review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Keith Gull | Q6384431 |
Bill Wickstead | Q43078779 | ||
P2093 | author name string | Jan-Peter Daniels | |
P2860 | cites work | Telomeric expression sites are highly conserved in Trypanosoma brucei | Q21144222 |
Psiscan: a computational approach to identify H/ACA-like and AGA-like non-coding RNA in trypanosomatid genomes | Q21284197 | ||
Signal recognition particle components in the nucleolus | Q22011006 | ||
The genome of the kinetoplastid parasite, Leishmania major | Q22065797 | ||
The Genome of the African Trypanosome Trypanosoma brucei | Q22065798 | ||
The Genome Sequence of Trypanosoma cruzi, Etiologic Agent of Chagas Disease | Q22065799 | ||
Nuclear speckles: a model for nuclear organelles | Q22121993 | ||
A genome-wide analysis of C/D and H/ACA-like small nucleolar RNAs in Trypanosoma brucei reveals a trypanosome-specific pattern of rRNA modification | Q24537378 | ||
The spliced leader-associated RNA is a trypanosome-specific sn(o) RNA that has the potential to guide pseudouridine formation on the SL RNA. | Q24540083 | ||
Flagellar and ciliary beating in trypanosome motility | Q80430662 | ||
Identification of the heptameric Lsm complex that binds U6 snRNA in Trypanosoma brucei | Q81145154 | ||
Functional characterization of cohesin SMC3 and separase and their roles in the segregation of large and minichromosomes in Trypanosoma brucei | Q83272779 | ||
Trypanosome spliced-leader-associated RNA (SLA1) localization and implications for spliced-leader RNA biogenesis | Q24651132 | ||
Cajal bodies and coilin--moving towards function | Q24672790 | ||
Analysis of the VSG gene silent archive in Trypanosoma brucei reveals that mosaic gene expression is prominent in antigenic variation and is favored by archive substructure | Q24676882 | ||
Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy | Q24681029 | ||
Tissue-specific spatial organization of genomes | Q24805135 | ||
Automated nuclear analysis of Leishmania major telomeric clusters reveals changes in their organization during the parasite's life cycle | Q27301285 | ||
Regulation of antigen gene expression in Trypanosoma brucei | Q28269366 | ||
Nuclear organization of the genome and the potential for gene regulation | Q28303751 | ||
Why are parasite contingency genes often associated with telomeres? | Q29036018 | ||
Comparative genomics of trypanosomatid parasitic protozoa | Q29617953 | ||
Nuclear repositioning of the VSG promoter during developmental silencing in Trypanosoma brucei | Q30480413 | ||
Evaluation of differential gene expression in Leishmania major Friedlin procyclics and metacyclics using DNA microarray analysis | Q30947082 | ||
Microarray profiling of gene expression during trypomastigote to amastigote transition in Trypanosoma cruzi | Q30981253 | ||
Timing of nuclear and kinetoplast DNA replication and early morphological events in the cell cycle of Trypanosoma brucei | Q31030771 | ||
Analysis of stage-specific gene expression in the bloodstream and the procyclic form of Trypanosoma brucei using a genomic DNA-microarray | Q31110518 | ||
Tetracycline regulated gene expression in Leishmania donovani | Q31883292 | ||
What the genome sequence is revealing about trypanosome antigenic variation | Q33225833 | ||
The promoter and transcribed regions of the Leishmania tarentolae spliced leader RNA gene array are devoid of nucleosomes | Q33285316 | ||
Isolation and analysis of the genetic diversity of repertoires of VSG expression site containing telomeres from Trypanosoma brucei gambiense, T. b. brucei and T. equiperdum. | Q33359774 | ||
The burden of human African trypanosomiasis | Q33395338 | ||
Histone acetylations mark origins of polycistronic transcription in Leishmania major | Q33428336 | ||
Key role of the 3' untranslated region in the cell cycle regulated expression of the Leishmania infantum histone H2A genes: minor synergistic effect of the 5' untranslated region | Q33449914 | ||
Trypanosoma brucei PUF9 regulates mRNAs for proteins involved in replicative processes over the cell cycle | Q33497916 | ||
