scholarly article | Q13442814 |
P819 | ADS bibcode | 2008PNAS..10510125K |
P356 | DOI | 10.1073/PNAS.0802331105 |
P932 | PMC publication ID | 2481378 |
P698 | PubMed publication ID | 18626016 |
P5875 | ResearchGate publication ID | 5226392 |
P50 | author | Jackson Egen | Q54152493 |
Michael P. Fay | Q48691498 | ||
P2093 | author name string | Shaden Kamhawi | |
David Sacks | |||
Alain Debrabant | |||
Phillip Lawyer | |||
Nathan Peters | |||
Nagila Secundino | |||
Nicola Kimblin | |||
P2860 | cites work | Salivary gland lysates from the sand fly Lutzomyia longipalpis enhance Leishmania infectivity. | Q52461534 |
The effect of post-bloodmeal nutrition of Phlebotomus papatasi on the transmission of Leishmania major. | Q52464926 | ||
An analysis of T cell responsiveness in Indian kala-azar. | Q54412738 | ||
Filamentous proteophosphoglycan secreted by Leishmania promastigotes forms gel-like three-dimensional networks that obstruct the digestive tract of infected sandfly vectors | Q58867616 | ||
Dissection of the functional domains of the Leishmania surface membrane 3'-nucleotidase/nuclease, a unique member of the class I nuclease family | Q73626691 | ||
Evolution of lesion formation, parasitic load, immune response, and reservoir potential in C57BL/6 mice following high- and low-dose challenge with Leishmania major | Q33599537 | ||
Transmission of cutaneous leishmaniasis by sand flies is enhanced by regurgitation of fPPG. | Q33714994 | ||
Synthetic glycovaccine protects against the bite of leishmania-infected sand flies. | Q33732035 | ||
Molecular aspects of parasite-vector and vector-host interactions in leishmaniasis | Q34360809 | ||
Leishmania manipulation of sand fly feeding behavior results in enhanced transmission | Q35865489 | ||
New insights into the developmental biology and transmission mechanisms of Leishmania. | Q35882552 | ||
Leishmania chitinase facilitates colonization of sand fly vectors and enhances transmission to mice. | Q36691534 | ||
Leishmania infections damage the feeding mechanism of the sandfly vector and implement parasite transmission by bite | Q37259413 | ||
Metacyclogenesis in Leishmania promastigotes | Q38643070 | ||
Leishmania in phlebotomid sandflies - IV. The transmission of Leishmania mexicana amazonensis to hamsters by the bite of experimentally infected Lutzomyia longipalpis | Q39141908 | ||
The role of promastigote secretory gel in the origin and transmission of the infective stage of Leishmania mexicana by the sandfly Lutzomyia longipalpis. | Q39405769 | ||
Leishmanin skin test lymphoproliferative responses and cytokine production after symptomatic or asymptomatic Leishmania major infection in Tunisia | Q39432514 | ||
Modification of sand fly biting behavior by Leishmania leads to increased parasite transmission | Q41496808 | ||
Blocked stomodeal valve of the insect vector: similar mechanism of transmission in two trypanosomatid models | Q44162617 | ||
A prospective study of visceral leishmaniasis in an endemic area of Brazil. | Q50575676 | ||
Identification and overexpression of the A2 amastigote-specific protein in Leishmania donovani. | Q52201228 | ||
Changes in lipophosphoglycan and gene expression associated with the development of Leishmania major in Phlebotomus papatasi. | Q52206417 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 29 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Leishmania major | Q1950715 |
P1104 | number of pages | 6 | |
P304 | page(s) | 10125-10130 | |
P577 | publication date | 2008-07-14 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Quantification of the infectious dose of Leishmania major transmitted to the skin by single sand flies | |
P478 | volume | 105 |
Q36702606 | A new model of progressive visceral leishmaniasis in hamsters by natural transmission via bites of vector sand flies |
Q41186389 | A sand fly salivary protein vaccine shows efficacy against vector-transmitted cutaneous leishmaniasis in nonhuman primates. |
Q46248277 | All-Trans Retinoic Acid Promotes an M1- to M2-Phenotype Shift and Inhibits Macrophage-Mediated Immunity to Leishmania major |
Q33859617 | Animal models for the study of leishmaniasis immunology. |
Q28540810 | Antimony resistant Leishmania donovani but not sensitive ones drives greater frequency of potent T-regulatory cells upon interaction with human PBMCs: role of IL-10 and TGF-β in early immune response |
Q36485150 | Apoptotic cell clearance of Leishmania major-infected neutrophils by dendritic cells inhibits CD8⁺ T-cell priming in vitro by Mer tyrosine kinase-dependent signaling |
Q40122780 | Apoptotic induction induces Leishmania aethiopica and L. mexicana spreading in terminally differentiated THP-1 cells |
Q28485377 | Appraisal of a Leishmania major strain stably expressing mCherry fluorescent protein for both in vitro and in vivo studies of potential drugs and vaccine against cutaneous leishmaniasis |
Q33557765 | CXCL10 production by human monocytes in response to Leishmania braziliensis infection |
Q38852454 | Causes and consequences of higher Leishmania infantum burden in patients with kala-azar: a study of 625 patients |
