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429 results on '"Ferdig, Michael T"'

1. Chloroquine resistance evolution in Plasmodium falciparum is mediated by the putative amino acid transporter AAT1

Author

Amambua-Ngwa, Alfred, Button-Simons, Katrina A., Li, Xue, Kumar, Sudhir, Brenneman, Katelyn Vendrely, Ferrari, Marco, Checkley, Lisa A., Haile, Meseret T., Shoue, Douglas A., McDew-White, Marina, Tindall, Sarah M., Reyes, Ann, Delgado, Elizabeth, Dalhoff, Haley, Larbalestier, James K., Amato, Roberto, Pearson, Richard D., Taylor, Alexander B., Nosten, François H., D’Alessandro, Umberto, Kwiatkowski, Dominic, Cheeseman, Ian H., Kappe, Stefan H. I., Avery, Simon V., Conway, David J., Vaughan, Ashley M., Ferdig, Michael T., and Anderson, Timothy J. C.

Published
2023
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6. Open Source Drug Discovery with the Malaria Box Compound Collection for Neglected Diseases and Beyond.

Author

Van Voorhis, Wesley C, Adams, John H, Adelfio, Roberto, Ahyong, Vida, Akabas, Myles H, Alano, Pietro, Alday, Aintzane, Alemán Resto, Yesmalie, Alsibaee, Aishah, Alzualde, Ainhoa, Andrews, Katherine T, Avery, Simon V, Avery, Vicky M, Ayong, Lawrence, Baker, Mark, Baker, Stephen, Ben Mamoun, Choukri, Bhatia, Sangeeta, Bickle, Quentin, Bounaadja, Lotfi, Bowling, Tana, Bosch, Jürgen, Boucher, Lauren E, Boyom, Fabrice F, Brea, Jose, Brennan, Marian, Burton, Audrey, Caffrey, Conor R, Camarda, Grazia, Carrasquilla, Manuela, Carter, Dee, Belen Cassera, Maria, Chih-Chien Cheng, Ken, Chindaudomsate, Worathad, Chubb, Anthony, Colon, Beatrice L, Colón-López, Daisy D, Corbett, Yolanda, Crowther, Gregory J, Cowan, Noemi, D'Alessandro, Sarah, Le Dang, Na, Delves, Michael, DeRisi, Joseph L, Du, Alan Y, Duffy, Sandra, Abd El-Salam El-Sayed, Shimaa, Ferdig, Michael T, Fernández Robledo, José A, Fidock, David A, Florent, Isabelle, Fokou, Patrick VT, Galstian, Ani, Gamo, Francisco Javier, Gokool, Suzanne, Gold, Ben, Golub, Todd, Goldgof, Gregory M, Guha, Rajarshi, Guiguemde, W Armand, Gural, Nil, Guy, R Kiplin, Hansen, Michael AE, Hanson, Kirsten K, Hemphill, Andrew, Hooft van Huijsduijnen, Rob, Horii, Takaaki, Horrocks, Paul, Hughes, Tyler B, Huston, Christopher, Igarashi, Ikuo, Ingram-Sieber, Katrin, Itoe, Maurice A, Jadhav, Ajit, Naranuntarat Jensen, Amornrat, Jensen, Laran T, Jiang, Rays HY, Kaiser, Annette, Keiser, Jennifer, Ketas, Thomas, Kicka, Sebastien, Kim, Sunyoung, Kirk, Kiaran, Kumar, Vidya P, Kyle, Dennis E, Lafuente, Maria Jose, Landfear, Scott, Lee, Nathan, Lee, Sukjun, Lehane, Adele M, Li, Fengwu, Little, David, Liu, Liqiong, Llinás, Manuel, Loza, Maria I, Lubar, Aristea, Lucantoni, Leonardo, Lucet, Isabelle, and Maes, Louis

Subjects
Humans, Malaria, Antimalarials, Drug Evaluation, Preclinical, Small Molecule Libraries, Drug Discovery, Neglected Diseases, Datasets as Topic, Drug Evaluation, Preclinical, Virology, Microbiology, Immunology, Medical Microbiology
Abstract