Widespread variation in transcript abundance within and across developmental stages of Trypanosoma brucei | Q33511368 | ||
Digital gene expression analysis of two life cycle stages of the human-infective parasite, Trypanosoma brucei gambiense reveals differentially expressed clusters of co-regulated genes | Q33533454 | ||
Nuclear and genome organization of Trypanosoma brucei | Q33611130 | ||
Gene expression in trypanosomatid parasites | Q33651870 | ||
The organization of replication and transcription | Q33655131 | ||
The Transcriptome of the Human Pathogen Trypanosoma brucei at Single-Nucleotide Resolution | Q33691492 | ||
Exonic sequences in the 5' untranslated region of alpha-tubulin mRNA modulate trans splicing in Trypanosoma brucei | Q33775334 | ||
Histone H3 trimethylated at lysine 4 is enriched at probable transcription start sites in Trypanosoma brucei | Q33875106 | ||
Architecture of the Trypanosoma brucei nucleus during interphase and mitosis | Q33900426 | ||
Architectural organization in the interphase nucleus of the protozoan Trypanosoma brucei: location of telomeres and mini-chromosomes | Q33924213 | ||
Chromatin remodelling during the life cycle of trypanosomatids. | Q33944576 | ||
Concepts in nuclear architecture | Q36098945 | ||
Characterization of the Trypanosoma brucei cap hypermethylase Tgs1 | Q36137733 | ||
Multifunctional class I transcription in Trypanosoma brucei depends on a novel protein complex | Q36177213 | ||
Disruption of nuclear lamin organization alters the distribution of replication factors and inhibits DNA synthesis | Q36254659 | ||
Golgi duplication in Trypanosoma brucei | Q36322124 | ||
Gene transcription in trypanosomes | Q36374333 | ||
Structure and function of the nucleolus in the spotlight | Q36474418 | ||
Acetylation of histone H4K4 is cell cycle regulated and mediated by HAT3 in Trypanosoma brucei. | Q36477552 | ||
Subnuclear localization of the active variant surface glycoprotein gene expression site in Trypanosoma brucei. | Q36523556 | ||
Increased expression of LD1 genes transcribed by RNA polymerase I in Leishmania donovani as a result of duplication into the rRNA gene locus. | Q36556343 | ||
An RNA polymerase II promoter in the hsp70 locus of Trypanosoma brucei | Q36557602 | ||
Trypanosome mRNAs share a common 5' spliced leader sequence. | Q36586711 | ||
Accurate polyadenylation of procyclin mRNAs in Trypanosoma brucei is determined by pyrimidine-rich elements in the intergenic regions | Q36654188 | ||
Upstream tRNA genes are essential for expression of small nuclear and cytoplasmic RNA genes in trypanosomes | Q36667500 | ||
Structural alterations of the nucleolus in mutants of Saccharomyces cerevisiae defective in RNA polymerase I. | Q36678953 | ||
Maturation of polycistronic pre-mRNA in Trypanosoma brucei: analysis of trans splicing and poly(A) addition at nascent RNA transcripts from the hsp70 locus | Q36696804 | ||
Beyond the sequence: cellular organization of genome function | Q36744492 | ||
Nuclear architecture underlying gene expression in Trypanosoma brucei | Q36811798 | ||
Polycistronic transcripts in trypanosomes and their accumulation during heat shock: evidence for a precursor role in mRNA synthesis | Q36845306 | ||
Two essential MYST-family proteins display distinct roles in histone H4K10 acetylation and telomeric silencing in trypanosomes. | Q36916497 | ||
Post-transcriptional regulation of gene expression in trypanosomes and leishmanias | Q36927117 | ||
Rapamycin inhibits trypanosome cell growth by preventing TOR complex 2 formation | Q36936439 | ||
Identification and characterization of two trypanosome TFIIS proteins exhibiting particular domain architectures and differential nuclear localizations | Q37029482 | ||
Differential trypanosome surface coat regulation by a CCCH protein that co-associates with procyclin mRNA cis-elements. | Q37097303 | ||
RAP1 is essential for silencing telomeric variant surface glycoprotein genes in Trypanosoma brucei. | Q37169037 | ||
