J. Barale

发表

A Key Role for Plasmodium Subtilisin-like SUB1 Protease in Egress of Malaria Parasites from Host Hepatocytes*

S. Thiberge, R. Ménard, C. Lacroix, 2013, The Journal of Biological Chemistry.

A molecular marker of artemisinin-resistant Plasmodium falciparum malaria

B. Genton, Saorin Kim, N. Khim, 2013, Nature.

In Silico Screening on the Three-dimensional Model of the Plasmodium vivax SUB1 Protease Leads to the Validation of a Novel Anti-parasite Compound*

M. Nilges, D. Giganti, D. Ménard, 2013, The Journal of Biological Chemistry.

Screening and evaluation of inhibitors of Plasmodium falciparum merozoite egress and invasion using cytometry.

O. Mercereau‐Puijalon, O. Gorgette, J. Barale, 2012, Methods in molecular biology.

Mammalian subtilisin/kexin isozyme SKI-1: A widely expressed proprotein convertase with a unique cleavage specificity and cellular localization.

N. Seidah, R. A. Murphy, M. Marcinkiewicz, 1999, Proceedings of the National Academy of Sciences of the United States of America.

A surrogate marker of piperaquine-resistant Plasmodium falciparum malaria: a phenotype–genotype association study

D. Fidock, L. Ross, E. Legrand, 2017, The Lancet. Infectious diseases.

The LIM homeobox protein mLIM3/Lhx3 induces expression of the prolactin gene by a Pit‐1/GHF‐1‐independent pathway in corticotroph AtT20 cells

N. Seidah, S. Girardin, S. Benjannet, 1998, FEBS letters.

the Validation of a Novel Anti-parasite Plasmodium vivax SUB1 Protease Leads to Three-dimensional Model of the In Silico Screening on the Computational Biology:

M. Nilges, D. Giganti, D. Ménard, 2013 .

Gene targeting demonstrates that the Plasmodium berghei subtilisin PbSUB2 is essential for red cell invasion and reveals spontaneous genetic recombination events

C. Janse, A. Waters, P. Uzureau, 2004, Cellular microbiology.

Artemisinin-independent inhibitory activity of Artemisia sp. infusions against different Plasmodium stages including relapse-causing hypnozoites

T. Bousema, G. van Gemert, G. Snounou, 2021, Life Science Alliance.

Human peroxiredoxin 6 is essential for malaria parasites and provides a host-based drug target

Zbynek Bozdech, S. Rahlfs, L. Touqui, 2022, bioRxiv.

Computational Design of Protein-Based Inhibitors of Plasmodium vivax Subtilisin-Like 1 Protease

M. Nilges, D. Le-Nguyen, J. Barale, 2014, PloS one.

CyProQuant-PCR: a real time RT-PCR technique for profiling human cytokines, based on external RNA standards, readily automatable for clinical use

D. Jublot, O. Mercereau‐Puijalon, I. Vigan-Womas, 2005, BMC Immunology.

Malarial proteases: assignment of function to activity.

W. Mangel, G. Langsley, J. Barale, 1991, Research in immunology.

The C-terminal domain of RNA polymerase II of the malaria parasite Plasmodium berghei.

G. Langsley, J. Barale, A. Cornelissen, 1991, Biochemical and biophysical research communications.

Trypanosoma cruzi proline racemases are involved in parasite differentiation and infectivity

W. Degrave, P. Minoprio, N. Chamond, 2005, Molecular microbiology.

Cytometric measurement of in vitro inhibition of Plasmodium falciparum field isolates by drugs: a new approach for re-invasion inhibition study

J. Barale, D. Aldebert, R. Jambou, 2014, Malaria Journal.

Plasmodium falciparum subtilisin-like protease 2, a merozoite candidate for the merozoite surface protein 1-42 maturase.

P. Alzari, G. Langsley, J. Barale, 1999, Proceedings of the National Academy of Sciences of the United States of America.

A Worldwide Map of Plasmodium falciparum K13-Propeller Polymorphisms.

C. Rogier, D. Fidock, B. Pradines, 2016, The New England journal of medicine.

Three multigene families in Plasmodium parasites: facts and questions.

E. Bischoff, O. Mercereau‐Puijalon, J. Barale, 2002, International journal for parasitology.

Pfsbp1, a Maurer's cleft Plasmodium falciparum protein, is associated with the erythrocyte skeleton.

