J. P. Hall

发表

Alginate-poly-L-lysine microcapsule biocompatibility: a novel RT-PCR method for cytokine gene expression analysis in pericapsular infiltrates.

R. Robitaille, F. Leblond, E. Drobetsky, 1999, Journal of biomedical materials research.

Pharmacologic Inhibition of Tpl2 Blocks Inflammatory Responses in Primary Human Monocytes, Synoviocytes, and Blood*

K. Seidl, J. D. Clark, J. Telliez, 2007, Journal of Biological Chemistry.

Inhibition of Tpl2 kinase and TNFalpha production with quinoline-3-carbonitriles for the treatment of rheumatoid arthritis.

J. Telliez, J. Cuozzo, Lih-Ling Lin, 2006, Bioorganic & medicinal chemistry letters.

Identification and SAR of a new series of thieno[3,2-d]pyrimidines as Tpl2 kinase inhibitors.

Y. Ni, R. Denny, J. Telliez, 2011, Bioorganic & medicinal chemistry letters.

NAK is recruited to the TNFR1 complex in a TNFalpha-dependent manner and mediates the production of RANTES: identification of endogenous TNFR-interacting proteins by a proteomic approach.

V. Rao, Lih-Ling Lin, Y. Qiu, 2004, The Journal of biological chemistry.

Human Recombinant Alkaline Phosphatase (Ilofotase Alfa) Protects Against Kidney Ischemia-Reperfusion Injury in Mice and Rats Through Adenosine Receptors

B. Molitoris, Liping Huang, K. Beaumont, 2022, Frontiers in Medicine.

Analysis of c-Jun N-terminal kinase regulation and function.

J. P. Hall, R. Davis, 2002, Methods in enzymology.

Optimized protocols for studying the NLRP3 inflammasome and assessment of potential targets of CP-453,773 in undifferentiated THP1 cells.

J. Stock, J. Guzova, J. P. Hall, 2019, Journal of immunological methods.

Discovery of indazoles as inhibitors of Tpl2 kinase.

David R. Anderson, Y. Ni, R. Denny, 2011, Bioorganic & medicinal chemistry letters.

Identification of a novel class of selective Tpl2 kinase inhibitors: 4-Alkylamino-[1,7]naphthyridine-3-carbonitriles.

J. Telliez, D. Powell, J. Cuozzo, 2007, Bioorganic & medicinal chemistry.

A rat pharmacokinetic/pharmacodynamic model for assessment of lipopolysaccharide-induced tumor necrosis factor-alpha production.

Xin Xu, J. Levin, J. Cuozzo, 2007, Journal of pharmacological and toxicological methods.

Inhibition of Tpl2 kinase and TNF-alpha production with 1,7-naphthyridine-3-carbonitriles: synthesis and structure-activity relationships.

J. Telliez, A. Gopalsamy, G. Ciszewski, 2005, Bioorganic & medicinal chemistry letters.

TRIL Is Involved in Cytokine Production in the Brain following Escherichia coli Infection

K. Seidl, K. Fitzgerald, A. Dunne, 2014, The Journal of Immunology.

Stimulation of TLR4 by recombinant HSP70 requires structural integrity of the HSP70 protein itself

Jill F. Wright, J. P. Hall, Michael Luong, 2012, Journal of Inflammation.

A selenopyrylium photosensitizer for photodynamic therapy related in structure to the antitumor agent AA1 with potent in vivo activity and no long-term skin photosensitization.

A. Oseroff, S. Gollnick, S. Gibson, 2000, Journal of medicinal chemistry.

The osmoregulatory pathway represses mating pathway activity in Saccharomyces cerevisiae: isolation of a FUS3 mutant that is insensitive to the repression mechanism

E. Elion, E. Winter, V. Cherkasova, 1996, Molecular and cellular biology.

An NLRP3-specific inflammasome inhibitor attenuates crystal-induced kidney fibrosis in mice.

P. Boor, V. Hornung, G. Hartmann, 2016, Kidney international.

Efficacy and Pharmacology of the NLRP3 Inflammasome Inhibitor CP-456,773 (CRID3) in Murine Models of Dermal and Pulmonary Inflammation

B. Monks, E. Latz, D. Hepworth, 2016, The Journal of Immunology.

SMK1, a developmentally regulated MAP kinase, is required for spore wall assembly in Saccharomyces cerevisiae.

E. Winter, M. J. Mallory, R. Tuan, 1994, Genes & development.

Innate immune recognition of an AT-rich stem-loop DNA motif in the Plasmodium falciparum genome.

D. Golenbock, G. Barber, D. Bartholomeu, 2011, Immunity.

JNK initiates a cytokine cascade that causes Pax2 expression and closure of the optic fissure.

R. Flavell, C. Weston, J. P. Hall, 2003, Genes & development.

The c-Jun NH2-terminal kinase is essential for epidermal growth factor expression during epidermal morphogenesis.

R. Flavell, C. Weston, J. P. Hall, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Inhibition of the p38 pathway upregulates macrophage JNK and ERK activities, and the ERK, JNK, and p38 MAP kinase pathways are reprogrammed during differentiation of the murine myeloid M1 cell line

J. P. Hall, R. Davis, 2002, Journal of cellular biochemistry.

Pulmonary Inflammation ( CRID 3 ) in Murine Models of Dermal and Inflammasome Inhibitor CP-456 , 773 Efficacy and Pharmacology of the NLRP 3

B. Monks, E. Latz, D. Hepworth, 2016 .

c-Jun N-terminal kinase (JNK) repression during the inflammatory response? Just say NO.

R. Davis, J. P. Hall, E. Merithew, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Inhibitors of tumor progression loci-2 (Tpl2) kinase and tumor necrosis factor alpha (TNF-alpha) production: selectivity and in vivo antiinflammatory activity of novel 8-substituted-4-anilino-6-aminoquinoline-3-carbonitriles.

D. Joseph-McCarthy, J. Telliez, J. Cuozzo, 2007, Journal of medicinal chemistry.

Identification of a Novel Human Kinase Supporter of Ras (hKSR-2) That Functions as a Negative Regulator of Cot (Tpl2) Signaling*

J. Cuozzo, Lih-Ling Lin, Leeying Wu, 2003, Journal of Biological Chemistry.

Metformin and 2-Deoxyglucose Collaboratively Suppress Human CD4+ T Cell Effector Functions and Activation-Induced Metabolic Reprogramming

A. Hadjipanayis, Y. Kelkar, T. Wynn, 2020, The Journal of Immunology.

Mice lacking Tbk1 activity exhibit immune cell infiltrates in multiple tissues and increased susceptibility to LPS‐induced lethality

K. Fitzgerald, V. Ling, Lih-Ling Lin, 2010, Journal of leukocyte biology.