Four histone variants mark the boundaries of polycistronic transcription units in Trypanosoma brucei | Q37194366 | ||
Cohesin regulates VSG monoallelic expression in trypanosomes | Q37280418 | ||
Eukaryotic gene regulation in three dimensions and its impact on genome evolution | Q37325165 | ||
A new model for nuclear lamina organization. | Q37330441 | ||
The 3'-terminal region of the mRNAs for VSG and procyclin can confer stage specificity to gene expression in Trypanosoma brucei | Q37698670 | ||
Identification of cis and trans elements involved in the cell cycle regulation of multiple genes in Crithidia fasciculata | Q38321472 | ||
The NOG1 GTP-binding protein is required for biogenesis of the 60 S ribosomal subunit | Q38353907 | ||
Trypanosome spliced leader RNA genes contain the first identified RNA polymerase II gene promoter in these organisms | Q38678733 | ||
The chromatin of trypanosomes | Q39061836 | ||
A cathepsin B-like protease is required for host protein degradation in Trypanosoma brucei | Q39200840 | ||
Validation of a new method for immobilising kinetoplastid parasites for live cell imaging | Q39368756 | ||
The genes for small nucleolar RNAs in Trypanosoma brucei are organized in clusters and are transcribed as a polycistronic RNA. | Q39543027 | ||
Cell cycle regulation of RPA1 transcript levels in the trypanosomatid Crithidia fasciculata | Q39720866 | ||
RNA polymerase I transcribes procyclin genes and variant surface glycoprotein gene expression sites in Trypanosoma brucei | Q39774504 | ||
Sequences within the 5' untranslated region regulate the levels of a kinetoplast DNA topoisomerase mRNA during the cell cycle | Q40020383 | ||
The subcellular localisation of trypanosome RRP6 and its association with the exosome | Q40205921 | ||
Mitosis and genome partition in trypanosomes | Q40407472 | ||
Histone acetylation and methylation at sites initiating divergent polycistronic transcription in Trypanosoma cruzi | Q40446211 | ||
Alpha-amanitin-insensitive transcription of variant surface glycoprotein genes provides further evidence for discontinuous transcription in trypanosomes. | Q40463422 | ||
A variant histone H3 is enriched at telomeres in Trypanosoma brucei. | Q40496499 | ||
The actin gene promoter of Trypanosoma brucei | Q40508223 | ||
A ribosomal RNA gene promoter at the telomere of a mini-chromosome in Trypanosoma brucei | Q40547756 | ||
The small chromosomes of Trypanosoma brucei involved in antigenic variation are constructed around repetitive palindromes | Q40550000 | ||
Transcription initiation and termination on Leishmania major chromosome 3. | Q40762912 | ||
VSG gene expression site control in insect form Trypanosoma brucei | Q40793913 | ||
Transcription rate modulation through the Trypanosoma cruzi life cycle occurs in parallel with changes in nuclear organisation | Q40829033 | ||
Identification of novel snRNA-specific Sm proteins that bind selectively to U2 and U4 snRNAs in Trypanosoma brucei | Q41500612 | ||
Actively transcribing RNA polymerase II concentrates on spliced leader genes in the nucleus of Trypanosoma cruzi | Q41880279 | ||
Dyneins across eukaryotes: a comparative genomic analysis | Q41996465 | ||
Systematic study of sequence motifs for RNA trans splicing in Trypanosoma brucei | Q41997223 | ||
Nucleolar clustering of dispersed tRNA genes. | Q42116159 | ||
Trypanosoma brucei: a putative RNA polymerase II promoter | Q42458952 | ||
Characterization and differential nuclear localization of Nopp140 and a novel Nopp140-like protein in trypanosomes. | Q42582654 | ||
Overlapping sense and antisense transcription units in Trypanosoma brucei | Q42651879 | ||
Control of variant surface glycoprotein gene-expression sites in Trypanosoma brucei | Q42680578 | ||
Processing of a phosphoglycerate kinase reporter mRNA in Trypanosoma brucei is not coupled to transcription by RNA polymerase II. | Q43110489 | ||
Histone H1 of Trypanosoma cruzi is concentrated in the nucleolus region and disperses upon phosphorylation during progression to mitosis | Q43111881 | ||