A major cause of the paucity of new starting points for drug discovery is the lack of interaction between academia and industry. Much of the global resource in biology is present in universities, whereas the focus of medicinal chemistry is still largely within industry. Open source drug discovery, with sharing of information, is clearly a first step towards overcoming this gap. But the interface could especially be bridged through a scale-up of open sharing of physical compounds, which would accelerate the finding of new starting points for drug discovery. The Medicines for Malaria Venture Malaria Box is a collection of over 400 compounds representing families of structures identified in phenotypic screens of pharmaceutical and academic libraries against the Plasmodium falciparum malaria parasite. The set has now been distributed to almost 200 research groups globally in the last two years, with the only stipulation that information from the screens is deposited in the public domain. This paper reports for the first time on 236 screens that have been carried out against the Malaria Box and compares these results with 55 assays that were previously published, in a format that allows a meta-analysis of the combined dataset. The combined biochemical and cellular assays presented here suggest mechanisms of action for 135 (34%) of the compounds active in killing multiple life-cycle stages of the malaria parasite, including asexual blood, liver, gametocyte, gametes and insect ookinete stages. In addition, many compounds demonstrated activity against other pathogens, showing hits in assays with 16 protozoa, 7 helminths, 9 bacterial and mycobacterial species, the dengue fever mosquito vector, and the NCI60 human cancer cell line panel of 60 human tumor cell lines. Toxicological, pharmacokinetic and metabolic properties were collected on all the compounds, assisting in the selection of the most promising candidates for murine proof-of-concept experiments and medicinal chemistry programs. The data for all of these assays are presented and analyzed to show how outstanding leads for many indications can be selected. These results reveal the immense potential for translating the dispersed expertise in biological assays involving human pathogens into drug discovery starting points, by providing open access to new families of molecules, and emphasize how a small additional investment made to help acquire and distribute compounds, and sharing the data, can catalyze drug discovery for dozens of different indications. Another lesson is that when multiple screens from different groups are run on the same library, results can be integrated quickly to select the most valuable starting points for subsequent medicinal chemistry efforts.

Published
2016

7. The power and promise of genetic mapping from Plasmodium falciparum crosses utilizing human liver-chimeric mice

Author

Button-Simons, Katrina A., Kumar, Sudhir, Carmago, Nelly, Haile, Meseret T., Jett, Catherine, Checkley, Lisa A., Kennedy, Spencer Y., Pinapati, Richard S., Shoue, Douglas A., McDew-White, Marina, Li, Xue, Nosten, François H., Kappe, Stefan H., Anderson, Timothy J. C., Romero-Severson, Jeanne, Ferdig, Michael T., Emrich, Scott J., Vaughan, Ashley M., and Cheeseman, Ian H.

Published
2021
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9. An apicoplast localized ubiquitylation system is required for the import of nuclear-encoded plastid proteins.

Author

Agrawal, Swati, Chung, Duk-Won D, Ponts, Nadia, van Dooren, Giel G, Prudhomme, Jacques, Brooks, Carrie F, Rodrigues, Elisadra M, Tan, John C, Ferdig, Michael T, Striepen, Boris, and Le Roch, Karine G

Subjects
Cell Line, Humans, Toxoplasma, Plasmodium falciparum, Proteasome Endopeptidase Complex, Protozoan Proteins, Protein Transport, Ubiquitination, Chloroplast Proteins, Endoplasmic Reticulum-Associated Degradation, Virology, Microbiology, Immunology, Medical Microbiology
Abstract

Apicomplexan parasites are responsible for numerous important human diseases including toxoplasmosis, cryptosporidiosis, and most importantly malaria. There is a constant need for new antimalarials, and one of most keenly pursued drug targets is an ancient algal endosymbiont, the apicoplast. The apicoplast is essential for parasite survival, and several aspects of its metabolism and maintenance have been validated as targets of anti-parasitic drug treatment. Most apicoplast proteins are nuclear encoded and have to be imported into the organelle. Recently, a protein translocon typically required for endoplasmic reticulum associated protein degradation (ERAD) has been proposed to act in apicoplast protein import. Here, we show ubiquitylation to be a conserved and essential component of this process. We identify apicoplast localized ubiquitin activating, conjugating and ligating enzymes in Toxoplasma gondii and Plasmodium falciparum and observe biochemical activity by in vitro reconstitution. Using conditional gene ablation and complementation analysis we link this activity to apicoplast protein import and parasite survival. Our studies suggest ubiquitylation to be a mechanistic requirement of apicoplast protein import independent to the proteasomal degradation pathway.

