Search Results - "GAMARRO, Francisco"
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Drug resistance and treatment failure in leishmaniasis: A 21st century challenge
Published in PLoS neglected tropical diseases (14-12-2017)“…Reevaluation of treatment guidelines for Old and New World leishmaniasis is urgently needed on a global basis because treatment failure is an increasing…”
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Genomic and Molecular Characterization of Miltefosine Resistance in Leishmania infantum Strains with Either Natural or Acquired Resistance through Experimental Selection of Intracellular Amastigotes
Published in PloS one (28-04-2016)“…During the last decade miltefosine (MIL) has been used as first-line treatment for visceral leishmaniasis in endemic areas with antimonial resistance, but a…”
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Leishmania donovani develops resistance to drug combinations
Published in PLoS neglected tropical diseases (01-12-2012)“…Drug combinations for the treatment of leishmaniasis represent a promising and challenging chemotherapeutic strategy that has recently been implemented in…”
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Complete assembly of the Leishmania donovani (HU3 strain) genome and transcriptome annotation
Published in Scientific reports (16-04-2019)“…Leishmania donovani is a unicellular parasite that causes visceral leishmaniasis, a fatal disease in humans. In this study, a complete assembly of the genome…”
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Genomic and transcriptomic alterations in Leishmania donovani lines experimentally resistant to antileishmanial drugs
Published in International journal for parasitology -- drugs and drug resistance (01-08-2018)“…Leishmaniasis is a serious medical issue in many countries around the World, but it remains largely neglected in terms of research investment for developing…”
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Strasseriolides display in vitro and in vivo activity against trypanosomal parasites and cause morphological and size defects in Trypanosoma cruzi
Published in PLoS neglected tropical diseases (01-09-2023)“…Neglected diseases caused by kinetoplastid parasites are a health burden in tropical and subtropical countries. The need to create safe and effective medicines…”
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Fitness of Leishmania donovani parasites resistant to drug combinations
Published in PLoS neglected tropical diseases (01-04-2015)“…Drug resistance represents one of the main problems for the use of chemotherapy to treat leishmaniasis. Additionally, it could provide some advantages to…”
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Synthesis of sp2-Iminosugar Selenoglycolipids as Multitarget Drug Candidates with Antiproliferative, Leishmanicidal and Anti-Inflammatory Properties
Published in Molecules (Basel, Switzerland) (11-12-2021)“…sp2-Iminosugar glycolipids (sp2-IGLs) represent a consolidated family of glycoconjugate mimetics encompassing a monosaccharide-like glycone moiety with a…”
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The 8-Aminoquinoline Analogue Sitamaquine Causes Oxidative Stress in Leishmania donovani Promastigotes by Targeting Succinate Dehydrogenase
Published in Antimicrobial Agents and Chemotherapy (01-09-2011)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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Antileishmanial and Antitrypanosomal Activities of the 8-Aminoquinoline Tafenoquine
Published in Antimicrobial Agents and Chemotherapy (01-12-2010)“…ERRATUM ( vol. 55 , p. 458 ) Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg…”
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Arylthiosemicarbazones as antileishmanial agents
Published in European journal of medicinal chemistry (10-11-2016)“…Based on a screening process, we targeted substituted thiosemicarbazone as potential antileishmanial agents. Our objective was to identify the key structural…”
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The Oral Antimalarial Drug Tafenoquine Shows Activity against Trypanosoma brucei
Published in Antimicrobial agents and chemotherapy (01-10-2015)“…The protozoan parasite Trypanosoma brucei causes human African trypanosomiasis, or sleeping sickness, a neglected tropical disease that requires new, safer,…”
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Tafenoquine, an Antiplasmodial 8-Aminoquinoline, Targets Leishmania Respiratory Complex III and Induces Apoptosis
Published in Antimicrobial Agents and Chemotherapy (01-12-2010)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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Discovery of potent pteridine reductase inhibitors to guide antiparasite drug development
Published in Proceedings of the National Academy of Sciences - PNAS (05-02-2008)“…Pteridine reductase (PTR1) is essential for salvage of pterins by parasitic trypanosomatids and is a target for the development of improved therapies. To…”
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Identification of novel anti-amoebic pharmacophores from kinase inhibitor chemotypes
Published in Frontiers in microbiology (10-05-2023)“…species, , and are opportunistic pathogens that cause a range of brain, skin, eye, and disseminated diseases in humans and animals. These pathogenic…”
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Modulation of Cholesterol Pathways in Human Macrophages Infected by Clinical Isolates of Leishmania infantum
Published in Frontiers in cellular and infection microbiology (29-04-2022)“…To increase our understanding of factors contributing to therapeutic failure (TF) in leishmaniasis, we have studied some plasma membrane features of host THP-1…”
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Corrigendum: Identification of novel anti-amoebic pharmacophores from kinase inhibitor chemotypes
Published in Frontiers in microbiology (25-10-2023)“…[This corrects the article DOI: 10.3389/fmicb.2023.1149145.]…”
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Phospholipid Translocation and Miltefosine Potency Require Both L. donovani Miltefosine Transporter and the New Protein LdRos3 in Leishmania Parasites
Published in The Journal of biological chemistry (18-08-2006)“…The antitumor drug miltefosine has been recently approved as the first oral drug active against visceral leishmaniasis. We have previously identified the L…”
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Functional role of evolutionarily highly conserved residues, N-glycosylation level and domains of the Leishmania miltefosine transporter-Cdc50 subunit
Published in Biochemical journal (01-04-2014)“…Cdc50 (cell-cycle control protein 50) is a family of conserved eukaryotic proteins that interact with P4-ATPases (phospholipid translocases). Cdc50 association…”
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Thiol-ene "Click" Synthesis and Pharmacological Evaluation of C-Glycoside sp2-Iminosugar Glycolipids
Published in Molecules (Basel, Switzerland) (08-08-2019)“…The unique stereoelectronic properties of sp2-iminosugars enable their participation in glycosylation reactions, thereby behaving as true carbohydrate chemical…”
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