TcUBP-1, a developmentally regulated U-rich RNA-binding protein involved in selective mRNA destabilization in trypanosomes | Q43660542 | ||
RNA polymerase I-mediated transcription of a reporter gene integrated into different loci of Leishmania | Q43832482 | ||
Characterization of the Crithidia fasciculata mRNA cycling sequence binding proteins | Q33968635 | ||
A haptoglobin-hemoglobin receptor conveys innate immunity to Trypanosoma brucei in humans | Q34011441 | ||
Genome-wide analysis of mRNA abundance in two life-cycle stages of Trypanosoma brucei and identification of splicing and polyadenylation sites | Q34080058 | ||
Life without transcriptional control? From fly to man and back again | Q34086628 | ||
A global analysis of Caenorhabditis elegans operons | Q34134326 | ||
Protein dynamics: implications for nuclear architecture and gene expression. | Q34166236 | ||
RNA-binding domain proteins in Kinetoplastids: a comparative analysis | Q34232882 | ||
The evolutionary dynamics of eukaryotic gene order | Q34319346 | ||
Leishmaniasis: current situation and new perspectives | Q34330071 | ||
A new twist in trypanosome RNA metabolism: cis-splicing of pre-mRNA. | Q34362380 | ||
The switch region on Leishmania major chromosome 1 is not required for mitotic stability or gene expression, but appears to be essential. | Q34377296 | ||
The concept of self-organization in cellular architecture | Q34403925 | ||
Birth of a nucleolus: the evolution of nucleolar compartments | Q34409658 | ||
Chromosome localization changes in the Trypanosoma cruzi nucleus | Q34420514 | ||
Ex vivo and in vitro identification of a consensus promoter for VSG genes expressed by metacyclic-stage trypanosomes in the tsetse fly. | Q34420645 | ||
Chromosome territories--a functional nuclear landscape. | Q34523990 | ||
Negative Feedback Regulation Ensures the One Receptor-One Olfactory Neuron Rule in Mouse | Q34542975 | ||
Unconventional rules of small nuclear RNA transcription and cap modification in trypanosomatids | Q34546175 | ||
Antigenic variation and allelic exclusion | Q34602633 | ||
Transcription of the intergenic regions of the tubulin gene cluster of Trypanosoma brucei: evidence for a polycistronic transcription unit in a eukaryote | Q34708187 | ||
Stimuli of differentiation regulate RNA elongation in the transcription units for the major stage-specific antigens ofTrypanosoma brucei | Q34753220 | ||
Exportin 1 mediates nuclear export of the kinetoplastid spliced leader RNA. | Q34993951 | ||
Leishmania major Friedlin chromosome 1 has an unusual distribution of protein-coding genes | Q35062825 | ||
Spatial organization of transcription by RNA polymerase III. | Q35128056 | ||
The Dynamics of Chromosome Organization and Gene Regulation | Q35550688 | ||
Transcription in kinetoplastid protozoa: why be normal? | Q35586470 | ||
Sequence elements in both the intergenic space and the 3' untranslated region of the Crithidia fasciculata KAP3 gene are required for cell cycle regulation of KAP3 mRNA. | Q35612226 | ||
Diversification of function by different isoforms of conventionally shared RNA polymerase subunits | Q35723715 | ||
Spatial genome organization | Q35761807 | ||
Form follows function: The genomic organization of cellular differentiation | Q35806109 | ||
Antigenic variation in Trypanosoma brucei: facts, challenges and mysteries | Q35853298 | ||
Analysis of the Leishmania donovani transcriptome reveals an ordered progression of transient and permanent changes in gene expression during differentiation | Q35866090 | ||
Spatial positioning; a new dimension in genome function | Q35915886 | ||
The nucleolus and transcription of ribosomal genes | Q35935633 | ||
Expression site activation in Trypanosoma brucei with three marked variant surface glycoprotein gene expression sites | Q43919504 | ||
Organization of telomeres during the cell and life cycles of Trypanosoma brucei | Q44048505 | ||
Distinct, developmental stage-specific activation mechanisms of trypanosome VSG genes. | Q44093635 | ||