Published
2013

11. Leveraging crowdsourcing to accelerate global health solutions

Author

Davis, Sage, Button-Simons, Katrina, Bensellak, Taoufik, Ahsen, Eren Mehmet, Checkley, Lisa, Foster, Gabriel J., Su, Xinzhuan, Moussa, Ahmed, Mapiye, Darlington, Khoo, Sok Kean, Nosten, Francois, Anderson, Timothy J. C., Vendrely, Katelyn, Bletz, Julie, Yu, Thomas, Panji, Sumir, Ghouila, Amel, Mulder, Nicola, Norman, Thea, Kern, Steven, Meyer, Pablo, Stolovitzky, Gustavo, Ferdig, Michael T., and Siwo, Geoffrey H.

Published
2019
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12. APlasmodium falciparumgenetic cross reveals the contributions ofpfcrtandplasmepsin II/IIIto piperaquine drug resistance

Author

Kane, John, primary, Li, Xue, additional, Kumar, Sudhir, additional, Button-Simons, Katrina A., additional, Vendrely Brenneman, Katelyn M., additional, Dahlhoff, Haley, additional, Sievert, Mackenzie A.C., additional, Checkley, Lisa A., additional, Shoue, Douglas A., additional, Singh, Puspendra P., additional, Abatiyow, Biley A., additional, Haile, Meseret T., additional, Nair, Shalini, additional, Reyes, Ann, additional, Tripura, Rupam, additional, Peto, Tom, additional, Lek, Dysoley, additional, Kappe, Stefan H.I., additional, Dhorda, Mehul, additional, Nkhoma, Standwell C, additional, Cheeseman, Ian H., additional, Vaughan, Ashley M., additional, Anderson, Timothy J. C., additional, and Ferdig, Michael T., additional

Published
2023
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15. Chemogenomic Profiling of a Plasmodium falciparum Transposon Mutant Library Reveals Shared Effects of Dihydroartemisinin and Bortezomib on Lipid Metabolism and Exported Proteins

Author

Pires, Camilla Valente, primary, Oberstaller, Jenna, additional, Wang, Chengqi, additional, Casandra, Debora, additional, Zhang, Min, additional, Chawla, Jyotsna, additional, Adapa, Swamy Rakesh, additional, Otto, Thomas D., additional, Ferdig, Michael T., additional, Rayner, Julian C., additional, Jiang, Rays H. Y., additional, and Adams, John H., additional

Published
2023
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16. Independent Emergence of Artemisinin Resistance Mutations Among Plasmodium falciparum in Southeast Asia

Author

Takala-Harrison, Shannon, Jacob, Christopher G., Arze, Cesar, Cummings, Michael P., Silva, Joana C., Dondorp, Arjen M., Fukuda, Mark M., Hien, Tran Tinh, Mayxay, Mayfong, Noedl, Harald, Nosten, Francois, Kyaw, Myat P., Nhien, Nguyen Thanh Thuy, Imwong, Mallika, Bethell, Delia, Se, Youry, Lon, Chanthap, Tyner, Stuart D., Saunders, David L., Ariey, Frederic, Mercereau-Puijalon, Odile, Menard, Didier, Newton, Paul N., Khanthavong, Maniphone, Hongvanthong, Bouasy, Starzengruber, Peter, Fuehrer, Hans-Peter, Swoboda, Paul, Khan, Wasif A., Phyo, Aung Pyae, Nyunt, Myaing M., Nyunt, Myat H., Brown, Tyler S., Adams, Matthew, Pepin, Christopher S., Bailey, Jason, Tan, John C., Ferdig, Michael T., Clark, Taane G., Miotto, Olivo, MacInnis, Bronwyn, Kwiatkowski, Dominic P., White, Nicholas J., Ringwald, Pascal, and Plowe, Christopher V.

Published
2015

18. A Major Genome Region Underlying Artemisinin Resistance in Malaria

Author

Cheeseman, Ian H., Miller, Becky A., Nair, Shalini, Nkhoma, Standwell, Tan, Asako, Tan, John C., Saai, Salma Al, Phyo, Aung Pyae, Moo, Carit Ler, Lwin, Khin Maung, McGready, Rose, Ashley, Elizabeth, Imwong, Mallika, Stepniewska, Kasia, Yi, Poravuth, Dondorp, Arjen M., Mayxay, Mayfong, Newton, Paul N., White, Nicholas J., Nosten, François, Ferdig, Michael T., and Anderson, Timothy J. C.

