p62 is involved in the mechanism of Mallory body formation.

scientific article published in December 2004

p62 is involved in the mechanism of Mallory body formation. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.YEXMP.2004.06.003
P698PubMed publication ID15507232

P2093author name stringJun Li
Samuel W French
Yong Wu
Li Nan
Fawzia Bardag-Gorce
Alan N Fu
Jennifer Vu
Barbara A French
Tricia Francis
P2860cites workThe interaction of p62 with RIP links the atypical PKCs to NF-kappaB activationQ22009927
Structure and functional properties of the ubiquitin binding protein p62Q24292324
Molecular cloning of a phosphotyrosine-independent ligand of the p56lck SH2 domainQ24316893
Ubiquitin-associated (UBA) domains in Rad23 bind ubiquitin and promote inhibition of multi-ubiquitin chain assemblyQ24522596
Localization of atypical protein kinase C isoforms into lysosome-targeted endosomes through interaction with p62.Q24523784
Analysis of intracytoplasmic hyaline bodies in a hepatocellular carcinoma. Demonstration of p62 as major constituentQ24671478
A method to identify p62’s UBA domain interacting proteinsQ24801013
UBA domains of DNA damage-inducible proteins interact with ubiquitinQ27935487
Cytokeratin 8 protects from hepatotoxicity, and its ratio to cytokeratin 18 determines the ability of hepatocytes to form Mallory bodiesQ28344098
Interaction of protein kinase C zeta with ZIP, a novel protein kinase C-binding proteinQ28579361
Cloning, expression profile, and genomic organization of the mouse STAP/A170 geneQ28588942
Ubiquitin-binding protein p62 expression is induced during apoptosis and proteasomal inhibition in neuronal cellsQ31855203
Roles of nuclear factor kappaB in neuronal survival and plasticityQ33824008
Binding of non-native protein to Hsp25 during heat shock creates a reservoir of folding intermediates for reactivation.Q33885969
The atypical protein kinase Cs. Functional specificity mediated by specific protein adaptersQ34189807
Structure of a human DNA repair protein UBA domain that interacts with HIV-1 Vpr.Q34482838
NF-kappaB activation by protein kinase C isoforms and B-cell functionQ35043854
p62 Is a common component of cytoplasmic inclusions in protein aggregation diseasesQ42184099
Aggresome formation in liver cells in response to different toxic mechanisms: role of the ubiquitin-proteasome pathway and the frameshift mutant of ubiquitinQ43816065
Mallory body--a disease-associated type of sequestosomeQ43974815
The role of the ubiquitin-proteasome pathway in the formation of mallory bodiesQ44136423
The mechanism of cytokeratin aggresome formation: the role of mutant ubiquitin (UBB+1)Q44413773
Microtubules are required for cytokeratin aggresome (Mallory body) formation in hepatocytes: an in vitro studyQ44413775
Proteasome inhibition induces cytokeratin accumulation in vivoQ44792746
Molecular misreading of the ubiquitin B gene and hepatic mallory body formationQ44882036
Murine peritoneal macrophages induce a novel 60-kDa protein with structural similarity to a tyrosine kinase p56lck-associated protein in response to oxidative stressQ48060160
Insulin-like growth factor-1-mediated neuroprotection against oxidative stress is associated with activation of nuclear factor kappaB.Q48254872
The atypical PKC-interacting protein p62 is an important mediator of RANK-activated osteoclastogenesis.Q51040187
Early accumulation of p62 in neurofibrillary tangles in Alzheimer's disease: possible role in tangle formation.Q53352974
P62 and the sequestosome, a novel mechanism for protein metabolismQ77735047
P433issue3
P304page(s)168-175
P577publication date2004-12-01
P1433published inExperimental and Molecular PathologyQ15767470
P1476titlep62 is involved in the mechanism of Mallory body formation.
P478volume77