Literature DB >> 11790549

The JNK signal transduction pathway.

Claire R Weston1, Roger J Davis.   

Abstract

The c-Jun NH(2)-terminal kinase (JNK) is a member of an evolutionarily conserved sub-family of mitogen-activated protein (MAP) kinases. Recent studies have led to progress towards understanding the physiological function of the JNK signaling pathway, including the analysis of the phenotype of knockout mice. An important role for JNK in the non-canonical Wnt-signaling pathway has been established. Insight into the role of scaffold proteins that may assemble functional JNK modules has been achieved. In addition, a small molecule pharmacological inhibitor of JNK has been described and it is likely that this drug will facilitate future studies of JNK function.

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Year:  2002        PMID: 11790549     DOI: 10.1016/s0959-437x(01)00258-1

Source DB:  PubMed          Journal:  Curr Opin Genet Dev        ISSN: 0959-437X            Impact factor:   5.578


  206 in total

Review 1.  Mitogen activated protein (MAP) kinase signal transduction pathways and novel anti-inflammatory targets.

Authors:  D W Hommes; M P Peppelenbosch; S J H van Deventer
Journal:  Gut       Date:  2003-01       Impact factor: 23.059

2.  Distinct roles of c-Jun N-terminal kinase isoforms in neurite initiation and elongation during axonal regeneration.

Authors:  Monia Barnat; Hervé Enslen; Friedrich Propst; Roger J Davis; Sylvia Soares; Fatiha Nothias
Journal:  J Neurosci       Date:  2010-06-09       Impact factor: 6.167

Review 3.  Signal transduction networks in rheumatoid arthritis.

Authors:  D Hammaker; S Sweeney; G S Firestein
Journal:  Ann Rheum Dis       Date:  2003-11       Impact factor: 19.103

Review 4.  ERK and p38 MAPK-activated protein kinases: a family of protein kinases with diverse biological functions.

Authors:  Philippe P Roux; John Blenis
Journal:  Microbiol Mol Biol Rev       Date:  2004-06       Impact factor: 11.056

5.  Differential input by Ste5 scaffold and Msg5 phosphatase route a MAPK cascade to multiple outcomes.

Authors:  Jessica Andersson; David M Simpson; Maosong Qi; Yunmei Wang; Elaine A Elion
Journal:  EMBO J       Date:  2004-06-10       Impact factor: 11.598

Review 6.  The various roles of ubiquitin in Wnt pathway regulation.

Authors:  Daniele V F Tauriello; Madelon M Maurice
Journal:  Cell Cycle       Date:  2010-09-25       Impact factor: 4.534

7.  Apoptosis Repressor With Caspase Recruitment Domain Ameliorates Amyloid-Induced β-Cell Apoptosis and JNK Pathway Activation.

Authors:  Andrew T Templin; Tanya Samarasekera; Daniel T Meier; Meghan F Hogan; Mahnaz Mellati; Michael T Crow; Richard N Kitsis; Sakeneh Zraika; Rebecca L Hull; Steven E Kahn
Journal:  Diabetes       Date:  2017-07-20       Impact factor: 9.461

8.  Norcantharidin-induced apoptosis is via the extracellular signal-regulated kinase and c-Jun-NH2-terminal kinase signaling pathways in human hepatoma HepG2 cells.

Authors:  Yan-Nian Chen; Chi-Chih Cheng; Jung-Chou Chen; Wei Tsauer; Shih-Lan Hsu
Journal:  Br J Pharmacol       Date:  2003-09-01       Impact factor: 8.739

9.  c-Jun N-terminal kinases (JNK) antagonize cardiac growth through cross-talk with calcineurin-NFAT signaling.

Authors:  Qiangrong Liang; Orlando F Bueno; Benjamin J Wilkins; Chia-Yi Kuan; Ying Xia; Jeffery D Molkentin
Journal:  EMBO J       Date:  2003-10-01       Impact factor: 11.598

10.  c-Jun N-Terminal Kinases (JNKs) Are Critical Mediators of Osteoblast Activity In Vivo.

Authors:  Ren Xu; Chao Zhang; Dong Yeon Shin; Jung-Min Kim; Sarfaraz Lalani; Na Li; Yeon-Suk Yang; Yifang Liu; Mark Eiseman; Roger J Davis; Jae-Hyuck Shim; Matthew B Greenblatt
Journal:  J Bone Miner Res       Date:  2017-09       Impact factor: 6.741

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