Published
2012
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19. A Malaria Parasite Cross Reveals Genetic Determinants of Plasmodium falciparum Growth in Different Culture Media

Author

Kumar, Sudhir, primary, Li, Xue, additional, McDew-White, Marina, additional, Reyes, Ann, additional, Delgado, Elizabeth, additional, Sayeed, Abeer, additional, Haile, Meseret T., additional, Abatiyow, Biley A., additional, Kennedy, Spencer Y., additional, Camargo, Nelly, additional, Checkley, Lisa A., additional, Brenneman, Katelyn V., additional, Button-Simons, Katrina A., additional, Duraisingh, Manoj T., additional, Cheeseman, Ian H., additional, Kappe, Stefan H. I., additional, Nosten, François, additional, Ferdig, Michael T., additional, Vaughan, Ashley M., additional, and Anderson, Tim J. C., additional

Published
2022
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20. An amino acid transporter AAT1 plays a pivotal role in chloroquine resistance evolution in malaria parasites

Author

Amambua-Ngwa, Alfred, primary, Button-Simons, Katrina A., additional, Li, Xue, additional, Kumar, Sudhir, additional, Brenneman, Katelyn Vendrely, additional, Ferrari, Marco, additional, Checkley, Lisa A., additional, Haile, Meseret T., additional, Shoue, Douglas A., additional, McDew-White, Marina, additional, Tindall, Sarah M., additional, Reyes, Ann, additional, Delgado, Elizabeth, additional, Dalhoff, Haley, additional, Larbalestier, James K., additional, Amato, Roberto, additional, Pearson, Richard D., additional, Taylor, Alexander B., additional, Nosten, François H., additional, D’Alessandro, Umberto, additional, Kwiatkowski, Dominic, additional, Cheeseman, Ian H., additional, Kappe, Stefan H. I., additional, Avery, Simon V., additional, Conway, David J., additional, Vaughan, Ashley M., additional, Ferdig, Michael T., additional, and Anderson, Timothy J. C., additional

Published
2022
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22. Optimizing bulk segregant analysis of drug resistance using Plasmodium falciparum genetic crosses conducted in humanized mice

Author

Brenneman, Katelyn Vendrely, primary, Li, Xue, additional, Kumar, Sudhir, additional, Delgado, Elizabeth, additional, Checkley, Lisa A., additional, Shoue, Douglas A., additional, Reyes, Ann, additional, Abatiyow, Biley A., additional, Haile, Meseret T., additional, Tripura, Rupam, additional, Peto, Tom, additional, Lek, Dysoley, additional, Button-Simons, Katrina A., additional, Kappe, Stefan H.I., additional, Dhorda, Mehul, additional, Nosten, François, additional, Nkhoma, Standwell C., additional, Cheeseman, Ian H., additional, Vaughan, Ashley M., additional, Ferdig, Michael T., additional, and Anderson, Tim J.C., additional

Published
2022
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24. Additional file 2 of Cyclical regression covariates remove the major confounding effect of cyclical developmental gene expression with strain-specific drug response in the malaria parasite Plasmodium falciparum

Author

Foster, Gabriel J., Sievert, Mackenzie A. C., Button-Simons, Katrina, Vendrely, Katelyn M., Romero-Severson, Jeanne, and Ferdig, Michael T.

Subjects
Data_GENERAL
Abstract

Additional file 2. Provides quality control comparisons between our curation and analysis of the Mok et al. data and the originally published results.

Published
2022
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25. Optimizing bulk segregant analysis of drug resistance using Plasmodium falciparum genetic crosses conducted in humanized mice

Author

Brenneman, Katelyn Vendrely, primary, Li, Xue, additional, Kumar, Sudhir, additional, Delgado, Elizabeth, additional, Checkley, Lisa A., additional, Shoue, Douglas A., additional, Reyes, Ann, additional, Abatiyow, Biley, additional, Haile, Meseret, additional, Tripura, Rupam, additional, Peto, Tom, additional, Lek, Dysoley, additional, Button-Simons, Katrina A., additional, Kappe, Stefan H.I., additional, Dhorda, Mehul, additional, Nosten, Francois, additional, Nkhoma, Standwell C., additional, Cheeseman, Ian H, additional, Vaughan, Ashley M, additional, Ferdig, Michael T, additional, and Anderson, Tim JC, additional

Published
2021
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29. Analysis of Plasmodium falciparum diversity in natural infections by deep sequencing

