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The Pathways Underlying the Multiple Roles of p62 in Inflammation and

Autophagic Regulation of p62 is Critical for Cancer Therapy

The Pathways Underlying the Multiple Roles of p62 in Inflammation and

S-Nitrosylation of p62 Inhibits Autophagic Flux to Promote α-Synuclein ...

SNitrosylation of p62 Inhibits Autophagic Flux to Promote Synuclein

Sacylation of p62 promotes p62 droplet recruitment into autophagosomes

Autophagy and p62 in Cardiac Proteinopathy Circulation Research

Arsenic Induces p62 Expression to Form a Positive Feedback Loop with

Rapid activation of p62 bodymediated autophagy in human cells under

Autophagic Regulation of p62 is Critical for Cancer Therapy

Rapid activation of p62 bodymediated autophagy in human cells under

p62 improves ADlike pathology by increasing autophagy Abstract

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Arsenic Induces p62 Expression to Form a Positive Feedback Loop with

p62 Is a Potential Biomarker for Risk of Malignant Transformation of

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多功能 p62 效应是多种代谢疾病的基础,Trends in Endocrinology & Metabolism - X-MOL

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Frontiers Expression Pattern of p62 in Primary AgeRelated Tauopathy

The Pathways Underlying the Multiple Roles of p62 in Inflammation and

Arsenic Induces p62 Expression to Form a Positive Feedback Loop with

p62 Is a Potential Biomarker for Risk of Malignant Transformation of

Sensing Protein Quality in Cardiac Myocytes p62 Triggers a Lysosomal

Investigating p62 Concentrations in Cerebrospinal Fluid of Patients

A SexSpecific AntiInflammatory Role for p62 in PsoriasisLike Disease

Autophagy and p62 in Cardiac Proteinopathy Circulation Research

Rapid activation of p62 bodymediated autophagy in human cells under

p62 is a key regulator of nutrient sensing in the mTORC1 pathway

p62 Association with RNA Is Regulated by Tyrosine Phosphorylation

Arsenic Induces p62 Expression to Form a Positive Feedback Loop with

An Alternatively Spliced p62 Isoform Confers Resistance to Chemotherapy

A SexSpecific AntiInflammatory Role for p62 in PsoriasisLike Disease

Prognostic Impact of p62 Expression in Cutaneous Malignant Melanoma

Arsenic Induces p62 Expression to Form a Positive Feedback Loop with

Cucurbitacin E Exerts AntiProliferative Activity via Promoting p62

p62 Is a Potential Biomarker for Risk of Malignant Transformation of

Phosphorylation of phaseseparated p62 bodies by ULK1 activates a redox

Investigating p62 Concentrations in Cerebrospinal Fluid of Patients

p62 condensates are a hub for proteasomemediated protein turnover in

p62 Binding to Protein Kinase C ζ Regulates Tumor Necrosis Factor α ...

p62 Binding to Protein Kinase C Regulates Tumor Necrosis Factor

The pR321C mutation in the p62 protein is associated with

Autophagy Receptor p62 Regulates SARSCoV2Induced Inflammation in

Prognostic Impact of p62 Expression in Cutaneous Malignant Melanoma

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Frontiers BioinformaticsDriven Identification of p62 as A Crucial

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p62 at the Crossroads of Autophagy Apoptosis and Cancer Cell

p62 mediated phase separation at the intersection of the ubiquitin

Structural and dynamical insights into the PH domain of p62 in human

p62 Stages an Interplay between the UbiquitinProteasome System and

p62 in cancer signaling adaptor beyond autophagy PMC

p62 improves ADlike pathology by increasing autophagy PMC

A P62 mRNA expression in human cancers compared to corresponding

The autophagic protein p62 is a target of reactive aldehydes in human

Sacylation of p62 promotes p62 droplet recruitment into autophagosomes

p62 filaments capture and present ubiquitinated cargos for autophagy PMC

Expression and clinical significance of p62 protein in colon cancer PMC

Pituitary P62 deficiency leads to female infertility by impairing

PostTranslational Modification of p62 Roles and Regulations in Autophagy

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PostTranslational Modification of p62 Roles and Regulations in Autophagy

Exploring the Regulatory Mechanism and Physiological Significance of

p62 Upregulated during Preneoplasia Induces Hepatocellular

B1b Cells Possess Unique bHLHDriven P62Dependent SelfRenewal and

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A p62dependent rheostat dictates micronuclei catastrophe and

Coxiella burnetii Subverts p62Sequestosome 1 and Activates Nrf2

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Coxiella burnetii Subverts p62Sequestosome 1 and Activates Nrf2

Experimental and Therapeutic Medicine

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Frontiers Selective Autophagy Receptor p62SQSTM1 a Pivotal Player

Generation and Characterization of Novel Monoclonal Antibodies

PostTranslational Modification of p62 Roles and Regulations in Autophagy

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A p62dependent rheostat dictates micronuclei catastrophe and

TAK1 将 Sequestosome 1/p62 从自噬受体转化为信号平台。,EMBO Reports - X-MOL

TAK1 Sequestosome 1p62 EMBO Reports XMOL

PostTranslational Modification of p62 Roles and Regulations in Autophagy

P62SQSTM1 antibody 661841Ig Proteintech

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Coxiella burnetii Subverts p62Sequestosome 1 and Activates Nrf2

An inhibition of p62SQSTM1 caused autophagic cell death of several

p62 Friend or Foe Evidences for OncoJanus and NeuroJanus Roles

P62SQSTM1 antibody 184201AP Proteintech

HumanMouseRat p62SQSTM1 Antibody MAB8028 RD Systems

P62SQSTM1 antibody 184201AP Proteintech

Sequestosome 1p62 a Scaffolding Protein Is a Newly Identified

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IMP2p62 induces genomic instability and an aggressive hepatocellular

International Journal of Oncology

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A p62dependent rheostat dictates micronuclei catastrophe and

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TRIM72mediated degradation of the short form of p62SQSTM1

Oncology Reports

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Molecular mechanisms underlying p62dependent secretion of the

A p62dependent rheostat dictates micronuclei catastrophe and

p62 Friend or Foe Evidences for OncoJanus and NeuroJanus Roles

p62SQSTM1 Differentially Removes the Toxic Mutant Androgen Receptor

p62 a versatile multitasker takes on cancer PMC

Finding Vault Unravelling the Mysteries of p62Bodies and the

COOHterminal fragment of APP interacts with p62 forms an aggregate

p62SQSTM1 by binding to vitamin D receptor inhibits hepatic stellate

p62Sqstm1 promotes malignancy of HCVpositive hepatocellular carcinoma

Escininduced DNA damage promotes escininduced apoptosis in human

p62 a versatile multitasker takes on cancer PMC

p62sequestosome 1 in human colorectal carcinoma as a potent prognostic

NRBF2 regulates the chemoresistance of small cell lung cancer by

COOHterminal fragment of APP interacts with p62 forms an aggregate

Metabolic reprogramming of stromal fibroblasts through p62mTORC1

Antip62 Cterminal Human pAb Catalog No MBLPM066

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