scholarly article | Q13442814 |
P2093 | author name string | Richard McCulloch | |
Catarina A Marques | |||
P2860 | cites work | 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 | ||
Regulation of replication licensing by acetyltransferase Hbo1. | Q24537658 | ||
Interactions between BRCA2 and RAD51 for promoting homologous recombination in Leishmania infantum | Q24622502 | ||
ATPase-dependent cooperative binding of ORC and Cdc6 to origin DNA. | Q24633457 | ||
Mechanisms for initiating cellular DNA replication | Q26827264 | ||
Peaks cloaked in the mist: the landscape of mammalian replication origins | Q26829115 | ||
Deciphering the evolutionary history of open and closed mitosis | Q27014064 | ||
Structural analysis of human Orc6 protein reveals a homology with transcription factor TFIIB | Q27667555 | ||
The BAH domain of ORC1 links H4K20me2 to DNA replication licensing and Meier–Gorlin syndrome | Q27677935 | ||
Break-induced replication requires all essential DNA replication factors except those specific for pre-RC assembly. | Q27930164 | ||
How MCM loading and spreading specify eukaryotic DNA replication initiation sites | Q28066336 | ||
ATP-dependent recognition of eukaryotic origins of DNA replication by a multiprotein complex | Q28241786 | ||
Protein-RNA interactions: new genomic technologies and perspectives | Q28257664 | ||
HBO1 histone acetylase activity is essential for DNA replication licensing and inhibited by Geminin | Q28272275 | ||
Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions | Q28279406 | ||
The multidomain structure of Orc1p reveals similarity to regulators of DNA replication and transcriptional silencing | Q28291160 | ||
Formation of linear amplicons with inverted duplications in Leishmania requires the MRE11 nuclease | Q28542480 | ||
Transcription initiation activity sets replication origin efficiency in mammalian cells | Q28754949 | ||
Evolutionary history and higher order classification of AAA+ ATPases | Q29615260 | ||
ChIP-seq: advantages and challenges of a maturing technology | Q29615336 | ||
Comparative genomics of trypanosomatid parasitic protozoa | Q29617953 | ||
RNA sequencing: advances, challenges and opportunities | Q29619605 | ||
Charting histone modifications and the functional organization of mammalian genomes | Q29620707 | ||
Archaeal DNA replication. | Q30368911 | ||
Chromosome structure: DNA nucleotide sequence elements of a subset of the minichromosomes of the protozoan Trypanosoma brucei | Q30450327 | ||
A cytokinetic function of Drosophila ORC6 protein resides in a domain distinct from its replication activity | Q30968824 | ||
Trypanosome outer kinetochore proteins suggest conservation of chromosome segregation machinery across eukaryotes. | Q31152005 | ||
Conserved linkage groups associated with large-scale chromosomal rearrangements between Old World and New World Leishmania genomes | Q31976283 | ||
G-Quadruplexes in DNA Replication: A Problem or a Necessity? | Q38963148 | ||
Does DNA replication direct locus-specific recombination during host immune evasion by antigenic variation in the African trypanosome? | Q39002369 | ||
Nuclear DNA replication and repair in parasites of the genus Leishmania: Exploiting differences to develop innovative therapeutic approaches | Q39037726 | ||
Repetitive DNA is associated with centromeric domains in Trypanosoma brucei but not Trypanosoma cruzi. | Q39315224 | ||
Unraveling cell type-specific and reprogrammable human replication origin signatures associated with G-quadruplex consensus motifs. | Q39321886 | ||
The Leishmania genome comprises 36 chromosomes conserved across widely divergent human pathogenic species | Q39716216 | ||
Divergent polo box domains underpin the unique kinetoplastid kinetochore | Q39879158 | ||
ATPase-dependent quality control of DNA replication origin licensing | Q39989632 | ||
Mechanism of Archaeal MCM Helicase Recruitment to DNA Replication Origins | Q40150794 | ||
The chromatin environment shapes DNA replication origin organization and defines origin classes | Q40330362 | ||
Genome-wide mapping reveals single-origin chromosome replication in Leishmania, a eukaryotic microbe. | Q40945987 | ||
Structure of the active form of human origin recognition complex and its ATPase motor module | Q41599238 | ||
Coordination of replication and transcription along a Drosophila chromosome. | Q41711507 | ||
Genome-wide mapping of human DNA-replication origins: levels of transcription at ORC1 sites regulate origin selection and replication timing. | Q41868711 | ||
The dynamics of genome replication using deep sequencing. | Q42090523 | ||