Author

Manske, Magnus, Miotto, Olivo, Campino, Susana, Auburn, Sarah, Almagro-Garcia, Jacob, Maslen, Gareth, O’Brien, Jack, Djimde, Abdoulaye, Doumbo, Ogobara, Zongo, Issaka, Ouedraogo, Jean-Bosco, Michon, Pascal, Mueller, Ivo, Siba, Peter, Nzila, Alexis, Borrmann, Steffen, Kiara, Steven M., Marsh, Kevin, Jiang, Hongying, Su, Xin-Zhuan, Amaratunga, Chanaki, Fairhurst, Rick, Socheat, Duong, Nosten, Francois, Imwong, Mallika, White, Nicholas J., Sanders, Mandy, Anastasi, Elisa, Alcock, Dan, Drury, Eleanor, Oyola, Samuel, Quail, Michael A., Turner, Daniel J., Ruano-Rubio, Valentin, Jyothi, Dushyanth, Amenga-Etego, Lucas, Hubbart, Christina, Jeffreys, Anna, Rowlands, Kate, Sutherland, Colin, Roper, Cally, Mangano, Valentina, Modiano, David, Tan, John C., Ferdig, Michael T., Amambua-Ngwa, Alfred, Conway, David J., Takala-Harrison, Shannon, Plowe, Christopher V., Rayner, Julian C., Rockett, Kirk A., Clark, Taane G., Newbold, Chris I., Berriman, Matthew, MacInnis, Bronwyn, and Kwiatkowski, Dominic P.

Published
2012
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31. Additional file 2 of Quantitative trait loci mapping reveals candidate pathways regulating cell cycle duration in Plasmodium falciparum

Author

Ayala, Heather B Reilly, Wacker, Mark A, Siwo, Geoffrey, and Ferdig, Michael T

Abstract

Additional file 2: Scatter plots of criteria used to refine gene listThe x-axis represents the 104 genes in the preliminary gene list. They are arranged in ascending order for each of the three criteria used. A) SNP density between HB3 and Dd2 taken from PlasmoDB. B) Correlations of transcriptome for each gene between HB3 and Dd2 [47] C) Correlation of gene expression at 18 hours post-invasion between HB3 and Dd2 [30]. (PDF 24 KB)

Published
2021
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32. Additional file 6 of High-throughput 454 resequencing for allele discovery and recombination mapping in Plasmodium falciparum

Author

Upeka Samarakoon, Regier, Allison, Tan, Asako, Desany, Brian A, Collins, Brendan, Tan, John C, Emrich, Scott J, and Ferdig, Michael T

Abstract

Additional file 6:Distance between consecutive de novo SNPs. The distance between consecutive de novo SNPs were calculated to detect SNP clustering characteristic of sequencing errors or mis-mapping errors. 35% of the de novo SNPs were clustered in distances of less than 5 bps. (DOC 42 KB)

Published
2021
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34. Additional file 3 of High-throughput 454 resequencing for allele discovery and recombination mapping in Plasmodium falciparum

Author

Upeka Samarakoon, Regier, Allison, Tan, Asako, Desany, Brian A, Collins, Brendan, Tan, John C, Emrich, Scott J, and Ferdig, Michael T

Abstract

Additional file 3:Refined views of previously unknown COs shown in Figure3. Previously unknown COs detected in the progeny lines (highlighted with black bars in Figure 3) are indicated by double arrows in the chromosomal view (top) and zoomed-in view (boxed, bottom). (A-D) previously unknown COs in 7C126, (E-H) previously unknown COs in SC05. SNP map by 454 sequencing is presented in comparison with the MS marker linkage map in P. falciparum[4]. Each line represents a single SNP marker. HB3 alleles are shown in green bars and Dd2 alleles are shown in red. (PDF 183 KB)

Published
2021
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35. Additional file 8 of High-throughput 454 resequencing for allele discovery and recombination mapping in Plasmodium falciparum

Author

Upeka Samarakoon, Regier, Allison, Tan, Asako, Desany, Brian A, Collins, Brendan, Tan, John C, Emrich, Scott J, and Ferdig, Michael T

Subjects
mental disorders
Abstract

Additional file 8:Alternate SNP positions. The alternate SNP positions were assessed for their primary and secondary positions base call identity. Most primary base calls reflected the parental base call. The secondary base call position varied in the 2 progeny genomes in base call identity. Majority of the secondary base calls were parental in 7C126, whereas majority of the secondary base calls were non-parental in SC05 (A). Majority of the primary base calls were transitions in 7C126, while they were transversions in SC05 (B, C). (DOC 45 KB)

Published
2021
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37. Additional file 7 of High-throughput 454 resequencing for allele discovery and recombination mapping in Plasmodium falciparum

Author

Upeka Samarakoon, Regier, Allison, Tan, Asako, Desany, Brian A, Collins, Brendan, Tan, John C, Emrich, Scott J, and Ferdig, Michael T