Distinct acetylation of Trypanosoma cruzi histone H4 during cell cycle, parasite differentiation, and after DNA damage. | Q46035731 | ||
A structural and transcription pattern for variant surface glycoprotein gene expression sites used in metacyclic stage Trypanosoma brucei. | Q46406717 | ||
Loss of the mono-allelic control of the VSG expression sites during the development of Trypanosoma brucei in the bloodstream | Q46794890 | ||
The taxonomic position and evolutionary relationships of Trypanosoma rangeli | Q47947825 | ||
Novel organization and sequences of five genes encoding all six enzymes for de novo pyrimidine biosynthesis in Trypanosoma cruzi | Q47996996 | ||
The Trypanosoma brucei signal recognition particle lacks the Alu-domain-binding proteins: purification and functional analysis of its binding proteins by RNAi | Q48119826 | ||
The architecture of variant surface glycoprotein gene expression sites in Trypanosoma brucei | Q48294559 | ||
Diversity and dynamics of the minichromosomal karyotype in Trypanosoma brucei | Q48375777 | ||
Regulation of a transmembrane protein gene family by the small RNA-binding proteins TbUBP1 and TbUBP2. | Q51971969 | ||
Regulated expression of glycosomal phosphoglycerate kinase in Trypanosoma brucei. | Q51998546 | ||
Isolation and characterization of subnuclear compartments from Trypanosoma brucei. Identification of a major repetitive nuclear lamina component. | Q52131872 | ||
Developmental regulation of pp44/46, tyrosine-phosphorylated proteins associated with tyrosine/serine kinase activity in Trypanosoma brucei. | Q52219612 | ||
Post-transcriptional control of the differential expression of phosphoglycerate kinase genes in Trypanosoma brucei. | Q52452308 | ||
A Drosophila rRNA gene located in euchromatin is active in transcription and nucleolus formation. | Q52459985 | ||
Dynein light chain LC8 is a dimerization hub essential in diverse protein networks. | Q53509938 | ||
Histone genes in trypanosomatids. | Q53593862 | ||
Predicting three-dimensional genome structure from transcriptional activity. | Q53663300 | ||
Targeted integration into a rRNA locus results in uniform and high level expression of transgenes in Leishmania amastigotes. | Q54054140 | ||
Transcription of Leishmania major Friedlin chromosome 1 initiates in both directions within a single region. | Q55036574 | ||
Cell biology: chromosome territories. | Q55042988 | ||
Transcription of the Trypanosoma brucei spliced leader RNA gene is dependent only on the presence of upstream regulatory elements | Q55339844 | ||
Gene synteny and evolution of genome architecture in trypanosomatids | Q56877837 | ||
Electron Microscopy Analysis of the Nucleolus of Trypanosoma cruzi | Q57881589 | ||
High-Yield Isolation and Subcellular Proteomic Characterization of Nuclear and Subnuclear Structures from Trypanosomes | Q58425579 | ||
Potential regulatory elements in the Trypanosoma cruzi rRNA gene promoter | Q58811071 | ||
A pol I transcriptional body associated with VSG mono-allelic expression in Trypanosoma brucei | Q58846342 | ||
Testing Promoter Activity in the Trypanosome Genome: Isolation of a Metacyclic-Type VSG Promoter, and Unexpected Insights into RNA Polymerase II Transcription | Q60181046 | ||
Selective di- or trimethylation of histone H3 lysine 76 by two DOT1 homologs is important for cell cycle regulation in Trypanosoma brucei | Q61485153 | ||
Analysis of spliceosomal complexes in Trypanosoma brucei and silencing of two splicing factors Prp31 and Prp43 | Q61509322 | ||
Histone H2AZ dimerizes with a novel variant H2B and is enriched at repetitive DNA in Trypanosoma brucei | Q61530543 | ||
TbRAB23; a nuclear-associated Rab protein from Trypanosoma brucei | Q61569146 | ||
Inactivation of transcription by UV irradiation of T. brucei provides evidence for a multicistronic transcription unit including a VSG gene | Q69419190 | ||
DNA contents and molecular karyotypes of hybrid Trypanosoma brucei | Q69903624 | ||
Evidence for trans splicing in trypanosomes | Q70153492 | ||
Coupling of poly(A) site selection and trans-splicing in Leishmania | Q70744396 | ||
