| scholarly article | Q13442814 |
| P2093 | author name string | Modi G | |
| Sacks DL | |||
| McMaster WR | |||
| Joshi PB | |||
| P2860 | cites work | Plasmid-encoded hygromycin B resistance: the sequence of hygromycin B phosphotransferase gene and its expression in Escherichia coli and Saccharomyces cerevisiae | Q28265770 |
| Molecular cloning of the major surface antigen of leishmania | Q34175378 | ||
| Characterization of the promastigote surface protease of Leishmania as a membrane-bound zinc endopeptidase | Q34481004 | ||
| Evidence that the vectorial competence of phlebotomine sand flies for different species of Leishmania is controlled by structural polymorphisms in the surface lipophosphoglycan | Q35766941 | ||
| The nucleotide sequence of leuA from Salmonella typhimurium. | Q35832726 | ||
| Deletion of an immunodominant Trypanosoma cruzi surface glycoprotein disrupts flagellum-cell adhesion | Q36232637 | ||
| Identification of Leishmania genes encoding proteins containing tandemly repeating peptides | Q36354280 | ||
| Complement binding by two developmental stages of Leishmania major promastigotes varying in expression of a surface lipophosphoglycan | Q36354656 | ||
| Stage-specific binding of Leishmania donovani to the sand fly vector midgut is regulated by conformational changes in the abundant surface lipophosphoglycan. | Q36364463 | ||
| Stable transfection of the human parasite Leishmania major delineates a 30-kilobase region sufficient for extrachromosomal replication and expression | Q36721065 | ||
| Double targeted gene replacement for creating null mutants | Q37578939 | ||
| Nucleotide sequence of a plasmid born streptothricin-acetyl-transferase gene (sat-1). | Q40453528 | ||
| Mutational and functional analysis of the Leishmania surface metalloproteinase GP63: similarities to matrix metalloproteinases | Q40701933 | ||
| Modification of GP63 genes from diverse species of Leishmania for expression of recombinant protein at high levels in Escherichia coli | Q41161332 | ||
| Null mutants for the lmcpa cysteine proteinase gene in Leishmania mexicana | Q41491846 | ||
| The major surface glycoprotein (GP63) is present in both life stages of Leishmania | Q41752302 | ||
| Recombinant Leishmania surface glycoprotein GP63 is secreted in the baculovirus expression system as a latent metalloproteinase | Q42069351 | ||
| The promastigote surface protease (gp63) of Leishmania is expressed but differentially processed and localized in the amastigote stage | Q43985877 | ||
| Acid protease activity of a major surface membrane glycoprotein (gp63) from Leishmania mexicana promastigotes | Q44082213 | ||
| Identification of a surface metalloproteinase on 13 species of Leishmania isolated from humans, Crithidia fasciculata, and Herpetomonas samuelpessoai | Q44918539 | ||
| Crithidia fasciculata contains a transcribed leishmanial surface proteinase (gp63) gene homologue | Q48139130 | ||
| Structurally distinct genes for the surface protease of Leishmania mexicana are developmentally regulated | Q48139144 | ||
| Stage-specific adhesion of Leishmania promastigotes to the sandfly midgut. | Q52231087 | ||
| Developmental modification of the lipophosphoglycan from Leishmania major promastigotes during metacyclogenesis. | Q52240329 | ||
| Released glycoconjugate of indigenous Leishmania major enhances survival of a foreign L. major in Phlebotomus papatasi. | Q52450385 | ||
| Leishmania major and L. donovani: effects on proteolytic enzymes of Phlebotomus papatasi (Diptera, Psychodidae). | Q52465092 | ||
| Analysis of the active site and activation mechanism of the Leishmania surface metalloproteinase GP63. | Q52546385 | ||
| The gene encoding streptothricin acetyltransferase (sat) as a selectable marker for Leishmania expression vectors. | Q54175146 | ||
| Leishmania major HEXBP deletion mutants generated by double targeted gene replacement. | Q54216121 | ||
| Rapid isolation of DNA from trypanosomatid protozoa using a simple 'mini-prep' procedure. | Q54656629 | ||
| Genes encoding the major surface glycoprotein in Leishmania are tandemly linked at a single chromosomal locus and are constitutively transcribed | Q56762906 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Leishmania major | Q1950715 |
| P304 | page(s) | 519-530 | |
| P577 | publication date | 1998-02-01 | |
| P1433 | published in | Molecular Microbiology | Q6895967 |
| P1476 | title | Targeted gene deletion of Leishmania major genes encoding developmental stage-specific leishmanolysin (GP63). | |
| P478 | volume | 27 |
| Q39996005 | A novel form of NF-kappaB is induced by Leishmania infection: involvement in macrophage gene expression. |
| Q35433080 | A perspective on the emergence of sialic acids as potent determinants affecting leishmania biology |
| Q35188674 | Animal models for the analysis of immune responses to leishmaniasis |
| Q33279371 | Bis-acridines as lead antiparasitic agents: structure-activity analysis of a discrete compound library in vitro |
| Q35745876 | Centrin gene disruption impairs stage-specific basal body duplication and cell cycle progression in Leishmania |
| Q33397068 | Characterization of DNA sequences that confer complement resistance in Leishmania chagasi |
| Q39098197 | Complement C3 is required for the progression of cutaneous lesions and neutrophil attraction in Leishmania major infection |
| Q45374298 | Design of protease-resistant pexiganan enhances antileishmanial activity |
| Q45209464 | Development of a recombinant Leishmania major strain sensitive to ganciclovir and 5-fluorocytosine for use as a live vaccine challenge in clinical trials |
| Q47815725 | Differential expression of GP63 genes in Trypanosoma cruzi |
| Q36778915 | Differential surface deposition of complement proteins on logarithmic and stationary phase Leishmania chagasi promastigotes. |
