Gene expression regulation in trypanosomatids

The Genome of the African Trypanosome Trypanosoma brucei

Berriman, M., Ghedin, E., Hertz‐Fowler, C., Blandin, G., Renauld, H., Bartholomeu, D. C., Lennard, N. J., Caler, E. V., Hamlin, N. E., Haas, B. J., et al. (2005) · Science · doi:10.1126/science.1112642 · Cited by 1,634 · see citing works

The Genome Sequence of Trypanosoma cruzi , Etiologic Agent of Chagas Disease

El-Sayed, N. M., Myler, P. J., Bartholomeu, D. C., Nilsson, D., Aggarwal, G., Tran, A.-N., Ghedin, E., Worthey, E. A., Delcher, A. L., Blandin, G., et al. (2005) · Science · doi:10.1126/science.1112631 · Cited by 1,394 · see citing works

The Genome of the Kinetoplastid Parasite, Leishmania major

Ivens, A. C., Peacock, C. S., Worthey, E. A., Murphy, L., Aggarwal, G., Berriman, M., Sisk, E. C., Rajandream, M., Adlem, E., Aert, R., et al. (2005) · Science · doi:10.1126/science.1112680 · Cited by 1,347 · see citing works

RNA regulons: coordination of post-transcriptional events

Keene, J. D. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2111 · Cited by 1,321 · see citing works

Comparative Genomics of Trypanosomatid Parasitic Protozoa

El-Sayed, N. M., Myler, P. J., Blandin, G., Berriman, M., Crabtree, J., Aggarwal, G., Caler, E. V., Renauld, H., Worthey, E. A., Hertz‐Fowler, C., et al. (2005) · Science · doi:10.1126/science.1112181 · Cited by 818 · see citing works

The trypanosomiases

Barrett, M. P., Burchmore, R., Stich, A., Lázzari, J. O., Frasch, A. C. C., Cazzulo, J. J., & Krishna, S. (2003) · The Lancet · doi:10.1016/s0140-6736(03)14694-6 · Cited by 673 · see citing works

Post-transcriptional regulation of gene expression in trypanosomes and leishmanias

CLAYTON, C. E., & Shapira, M. (2007) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2007.07.007 · Cited by 414 · see citing works

The Control of mRNA Decapping and P-Body Formation

Franks, T. M., & Lykke‐Andersen, J. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.11.001 · Cited by 399 · see citing works

Polysomes, P bodies and stress granules: states and fates of eukaryotic mRNAs

Balagopal, V., & Parker, R. (2009) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2009.03.005 · Cited by 391 · see citing works

Complex management: RNA editing in trypanosomes

Stuart, K. D., Schnaufer, A. C., Ernst, N. L., & Panigrahi, A. K. (2005) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2004.12.006 · Cited by 367 · see citing works

trans and cis Splicing in Trypanosomatids: Mechanism, Factors, and Regulation

Liang, X., Haritan, A., Uliel, S., & Michaeli, S. (2003) · Eukaryotic Cell · doi:10.1128/ec.2.5.830-840.2003 · Cited by 326 · see citing works

RNA interference in protozoan parasites

Ullu, E., Tschudi, C., & Chakraborty, T. (2004) · Cellular Microbiology · doi:10.1111/j.1462-5822.2004.00399.x · Cited by 294 · see citing works

Genome-wide analysis of mRNA abundance in two life-cycle stages of Trypanosoma brucei and identification of splicing and polyadenylation sites

Siegel, T. N., Hekstra, D. R., Wang, X., Dewell, S. B., & Cross, G. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq237 · Cited by 280 · see citing works

The Transcriptome of the Human Pathogen Trypanosoma brucei at Single-Nucleotide Resolution

Kolev, N. G., Franklin, J. B., Carmi, S., Shi, H., Michaeli, S., & Tschudi, C. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001090 · Cited by 256 · see citing works

The Genome of the African Trypanosome

Donelson, J. E. (2005) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-46894-8_11 · Cited by 239 · see citing works

Retention and Loss of RNA Interference Pathways in Trypanosomatid Protozoans

Lye, L., Owens, K. L., Shi, H., Murta, S. M. F., Vieira, A. C., Turco, S. J., Tschudi, C., Ullu, E., & Beverley, S. M. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001161 · Cited by 229 · see citing works

Developmental regulation of gene expression in trypanosomatid parasitic protozoa

Haile, S., & Papadopoulou, B. (2007) · Current Opinion in Microbiology · doi:10.1016/j.mib.2007.10.001 · Cited by 222 · see citing works

Switching trypanosome coats: what's in the wardrobe?

Taylor, J. W., & Rudenko, G. (2006) · Trends in Genetics · doi:10.1016/j.tig.2006.08.003 · Cited by 193 · see citing works

Spliced Leader Trapping Reveals Widespread Alternative Splicing Patterns in the Highly Dynamic Transcriptome of Trypanosoma brucei

Nilsson, D., Gunasekera, K., Mani, J., Østerås, M., Farinelli, L., Bærlocher, L., Roditi, I. J., & Ochsenreiter, T. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001037 · Cited by 183 · see citing works

Heat shock causes a decrease in polysomes and the appearance of stress granules in trypanosomes independently of eIF2α phosphorylation at Thr169

Krämer, S., Queiroz, R., Ellis, L., Webb, H., Hoheisel, J. D., CLAYTON, C. E., & Carrington, M. (2008) · Journal of Cell Science · doi:10.1242/jcs.031823 · Cited by 160 · see citing works

Elements in the 3′ Untranslated Region of Procyclin mRNA Regulate Expression in Insect Forms of Trypanosoma brucei by Modulating RNA Stability and Translation

Furger, A., Schürch, N., Kurath, U., & Roditi, I. J. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.8.4372 · Cited by 154 · see citing works

Genome-wide gene expression profiling analysis of Leishmania major and Leishmania infantum developmental stages reveals substantial differences between the two species

Rochette, A., Raymond, F., Ubeda, J.-M., Smith, M. A., Messier, N., Boisvert, S., Rigault, P., Corbeil, J., Ouellette, M., & Papadopoulou, B. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-255 · Cited by 143 · see citing works

