |
61 | Chelating efficiency and mechanisms of interaction of some toxic and biologically important cations with EDTA by isothermal titration calorimetry |
62 | Chelating efficiency and mechanisms of interaction of some toxic and biologically important cations with EDTA by isothermal titration calorimetry |
63 | Chelating efficiency and mechanisms of interaction of some toxic and biologically important cations with EDTA by isothermal titration calorimetry |
64 | Molecular dynamics and energetic perceptions of substrate recognition by thymidylate kinase |
65 | Molecular dynamics and energetic perceptions of substrate recognition by thymidylate kinase |
66 | Molecular dynamics and energetic perceptions of substrate recognition by thymidylate kinase |
67 | Molecular dynamics and energetic perceptions of substrate recognition by thymidylate kinase |
68 | Molecular dynamics and energetic perceptions of substrate recognition by thymidylate kinase |
69 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against< i> Plasmodium falciparum thymidylate kinase |
70 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against< i> Plasmodium falciparum thymidylate kinase |
71 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against< i> Plasmodium falciparum thymidylate kinase |
72 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against< i> Plasmodium falciparum thymidylate kinase |
73 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against< i> Plasmodium falciparum thymidylate kinase |
74 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against< i> Plasmodium falciparum thymidylate kinase |
75 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against< i> Plasmodium falciparum thymidylate kinase |
76 | Facile synthesis of 1?, 2?-< i> cis-$beta$-pyranosyladenine nucleosides |
77 | Facile synthesis of 1?, 2?-< i> cis-$beta$-pyranosyladenine nucleosides |
78 | Facile synthesis of 1?, 2?-< i> cis-$beta$-pyranosyladenine nucleosides |
79 | Facile synthesis of 1?, 2?-< i> cis-$beta$-pyranosyladenine nucleosides |
80 | Facile synthesis of 1?, 2?-< i> cis-$beta$-pyranosyladenine nucleosides |
81 | Bioinformatics analysis of the recent MERS-CoV with special reference to the virus-encoded Spike protein |
82 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against Plasmodium falciparum thymidylate kinase |
83 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against Plasmodium falciparum thymidylate kinase |
84 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against Plasmodium falciparum thymidylate kinase |
85 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against Plasmodium falciparum thymidylate kinase |
86 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against Plasmodium falciparum thymidylate kinase |
87 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against Plasmodium falciparum thymidylate kinase |
88 | Synthesis of carbocyclic pyrimidine nucleosides and their inhibitory activities against Plasmodium falciparum thymidylate kinase |