PRADIPSINH RATHOD

Summary

Affiliation: University of Washington
Country: USA

Publications

  1. ncbi DNA microarrays for malaria
    Pradipsinh K Rathod
    Dept of Chemistry, University of Washington, Seattle, WA 98195, USA
    Trends Parasitol 18:39-45. 2002
  2. ncbi A genetically hard-wired metabolic transcriptome in Plasmodium falciparum fails to mount protective responses to lethal antifolates
    Karthikeyan Ganesan
    Department of Chemistry and Global Health, University of Washington, Seattle, Washington, United States of America
    PLoS Pathog 4:e1000214. 2008
  3. ncbi Stochastic versus stable transcriptional differences on Plasmodium falciparum DNA microarrays
    Karthikeyan Ganesan
    Department of Chemistry, University of Washington, Seattle, WA 98105, USA
    Int J Parasitol 32:1543-50. 2002
  4. ncbi Resistance to a protein farnesyltransferase inhibitor in Plasmodium falciparum
    Richard T Eastman
    Department of Pathobiology, University of Washington, Seattle, Washington 98195, USA
    J Biol Chem 280:13554-9. 2005
  5. ncbi Resistance mutations at the lipid substrate binding site of Plasmodium falciparum protein farnesyltransferase
    Richard T Eastman
    Department of Pathobiology, University of Washington, Seattle, WA 98195 7185, USA
    Mol Biochem Parasitol 152:66-71. 2007
  6. ncbi Microfluidic modeling of cell-cell interactions in malaria pathogenesis
    Meher Antia
    Department of Chemistry, University of Washington, Seattle, Washington, United States of America
    PLoS Pathog 3:e99. 2007
  7. ncbi Regulatory hotspots in the malaria parasite genome dictate transcriptional variation
    JOSEPH M GONZALES
    The Eck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA
    PLoS Biol 6:e238. 2008
  8. ncbi Prized malaria drug target nailed
    Pradipsinh K Rathod
    Nat Struct Biol 10:316-8. 2003
  9. ncbi Histone acetyltransferase inhibitor anacardic acid causes changes in global gene expression during in vitro Plasmodium falciparum development
    Long Cui
    Department of Entomology, The Pennsylvania State University, 501 ASI Building, University Park, PA 16802, USA
    Eukaryot Cell 7:1200-10. 2008

Research Grants

  1. Microfluidic platforms for severe malaria
    PRADIPSINH RATHOD; Fiscal Year: 2007

Collaborators

  • M H Gelb
  • Zbynek Bozdech
  • Yongyuth Yuthavong
  • Xin Zhuan Su
  • Richard T Eastman
  • Karthikeyan Ganesan
  • John White
  • Lei Jiang
  • Napawan Ponmee
  • JOSEPH M GONZALES
  • Long Cui
  • Meher Antia
  • Kohei Yokoyama
  • Wesley C Van Voorhis
  • Oliver Hucke
  • Christophe L M J Verlinde
  • Asako Tan
  • Tetsuya Furuya
  • Jun Miao
  • Liwang Cui
  • Stefan Wuchty
  • Steven P Maher
  • Jigar J Patel
  • Qi Fan
  • Sumalee Kamchonwongpaisan
  • Michael T Ferdig
  • Xinyi Li
  • Joseph W Fowble
  • Prapon Wilairat
  • Michael A Hast
  • Thurston Herricks
  • Lorena S Beese
  • Kevin Bauer
  • Laxman Nallan
  • Debopam Chakrabarti

Detail Information

Publications9

  1. ncbi DNA microarrays for malaria
    Pradipsinh K Rathod
    Dept of Chemistry, University of Washington, Seattle, WA 98195, USA
    Trends Parasitol 18:39-45. 2002
    ....
  2. ncbi A genetically hard-wired metabolic transcriptome in Plasmodium falciparum fails to mount protective responses to lethal antifolates
    Karthikeyan Ganesan
    Department of Chemistry and Global Health, University of Washington, Seattle, Washington, United States of America
    PLoS Pathog 4:e1000214. 2008
    ..In addition, such regulation affects how DNA microarrays are used to understand the mode of action of antimetabolites...
  3. ncbi Stochastic versus stable transcriptional differences on Plasmodium falciparum DNA microarrays
    Karthikeyan Ganesan
    Department of Chemistry, University of Washington, Seattle, WA 98105, USA
    Int J Parasitol 32:1543-50. 2002
    ..Reliable RNA transcriptional differences between Dd2 and HB3 could be readily visualised using public algorithms for data normalisation and clustering...
  4. ncbi Resistance to a protein farnesyltransferase inhibitor in Plasmodium falciparum
    Richard T Eastman
    Department of Pathobiology, University of Washington, Seattle, Washington 98195, USA
    J Biol Chem 280:13554-9. 2005
    ..These data are consistent with PFT as the target of BMS-388891 in P. falciparum and suggest that PFT inhibitors should be combined with other antimalarial agents for effective therapy...
  5. ncbi Resistance mutations at the lipid substrate binding site of Plasmodium falciparum protein farnesyltransferase
    Richard T Eastman
    Department of Pathobiology, University of Washington, Seattle, WA 98195 7185, USA
    Mol Biochem Parasitol 152:66-71. 2007
    ..These data provide further support that PFT is the target of THQ inhibitors in P. falciparum and suggest that PFT inhibitors should be combined with other antimalarial agents to minimize the development of resistant parasites...
  6. ncbi Microfluidic modeling of cell-cell interactions in malaria pathogenesis
    Meher Antia
    Department of Chemistry, University of Washington, Seattle, Washington, United States of America
    PLoS Pathog 3:e99. 2007
    ..The devices are cheap and portable and require small sample volumes; thus, they have the potential to be widely used in research laboratories and at field sites with access to fresh patient samples...
  7. ncbi Regulatory hotspots in the malaria parasite genome dictate transcriptional variation
    JOSEPH M GONZALES
    The Eck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, Indiana, USA
    PLoS Biol 6:e238. 2008
    ....
  8. ncbi Prized malaria drug target nailed
    Pradipsinh K Rathod
    Nat Struct Biol 10:316-8. 2003
  9. ncbi Histone acetyltransferase inhibitor anacardic acid causes changes in global gene expression during in vitro Plasmodium falciparum development
    Long Cui
    Department of Entomology, The Pennsylvania State University, 501 ASI Building, University Park, PA 16802, USA
    Eukaryot Cell 7:1200-10. 2008
    ..This study suggests that the parasiticidal effect of AA is at least partially associated with its inhibition of PfGCN5 HAT, resulting in the disturbance of the transcription program in the parasites...

Research Grants11

  1. Microfluidic platforms for severe malaria
    PRADIPSINH RATHOD; Fiscal Year: 2007
    ..2.3. Develop a model to study pitting in obstructed capillaries. In the future, the devices developed here may also find utility in studying adhesion and natural immunity in malaria, and in control of other infectious diseases. ..