AU-rich Elements in the 3′-Untranslated Region of a New Mucin-type Gene Family of Trypanosoma cruzi Confers mRNA Instability and Modulates Translation Efficiency

Noia, J. M. D., D’Orso, I., Sánchez, D. O., & Frasch, A. C. C. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.14.10218 · Cited by 134 · see citing works

The steady-state transcriptome of the four major life-cycle stages of Trypanosoma cruzi

Minning, T. A., Weatherly, D. B., Atwood, J., Orlando, R., & Tarleton, R. L. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-370 · Cited by 133 · see citing works

RNA-Binding Domain Proteins in Kinetoplastids: a Comparative Analysis

Gaudenzi, J. G. D., Frasch, A. C. C., & CLAYTON, C. E. (2005) · Eukaryotic Cell · doi:10.1128/ec.4.12.2106-2114.2005 · Cited by 131 · see citing works

Recruitment of mRNAs to cytoplasmic ribonucleoprotein granules in trypanosomes

Cassola, A., Gaudenzi, J. G. D., & Frasch, A. C. C. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05833.x · Cited by 129 · see citing works

Gene transcription in trypanosomes

Palenchar, J. B., & Bellofatto, V. (2006) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2005.12.008 · Cited by 129 · see citing works

Chromosome level assembly of the hybrid Trypanosoma cruzi genome

Weatherly, D. B., Boehlke, C., & Tarleton, R. L. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-255 · Cited by 126 · see citing works

Epigenetic regulation in African trypanosomes: a new kid on the block

Figueiredo, L. M., Cross, G., & Janzen, C. J. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2149 · Cited by 119 · see citing works

Genome-wide in silico screen for CCCH-type zinc finger proteins of Trypanosoma brucei, Trypanosoma cruzi and Leishmania major

Krämer, S., Kimblin, N., & Carrington, M. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-283 · Cited by 118 · see citing works

Members of a Large Retroposon Family Are Determinants of Post-Transcriptional Gene Expression in Leishmania

Bringaud, F., Müller-McNicoll, M., Cerqueira, G. C., Smith, M. A., Rochette, A., El-Sayed, N. M., Papadopoulou, B., & Ghedin, E. (2007) · PLoS Pathogens · doi:10.1371/journal.ppat.0030136 · Cited by 112 · see citing works

Unravelling the procyclin coat of Trypanosoma brucei

Roditi, I. J. (1998) · Molecular and Biochemical Parasitology · doi:10.1016/s0166-6851(97)00195-3 · Cited by 108 · see citing works

Posttranscriptional control and the role of RNA‐binding proteins in gene regulation in trypanosomatid protozoan parasites

Moya, S. M. F., & Estévez, A. M. (2010) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.6 · Cited by 84 · see citing works

Differential Trypanosome Surface Coat Regulation by a CCCH Protein That Co-Associates with procyclin mRNA cis-Elements

Walrad, P. B., Paterou, A., Acosta-Serrano, Á., & Matthews, K. R. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000317 · Cited by 81 · see citing works

TcUBP-1, a Developmentally Regulated U-rich RNA-binding Protein Involved in Selective mRNA Destabilization in Trypanosomes

D’Orso, I., & Frasch, A. C. C. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m102120200 · Cited by 74 · see citing works

Repetitive Elements in Genomes of Parasitic Protozoa

Wickstead, B., Ersfeld, K., & Keith Gull, B. (2003) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.67.3.360-375.2003 · Cited by 74 · see citing works

Mobile genetic elements in protozoan parasites

Bhattacharya, S., Bakre, A. A., & Bhattacharya, A. (2002) · Journal of Genetics · doi:10.1007/bf02715903 · Cited by 61 · see citing works

Coordinated gene expression by post-transcriptional regulons in African trypanosomes

Ouellette, M., & Papadopoulou, B. (2009) · Journal of Biology · doi:10.1186/jbiol203 · Cited by 60 · see citing works

Functional Characterization of a Trypanosoma brucei TATA-Binding Protein-Related Factor Points to a Universal Regulator of Transcription in Trypanosomes

Ruan, J., Arhin, G. K., Ullu, E., & Tschudi, C. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.21.9610-9618.2004 · Cited by 58 · see citing works

Changes in polysome profiles accompany trypanosome development

Brecht, M., & Parsons, M. (1998) · Molecular and Biochemical Parasitology · doi:10.1016/s0166-6851(98)00151-0 · Cited by 57 · see citing works

mRNA maturation by two-step trans-splicing/polyadenylation processing in trypanosomes

Jäger, A. V., Gaudenzi, J. G. D., Cassola, A., D’Orso, I., & Frasch, A. C. C. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611125104 · Cited by 55 · see citing works

The trypanosome Pumilio‐domain protein PUF7 associates with a nuclear cyclophilin and is involved in ribosomal RNA maturation

Droll, D., Archer, S. K., Fenn, K., Delhi, P., Matthews, K. R., & CLAYTON, C. E. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.02.018 · Cited by 54 · see citing works

RNA-binding proteins and mRNA turnover in trypanosomes

D’Orso, I., Gaudenzi, J. G. D., & Frasch, A. C. C. (2003) · Trends in Parasitology · doi:10.1016/s1471-4922(03)00035-7 · Cited by 54 · see citing works

RNA Recognition Motif-type RNA-binding Proteins in Trypanosoma cruzi Form a Family Involved in the Interaction with Specific Transcripts in Vivo

Gaudenzi, J. G. D., D’Orso, I., & Frasch, A. C. C. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m301756200 · Cited by 52 · see citing works

Functionally related transcripts have common RNA motifs for specific RNA-binding proteins in trypanosomes

Noé, G., Gaudenzi, J. G. D., & Frasch, A. C. C. (2008) · BMC Molecular Biology · doi:10.1186/1471-2199-9-107 · Cited by 51 · see citing works

Why kinetoplast DNA networks?