Spindle Microtubules in the Dividing Nuclei of Trypanosomes | Q71435295 | ||
A fluorescence in situ hybridisation study of the regulation of histone mRNA levels during the cell cycle of Trypanosoma brucei | Q71739047 | ||
Essential components of the mini-exon gene promoter in the trypanosomatid Leptomonas seymouri | Q71945498 | ||
A common pyrimidine-rich motif governs trans-splicing and polyadenylation of tubulin polycistronic pre-mRNA in trypanosomes | Q72670719 | ||
Fine Structure and Cytochemistry of the Nucleus and the Kinetoplast of Epimastigotes ofTrypanosoma cruzi1 | Q72701917 | ||
Partitioning of large and minichromosomes in Trypanosoma brucei | Q73248175 | ||
Segregation of minichromosomes in trypanosomes: implications for mitotic mechanisms | Q77329368 | ||
Silencing of Sm proteins in Trypanosoma brucei by RNA interference captured a novel cytoplasmic intermediate in spliced leader RNA biogenesis | Q79130141 | ||
The mitotic stability of the minichromosomes of Trypanosoma brucei | Q79253027 | ||
RNAi interference of XPO1 and Sm genes and their effect on the spliced leader RNA in Trypanosoma brucei | Q80133507 | ||
P433 | issue | 4 | |
P921 | main subject | cell biology | Q7141 |
P304 | page(s) | 552-569 | |
P577 | publication date | 2010-12-01 | |
P1433 | published in | Microbiology and Molecular Biology Reviews | Q6839270 |
P1476 | title | Cell biology of the trypanosome genome | |
P478 | volume | 74 |
Q38388370 | A touch of Zen: post-translational regulation of the Leishmania stress response. |
Q28742742 | ALBA proteins are stage regulated during trypanosome development in the tsetse fly and participate in differentiation |
Q91617860 | African trypanosomes |
Q34322155 | Alternative cytoskeletal landscapes: cytoskeletal novelty and evolution in basal excavate protists |
Q38771703 | Bromodomains in Protozoan Parasites: Evolution, Function, and Opportunities for Drug Development |
Q42370276 | Cell cycle stage-specific transcriptional activation of cyclins mediated by HAT2-dependent H4K10 acetylation of promoters in Leishmania donovani. |
Q37507562 | Co-dependence between trypanosome nuclear lamina components in nuclear stability and control of gene expression. |
Q28553426 | Comparative Transcriptome Profiling of Human Foreskin Fibroblasts Infected with the Sylvio and Y Strains of Trypanosoma cruzi |
Q36263867 | Comprehensive Identification of mRNA-Binding Proteins of Leishmania donovani by Interactome Capture |
Q38048724 | Cytokinesis in trypanosomes |
Q28547740 | Differential Subcellular Localization of Leishmania Alba-Domain Proteins throughout the Parasite Development |
Q37690124 | Discovery of unconventional kinetochores in kinetoplastids. |
Q38013885 | Epigenetic mechanisms, nuclear architecture and the control of gene expression in trypanosomes. |
Q38103341 | Evolutionary cell biology of chromosome segregation: insights from trypanosomes |
Q24630129 | Genome hyperevolution and the success of a parasite |
Q36037491 | Genome organization is a major component of gene expression control in response to stress and during the cell division cycle in trypanosomes. |
Q41666787 | Genome wide occurrence and insertion preferences of INGI/RIME and SLACS CRE transposable elements in Trypanosoma brucei |
Q36713460 | Genome-wide analysis reveals extensive functional interaction between DNA replication initiation and transcription in the genome of Trypanosoma brucei. |
Q57285697 | Genome-wide mapping reveals conserved and diverged R-loop activities in the unusual genetic landscape of the African trypanosome genome |
Q42379576 | Genomic analysis of Isometamidium Chloride resistance in Trypanosoma congolense |
Q34469008 | Histone H1 plays a role in heterochromatin formation and VSG expression site silencing in Trypanosoma brucei. |
Q34193312 | Identification of ORC1/CDC6-interacting factors in Trypanosoma brucei reveals critical features of origin recognition complex architecture |