D. Mattei, P. Uzureau, J. Barale, 2000, Molecular and biochemical parasitology.

Drug inhibition of HDAC3 and epigenetic control of differentiation in Apicomplexa parasites

P. Baldacci, R. Ménard, A. Bougdour, 2009, The Journal of experimental medicine.

Whole Pichia pastoris Yeast Expressing Measles Virus Nucleoprotein as a Production and Delivery System to Multimerize Plasmodium Antigens

R. Ménard, F. Tangy, G. Péhau-Arnaudet, 2014, PloS one.

Reduced Artemisinin Susceptibility of Plasmodium falciparum Ring Stages in Western Cambodia

Saorin Kim, N. Khim, D. Ménard, 2012, Antimicrobial Agents and Chemotherapy.

The mouse homeoprotein mLIM-3 is expressed early in cells derived from the neuroepithelium and persists in adult pituitary.

M. Marcinkiewicz, M. Chrétien, M. Mattei, 1994, DNA and cell biology.

FLP/FRT-mediated conditional mutagenesis in pre-erythrocytic stages of Plasmodium berghei

S. Thiberge, R. Ménard, C. Lacroix, 2011, Nature Protocols.

A small-molecule cell-based screen led to the identification of biphenylimidazoazines with highly potent and broad-spectrum anti-apicomplexan activity.

F. Brossier, O. Gorgette, J. Barale, 2015, European journal of medicinal chemistry.

Isolation from a Plasmodium chabaudi chromosome 7 specific library of a novel gene encoding a protein with multiple GGMP repeats homologous to hsp70.

G. Langsley, D. Mattei, J. Barale, 1993, Molecular and biochemical parasitology (Print).

Computational Reverse-Engineering of a Spider-Venom Derived Peptide Active Against Plasmodium falciparum SUB1

Michael Nilges, M. Nilges, D. Le-Nguyen, 2011, PloS one.

Western Cambodia Plasmodium falciparum Ring Stages in Reduced Artemisinin Susceptibility of

Saorin Kim, N. Khim, P. Ringwald, 2013 .

Plasmodium falciparum AARP1, a giant protein containing repeated motifs rich in asparagine and aspartate residues, is associated with the infected erythrocyte membrane

G. Langsley, P. Dehoux, L. H. Pereira da Silva, 1997, Infection and immunity.

On the Knorr Synthesis of 6-Bromo-4-methylquinolin-2(1H)-one

M. Delepierre, J. Barale, C. Simenel, 2011 .

A novel Plasmodium-specific prodomain fold regulates the malaria drug target SUB1 subtilase

P. Alzari, D. Giganti, Jean‐François Hernandez, 2014, Nature Communications.

Prevalence and characterization of piperaquine, mefloquine and artemisinin derivatives triple-resistant Plasmodium falciparum in Cambodia

Saorin Kim, N. Khim, P. Ringwald, 2022, The Journal of antimicrobial chemotherapy.

In vitro activity of ferroquine against artemisinin-based combination therapy (ACT)-resistant Plasmodium falciparum isolates from Cambodia.

D. Leboulleux, D. Leroy, Saorin Kim, 2019, The Journal of antimicrobial chemotherapy.

Plasmodium falciparum asparagine and aspartate rich protein 2 is an evolutionary conserved protein whose repeats identify a new family of parasite antigens.

G. Langsley, L. H. Pereira da Silva, J. Barale, 1997, Molecular and biochemical parasitology.

LANCL1, an erythrocyte protein recruited to the Maurer's clefts during Plasmodium falciparum development.

A. Namane, J. Barale, T. Blisnick, 2005, Molecular and biochemical parasitology.

Plasmodium chabaudi p68 serine protease activity required for merozoite entry into mouse erythrocytes.

G. Langsley, T. Rabilloud, L. H. Pereira da Silva, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Reduced artemisinin susceptibility of Plasmodium falciparum ring

Saorin Kim, N. Khim, D. Ménard, 2012 .

Prodomain-driven enzyme dimerization, a potent pH-dependent autoinhibition mechanism to control Plasmodium Sub1 subtilisin-like activity prior to prime merozoite egress

P. Alzari, B. Raynal, A. Haouz, 2023, bioRxiv.

A Plasmodium falciparum gene coding for a 15-kilodalton antigen expressed in asexual stage parasites, gametocytes and gametes.

D. Kaslow, T. Ponnudurai, G. Langsley, 1992, Molecular and biochemical parasitology.

Compound the Validation of a Novel Anti-parasite SUB 1 Protease Leads to Plasmodium vivax Three-dimensional Model of the Screening on the In Silico Computational Biology :

M. Nilges, D. Giganti, D. Ménard, 2013 .

A novel Plasmodium-specific prodomain fold regulates the malaria drug target SUB1 subtilase

P. Alzari, D. Giganti, Jean‐François Hernandez, 2014, Nature Communications.

Insights from structure-activity relationships and the binding mode of peptidic α-ketoamide inhibitors of the malaria drug target subtilisin-like SUB1.

A. Haouz, J. Barale, Anthony Bouillon, 2024, European journal of medicinal chemistry.