Borst, P. (1991) · Trends in Genetics · doi:10.1016/0168-9525(91)90374-y · Cited by 48 · see citing works

Identification of mRNA decapping activities and an ARE-regulated 3' to 5' exonuclease activity in trypanosome extracts

Milone, J. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf521 · Cited by 39 · see citing works

Why kinetoplast DNA networks?

Borst, P. (1991) · Trends in Genetics · doi:10.1016/0168-9525(91)90091-4 · Cited by 39 · see citing works

Trypanosoma cruzi: Analysis of the complete PUF RNA-binding protein family

Caro, F., Bercovich, N., Atorrasagasti, C., Levin, M. J., & Vázquez, M. (2006) · Experimental Parasitology · doi:10.1016/j.exppara.2005.12.015 · Cited by 36 · see citing works

Chromatin-based transcriptional punctuation: Figure 1.Preprint

Talbert, P. B., & Henikoff, S. (2009) · Genes & Development · doi:10.1101/gad.1806409 · Cited by 29 · see citing works

Consequences of Telomere Shortening at an Active VSG Expression Site in Telomerase-Deficient Trypanosoma brucei

Dreesen, O., & Cross, G. (2006) · Eukaryotic Cell · doi:10.1128/ec.00059-06 · Cited by 26 · see citing works

Coordinate regulation of a family of promastigote-enriched mRNAs by the 3′UTR PRE element in Leishmania mexicana

Holzer, T. R., Mishra, K. K., LeBowitz, J. H., & FORNEY, J. D. (2007) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2007.10.001 · Cited by 21 · see citing works

A compendium of RNA-binding motifs for decoding gene regulation

Ray, D., Kazan, H., Cook, K. B., Weirauch, M. T., Najafabadi, H. S., Li, X., Gueroussov, S., Albu, M., Zheng, H., Yang, A., et al. (2013) · Nature · doi:10.1038/nature12311 · Cited by 1,480 · see citing works

Drug resistance and treatment failure in leishmaniasis: A 21st century challenge

Ponte‐Sucre, A., Gamarro, F., Dujardin, J., Barrett, M. P., López‐Vélez, R., García‐Hernández, R., Pountain, A. W., Mwenechanya, R., & Papadopoulou, B. (2017) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0006052 · Cited by 971 · see citing works

Proteomic Analysis of Trypanosoma cruzi Secretome: Characterization of Two Populations of Extracellular Vesicles and Soluble Proteins

Bayer‐Santos, E., Aguilar-Bonavides, C., Rodrigues, S. P., Cordero, E. M., Marques, A. F., Varela-Ramı́rez, A., Choi, H., Yoshida, N., da Silveira, J. F., & de Almeida, I. C. (2012) · Journal of Proteome Research · doi:10.1021/pr300947g · Cited by 257 · see citing works

Trypanosomatids Are Much More than Just Trypanosomes: Clues from the Expanded Family Tree

Lukeš, J., Butenko, A., Hashimi, H., Maslov, D. A., Votýpka, J., & Yurchenko, V. (2018) · Trends in Parasitology · doi:10.1016/j.pt.2018.03.002 · Cited by 200 · see citing works

Modulation of Aneuploidy in Leishmania donovani during Adaptation to Different In Vitro and In Vivo Environments and Its Impact on Gene Expression

Dumetz, F., Imamura, H., Sanders, M. J., Šeblová, V., Myšková, J., Pescher, P., Vanaerschot, M., Meehan, C. J., Cuypers, B., Muylder, G. D., et al. (2017) · mBio · doi:10.1128/mbio.00599-17 · Cited by 196 · see citing works

Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi

Smircich, P., Eastman, G., Poubel, S. B., Duhagon, M. A., Guerra-Slompo, E. P., Garat, B., Goldenberg, S., Munroe, D. J., Dallagiovanna, B., Holetz, F., et al. (2015) · BMC Genomics · doi:10.1186/s12864-015-1563-8 · Cited by 146 · see citing works

The mRNA-bound proteome of the human malaria parasite Plasmodium falciparum

Bunnik, E. M., Batugedara, G., Saraf, A., Prudhomme, J. G., Florens, L. A., & Roch, K. G. L. (2016) · Genome biology · doi:10.1186/s13059-016-1014-0 · Cited by 92 · see citing works

Characterization of the small RNA content of Trypanosoma cruzi extracellular vesicles

Bayer‐Santos, E., Lima, F. M., Ruiz, J. C., de Almeida, I. C., & da Silveira, J. F. (2014) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2014.02.004 · Cited by 86 · see citing works

Highly Sensitive In Vivo Imaging of Trypanosoma brucei Expressing “Red-Shifted” Luciferase

McLatchie, A. P., Burrell‐Saward, H., Myburgh, E., Lewis, M. D., Ward, T. H., Mottram, J. C., Croft, S. L., Kelly, J. M., & Taylor, M. C. (2013) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0002571 · Cited by 76 · see citing works

Genomic assemblies of newly sequenced Trypanosoma cruzi strains reveal new genomic expansion and greater complexity

Callejas‐Hernández, F., Rastrojo, A., Poveda, C., Gironès, N., & Fresno, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-32877-2 · Cited by 73 · see citing works

Transcriptionally Driven DNA Replication Program of the Human Parasite Leishmania major

Lombraña, R., Álvarez, A., Fernández-Justel, J. M., Almeida, R., Poza‐Carrión, C., Gomes, F., Calzada, A., Requena, J. M., & Gómez, M. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.007 · Cited by 71 · see citing works

Trypanosoma Cruzi Genome: Organization, Multi-Gene Families, Transcription, and Biological Implications

Herreros‐Cabello, A., Callejas‐Hernández, F., Gironès, N., & Fresno, M. (2020) · Genes · doi:10.3390/genes11101196 · Cited by 65 · see citing works

