J. Goldring

发表

Oligopeptidase B: a processing peptidase involved in pathogenesis.

J. D. Goldring, T. Coetzer, Laura. Huson, 2008, Biochimie.

Concentrating Proteins by Salt, Polyethylene Glycol, Solvent, SDS Precipitation, Three-Phase Partitioning, Dialysis, Centrifugation, Ultrafiltration, Lyophilization, Affinity Chromatography, Immunoprecipitation or Increased Temperature for Protein Isolation, Drug Interaction, and Proteomic and Pepti

J. D. Goldring, J. Goldring, J. P. Dean Goldring, 2018, Methods in molecular biology.

PfPK7, an atypical MEK‐related protein kinase, reflects the absence of classical three‐component MAPK pathways in the human malaria parasite Plasmodium falciparum

D. Chakrabarti, Shelley Patterson, Christina M. Whittle, 2004, Molecular microbiology.

Plasmodium glyceraldehyde-3-phosphate dehydrogenase: A potential malaria diagnostic target.

Jude M. Przyborski, J. Przyborski, T. Coetzer, 2017, Experimental parasitology.

Comparing Antibody Responses in Chickens Against Plasmodium falciparum Lactate Dehydrogenase and Glyceraldehyde-3-phosphate Dehydrogenase with Freund’s and Pheroid® Adjuvants

J. D. Goldring, A. Grobler, R. G. Krause, 2015, Immunological investigations.

Evaluation of immunotherapy to reverse sequestration in the treatment of severe Plasmodium falciparum malaria

J. D. Goldring, J. Goldring, 2004, Immunology and cell biology.

A Plasmodium falciparum copper-binding membrane protein with copper transport motifs

J. Przyborski, David L Choveaux, J. D. Goldring, 2012, Malaria Journal.

A novel protein kinase family in Plasmodium falciparum is differentially transcribed and secreted to various cellular compartments of the host cell

M. Nunes, A. Scherf, C. Doerig, 2007, Molecular microbiology.

Plasmodium falciparum malaria: rosettes are disrupted by quinine, artemisinin, mefloquine, primaquine, pyrimethamine, chloroquine and proguanil.

I. Ismail, T. Padayachee, J. D. Goldring, 1999, Memorias do Instituto Oswaldo Cruz.

Antimalarial drugs modulate the expression of monocyte receptors.

J. Goldring, S. Nemaorani, J. Goldring, 1999, International journal of immunopharmacology.

Phosphoethanolamine-N-methyltransferase is a potential biomarker for the diagnosis of P. knowlesi and P. falciparum malaria

J. D. Goldring, R. G. Krause, J. Goldring, 2018, PloS one.

Expression and copper binding characteristics of Plasmodium falciparum cytochrome c oxidase assembly factor 11, Cox11

J. D. Goldring, A. Salman, J. Goldring, 2022, Malaria journal.

Identification and initial characterisation of a Plasmodium falciparum Cox17 copper metallochaperone.

J. Przyborski, David L Choveaux, J. D. Goldring, 2015, Experimental parasitology.

Plasmodium falciparum: effect of antimalarial drugs, malaria pigment (β-haematin) and Plasmodium falciparum lysate on monocyte GTP-cyclohydrolase 1 gene expression.

J. D. Goldring, G. Watson, Bridgette M. Cumming, 2011, Experimental parasitology.

Monocyte phagocytosis of malaria β-haematin in the presence of artemisinin, amodiaquine, chloroquine, doxycycline, primaquine, pyrimethamine and quinine.

J. D. Goldring, Bridgette M. Cumming, J. Goldring, 2019, Experimental parasitology.

Plasmodium falciparum: diversity of isolates from Malawi in their cytoadherence to melanoma cells and monocytes in vitro

M. Molyneux, J. Wirima, T. Taylor, 1992, British journal of haematology.

Raising Antibodies in Chickens Against Primaquine, Pyrimethamine, Dapsone, Tetracycline, and Doxycycline

C. Thobakgale, T. Coetzer, J. D. Goldring, 2005, Immunological investigations.

Towards development of aptamers that specifically bind to lactate dehydrogenase of Plasmodium falciparum through epitopic targeting

Meesbah Jiwaji, J. D. Goldring, M. Khati, 2018, Malaria Journal.