Results 1 to 10 of about 1,936 (110)

African Trypanosomiasis Research at a Crossroads: Bibliometric and Systematic Insights for the Future. [PDF]

open access: yesJ Parasitol Res
Aim Despite a reduction in the overall incidence and prevalence in the last two decades, trypanosomiasis continues to be a public health concern in Africa. This study was designed to comprehensively evaluate current trends in trypanosomiasis research using bibliometric approaches to uncover emerging topics and knowledge gaps, thereby guiding future ...
Ogra IO   +7 more
europepmc   +2 more sources

Repurposing With Purpose: Treatment of Bachmann-Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies. [PDF]

open access: yesAm J Med Genet C Semin Med Genet
ABSTRACT Rare diseases impact approximately 1 in 10 people worldwide, and yet, less than 5% of all rare diseases currently have an approved treatment option available. This is due to many challenges unique to rare diseases, including small, diverse patient populations, the cost of drug development that is not proportionate to the number of patients who
Bupp CP   +7 more
europepmc   +2 more sources

ODC-Driven Polyamines Synthesis Sustains the Self-Renewal of Glioblastoma Stem Cells and Drives Tumor Aggressiveness. [PDF]

open access: yesCancer Sci
Our findings delineate a novel regulatory network that integrates metabolic and GSCs self‐renewal in GBM. By integrating genetic ODC ablation with multiomic profiling, we redefine polyamine metabolism as a linchpin of GSCs self‐renewal, a dependency exploitable through precision gene editing.
Wei XC   +7 more
europepmc   +2 more sources

Identification of transport systems involved in eflornithine delivery across the blood-brain barrier. [PDF]

open access: yesFront Drug Deliv, 2023
Human African Trypanosomiasis (HAT) is a neglected parasitic disease that continues to persist in sub-Saharan Africa. It is fatal if untreated. The first stage of the disease is associated with the presence of the parasite in the periphery and the second
Watson CP, Sekhar GN, Thomas SA.
europepmc   +2 more sources

Enantiospecific antitrypanosomal in vitro activity of eflornithine.

open access: yesPLoS Neglected Tropical Diseases, 2021
The polyamine synthesis inhibitor eflornithine is a recommended treatment for the neglected tropical disease Gambian human African trypanosomiasis in late stage.
Mikael Boberg   +5 more
doaj   +1 more source

The impact of thermophysical properties on eflornithine drug solute in acetone and ethyl acetate solvent interactions at varying concentrations and temperatures. [PDF]

open access: yesBMC Chem
The study was conducted on the impact of thermophysical properties on eflornithine drug solute–solvent interactions in aqueous ethyl acetate and acetone at different concentrations and temperatures.
Tegegn DF, Wirtu SF.
europepmc   +2 more sources

Application of Hantzsch reaction for sensitive determination of eflornithine in cream, plasma and urine samples

open access: yesRoyal Society Open Science, 2021
Eflornithine (EFN) is an anti-Trypanosoma brucei agent for the medication of sleeping sickness and widely distributed for the treatment of hirsutism (unwanted facial hair in women).
Albandary Almahri   +1 more
doaj   +1 more source

The First Insight Into the Supramolecular System of D,L-α-Difluoromethylornithine: A New Antiviral Perspective

open access: yesFrontiers in Chemistry, 2021
Targeting the polyamine biosynthetic pathway by inhibiting ornithine decarboxylase (ODC) is a powerful approach in the fight against diverse viruses, including SARS-CoV-2.
Joanna Bojarska   +8 more
doaj   +1 more source

An Update on African Trypanocide Pharmaceutics and Resistance

open access: yesFrontiers in Veterinary Science, 2022
African trypanosomiasis is associated with Trypanosoma evansi, T. vivax, T. congolense, and T. brucei pathogens in African animal trypanosomiasis (AAT) while T. b gambiense and T.
Keneth Iceland Kasozi   +5 more
doaj   +1 more source

Difluoromethylornithine rebalances aberrant polyamine ratios in Snyder–Robinson syndrome

open access: yesEMBO Molecular Medicine, 2023
Snyder–Robinson syndrome (SRS) results from mutations in spermine synthase (SMS), which converts the polyamine spermidine into spermine. Affecting primarily males, common manifestations of SRS include intellectual disability, osteoporosis, hypotonia, and
Tracy Murray Stewart   +8 more
doaj   +1 more source

Home - About - Disclaimer - Privacy