Accelerated growth in the absence of DNA replication origins | Q42258104 | ||
Trypanosoma brucei Orc1 is essential for nuclear DNA replication and affects both VSG silencing and VSG switching. | Q42283703 | ||
New insights into replication origin characteristics in metazoans | Q42559394 | ||
Conservation of replication timing reveals global and local regulation of replication origin activity | Q42573426 | ||
Trypanosome prereplication machinery contains a single functional orc1/cdc6 protein, which is typical of archaea | Q42576404 | ||
Initiation of DNA replication at CpG islands in mammalian chromosomes | Q42643271 | ||
Dynamic changes in histone acetylation regulate origins of DNA replication | Q42700642 | ||
Trypanosome prereplication machinery: a potential new target for an old problem. | Q42752722 | ||
Ribosome profiling: new views of translation, from single codons to genome scale | Q44759418 | ||
A highly basic sequence at the N-terminal region is essential for targeting the DNA replication protein ORC1 to the nucleus in Leishmania donovani | Q45326238 | ||
Nucleotide-dependent conformational changes in the DnaA-like core of the origin recognition complex. | Q46030233 | ||
Transcriptionally Driven DNA Replication Program of the Human Parasite Leishmania major | Q47287334 | ||
Replication timing of genes and middle repetitive sequences. | Q51233045 | ||
Expression and subcellular localization of ORC1 in Leishmania major. | Q53462170 | ||
An ARS element inhibits DNA replication through a SIR2-dependent mechanism. | Q53480696 | ||
Yeast origin recognition complex functions in transcription silencing and DNA replication | Q61942289 | ||
A telomere-mediated chromosome fragmentation approach to assess mitotic stability and ploidy alterations of Leishmania chromosomes | Q73384471 | ||
Studies with artificial extrachromosomal elements in trypanosomatids: could specificity in the initiation of DNA replication be linked to that in transcription? | Q80381253 | ||
Leishmania DNA Replication Timing: A Stochastic Event? | Q89354406 | ||
Sequencing newly replicated DNA reveals widespread plasticity in human replication timing | Q33591861 | ||
Expanded roles of the origin recognition complex in the architecture and function of silenced chromatin in Saccharomyces cerevisiae | Q33613997 | ||
Drosophila ORC localizes to open chromatin and marks sites of cohesin complex loading | Q33618928 | ||
Structural basis of the Sir1-origin recognition complex interaction in transcriptional silencing | Q33854091 | ||
Break-induced DNA replication | Q34037586 | ||
Principles and challenges of genomewide DNA methylation analysis | Q34096366 | ||
Eukaryotic DNA replication origins: many choices for appropriate answers | Q34139588 | ||
Orc6 involved in DNA replication, chromosome segregation, and cytokinesis. | Q34143699 | ||
The cell cycle of Leishmania: morphogenetic events and their implications for parasite biology | Q34160173 | ||
Trans-splicing in trypanosomes: machinery and its impact on the parasite transcriptome | Q34180921 | ||
Identification of ORC1/CDC6-interacting factors in Trypanosoma brucei reveals critical features of origin recognition complex architecture | Q34193312 | ||
Evaluating genome-scale approaches to eukaryotic DNA replication | Q34232735 | ||
Genome-wide distribution of DNA replication origins at A+T-rich islands in Schizosaccharomyces pombe | Q34250460 | ||
Evolutionary diversification of eukaryotic DNA replication machinery. | Q34392328 | ||
Replication stress and cancer | Q34473453 | ||
Coming of age: ten years of next-generation sequencing technologies | Q34526801 | ||
DNA replication timing | Q34654036 | ||
Genome-wide mapping of Arabidopsis thaliana origins of DNA replication and their associated epigenetic marks | Q34814221 | ||
Pre-replication complex proteins assemble at regions of low nucleosome occupancy within the Chinese hamster dihydrofolate reductase initiation zone | Q34865206 | ||
Motors and switches: AAA+ machines within the replisome. | Q34988324 | ||
The fission yeast homologue of Orc4p binds to replication origin DNA via multiple AT-hooks | Q35058094 | ||
The BAH domain facilitates the ability of human Orc1 protein to activate replication origins in vivo | Q35131006 | ||
The spatiotemporal program of DNA replication is associated with specific combinations of chromatin marks in human cells | Q35160747 | ||
Single molecule analysis of Trypanosoma brucei DNA replication dynamics | Q35171539 | ||
Genome-scale analysis of metazoan replication origins reveals their organization in specific but flexible sites defined by conserved features | Q35195952 | ||