Chromatin Proteomics Reveals Variable Histone Modifications during the Life Cycle of Trypanosoma cruzi

de Jesus, T. C. L., Nunes, V. S., Lopes, M. D. C., Martil, D. E., Iwai, L. K., Moretti, N. S., Machado, F. C., de Lima-Stein, M. L., Thiemann, O. H., Elias, M. C., et al. (2016) · Journal of Proteome Research · doi:10.1021/acs.jproteome.6b00208 · Cited by 61 · see citing works

Basal body multipotency and axonemal remodelling are two pathways to a 9+0 flagellum

Wheeler, R. J., Gluenz, E., & Keith Gull, B. (2015) · Nature Communications · doi:10.1038/ncomms9964 · Cited by 60 · see citing works

Metabolic adaptations of L eishmania donovani in relation to differentiation, drug resistance, and drug pressure

Berg, M., Vanaerschot, M., Jankevics, A., Cuypers, B., Maes, I., Mukherjee, S., Khanal, B., Rijal, S., Roy, S., Opperdoes, F. R., et al. (2013) · Molecular Microbiology · doi:10.1111/mmi.12374 · Cited by 59 · see citing works

The Role of Cytoplasmic mRNA Cap-Binding Protein Complexes in Trypanosoma brucei and Other Trypanosomatids

Freire, E. R., Sturm, N. R., Campbell, D. A., & Neto, O. P. D. M. (2017) · Pathogens · doi:10.3390/pathogens6040055 · Cited by 59 · see citing works

Regulation of Translation in the Protozoan Parasite Leishmania

Karamysheva, Z., Guarnizo, S. G. G., & Karamyshev, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21082981 · Cited by 45 · see citing works

Redox Balance Keepers and Possible Cell Functions Managed by Redox Homeostasis in Trypanosoma cruzi

Mesías, A. C., Garg, N. J., & Zago, M. P. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00435 · Cited by 53 · see citing works

LC-MS METABOLOMICS FROM STUDY DESIGN TO DATA-ANALYSIS – USING A VERSATILE PATHOGEN AS A TEST CASE

Berg, M., Vanaerschot, M., Jankevics, A., Cuypers, B., Rainer Breitling, A., & Dujardin, J. (2013) · Computational and Structural Biotechnology Journal · doi:10.5936/csbj.201301002 · Cited by 50 · see citing works

Comparative Proteomic Analysis of Lysine Acetylation in Trypanosomes

Moretti, N. S., Cestari, I. D. S., Anupama, A., Stuart, K., & Schenkman, S. (2017) · Journal of Proteome Research · doi:10.1021/acs.jproteome.7b00603 · Cited by 49 · see citing works

A Multiplatform Metabolomic Approach to the Basis of Antimonial Action and Resistance in Leishmania infantum

Rojo, D., Canuto, G. A. B., Castilho-Martins, E. A., Tavares, M. F. M., Barbas, C., López‐Gonzálvez, Á., & Rivas, L. (2015) · PLoS ONE · doi:10.1371/journal.pone.0130675 · Cited by 48 · see citing works

Secretome analysis of Trypanosoma cruzi by proteomics studies

Brossas, J., Gulin, J. E. N., Bisio, M. M. C., Chapelle, M., Marinach, C., Bordessoulles, M., Ruiz, G. P., Vion, J., Paris, L., Altcheh, J., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0185504 · Cited by 41 · see citing works

(Post-) Genomic approaches to tackle drug resistance in Leishmania

Berg, M., Mannaert, A., Vanaerschot, M., der Auwera, G. V., & Dujardin, J. (2013) · Parasitology · doi:10.1017/s0031182013000140 · Cited by 40 · see citing works

RNA in development: how ribonucleoprotein granules regulate the life cycles of pathogenic protozoa

Krämer, S. (2013) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1207 · Cited by 38 · see citing works

Parasite Prolyl Oligopeptidases and the Challenge of Designing Chemotherapeuticals for Chagas Disease, Leishmaniasis and African Trypanosomiasis

Bastos, I. M. D., Motta, F., Grellier, P., & Santana, J. M. (2013) · Current Medicinal Chemistry · doi:10.2174/0929867311320250006 · Cited by 38 · see citing works

Nutritional stress affects an atypical cap-binding protein in Leishmania

Zinoviev, A., Manor, S., & Shapira, M. (2012) · RNA Biology · doi:10.4161/rna.22709 · Cited by 38 · see citing works

Comparative transcriptomics in Leishmania braziliensis : disclosing differential gene expression of coding and putative noncoding RNAs across developmental stages

Ruy, P. D. C., Teles, N. M. M., Magalhães, R. D. M., Freitas-Castro, F., da Silva, L. D., Defina, T. P. A., Vasconcelos, E. J. R., Myler, P. J., & Cruz, Â. K. (2019) · RNA Biology · doi:10.1080/15476286.2019.1574161 · Cited by 37 · see citing works

Neglected Tropical Diseases in the Post-Genomic Era

Buscaglia, C. A., Kissinger, J. C., & Agüero, F. (2015) · Trends in Genetics · doi:10.1016/j.tig.2015.06.002 · Cited by 36 · see citing works

Genome-wide analysis of 3′-untranslated regions supports the existence of post-transcriptional regulons controlling gene expression in trypanosomes

Gaudenzi, J. G. D., Carmona, S. J., Agüero, F., & Frasch, A. C. C. (2013) · PeerJ · doi:10.7717/peerj.118 · Cited by 33 · see citing works

A MFS-like plasma membrane transporter required for Leishmania virulence protects the parasites from iron toxicity

Laranjeira‐Silva, M. F., Wang, W., Samuel, T. K., Maeda, F. Y., Michailowsky, V., Hamza, I., Liu, Z., & Andrews, N. W. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1007140 · Cited by 31 · see citing works

SCD6 induces ribonucleoprotein granule formation in trypanosomes in a translation-independent manner, regulated by its Lsm and RGG domains

Krüger, T., Hofweber, M., & Krämer, S. (2013) · Molecular Biology of the Cell · doi:10.1091/mbc.e13-01-0068 · Cited by 30 · see citing works