| Q34347500 | Does the Leishmania major paradigm of pathogenesis and protection hold for New World cutaneous leishmaniases or the visceral disease? |
| Q34543547 | Dressed for success: the surface coats of insect-borne protozoan parasites |
| Q34002959 | Episomal expression of specific sense and antisense mRNAs in Leishmania amazonensis: modulation of gp63 level in promastigotes and their infection of macrophages in vitro |
| Q90317136 | Establishment, optimisation and quantitation of a bioluminescent murine infection model of visceral leishmaniasis for systematic vaccine screening |
| Q48249997 | Expression and Function of the Trypanosoma brucei Major Surface Protease (GP63) Genes |
| Q43845834 | Extracellular release of the glycosylphosphatidylinositol (GPI)-linked Leishmania surface metalloprotease, gp63, is independent of GPI phospholipolysis: implications for parasite virulence |
| Q44552477 | Extracellular release of the surface metalloprotease, gp63, from Leishmania and insect trypanosomatids. |
| Q34282182 | Function and assembly of the Leishmania surface coat |
| Q43789213 | Functional glycosylphosphatidylinositol anchor signal sequences in the Pneumocystis carinii PRT1 protease family |
| Q52603674 | Functional identification of galactosyltransferases (SCGs) required for species-specific modifications of the lipophosphoglycan adhesin controlling Leishmania major-sand fly interactions. |
| Q43073222 | Gene regulation of pteridine reductase 1 in leishmania promastigotes and amastigotes using a full-length antisense construct |
| Q33231863 | Genetic complementation to identify DNA elements that influence complement resistance in Leishmania chagasi |
| Q39851491 | Genome-wide analysis reveals increased levels of transcripts related with infectivity in peanut lectin non-agglutinated promastigotes of Leishmania infantum. |
| Q33611111 | How do protozoan parasites survive inside macrophages? |
| Q34520491 | How to succeed in parasitic life without sex? Asking Leishmania |
| Q36915063 | Immune response regulation by leishmania secreted and nonsecreted antigens |
| Q27013029 | Impact of Leishmania metalloprotease GP63 on macrophage signaling |
| Q56449802 | In vitro cytocidal effects on Trypanosoma brucei and inhibition of Leishmania major GP63 by peptidomimetic metalloprotease inhibitors |
| Q36024566 | In vitro infectivity and differential gene expression of Leishmania infantum metacyclic promastigotes: negative selection with peanut agglutinin in culture versus isolation from the stomodeal valve of Phlebotomus perniciosus |
| Q53611497 | In vitro metacyclogenesis of Leishmania (Viannia) braziliensis and Leishmania (Leishmania) amazonensis clinical field isolates, as evaluated by morphology, complement resistance, and infectivity to human macrophages. |
| Q40529912 | Involvement of Leishmania donovani major surface glycoprotein gp63 in promastigote multiplication |
| Q34232557 | Is lipophosphoglycan a virulence factor? A surprising diversity between Leishmania species |
| Q34181208 | Leishmania Subtilisin Is a Maturase for the Trypanothione Reductase System and Contributes to Disease Pathology |
| Q36499194 | Leishmania development in sand flies: parasite-vector interactions overview |
| Q36371532 | Leishmania major LACK antigen is required for efficient vertebrate parasitization |
| Q33750020 | Leishmania major survival in selective Phlebotomus papatasi sand fly vector requires a specific SCG-encoded lipophosphoglycan galactosylation pattern |
| Q34701006 | Leishmania mexicana mutants lacking glycosylphosphatidylinositol (GPI):protein transamidase provide insights into the biosynthesis and functions of GPI-anchored proteins. |
| Q55002022 | Leishmania naiffi and Leishmania guyanensis reference genomes highlight genome structure and gene evolution in the Viannia subgenus. |
| Q58779353 | Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation |
| Q42177826 | Mammalian antimicrobial peptide influences control of cutaneous Leishmania infection |
| Q41825252 | Novel peptide inhibitors of Leishmania gp63 based on the cleavage site of MARCKS (myristoylated alanine-rich C kinase substrate)-related protein |
| Q33542293 | Recent advances in identifying and validating drug targets in trypanosomes and leishmanias. |
| Q36511643 | Recent developments in the molecular, biochemical and functional characterization of GPI8 and the GPI-anchoring mechanism [review]. |
| Q77361043 | Roles of free GPIs in amastigotes of Leishmania |
| Q33969495 | Secretory pathway of trypanosomatid parasites |
| Q48352877 | Stage-specific expression in Leishmania conferred by 3' untranslated regions of L. major leishmanolysin genes (GP63). |
| Q40049255 | Structural insights into leishmanolysins encoded on chromosome 10 of Leishmania (Viannia) braziliensis |
| Q33755221 | Subversion mechanisms by which Leishmania parasites can escape the host immune response: a signaling point of view. |
| Q37119803 | The Leishmania surface protease GP63 cleaves multiple intracellular proteins and actively participates in p38 mitogen-activated protein kinase inactivation |
| Q35623857 | The genetic toolbox for Leishmania parasites |
| Q35561779 | The major surface protease (MSP or GP63) of Leishmania sp. Biosynthesis, regulation of expression, and function. |
| Q34452594 | The oligopeptidase B of Leishmania regulates parasite enolase and immune evasion |
| Q51049940 | The role of surface glycoconjugates in Leishmania midgut attachment examined by competitive binding assays and experimental development in sand flies. |
| Q37081691 | Transgenic Leishmania and the immune response to infection |
| Q42002483 | gp63 in stable cationic liposomes confers sustained vaccine immunity to susceptible BALB/c mice infected with Leishmania donovani. |
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