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p62 Links beta-adrenergic input to mitochondrial function and thermogenesis
p62 expression and autophagy in alpha B-crystallin R120G mutant knock-in mouse model of hereditary cataract
p62 participates in the inhibition of NF-kappa B signaling and apoptosis induced by sulfasalazine in human glioma U251 cells
p62 Deficiency Enhances alpha-Synuclein Pathology in Mice
p62 Plays a Specific Role in Interferon-gamma-Induced Presentation of a Toxoplasma Vacuolar Antigen
p62 Plays a Protective Role in the Autophagic Degradation of Polyglutamine Protein Oligomers in Polyglutamine Disease Model Flies
p62 prevents carbonyl cyanide m-chlorophenyl hydrazine (CCCP)-induced apoptotic cell death by activating Nrf2
p62 links autophagy and Nrf2 signaling
p62 (SQSTM1) and cyclic AMP phosphodiesterase-4A4 (PDE4A4) locate to a novel, reversible protein aggregate with links to autophagy and proteasome degradation pathways
p62 (SQSTM1) forms part of a novel, reversible aggregate containing a specific conformer of the cAMP degrading phosphodiesterase, PDE4A4
p62 modulates the intrinsic signaling of UVB-induced apoptosis
p62 in Liver Disease: Good Guy or Bad Guy?
p62 Regulates the Proliferation of Molecular Apocrine Breast Cancer Cells
p62 at the Interface of Autophagy, Oxidative Stress Signaling, and Cancer
p62 provides dual cytoprotection against oxidative stress in the retinal pigment epithelium
P62 Regulates resveratrol-mediated Fas/Cav-1 complex formation and transition from autophagy to apoptosis
p62 Stages an Interplay Between the Ubiquitin-Proteasome System and Autophagy in the Heart of Defense Against Proteotoxic Stress
p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
p62 degradation by autophagy Another way for cancer cells to survive under hypoxia
p62 Is Required for Stem Cell/Progenitor Retention through Inhibition of IKK/NF-kappa B/Ccl4 Signaling at the Bone Marrow Macrophage-Osteoblast Niche
p62 targeting to the autophagosome formation site requires self-oligomerization but not LC3 binding
p62 at the Crossroads of Autophagy, Apoptosis, and Cancer
p62 Is a Key Regulator of Nutrient Sensing in the mTORC1 Pathway
p62 Binding to Protein Kinase C zeta Regulates Tumor Necrosis Factor alpha-Induced Apoptotic Pathway in Endothelial Cells
p62 Pathology Model in the Rat Substantia Nigra with Filamentous Inclusions and Progressive Neurodegeneration
p62 improves AD-like pathology by increasing autophagy
p62 Promotes Amino Acid Sensitivity of mTOR Pathway and Hepatic Differentiation in Adult Liver Stem/Progenitor Cells
P62 plasmid can alleviate diet-induced obesity and metabolic dysfunctions
p62 modulates the intrinsic signaling of UVB-induced apoptosis (vol 83, pg 226, 2016)
p62 links the autophagy pathway and the ubiqutin-proteasome system upon ubiquitinated protein degradation
p62 in Cancer: Signaling Adaptor Beyond Autophagy
p62 filaments capture and present ubiquitinated cargos for autophagy
p62 as a therapeutic target for inhibition of autophagy in prostate cancer
p62 is linked to mitophagy in oleic acid-induced adipogenesis in human adipose-derived stromal cells
p62+ Hyaline Inclusions in Intrahepatic Cholangiocarcinoma Associated With Viral Hepatitis or Alcoholic Liver Disease
p62, an autophagy hero or culprit?
p62, Upregulated during Preneoplasia, Induces Hepatocellular Carcinogenesis by Maintaining Survival of Stressed HCC-Initiating Cells
p62, Ref(2)P and ubiquitinated proteins are conserved markers of neuronal aging, aggregate formation and progressive autophagic defects
p62-RIP1泛素化调节人卵巢癌耐药细胞的存活与死亡
p62-Mediated mitochondrial clustering attenuates apoptosis induced by mitochondrial depolarization
p62-and ubiquitin-dependent stress-induced autophagy of the mammalian 26S proteasome
p62/SQSTM1 involved in cisplatin resistance in human ovarian cancer cells by clearing ubiquitinated proteins
p62/SQSTM1 cooperates with Parkin for perinuclear clustering of depolarized mitochondria
p62/SQSTM1 Is a Target Gene for Transcription Factor NRF2 and Creates a Positive Feedback Loop by Inducing Antioxidant Response Element-driven Gene Transcription
p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy
p62/sequestosome 1 binds to TDP-43 in brains with frontotemporal lobar degeneration with TDP-43 inclusions
p62/SQSTM1/A170: Physiology and pathology
p62/SQSTM1 Is Required for Cell Survival of Apoptosis-Resistant Bone Metastatic Prostate Cancer Cell Lines
p62/SQSTM1 at the interface of aging, autophagy, and disease
p62/SQSTM1 regulates cellular oxygen sensing by attenuating PHD3 activity through aggregate sequestration and enhanced degradation
p62/SQSTM1 is involved in caspase-8 associated cell death induced by proteasome inhibitor MG132 in U87MG cells
p62/SQSTM1 is involved in cisplatin resistance in human ovarian cancer cells via the Keap1-Nrf2-ARE system
p62/SQSTM1 Accumulation in Squamous Cell Carcinoma of Head and Neck Predicts Sensitivity to Phosphatidylinositol 3-Kinase Pathway Inhibitors
p62/SQSTM1 Differentially Removes the Toxic Mutant Androgen Receptor via Autophagy and Inclusion Formation in a Spinal and Bulbar Muscular Atrophy Mouse Model
p62/SQSTM1 Enhances NOD2-Mediated Signaling and Cytokine Production through Stabilizing NOD2 Oligomerization
p62/IMP2 stimulates cell migration and reduces cell adhesion in breast cancer
p62/SQSTM1 functions as a signaling hub and an autophagy adaptor
p62/Sequestosome-1, Autophagy-related Gene 8, and Autophagy in Drosophila Are Regulated by Nuclear Factor Erythroid 2-related Factor 2 (NRF2), Independent of Transcription Factor TFEB
p62/SQSTM1 analysis in frontotemporal lobar degeneration
p62/Sequestosome-1: Mapping Sites of Protein-Handling Stress in Canine Cutaneous Mast Cell Tumors
p62/Sequestosome-1 Associates with and Sustains the Expression of Retroviral Restriction Factor TRIM5 alpha
p62/SQSTM1 and ALFY interact to facilitate the formation of p62 bodies/ALIS and their degradation by autophagy
p62/SQSTM1 is required for Parkin-induced mitochondrial clustering but not mitophagy; VDAC1 is dispensable for both
p62/sequestosome 1 as a regulator of proteasome inhibitor-induced autophagy in human retinal pigment epithelial cells
p62/Sequestosome-1 Is Indispensable for Maturation and Stabilization of Mallory-Denk Bodies
p62/SQSTM1 but not LC3 is accumulated in sarcopenic muscle of mice
p62/Sqstm1 promotes malignancy of HCV-positive hepatocellular carcinoma through Nrf2-dependent metabolic reprogramming