Identification of novel proteins and mRNAs differentially bound to the Leishmania Poly(A) Binding Proteins reveals a direct association between PABP1, the RNA-binding protein RBP23 and mRNAs encoding ribosomal proteins

de Assis, L. A., Filho, M. D. V. C. S., Silva, J. R. D. C., Bezerra, M. J. R., de Aquino, I. R. P. U. C., Merlo, K. D. C., Holetz, F., Probst, C., Rezende, A. M., Papadopoulou, B., et al. (2021) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0009899 · Cited by 29 · see citing works

A 43-Nucleotide U-rich Element in 3′-Untranslated Region of Large Number of Trypanosoma cruzi Transcripts Is Important for mRNA Abundance in Intracellular Amastigotes

Li, Z., Gaudenzi, J. G. D., Álvarez, V. E., Mendiondo, N., Wang, H., Kissinger, J. C., Frasch, A. C. C., & Docampo, R. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.338699 · Cited by 29 · see citing works

RNA Binding Proteins and Gene Expression Regulation in Trypanosoma cruzi

Romagnoli, B. A. A., Holetz, F., Alves, L. R., & Goldenberg, S. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00056 · Cited by 27 · see citing works

Conservation and Variation in Strategies for DNA Replication of Kinetoplastid Nuclear Genomes

Marques, C. A., & McCulloch, R. (2017) · Current Genomics · doi:10.2174/1389202918666170815144627 · Cited by 25 · see citing works

Transcriptome-wide analysis of the Trypanosoma cruzi proliferative cycle identifies the periodically expressed mRNAs and their multiple levels of control

Chávez, S. S., Eastman, G., Smircich, P., Becco, L., Oliveira‐Rizzo, C., Fort, R. S., Potenza, M., Garat, B., Sotelo-Silveira, J. R., & Duhagon, M. A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0188441 · Cited by 24 · see citing works

Regulation of RNA binding proteins in trypanosomatid protozoan parasites

Romaniuk, M. A. (2016) · World Journal of Biological Chemistry · doi:10.4331/wjbc.v7.i1.146 · Cited by 22 · see citing works

Polysome Profiling in Leishmania, Human Cells and Mouse Testis

Karamysheva, Z. N., Tikhonova, E. B., Grozdanov, P. N., Huffman, J. C., Baca, K. R., Karamyshev, A., Denison, R. B., MacDonald, C. C., Zhang, K., & Karamyshev, A. L. (2018) · Journal of Visualized Experiments · doi:10.3791/57600 · Cited by 23 · see citing works

Quantitative phosphoproteome and proteome analyses emphasize the influence of phosphorylation events during the nutritional stress of Trypanosoma cruzi: the initial moments of in vitro metacyclogenesis

Lucena, A. C. R., Amorim, J. C., Lima, C. V. D. P., Batista, M., Krieger, M. A., de Godoy, L. M. F., & Marchini, F. K. (2019) · Cell Stress and Chaperones · doi:10.1007/s12192-019-01018-7 · Cited by 22 · see citing works

Knockout of the CCCH zinc finger protein TcZC3H31 blocks Trypanosoma cruzi differentiation into the infective metacyclic form

Alcântara, M. V., Kessler, R. L., Gonçalves, R. E. G., Marliére, N. P., Guarneri, A. A., Picchi, G. F. A., & Fragoso, S. P. (2018) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2018.01.006 · Cited by 18 · see citing works

The RNA-binding protein TcUBP1 up-regulates an RNA regulon for a cell surface–associated Trypanosoma cruzi glycoprotein and promotes parasite infectivity

Sabalette, K. B., Romaniuk, M. A., Noé, G., Cassola, A., Campo, V. A., & Gaudenzi, J. G. D. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.007123 · Cited by 18 · see citing works

Characterization of two different Asf1 histone chaperones with distinct cellular localizations and functions in Trypanosoma brucei

Pascoalino, B. S., Dindar, G., Vieira‐da‐Rocha, J. P., Machado, C. R., Janzen, C. J., & Schenkman, S. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt1267 · Cited by 18 · see citing works

Extensive Translational Regulation through the Proliferative Transition of Trypanosoma cruzi Revealed by Multi-Omics

Chávez, S., Urbaniak, M. D., Benz, C., Smircich, P., Garat, B., Sotelo-Silveira, J. R., & Duhagon, M. A. (2021) · mSphere · doi:10.1128/msphere.00366-21 · Cited by 17 · see citing works

Comparative high-throughput analysis of the Trypanosoma cruzi response to organometallic compounds

Mosquillo, M. F., Smircich, P., Ciganda, M., Lima, A. E., Gambino, D., Garat, B., & Pérez‐Díaz, L. (2020) · Metallomics · doi:10.1039/d0mt00030b · Cited by 17 · see citing works

Trypanosoma brucei: meet the system

Achcar, F., Kerkhoven, E. J., & Barrett, M. P. (2014) · Current Opinion in Microbiology · doi:10.1016/j.mib.2014.06.007 · Cited by 16 · see citing works

Genetic Structure and Expression of the Surface Glycoprotein GP82, the Main Adhesin of Trypanosoma cruzi Metacyclic Trypomastigotes

Corrêa, P. R. C., Cordero, E. M., Gentil, L. G., Bayer‐Santos, E., & da Silveira, J. F. (2013) · The Scientific World JOURNAL · doi:10.1155/2013/156734 · Cited by 15 · see citing works

A Host–Pathogen Interaction Reduced to First Principles: Antigenic Variation in T. brucei

Hovel-Miner, G. A., Mugnier, M. R., Papavasiliou, F. N., Pinger, J., & Schulz, D. (2015) · Results and problems in cell differentiation · doi:10.1007/978-3-319-20819-0_2 · Cited by 15 · see citing works

Phosphorylation and interactions associated with the control of theLeishmaniaPoly-A Binding Protein 1 (PABP1) function during translation initiation

Neto, O. P. D. M., Lima, T. D. C. D. C., Merlo, K. D. C., Romão, T. P., Rocha, P. O., de Assis, L. A., do Nascimento, L. M., Xavier, C. C., Rezende, A. M., Reis, C. R. D. S., et al. (2018) · RNA Biology · doi:10.1080/15476286.2018.1445958 · Cited by 15 · see citing works

