T. Hudson

发表

Brefeldin-A enhancement of ricin A-chain immunotoxins and blockade of intact ricin, modeccin, and abrin.

T. Hudson, F. Grillo, 1991, The Journal of biological chemistry.

Genetic Resistance/Susceptibility to Mycobacteria: Phenotypic Expression in Bone Marrow Derived Macrophage Lines

D. Radzioch, T. Hudson, L. Varesio, 1991, Journal of leukocyte biology.

New Class of Small Nonpeptidyl Compounds BlocksPlasmodium falciparum Development In Vitro by Inhibiting Plasmepsins

Dennis E. Kyle, John B. Dame, J. Dame, 2001, Antimicrobial Agents and Chemotherapy.

Synthesis and antimalarial activity of new isotebuquine analogues.

L. Gerena, D. Kyle, O. Miroshnikova, 2007, Journal of medicinal chemistry.

Temporal separation of protein toxin translocation from processing events.

D. Neville, T. Hudson, 1987, The Journal of biological chemistry.

Selection of Plasmodium falciparum Multidrug Resistance Gene 1 Alleles in Asexual Stages and Gametocytes by Artemether-Lumefantrine in Nigerian Children with Uncomplicated Falciparum Malaria

D. Wirth, W. Milhous, C. Happi, 2008, Antimicrobial Agents and Chemotherapy.

Point mutations in the pfcrt and pfmdr-1 genes of Plasmodium falciparum and clinical response to chloroquine, among malaria patients from Nigeria

L. Gerena, D. Wirth, D. Kyle, 2003, Annals of tropical medicine and parasitology.

Enhancement of immunotoxin action: manipulation of the cellular routing of proteins.

D. Neville, T. Hudson, 1988, Cancer treatment and research.

Forskolin as an activator of cyclic AMP accumulation and lipolysis in rat adipocytes.

T. Hudson, J. Fain, I. Litosch, 1982, Molecular pharmacology.

Antimalarial activity of novel 5-aryl-8-aminoquinoline derivatives.

A. Magill, T. Hudson, C. Ohrt, 2011, Journal of medicinal chemistry.

Adenosine 3',5'-monophosphate analogs promote a circular morphology of cultured Schwannoma cells.

T. Hudson, J. Sheppard, J. R. Larson, 1975, Science.

Analysis of stereoelectronic properties, mechanism of action and pharmacophore of synthetic indolo[2,1-b]quinazoline-6,12-dione derivatives in relation to antileishmanial activity using quantum chemical, cyclic voltammetry and 3-D-QSAR CATALYST procedures.

D. Skanchy, A. Bhattacharjee, K. Werbovetz, 2002, Bioorganic & medicinal chemistry.

The Antimalarial Potential of 4-Quinolinecarbinolamines May Be Limited due to Neurotoxicity and Cross-Resistance in Mefloquine-Resistant Plasmodium falciparum Strains

L. Gerena, A. Bhattacharjee, G. Dow, 2004, Antimicrobial Agents and Chemotherapy.

The acute neurotoxicity of mefloquine may be mediated through a disruption of calcium homeostasis and ER function in vitro

G. Dow, M. Vahey, T. Hudson, 2003, Malaria Journal.

Mefloquine-Induced Disruption of Calcium Homeostasis in Mammalian Cells Is Similar to That Induced by Ionomycin

D. Caridha, G. Dow, T. Hudson, 2007, Antimicrobial Agents and Chemotherapy.

Transmembrane transport of diphtheria toxin, related toxins, and colicins.

D. Neville, T. Hudson, 1986, Annual review of biochemistry.

Targeting the fatty acid biosynthesis enzyme, beta-ketoacyl-acyl carrier protein synthase III (PfKASIII), in the identification of novel antimalarial agents.

S. Prigge, L. Gerena, N. Waters, 2009, Journal of medicinal chemistry.

Direct Comparison of the Efficacy and Safety of Oral Treatments with Oleylphosphocholine (OlPC) and Miltefosine in a Mouse Model of L. major Cutaneous Leishmaniasis

D. Caridha, M. Grogl, M. Hickman, 2014, PLoS neglected tropical diseases.

Drug discovery algorithm for cutaneous leishmaniasis.

J. Berman, M. Grogl, J. Lazo, 2013, The American journal of tropical medicine and hygiene.

Review: Drug Discovery Algorithm for Cutaneous Leishmaniasis

J. Berman, M. Grogl, J. Lazo, 2013 .

Antileishmanial Activity of Compounds Derived from the Medicines for Malaria Venture Open Access Box against Intracellular Leishmania major Amastigotes

M. Grogl, R. Paris, Philip Smith, 2016, The American journal of tropical medicine and hygiene.

Quantal entry of diphtheria toxin to the cytosol.

D. Neville, T. Hudson, 1985, The Journal of biological chemistry.

Peptide mapping of adenylate cyclase regulatory proteins that are cholera toxin substrates.

G. Johnson, T. Hudson, 1980, The Journal of biological chemistry.

Forskolin-activated adenylate cyclase. Inhibition by guanyl-5'-yl imidodiphosphate.

T. Hudson, J. Fain, 1983, The Journal of biological chemistry.

Conformational changes of adenylate cyclase regulatory proteins mediated by guanine nucleotides.

G. Johnson, T. Hudson, J. Roeber, 1981, The Journal of biological chemistry.

Synthesis and in vitro studies of novel pyrimidinyl peptidomimetics as potential antimalarial therapeutic agents.

D. Kyle, T. Hudson, A. Lin, 2002, Journal of medicinal chemistry.

Use of Optical Imaging Technology in the Validation of a New, Rapid, Cost-Effective Drug Screen as Part of a Tiered In Vivo Screening Paradigm for Development of Drugs To Treat Cutaneous Leishmaniasis

D. Caridha, M. Grogl, M. Hickman, 2017, Antimicrobial Agents and Chemotherapy.

Energy requirements for diphtheria toxin translocation are coupled to the maintenance of a plasma membrane potential and a proton gradient.

D. Neville, J. Scharff, T. Hudson, 1988, The Journal of biological chemistry.

Auranofin is an apoptosis-simulating agent with in vitro and in vivo anti-leishmanial activity.

J. Lazo, M. Hickman, David A. Close, 2014, ACS chemical biology.

Functional alterations in components of pigeon erythrocyte adenylate cyclase following desensitization to isoproterenol.

G. Johnson, T. Hudson, 1981, Molecular pharmacology.

Review: Drug Discovery Algorithm for Cutaneous Leishmaniasis

J. Berman, M. Grogl, J. Lazo, 2013 .