Abstract

Additional file 7:Base conversion trends in de novo SNPs. The type of base conversion was investigated for positions at which the parental base calls were identical. More transversions were detected for SC05 compared to 7C126 (A), but did not show a predominant base conversion bias from 7C126 (B). (DOC 36 KB)

Published
2021
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38. Additional file 4 of High-throughput 454 resequencing for allele discovery and recombination mapping in Plasmodium falciparum

Author

Upeka Samarakoon, Regier, Allison, Tan, Asako, Desany, Brian A, Collins, Brendan, Tan, John C, Emrich, Scott J, and Ferdig, Michael T

Abstract

Additional file 4:Visual inspection of mapped WGS sequence at CO and NCO gene conversion breakpoints shown in Figure4. (A) simple CO breakpoint in 7C126, (B) NCO gene conversion in SC05 and (C) complex CO breakpoint accompanied by a conversion tract (defined by rapid allele changes at/near breakpoint) detected in 7C126. Chromosomal alignments at CO and NCO regions were visually inspected in comparison with the parental genomes, using Integrative Genomics Viewer [45]. (i) SNPs detected by 454 sequencing are ordered according to the chromosomal location (PlasmoDB v5.4 [27]). Each line represents a single SNP marker. HB3 alleles are shown in green bars and Dd2 alleles are shown in red. (ii) Comparison of SNPS and read alignments at selected SNP loci (arrow). SNPs are highlighted in blue [C], red [T], green [A] and brown [G]. (PDF 486 KB)

Published
2021
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44. Genetic diversity and chloroquine selective sweeps in Plasmodium falciparum

Author

Wootton, John C., Feng, Xiaorong, Ferdig, Michael T., Cooper, Roland A., Mu, Jianbing, Baruch, Dror I., Magill, Alan J., and Su, Xin-zhuan

Subjects
Environmental issues, Science and technology, Zoology and wildlife conservation
Abstract

Author(s): John C. Wootton [1]; Xiaorong Feng [2]; Michael T. Ferdig [3]; Roland A. Cooper [2]; Jianbing Mu [2]; Dror I. Baruch [2]; Alan J. Magill [2, 4]; Xin-zhuan Su [...]

Published
2002
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45. Optimizing Bulk Segregant Analysis of Drug Resistance Using Plasmodium Falciparum Genetic Crosses Conducted in Humanized Mice

Author

Brenneman, Katelyn V., primary, Li, Xue, additional, Kumar, Sudhir, additional, Delgado, Elizabeth, additional, Checkley, Lisa A., additional, Shoue, Douglas A., additional, Reyes, Ann, additional, Abatiyow, Biley A., additional, Haile, Meseret T., additional, Tripura, Rupam, additional, Peto, Tom, additional, Lek, Dysoley, additional, Button-Simons, Katrina A., additional, Kappe, Stefan H., additional, Dhorda, Mehul, additional, Nosten, François, additional, Nkhoma, Standwell C., additional, Cheeseman, Ian, additional, Vaughan, Ashley M., additional, Ferdig, Michael T., additional, and Anderson, Timothy JC, additional

Published
2021
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46. The apicoplast link to fever-survival and artemisinin-resistance in the malaria parasite

Author

Zhang, Min, primary, Wang, Chengqi, additional, Oberstaller, Jenna, additional, Thomas, Phaedra, additional, Otto, Thomas D., additional, Casandra, Debora, additional, Boyapalle, Sandhya, additional, Adapa, Swamy R., additional, Xu, Shulin, additional, Button-Simons, Katrina, additional, Mayho, Matthew, additional, Rayner, Julian C., additional, Ferdig, Michael T., additional, Jiang, Rays H. Y., additional, and Adams, John H., additional

Published
2020
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47. Bulk segregant analysis reveals environment × genotype interactions determining malaria parasite growth

Author

Kumar, Sudhir, primary, Li, Xue, additional, McDew-White, Marina, additional, Reyes, Ann, additional, Delgado, Elizabeth, additional, Sayeed, Abeer, additional, Haile, Meseret T., additional, Abatiyow, Biley A., additional, Kennedy, Spencer Y., additional, Camargo, Nelly M., additional, Checkley, Lisa A., additional, Brenneman, Katelyn V., additional, Button-Simons, Katrina A., additional, Duraisingh, Manoj T., additional, Cheeseman, Ian H., additional, Kappe, Stefan H. I., additional, Nosten, François, additional, Ferdig, Michael T., additional, Vaughan, Ashley M., additional, and Anderson, Tim J. C., additional

Published
2020
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