Proteins involved in the biosynthesis of lipophosphoglycan in Leishmania: a comparative genomic and evolutionary analysis

Azevedo, L. G., Queiroz, A. T. L., Barral, A. M. P., Santos, L. A., & Ramos, P. I. P. (2020) · Parasites & Vectors · doi:10.1186/s13071-020-3914-9 · Cited by 15 · see citing works

Trypanosoma cruzi: Genomic Diversity and Structure

Herreros‐Cabello, A., Callejas‐Hernández, F., Gironès, N., & Fresno, M. (2025) · Pathogens · doi:10.3390/pathogens14010061 · Cited by 14 · see citing works

A proteomics approach reveals molecular manipulators of distinct cellular processes in the salivary glands of Glossina m. morsitans in response to Trypanosoma b. brucei infections

Kariithi, H. M., Boeren, S. A., Murungi, E. K., Vlak, J. M., & Abd‐Alla, A. M. M. (2016) · Parasites & Vectors · doi:10.1186/s13071-016-1714-z · Cited by 14 · see citing works

Computational study on the allosteric mechanism of Leishmania major IF4E-1 by 4E-interacting protein-1: Unravelling the determinants of m 7 GTP cap recognition

Alvarez, L. H., Junior, A. B. D. O., González, J. E. H., Chahine, J., Pascutti, P. G., de Araújo, A. S., & de Souza, F. P. (2021) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2021.03.036 · Cited by 13 · see citing works

Current Status of Regulatory Non-Coding RNAs Research in the Tritryp

Fort, R. S., Chavez, S., Trinidad-Barnech, J. M., Oliveira‐Rizzo, C., Smircich, P., Sotelo-Silveira, J. R., & Duhagon, M. A. (2022) · Non-Coding RNA · doi:10.3390/ncrna8040054 · Cited by 13 · see citing works

Insights into the Regulation of mRNA Processing of Polycistronic Transcripts Mediated by DRBD 4/ PTB 2, a Trypanosome Homolog of the Polypyrimidine Tract‐Binding Protein

Gaudenzi, J. G. D., Jäger, A. V., Izcovich, R., & Campo, V. A. (2015) · Journal of Eukaryotic Microbiology · doi:10.1111/jeu.12288 · Cited by 13 · see citing works

The phosphoinositide regulatory network in Trypanosoma brucei: Implications for cell-wide regulation in eukaryotes

Cestari, I. D. S., & Stuart, K. D. (2020) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0008689 · Cited by 12 · see citing works

Involvement of an RNA binding protein containing Alba domain in the stage-specific regulation of beta-amastin expression in Trypanosoma cruzi

Pérez‐Díaz, L., Silva, T. C., & Teixeira, S. M. R. (2016) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2016.12.005 · Cited by 12 · see citing works

Exploring the genomic landscape of the GP63 family in Trypanosoma cruzi: Evolutionary dynamics and functional peculiarities

Berná, L., Chiribao, M. L., Pita, S., Álvarez-Valín, F., & Parodi‐Talice, A. (2025) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0012950 · Cited by 11 · see citing works

Dynamic composition of stress granules in Trypanosoma brucei

Aye, H. M., Li, F., & He, C. Y. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012666 · Cited by 10 · see citing works

Comparative and systems analyses of Leishmania spp. non-coding RNAs through developmental stages

Martinez-Hernandez, J. E., Aliaga-Tobar, V., González, C., do Monte‐Neto, R. L., Martín, A. J. M., & Maracaja‐Coutinho, V. (2025) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0013108 · Cited by 10 · see citing works

Modulation of Virulence Factors during Trypanosoma cruzi Differentiation

de Oliveira, C. I., Holetz, F., Alves, L. R., & Ávila, A. R. (2022) · Pathogens · doi:10.3390/pathogens12010032 · Cited by 10 · see citing works

Implication of CA repeated tracts on post-transcriptional regulation in Trypanosoma cruzi

Pastro, L., Smircich, P., Pérez‐Díaz, L., Duhagon, M. A., & Garat, B. (2013) · Experimental Parasitology · doi:10.1016/j.exppara.2013.04.004 · Cited by 10 · see citing works

The Role of the Trypanosoma cruzi TcNRBD1 Protein in Translation

de Oliveira, C. I., Carvalho, P. C., Alves, L. R., & Goldenberg, S. (2016) · PLoS ONE · doi:10.1371/journal.pone.0164650 · Cited by 10 · see citing works

A Novel Trypanosoma cruzi Protein Associated to the Flagellar Pocket of Replicative Stages and Involved in Parasite Growth

Durante, I. M., Cámara, M. D. L. M., & Buscaglia, C. A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0130099 · Cited by 10 · see citing works

A Genome-Wide Analysis of Genetic Diversity in Trypanosoma cruzi Intergenic Regions

Panunzi, L. G., & Agüero, F. (2014) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0002839 · Cited by 10 · see citing works

TbRRM1 knockdown produces abnormal cell morphology and apoptotic-like death in the bloodstream form of T. brucei

Níttolo, A. G., Bañuelos, C. P., Saborit, J. I., Tekiel, V., Sánchez, D. O., & Levy, G. V. (2018) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2018.07.006 · Cited by 9 · see citing works

Identification and subcellular localization of TcHIP, a putative Golgi zDHHC palmitoyl transferase of Trypanosoma cruzi

Batista, C. M., Kalb, L. C., Moreira, C. M. D. N., Batista, G. T. H., Eger, I., & Soares, M. J. (2013) · Experimental Parasitology · doi:10.1016/j.exppara.2013.01.023 · Cited by 9 · see citing works

Unique and Conserved Features of the Protein Synthesis Apparatus in Parasitic Trypanosomatid (Trypanosoma and Leishmania) Species

Neto, O. P. D. M., Reis, C. R. D. S., Moura, D. M. N., Freire, E. R., & Carrington, M. (2016) · Springer eBooks · doi:10.1007/978-3-319-39468-8_17 · Cited by 9 · see citing works