Q37846878 | Cell biology and immunology of Leishmania |
Q45980979 | Combining epidemiology with basic biology of sand flies, parasites, and hosts to inform leishmaniasis transmission dynamics and control. |
Q90316284 | Commensal-specific T cell plasticity promotes rapid tissue adaptation to injury |
Q34595909 | Comparative evaluation of lesion development, tissue damage, and cytokine expression in golden hamsters (Mesocricetus auratus) infected by inocula with different Leishmania (Viannia) braziliensis concentrations |
Q36970884 | Complement-mediated 'bystander' damage initiates host NLRP3 inflammasome activation. |
Q36063251 | Concomitant Immunity Induced by Persistent Leishmania major Does Not Preclude Secondary Re-Infection: Implications for Genetic Exchange, Diversity and Vaccination |
Q39016116 | Continual renewal and replication of persistent Leishmania major parasites in concomitantly immune hosts |
Q36331305 | Cutaneous Infection with Leishmania major Mediates Heterologous Protection against Visceral Infection with Leishmania infantum |
Q33523524 | Detection and identification of old world Leishmania by high resolution melt analysis |
Q37256528 | Distinct roles for MyD88 and Toll-like receptor 2 during Leishmania braziliensis infection in mice |
Q36302981 | Effect of ambient temperature on the clinical manifestations of experimental diffuse cutaneous leishmaniasis in a rodent model |
Q34167908 | Efficient capture of infected neutrophils by dendritic cells in the skin inhibits the early anti-leishmania response |
Q52769819 | Epidemiological survey of Lutzomyia longipalpis infected by Leishmania infantum in an endemic area of Brazil. |
Q52716429 | Establishment and maintenance of sand fly colonies. |
Q37270131 | Evaluation of T cell responses in healing and nonhealing leishmaniasis reveals differences in T helper cell polarization ex vivo and in vitro |
Q36682576 | Evaluation of recombinant Leishmania polyprotein plus glucopyranosyl lipid A stable emulsion vaccines against sand fly-transmitted Leishmania major in C57BL/6 mice |
Q37167717 | Experimental infection of Phlebotomus perniciosus by bioluminescent Leishmania infantum using murine model and artificial feeder |
Q33939315 | Experimental transmission of Leishmania infantum by two major vectors: a comparison between a viscerotropic and a dermotropic strain |
Q64060584 | Functional genomics in sand fly-derived Leishmania promastigotes |
Q38862609 | Genes that encodes NAGT, MIF1 and MIF2 are not virulence factors for kala-azar caused by Leishmania infantum |
Q61810435 | Host competence of African rodents and for |
Q38869588 | Human immune response to salivary proteins of wild-caught Phlebotomus papatasi. |
Q33979932 | IL-10 production differentially influences the magnitude, quality, and protective capacity of Th1 responses depending on the vaccine platform |
Q42654168 | IL-4Rα Signaling in Keratinocytes and Early IL-4 Production Are Dispensable for Generating a Curative T Helper 1 Response in Leishmania major-Infected C57BL/6 Mice. |
Q37760628 | Imaging of the host/parasite interplay in cutaneous leishmaniasis |
Q47094812 | Immunization against full-length protein and peptides from the Lutzomyia longipalpis sand fly salivary component maxadilan protects against Leishmania major infection in a murine model |
Q48546496 | Immunization with Live Attenuated Leishmania donovani Centrin-/- Parasites Is Efficacious in Asymptomatic Infection |
Q44190665 | In vitro isolation and infection intensity of Rickettsia parkeri in Amblyomma triste ticks from the Paraná River Delta region, Argentina |
Q37021689 | In vivo imaging reveals an essential role for neutrophils in leishmaniasis transmitted by sand flies. |
Q35788474 | Indigenous microbiota and Leishmaniasis. |
Q34009085 | Infection parameters in the sand fly vector that predict transmission of Leishmania major |
Q36013075 | Influence of the Microenvironment in the Transcriptome of Leishmania infantum Promastigotes: Sand Fly versus Culture. |
Q52818211 | Inhibitor of serine peptidase 2 enhances Leishmania major survival in the skin through control of monocytes and monocyte-derived cells. |
Q63246497 | Inward rectifier potassium (Kir) channels mediate salivary gland function and blood feeding in the lone star tick, Amblyomma americanum |
Q33991563 | Kinetic analysis of ex vivo human blood infection by Leishmania |
Q26777203 | Kinetoplastid Membrane Protein-11 as a Vaccine Candidate and a Virulence Factor in Leishmania |
Q33706138 | Leishmania Exosomes Modulate Innate and Adaptive Immune Responses through Effects on Monocytes and Dendritic Cells |
Q36251327 | Leishmania HASP and SHERP Genes Are Required for In Vivo Differentiation, Parasite Transmission and Virulence Attenuation in the Host. |
Q37675356 | Leishmania amazonensis exhibits phosphatidylserine-dependent procoagulant activity, a process that is counteracted by sandfly saliva. |
Q36499194 | Leishmania development in sand flies: parasite-vector interactions overview |
Q37724087 | Leishmania donovani development in Phlebotomus argentipes: comparison of promastigote- and amastigote-initiated infections |
