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A single early activation of invariant NK T cells confers long-term protection against collagen-induced arthritis in a ligand-specific manner
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- Journal Article
- A1
- open access
Rational design of 5'-thiourea-substituted α-thymidine analogues as thymidine monophosphate kinase inhibitors capable of inhibiting mycobacterial growth
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- Journal Article
- A1
- open access
Divergent strategy for the synthesis of α-aryl-substituted fosmidomycin analogues
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- Journal Article
- A1
- open access
Synthesis and evaluation of α,β-unsaturated α-aryl-substituted fosmidomycin analogues as DXR inhibitors
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Abnormal first trimester screen in partial deletion of chromosome 6p21: A case-report
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Molecular modeling of the human P2Y(2) receptor and design of a selective agonist, 2 '-amino-2 '-deoxy-2-thiouridine 5 '-triphosphate
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- Journal Article
- A1
- open access
Synthesis of α-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors
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- Journal Article
- A1
- open access
Synthesis and biological evaluation of cyclopropyl analogues of fosmidomycin as potent Plasmodium falciparum growth inhibitors
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- Journal Article
- A1
- open access
2-Triazole-substituted adenosines: a new class of selective A₃ adenosine receptor agonists, partial agonists, and antagonists
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- Journal Article
- A1
- open access
Synthesis of α-aryl-substituted and conformationally restricted fosmidomycin analogues as promising antimalarials