Analysis of mRNA processing at whole transcriptome level, transcriptomic profile and genome sequence refinement of Trypanosoma cruzi

Callejas‐Hernández, F., Gutierrez‐Nogués, Á., Rastrojo, A., Gironès, N., & Fresno, M. (2019) · Scientific Reports · doi:10.1038/s41598-019-53924-6 · Cited by 9 · see citing works

Parasite Prolyl Oligopeptidases and the Challenge of Designing Chemotherapeuticals for Chagas Disease, Leishmaniasis and African Trypanosomiasis

Bastos, I. M. D., Motta, F. N., Grellier, P., & Santana, J. M. (2013) · Current Medicinal Chemistry · doi:10.2174/09298673113209990121 · Cited by 9 · see citing works

Aim for the Readers! Bromodomains As New Targets Against Chagas’ Disease

Alonso, V. L., Tavernelli, L. E., Pezza, A., Cribb, P., Ritagliati, C., & Serra, E. C. (2018) · Current Medicinal Chemistry · doi:10.2174/0929867325666181031132007 · Cited by 9 · see citing works

Disclosing 3' UTR cis-elements and putative partners involved in gene expression regulation in Leishmania spp.

Terrão, M. C., Vasconcelos, E. J. R., Defina, T. P. A., Myler, P. J., & Cruz, Â. K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0183401 · Cited by 9 · see citing works

Insights on genomic profiles of drug resistance and virulence in a cohort of Leishmania infantum isolates from the Mediterranean area

Carrasco-Martin, M., Martí‐Carreras, J., Gómez-Ponce, M., Alcover, M. M., Roura, X., Ferrer, L., Baneth, G., Bruno, F., Chicharro, C., Cordeiro‐da‐Silva, A., et al. (2025) · Parasites & Vectors · doi:10.1186/s13071-025-07105-2 · Cited by 8 · see citing works

RNA-Seq reveals that overexpression of TcUBP1 switches the gene expression pattern toward that of the infective form of Trypanosoma cruzi

Sabalette, K. B., Sotelo-Silveira, J. R., Smircich, P., & Gaudenzi, J. G. D. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104623 · Cited by 8 · see citing works

Siccanin Is a Novel Selective Inhibitor of Trypanosomatid Complex II (Succinate-Ubiquinone Reductase) and a Potent Broad-Spectrum Anti-trypanosomatid Drug Candidate

Nihashi, N., Inaoka, D. K., Tsuge, C., Balogun, E. O., Osada, Y., Goto, Y., Matsumoto, Y., Nara, T., Mogi, T., Harada, S., et al. (2016) · Springer eBooks · doi:10.1007/978-3-319-47101-3_9 · Cited by 8 · see citing works

Deciphering Divergent Trypanosomatid Nuclear Complexes by Analyzing Interactomic Datasets with AlphaFold2 and Genetic Approaches

Araya, E. R., Merli, M. L., Cribb, P., de Souza, V. C., & Serra, E. C. (2023) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.3c00148 · Cited by 7 · see citing works

Trypanosoma cruzi Genomic Variability: Array Comparative Genomic Hybridization Analysis of Clone and Parental Strain

Cortez, D. R., Lima, F. M., Reis-Cunha, J. L., Bartholomeu, D. C., Villacis, R. A. R., Rogatto, S. R., Costa-Martins, A. G., Marchiano, F. S., do Carmo, R. A., da Silveira, J. F., et al. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.760830 · Cited by 5 · see citing works

Advances in euglenoid genomics: unravelling the fascinating biology of a complex clade

Fields, O., Hammond, M., Xu, X., & O’Neill, E. C. (2024) · Trends in Genetics · doi:10.1016/j.tig.2024.07.007 · Cited by 5 · see citing works

Subcellular protein localisation of Trypanosoma brucei bloodstream form-upregulated proteins maps stage-specific adaptations

Halliday, C., Dean, S., Sunter, J. D., & Wheeler, R. J. (2023) · Wellcome Open Research · doi:10.12688/wellcomeopenres.18586.2 · Cited by 5 · see citing works

Optimization of a Bioluminescence Resonance Energy Transfer-Based Assay for Screening of Trypanosoma cruzi Protein/Protein Interaction Inhibitors

Mild, J. G., Fernández, L. R., Gayet, O., Iovanna, J., Dusetti, N., & Edreira, M. M. (2018) · Molecular Biotechnology · doi:10.1007/s12033-018-0078-3 · Cited by 5 · see citing works

Diversity and genome mapping assessment of disordered and functional domains in trypanosomatids

Tavares, G. S., Gonçalves, L. O., Guimarães, F. G., Guimarães, P. A. S., Rocha, L. G. D. N., Carvalho, M. G. R., Resende, D. D. M., & Ruiz, J. C. (2020) · Journal of Proteomics · doi:10.1016/j.jprot.2020.103919 · Cited by 5 · see citing works

Suspension Culture of Protozoan Organisms

Hartmann, M., & Breitling, R. (2014) · doi:10.1002/9783527683321.ch09 · Cited by 5 · see citing works

The epimastigote stage-specific gene expression of CESP is tightly regulated by its 3′ UTR

Suganuma, K., Yamasaki, S., Asada, M., Kawazu, S., & Inoue, N. (2012) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2012.09.010 · Cited by 4 · see citing works

Adenosine–uridine-rich element is one of the required cis-elements for epimastigote form stage-specific gene expression of the congolense epimastigote specific protein

Suganuma, K., Mochabo, K. M., Hakimi, H., Yamasaki, S., Yamagishi, J., Asada, M., Kawazu, S.-I., & Inoue, N. (2013) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2013.09.001 · Cited by 4 · see citing works

Polycistronic Expression of Multi-Subunit Complexes in the Eukaryotic Environment: A Narrative Review

Ghavidel, A. A., Jajarmi, V., Bandehpour, M., & Kazemi, B. (2022) · Iranian Journal of Parasitology · doi:10.18502/ijpa.v17i3.10618 · Cited by 4 · see citing works