Q36000301 | Integrative analysis of the Trypanosoma brucei gene expression cascade predicts differential regulation of mRNA processing and unusual control of ribosomal protein expression |
Q38834177 | Interactions between RNA-binding proteins and P32 homologues in trypanosomes and human cells. |
Q52370221 | Involvement in surface antigen expression by a moonlighting FG-repeat nucleoporin in trypanosomes. |
Q33588730 | Lineage-specific proteins essential for endocytosis in trypanosomes |
Q36316016 | Lysine acetylation: elucidating the components of an emerging global signaling pathway in trypanosomes |
Q28676963 | Molecular paleontology and complexity in the last eukaryotic common ancestor |
Q39037726 | Nuclear DNA replication and repair in parasites of the genus Leishmania: Exploiting differences to develop innovative therapeutic approaches |
Q34069546 | Nucleotide excision repair in Trypanosoma brucei: specialization of transcription-coupled repair due to multigenic transcription |
Q36108560 | Opportunities and challenges in chronic Chagas cardiomyopathy |
Q39695613 | Organization of the smallest eukaryotic spindle |
Q21146630 | OrthoFinder: solving fundamental biases in whole genome comparisons dramatically improves orthogroup inference accuracy |
Q91816847 | PhyloToL: A Taxon/Gene-Rich Phylogenomic Pipeline to Explore Genome Evolution of Diverse Eukaryotes |
Q31115343 | Post-transcriptional regulation of the trypanosome heat shock response by a zinc finger protein |
Q42778313 | RNA-seq transcriptional profiling of Leishmania amazonensis reveals an arginase-dependent gene expression regulation. |
Q58842888 | Recent advances in trypanosomatid research: genome organization, expression, metabolism, taxonomy and evolution |
Q26765180 | Regulation of RNA binding proteins in trypanosomatid protozoan parasites |
Q35171539 | Single molecule analysis of Trypanosoma brucei DNA replication dynamics |
Q36686405 | Single-molecule analysis of DNA replication reveals novel features in the divergent eukaryotes Leishmania and Trypanosoma brucei versus mammalian cells |
Q36448548 | Telomeres, tethers and trypanosomes |
Q38178666 | The CAF1-NOT complex of trypanosomes |
Q38725177 | The Major Protein Arginine Methyltransferase in Trypanosoma brucei Functions as an Enzyme-Prozyme Complex. |
Q34067812 | The epigenome of Trypanosoma brucei: a regulatory interface to an unconventional transcriptional machine |
Q88130476 | The general mRNA exporters Mex67 and Mtr2 play distinct roles in nuclear export of tRNAs in Trypanosoma brucei. |
Q48302987 | The genomes of Crithidia bombi and C. expoeki, common parasites of bumblebees. |
Q40109240 | The proteome and transcriptome of the infectious metacyclic form of Trypanosoma brucei define quiescent cells primed for mammalian invasion. |
Q36932921 | The roles of 3'-exoribonucleases and the exosome in trypanosome mRNA degradation |
Q35091250 | The streamlined genome of Phytomonas spp. relative to human pathogenic kinetoplastids reveals a parasite tailored for plants |
Q36791484 | The unique Leishmania EIF4E4 N-terminus is a target for multiple phosphorylation events and participates in critical interactions required for translation initiation |
Q34842023 | Transcriptome-wide analysis of trypanosome mRNA decay reveals complex degradation kinetics and suggests a role for co-transcriptional degradation in determining mRNA levels |
Q37692788 | Transcriptomic analysis reveals metabolic switches and surface remodeling as key processes for stage transition in Trypanosoma cruzi |
Q42035252 | Trypanosome CNOT10 is essential for the integrity of the NOT deadenylase complex and for degradation of many mRNAs |
Q31152005 | Trypanosome outer kinetochore proteins suggest conservation of chromosome segregation machinery across eukaryotes. |
Q41135322 | Two related trypanosomatid eIF4G homologues have functional differences compatible with distinct roles during translation initiation |
Q37713544 | Well-positioned nucleosomes punctuate polycistronic pol II transcription units and flank silent VSG gene arrays in Trypanosoma brucei. |
Search more.