User profiles for Jason D. Graci
Jason D. GraciPrincipal Scientist, PTC Therapeutics Inc. Verified email at ptcbio.com Cited by 1839 |
Mechanisms of action of ribavirin against distinct viruses
JD Graci, CE Cameron - Reviews in medical virology, 2006 - Wiley Online Library
The nucleoside analogue ribavirin has antiviral activity against many distinct viruses both in
vitro and in vivo. Five distinct mechanisms have been proposed to explain the antiviral …
vitro and in vivo. Five distinct mechanisms have been proposed to explain the antiviral …
[HTML][HTML] Small molecule splicing modifiers with systemic HTT-lowering activity
…, A Dakka, V Gabbeta, NA Naryshkin, JD Graci… - Nature …, 2021 - nature.com
Huntington’s disease (HD) is a hereditary neurodegenerative disorder caused by expansion
of cytosine-adenine-guanine (CAG) trinucleotide repeats in the huntingtin (HTT) gene. …
of cytosine-adenine-guanine (CAG) trinucleotide repeats in the huntingtin (HTT) gene. …
[HTML][HTML] RNA virus population diversity, an optimum for maximal fitness and virulence
The ability of an RNA virus to exist as a population of genetically distinct variants permits the
virus to overcome events during infections that would otherwise limit virus multiplication or …
virus to overcome events during infections that would otherwise limit virus multiplication or …
Quasispecies, error catastrophe, and the antiviral activity of ribavirin
JD Graci, CE Cameron - Virology, 2002 - Elsevier
Ribavirin is the first synthetic, broad-spectrum antiviral nucleoside. Despite its more than 30
year history, the mechanism of action of this compound remains unclear and somewhat …
year history, the mechanism of action of this compound remains unclear and somewhat …
The DHODH inhibitor PTC299 arrests SARS-CoV-2 replication and suppresses induction of inflammatory cytokines
The coronavirus disease 2019 (COVID-19) pandemic has created an urgent need for
therapeutics that inhibit the SARS−COV-2 virus and suppress the fulminant inflammation …
therapeutics that inhibit the SARS−COV-2 virus and suppress the fulminant inflammation …
Targeting of hematologic malignancies with PTC299, a novel potent inhibitor of dihydroorotate dehydrogenase with favorable pharmaceutical properties
…, J Ma, MJ Kim, B Furia, C Romfo, JD Graci… - Molecular cancer …, 2019 - AACR
PTC299 was identified as an inhibitor of VEGFA mRNA translation in a phenotypic screen
and evaluated in the clinic for treatment of solid tumors. To guide precision cancer treatment, …
and evaluated in the clinic for treatment of solid tumors. To guide precision cancer treatment, …
Therapeutically targeting RNA viruses via lethal mutagenesis
JD Graci, CE Cameron - 2008 - Future Medicine
RNA viruses exhibit increased mutation frequencies relative to other organisms. Recent
work has attempted to exploit this unique feature by increasing the viral mutation frequency …
work has attempted to exploit this unique feature by increasing the viral mutation frequency …
Mutational robustness of an RNA virus influences sensitivity to lethal mutagenesis
The ability to extinguish a viral population of fixed reproductive capacity by causing small
changes in the mutation rate is referred to as lethal mutagenesis and is a corollary of …
changes in the mutation rate is referred to as lethal mutagenesis and is a corollary of …
Lethal mutagenesis of picornaviruses with N-6-modified purine nucleoside analogues
JD Graci, K Too, ED Smidansky… - Antimicrobial agents …, 2008 - Am Soc Microbiol
RNA viruses exhibit extraordinarily high mutation rates during genome replication.
Nonnatural ribonucleosides that can increase the mutation rate of RNA viruses by acting as …
Nonnatural ribonucleosides that can increase the mutation rate of RNA viruses by acting as …
Synthesis and antiviral activity of 5-substituted cytidine analogues: identification of a potent inhibitor of viral RNA-dependent RNA polymerases
As part of our studies of lethal viral mutagens, a series of 5-substituted cytidine analogues
were synthesized and evaluated for antiviral activity. Among the compounds examined, 5-…
were synthesized and evaluated for antiviral activity. Among the compounds examined, 5-…