Comparative genomic analysis of three Leishmania species that cause diverse human disease - Test2 - elhamkhani - TriplyDB

Comparative genomic analysis of three Leishmania species that cause diverse human disease

Comparative genomic analysis of three Leishmania species that cause diverse human disease

http://www.wikidata.org/entity/Q21972828

about

Genome of the avirulent human-infective trypanosome--Trypanosoma rangeli Leishmania RNA virus: when the host pays the toll Genomic confirmation of hybridisation and recent inbreeding in a vector-isolated Leishmania population Insights into the genome sequence of a free-living Kinetoplastid: Bodo saltans (Kinetoplastida: Euglenozoa)Whole genome sequencing of multiple Leishmania donovani clinical isolates provides insights into population structure and mechanisms of drug resistance The evolution of amastin surface glycoproteins in trypanosomatid parasites Cutaneous Leishmaniasis Vaccination: A Matter of Quality Post-Genomics and Vaccine Improvement for Leishmania Dendritic Cells and Leishmania Infection: Adding Layers of Complexity to a Complex Disease Drug resistance analysis by next generation sequencing in Leishmania Drug repurposing and human parasitic protozoan diseases Unveiling the intracellular survival gene kit of trypanosomatid parasites Comparative analysis of the omics technologies used to study antimonial, amphotericin B, and pentamidine resistance in leishmania Impact of Leishmania metalloprotease GP63 on macrophage signaling Functional genomics of trypanosomatids Determinants for the development of visceral leishmaniasis disease Automated nuclear analysis of Leishmania major telomeric clusters reveals changes in their organization during the parasite's life cycle Studies of the Effectiveness of Bisphosphonate and Vanadium-Bisphosphonate Compounds In Vitro against Axenic Leishmania tarentolae.Structures of Leishmania major orthologues of macrophage migration inhibitory factor N-Myristoyltransferase from Leishmania donovani: Structural and Functional Characterisation of a Potential Drug Target for Visceral Leishmaniasis Structural Basis of Molecular Recognition of the Leishmania Small Hydrophilic Endoplasmic Reticulum-associated Protein (SHERP) at Membrane Surfaces Substrate Preferences and Catalytic Parameters Determined by Structural Characteristics of Sterol 14α-Demethylase (CYP51) from Leishmania infantum Plasticity of the Leishmania genome leading to gene copy number variations and drug resistance Artemis: an integrated platform for visualization and analysis of high-throughput sequence-based experimental data The TriTryp phosphatome: analysis of the protein phosphatase catalytic domains Identification of potent chemotypes targeting Leishmania major using a high-throughput, low-stringency, computationally enhanced, small molecule screen Leishmania-specific surface antigens show sub-genus sequence variation and immune recognition Retention and loss of RNA interference pathways in trypanosomatid protozoans Shotgun sequencing analysis of Trypanosoma cruzi I Sylvio X10/1 and comparison with T. cruzi VI CL Brener Identification of putative potassium channel homologues in pathogenic protozoa Generation of Leishmania hybrids by whole genomic DNA transformation Computational prediction of protein-protein interactions in Leishmania predicted proteomes Transcriptomic study reveals widespread spliced leader trans-splicing, short 5'-UTRs and potential complex carbon fixation mechanisms in the euglenoid Alga Eutreptiella sp Genetic structure and evolution of the Leishmania genus in Africa and Eurasia: what does MLSA tell us Proteomic and genomic analyses of antimony resistant Leishmania infantum mutant Genetic profiling of the isoprenoid and sterol biosynthesis pathway genes of Trypanosoma cruzi Golgi-located NTPDase1 of Leishmania major is required for lipophosphoglycan elongation and normal lesion development whereas secreted NTPDase2 is dispensable for virulence Differential Subcellular Localization of Leishmania Alba-Domain Proteins throughout the Parasite Development Metabolomic Analyses of Leishmania Reveal Multiple Species Differences and Large Differences in Amino Acid Metabolism Comparative Life Cycle Transcriptomics Revises Leishmania mexicana Genome Annotation and Links a Chromosome Duplication with Parasitism of Vertebrates

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Comparative genomic analysis of three Leishmania species that cause diverse human disease

http://www.wikidata.org/entity/Q21972828

description

2007 nî lūn-bûn

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2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2007 թվականի հուլիսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Comparative genomic analysis of three Leishmania species that cause diverse human disease

@ast

Comparative genomic analysis of three Leishmania species that cause diverse human disease

@en

Comparative genomic analysis of three Leishmania species that cause diverse human disease

@en-gb

Comparative genomic analysis of three Leishmania species that cause diverse human disease

@nl

type

label

Comparative genomic analysis of three Leishmania species that cause diverse human disease

@ast

Comparative genomic analysis of three Leishmania species that cause diverse human disease

@en

Comparative genomic analysis of three Leishmania species that cause diverse human disease

@en-gb

Comparative genomic analysis of three Leishmania species that cause diverse human disease

@nl

prefLabel

Comparative genomic analysis of three Leishmania species that cause diverse human disease

@ast

Comparative genomic analysis of three Leishmania species that cause diverse human disease

@en

Comparative genomic analysis of three Leishmania species that cause diverse human disease

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Comparative genomic analysis of three Leishmania species that cause diverse human disease

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Nature Genetics

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Comparative genomic analysis of three Leishmania species that cause diverse human disease

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Audrey Fraser

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Barclay Barrell

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Christopher S Peacock

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Claire Arrowsmith

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Daniel P Depledge

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Deborah F Smith

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Doug Ormond

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P2860

The genome of the kinetoplastid parasite, Leishmania major

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

Initial sequencing and comparative analysis of the mouse genome

Functional replacement of Trypanosoma brucei Argonaute by the human slicer Argonaute2

A Plasmodium whole-genome synteny map: indels and synteny breakpoints as foci for species-specific genes

Artemis: sequence visualization and annotation

PAML: a program package for phylogenetic analysis by maximum likelihood

A phosphatidylinositol 3-kinase and phosphatidylinositol transfer protein act synergistically in formation of constitutive transport vesicles from the trans-Golgi network.

The Saccharomyces cerevisiae SEC14 gene encodes a cytosolic factor that is required for transport of secretory proteins from the yeast Golgi complex.

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10.1038/NG2053

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7

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39

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Sandra L. Baldauf

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Sally Whitehead

Tracey Chillingworth

Adam Faulconbridge

Halina Norbertczak

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2007-07-01T00:00:00Z

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