Q33750020 | Leishmania major survival in selective Phlebotomus papatasi sand fly vector requires a specific SCG-encoded lipophosphoglycan galactosylation pattern |
Q47551102 | Leishmania proteophosphoglycans regurgitated from infected sand flies accelerate dermal wound repair and exacerbate leishmaniasis via insulin-like growth factor 1-dependent signalling |
Q89441148 | Leishmania tropica: suggestive evidences for the effect of infectious dose on pathogenicity and immunogenicity in an experimental model |
Q35091237 | Lundep, a sand fly salivary endonuclease increases Leishmania parasite survival in neutrophils and inhibits XIIa contact activation in human plasma |
Q35685422 | Lymph node hypertrophy following Leishmania major infection is dependent on TLR9. |
Q27010243 | Mechanisms of cellular invasion by intracellular parasites |
Q59136686 | More than just exosomes: distinct extracellular products potentiate the establishment of infection |
Q36321924 | Natural hybrid of Leishmania infantum/L. donovani: development in Phlebotomus tobbi, P. perniciosus and Lutzomyia longipalpis and comparison with non-hybrid strains differing in tissue tropism. |
Q36357924 | Natural transmission of Leishmania infantum through experimentally infected Phlebotomus perniciosus highlights the virulence of Leishmania parasites circulating in the human visceral leishmaniasis outbreak in Madrid, Spain |
Q36871944 | New Insights Into the Transmissibility of Leishmania infantum From Dogs to Sand Flies: Experimental Vector-Transmission Reveals Persistent Parasite Depots at Bite Sites |
Q37224067 | Perpetuation of Leishmania: some novel insight into elegant developmental programs |
Q35213593 | Platelet activation attracts a subpopulation of effector monocytes to sites of Leishmania major infection |
Q44369661 | Preliminary study towards a novel experimental model to study localized cutaneous leishmaniasis caused by Leishmania (Leishmania) mexicana |
Q92888016 | Promastigote secretory gel from natural and unnatural sand fly vectors exacerbate Leishmania major and Leishmania tropica cutaneous leishmaniasis in mice |
Q92049458 | Protective or Detrimental? Understanding the Role of Host Immunity in Leishmaniasis |
Q33495567 | Proteophosophoglycans regurgitated by Leishmania-infected sand flies target the L-arginine metabolism of host macrophages to promote parasite survival |
Q64086882 | Quantifying Leishmania Metacyclic Promastigotes from Individual Sandfly Bites Reveals the Efficiency of Vector Transmission |
Q34428157 | Quantifying the contribution of hosts with different parasite concentrations to the transmission of visceral leishmaniasis in Ethiopia |
Q27319532 | Rapid Sequestration of Leishmania mexicana by Neutrophils Contributes to the Development of Chronic Lesion |
Q55311477 | Real-time PCR applications for diagnosis of leishmaniasis. |
Q34034024 | Risk factors for severe Rift Valley fever infection in Kenya, 2007. |
Q91999810 | Route map for the discovery and pre-clinical development of new drugs and treatments for cutaneous leishmaniasis |
Q33450546 | Sand fly salivary proteins induce strong cellular immunity in a natural reservoir of visceral leishmaniasis with adverse consequences for Leishmania |
Q28662255 | Sand fly-Leishmania interactions: long relationships are not necessarily easy |
Q54253014 | Sequential blood meals promote Leishmania replication and reverse metacyclogenesis augmenting vector infectivity. |
Q33899666 | Site-dependent recruitment of inflammatory cells determines the effective dose of Leishmania major |
Q33614998 | Skin-resident CD4+ T cells protect against Leishmania major by recruiting and activating inflammatory monocytes. |
Q41982110 | The PCR-based detection of Leishmania major in Mus musculus and other rodents caught in southern Iran: a guide to sample selection |
Q37288849 | The improbable transmission of Trypanosoma cruzi to human: the missing link in the dynamics and control of Chagas disease |
Q38744345 | The midgut microbiota plays an essential role in sand fly vector competence for Leishmania major. |
Q36063617 | The role of leishmania proteophosphoglycans in sand fly transmission and infection of the Mammalian host |
Q35800263 | The transmission of Leishmania infantum chagasi by the bite of the Lutzomyia longipalpis to two different vertebrates |
Q47290243 | Use of In Vivo Imaging System Technology in Leishmania major BALB/c Mouse Ear Infection Studies |
Q39257463 | Use of two-photon microscopy to study Leishmania major infection of the skin |
Q34019064 | Vector saliva in vaccines for visceral leishmaniasis: a brief encounter of high consequence? |
Q27316727 | Vector transmission of leishmania abrogates vaccine-induced protective immunity |
Q37988648 | What has proteomics taught us about Leishmania development? |
Q35190896 | Xenodiagnosis of Leishmania donovani in BALB/c mice using Phlebotomus orientalis: a new laboratory model. |
Q33921586 | Zika virus transmission to mouse ear by mosquito bite: a laboratory model that replicates the natural transmission process |
Search more.