Crystal structure of the eukaryotic origin recognition complex | Q35202495 | ||
The Cdc45·Mcm2-7·GINS protein complex in trypanosomes regulates DNA replication and interacts with two Orc1-like proteins in the origin recognition complex. | Q35213348 | ||
Different nucleosomal architectures at early and late replicating origins in Saccharomyces cerevisiae. | Q35251268 | ||
Genome evolution in trypanosomatid parasites | Q35550761 | ||
Chromosome and gene copy number variation allow major structural change between species and strains of Leishmania | Q35581571 | ||
Multiple Cdt1 molecules act at each origin to load replication-competent Mcm2-7 helicases | Q35626395 | ||
Cdc6-induced conformational changes in ORC bound to origin DNA revealed by cryo-electron microscopy | Q35823597 | ||
25 years of African trypanosome research: From description to molecular dissection and new drug discovery | Q35875131 | ||
High-resolution profiling of Drosophila replication start sites reveals a DNA shape and chromatin signature of metazoan origins | Q36035868 | ||
Chromosomal Translocations in the Parasite Leishmania by a MRE11/RAD50-Independent Microhomology-Mediated End Joining Mechanism | Q36055419 | ||
The positioning and dynamics of origins of replication in the budding yeast nucleus. | Q36381904 | ||
Replication landscape of the human genome | Q36511235 | ||
Single-molecule analysis of DNA replication reveals novel features in the divergent eukaryotes Leishmania and Trypanosoma brucei versus mammalian cells | Q36686405 | ||
Genome-wide analysis reveals extensive functional interaction between DNA replication initiation and transcription in the genome of Trypanosoma brucei. | Q36713460 | ||
Quantitative, genome-wide analysis of eukaryotic replication initiation and termination | Q36771862 | ||
Principles and concepts of DNA replication in bacteria, archaea, and eukarya | Q36938523 | ||
Genome-wide studies highlight indirect links between human replication origins and gene regulation. | Q36948921 | ||
Diverged composition and regulation of the Trypanosoma brucei origin recognition complex that mediates DNA replication initiation | Q36959024 | ||
Mapping replication dynamics in Trypanosoma brucei reveals a link with telomere transcription and antigenic variation. | Q37098846 | ||
DNA replication origins. | Q37197487 | ||
The origin recognition complex protein family | Q37213779 | ||
A Meier-Gorlin syndrome mutation in a conserved C-terminal helix of Orc6 impedes origin recognition complex formation | Q37217690 | ||
DNA topology, not DNA sequence, is a critical determinant for Drosophila ORC-DNA binding | Q37259735 | ||
The emerging role of RNA-binding proteins in the life cycle of Trypanosoma brucei | Q37682671 | ||
DnaA, ORC, and Cdc6: similarity beyond the domains of life and diversity. | Q37687102 | ||
Discovery of unconventional kinetochores in kinetoplastids. | Q37690124 | ||
G4 motifs affect origin positioning and efficiency in two vertebrate replicators | Q37723984 | ||
Eukaryotic chromosome DNA replication: where, when, and how? | Q37725931 | ||
Nuclear architecture, genome and chromatin organisation in Trypanosoma brucei | Q37851644 | ||
Gene expression regulation in trypanosomatids | Q37948933 | ||
On the opportunistic nature of transcription and replication initiation in the metazoan genome | Q37956564 | ||
Adaptive mechanisms in pathogens: universal aneuploidy in Leishmania | Q38025763 | ||
Dormant origins, the licensing checkpoint, and the response to replicative stresses | Q38035836 | ||
Relationship between DNA replication and the nuclear matrix. | Q38058379 | ||
Regulating DNA replication in bacteria | Q38087526 | ||
Transcription-replication encounters, consequences and genomic instability | Q38095707 | ||
Cell cycle control across the eukaryotic kingdom | Q38097151 | ||
Regulating DNA replication in eukarya | Q38120365 | ||
Antigenic variation in African trypanosomes: the importance of chromosomal and nuclear context in VSG expression control | Q38139125 | ||
Nuclear DNA replication initiation in kinetoplastid parasites: new insights into an ancient process. | Q38167180 | ||
High-resolution digital profiling of the epigenome | Q38258264 | ||
DNA replication origin activation in space and time | Q38496732 | ||
Programmed Genome Rearrangements in Tetrahymena | Q38535927 | ||
P433 | issue | 2 | |
P304 | page(s) | 98-109 | |
P577 | publication date | 2018-02-01 | |
P1433 | published in | Current Genomics | Q5195047 |
P1476 | title | Conservation and Variation in Strategies for DNA Replication of Kinetoplastid Nuclear Genomes. | |
P478 | volume | 19 |