Marisol Ocampo

Monitoring the chromosome 2 intraerythrocytic transcriptome of Plasmodium falciparum using oligonucleotide arrays.

Prospects for prophylactic and therapeutic vaccines against the hepatitis C viruses

Stimuli-responsive nanocarriers for drug delivery

The Transcriptome of the Intraerythrocytic Developmental Cycle of Plasmodium falciparum

Delivery of siRNA mediated by histidine-containing reducible polycations

Ralph F. Hirschmann award address 2009: Merger of organic chemistry with peptide diversity

Structure and Function of the Hepatitis C Virus Envelope Glycoproteins E1 and E2: Antiviral and Vaccine Targets

Degradable Controlled-Release Polymers and Polymeric Nanoparticles: Mechanisms of Controlling Drug Release

Studying Hepatitis C Virus: Making the Best of a Bad Virus

Human Monoclonal Antibody to Hepatitis C Virus E1 Glycoprotein That Blocks Virus Attachment and Viral Infectivity

Versatile Peptide C-Terminal Functionalization via a Computationally Engineered Peptide Amidase

Peptide synthesis: chemical or enzymatic

One‐Step C‐Terminal Deprotection and Activation of Peptides with Peptide Amidase from Stenotrophomonas maltophilia in Neat Organic Solvent

Interaction of Hepatitis C Virus-Like Particles and Cells: a Model System for Studying Viral Binding and Entry

Mapping the anatomy of a Plasmodium falciparum MSP-1 epitope using pseudopeptide-induced mono- and polyclonal antibodies and CD and NMR conformation analysis

Plasmodium falciparum circumsporozoite (CS) protein peptides specifically bind to HepG2 cells

Hepatitis C virus (HCV) E1 and E2 protein regions that specifically bind to HepG2 cells

Two MSA 2 peptides that bind to human red blood cells are relevant to Plasmodium falciparum merozoite invasion