A versatile 2A peptide-based strategy for ectopic expression and endogenous gene tagging in Trypanosoma cruzi

Niemirowicz, G. T., Carlevaro, G., Campetella, O., Bouvier, L. A., & Mucci, J. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e24595 · Cited by 4 · see citing works

Metabolite‐dependent regulation of gene expression in T rypanosoma brucei

Kim, D., & Barrett, M. P. (2013) · Molecular Microbiology · doi:10.1111/mmi.12243 · Cited by 4 · see citing works

Characterization of the mRNA untranslated regions [UTR] of the Trypanosoma cruzi LYT1 isoforms derived by alternative trans-splicing

Ruíz, E., Ramirez-Segura, C. A., Casas-Vargas, J. C., Ospina, M. I., Requena, J. M., & Puerta, C. J. (2018) · Universitas Scientiarum · doi:10.11144/javeriana.sc23-2.cotm · Cited by 4 · see citing works

Interactions between RNA-binding proteins and P32 homologues in trypanosomes and human cells

Polledo, J. M., Cervini, G., Romaniuk, M. A., & Cassola, A. (2015) · Current Genetics · doi:10.1007/s00294-015-0519-5 · Cited by 3 · see citing works

Innovation through instability? Genome (dis)organisation in Trypanosoma cruzi

Dickson, K. P., Costales, J. A., Domagalska, M. A., Veken, F. V., & Llewellyn, M. S. (2025) · Trends in Parasitology · doi:10.1016/j.pt.2025.04.008 · Cited by 2 · see citing works

Calcium homeostasis in trypanosomatids: A review of molecular targets and inhibitors

Coelho, N. C. C., Velásquez, Á. M. A., de Lima, J. S., Ramos, A. L. D., Cilli, E. M., & Graminha, M. A. S. (2025) · Cell Calcium · doi:10.1016/j.ceca.2025.103086 · Cited by 2 · see citing works

Homologous Expression of Glycosylphosphatidylinositol-Anchored Glycoproteins in Trypanosoma cruzi

Balouz, V., Mesías, A. C., Cameán, C. C., Ducrey, I., Lobo, M. M., Durante, I. M., Cánepa, G. E., Buscaglia, C. A., & Cámara, M. D. L. M. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9148-8_9 · Cited by 2 · see citing works

Transcriptomic analysis of N-terminal mutated Trypanosoma cruzi UBP1 knockdown underlines the importance of this RNA-binding protein in parasite development

Sabalette, K. B., Campo, V. A., Sotelo-Silveira, J. R., Smircich, P., & Gaudenzi, J. G. D. (2024) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0012179 · Cited by 2 · see citing works

DNA lesions that block transcription induce the death of Trypanosoma cruzi via ATR activation, which is dependent on the presence of R-loops

Mendes, I. C., Bertoldo, W. D. R., Miranda-Junior, A. S., de Assis, A. V., Repolês, B. M., Ferreira, W. R. R., Chame, D. F., Souza, D. D. L., Pavani, R., Macedo, A. M., et al. (2024) · DNA repair · doi:10.1016/j.dnarep.2024.103726 · Cited by 2 · see citing works

Genome alteration of Leishmania orientalis under Amphotericin B inhibiting conditions

Anuntasomboon, P., Siripattanapipong, S., Unajak, S., Choowongkomon, K., Burchmore, R., Leelayoova, S., Mungthin, M., & E-kobon, T. (2024) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0012716 · Cited by 2 · see citing works

Exploring the Genomic Landscape of the GP63 family in Trypanosoma cruzi : Evolutionary Dynamics and Functional PeculiaritiesPreprint

Berná, L., Chiribao, M. L., Pita, S., Álvarez-Valín, F., & Parodi‐Talice, A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.17.580826 · Cited by 2 · see citing works

A divide-and-conquer approach to uncover the genomic structure of the highly virulent RA strain of Trypanosoma cruzi

Balouz, V., Dean, A. A. C., Romer, G., Robello, C., Berná, L., & Buscaglia, C. A. (2025) · Scientific Reports · doi:10.1038/s41598-025-23742-0 · Cited by 1 · see citing works

Beyond the transcript: Chromatin implications in trans-splicing in Trypanosomatids

Siri, R. T. Z., Beati, P., Inchausti, L., Smircich, P., Alonso, G., & Ocampo, J. (2026) · PLoS ONE · doi:10.1371/journal.pone.0343367 · Cited by 1 · see citing works

Comparative Anti-Leishmanial Effects of Two ssDNA Aptamers Targeting Poly(A)-Binding Protein in Leishmania donovani Amastigotes

Tawfiq, H. A., Mohammed, A. A., & Hummadi, Y. M. K. A. M. (2026) · Journal Of Biochemical Technology · doi:10.51847/g8pt52l1nd · Cited by 1 · see citing works

Peer Review #2 of "Genome-wide analysis of 3′-untranslated regions supports the existence of post-transcriptional regulons controlling gene expression in trypanosomes (v0.1)"

(2013) · PeerJ · doi:10.7287/peerj.118v0.1/reviews/2 · Cited by 1 · see citing works

Regulatory mechanisms of Leishmania Aquaglyceroporin AQP1

Sharma, M. (2015) · doi:10.25148/etd.fidc000197

Functional Genomics and Insights into Trypanosoma cruziGene Expression Regulation

Ávila, A. R., & Goldenberg, S. (2010) · The Open Parasitology Journal · doi:10.2174/1874421401004010148

Mechanisms Controlling Gene Expression in Trypanosomatids

(2017) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9781681084053117010009 · Cited by 3 · see citing works

Open Access Functional Genomics and Insights into Trypanosoma cruzi Gene Expres- sion Regulation

Ávila, A. R., & Goldenberg, S. (2016)

Control of gene expression in Trypanosomatidae

Teixeira, S. M. R. (1998) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x1998001200001 · Cited by 69 · see citing works

Correspondence

Trypanosomatidae, I., & Teixeira, S. M. R. (1998)