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Structural Basis for Sorting Mechanism of p62 in Selective Autophagy

The Journal of biological chemistry, 2008-08, Vol.283 (33), p.22847-22857

2008

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Liver autophagy contributes to the maintenance of blood glucose and amino acid levels

Autophagy, 2011-07, Vol.7 (7), p.727-736

2011

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Homeostatic Levels of p62 Control Cytoplasmic Inclusion Body Formation in Autophagy-Deficient Mice

Cell, 2007-12, Vol.131 (6), p.1149-1163

2007

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Impairment of starvation-induced and constitutive autophagy in Atg7-deficient mice

The Journal of cell biology, 2005-05, Vol.169 (3), p.425-434

2005

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Crucial role for autophagy in degranulation of mast cells

Journal of allergy and clinical immunology, 2011-05, Vol.127 (5), p.1267-1276.e6

2011

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Lysosomal Storage of Subunit c of Mitochondrial ATP Synthase in Brain-Specific Atp13a2-Deficient Mice

The American journal of pathology, 2016-12, Vol.186 (12), p.3074-3082

2016

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HsAtg4B/HsApg4B/Autophagin-1 Cleaves the Carboxyl Termini of Three Human Atg8 Homologues and Delipidates Microtubule-associated Protein Light Chain 3- and GABAA Receptor-associated Protein-Phospholipid Conjugates

The Journal of biological chemistry, 2004-08, Vol.279 (35), p.36268-36276

2004

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Excess Peroxisomes Are Degraded by Autophagic Machinery in Mammals

The Journal of biological chemistry, 2006-02, Vol.281 (7), p.4035-4041

2006

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PARK2/Parkin-mediated mitochondrial clearance contributes to proteasome activation during slow-twitch muscle atrophy via NFE2L1 nuclear translocation

Autophagy, 2014-04, Vol.10 (4), p.631-641

2014

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Interleukin-11 links oxidative stress and compensatory proliferation

Science signaling, 2012-01, Vol.5 (207), p.ra5

2012

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Ferulic Acid Induces Mammalian Target of Rapamycin Inactivation in Cultured Mammalian Cells

Biological and Pharmaceutical Bulletin, 2013/01/01, Vol.36(1), pp.120-124

2013

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Differences in expression patterns of cathepsin C/dipeptidyl peptidase I in normal, pathological and aged mouse central nervous system

The European journal of neuroscience, 2013-03, Vol.37 (5), p.816-830

2013

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Metabolic contribution of hepatic autophagic proteolysis: Old wine in new bottles

Biochimica et biophysica acta, 2012-01, Vol.1824 (1), p.51-58

2012

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A treadmill exercise reactivates the signaling of the mammalian target of rapamycin (mTor) in the skeletal muscles of starved mice

Biochemical and biophysical research communications, 2015-01, Vol.456 (1), p.519-526

2015

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Peroxisome degradation in mammals

IUBMB life, 2011-11, Vol.63 (11), p.1001-1008

2011

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The Intracellular Location and Function Of Proteins Of Neuronal Ceroid Lipofuscinoses

Brain pathology (Zurich, Switzerland), 2004-01, Vol.14 (1), p.77-85

2004

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CLC‐3 deficiency leads to phenotypes similar to human neuronal ceroid lipofuscinosis

Genes to cells : devoted to molecular & cellular mechanisms, 2002-06, Vol.7 (6), p.597-605

2002

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A Lysosomal Proteinase, the Late Infantile Neuronal Ceroid Lipofuscinosis Gene (CLN2) Product, Is Essential for Degradation of a Hydrophobic Protein, the Subunit c of ATP Synthase

Journal of neurochemistry, 1999-06, Vol.72 (6), p.2573-2582

1999

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Tripeptidyl Peptidase I, the Late Infantile Neuronal Ceroid Lipofuscinosis Gene Product, Initiates the Lysosomal Degradation of Subunit c of ATP Synthase

Journal of biochemistry (Tokyo), 2000-09, Vol.128 (3), p.509-516

2000

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FAM83B is a novel biomarker for diagnosis and prognosis of lung squamous cell carcinoma

International journal of oncology, 2015-03, Vol.46 (3), p.999-1006

2015

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Establishment and Characterization of a Novel Human Clear-cell Sarcoma of Soft-tissue Cell Line, RSAR001, Derived from Pleural Effusion of a Patient with Pleural Dissemination

Anticancer research, 2018-09, Vol.38 (9), p.5035-5042

2018

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A novel gene expression scoring system for accurate diagnosis of basaloid squamous cell carcinoma of the esophagus

International journal of oncology, 2017-09, Vol.51 (3), p.877-886

2017

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Clinical and therapeutic impact of family with sequence similarity 83, member B in EGFR gene wild type-lung adenocarcinoma

Journal of clinical oncology, 2017-05, Vol.35 (15_suppl), p.e23136-e23136

2017

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Abstract 422: Functional analysis of family with sequence similarity 83, member B in lung adenocarcinoma

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (14_Supplement), p.422-422

2016

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Specific Delay in the Degradation of Mitochondrial ATP Synthase Subunit c in Late Infantile Neuronal Ceroid Lipofuscinosis Is Derived from Cellular Proteolytic Dysfunction Rather than Structural Alteration of Subunit c

Journal of neurochemistry, 1996-10, Vol.67 (4), p.1677-1687

1996

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Structural Basis for Sorting Mechanism of p62 in Selective Autophagy

Liver autophagy contributes to the maintenance of blood glucose and amino acid levels

Homeostatic Levels of p62 Control Cytoplasmic Inclusion Body Formation in Autophagy-Deficient Mice

Impairment of starvation-induced and constitutive autophagy in Atg7-deficient mice

Crucial role for autophagy in degranulation of mast cells

Lysosomal Storage of Subunit c of Mitochondrial ATP Synthase in Brain-Specific Atp13a2-Deficient Mice

HsAtg4B/HsApg4B/Autophagin-1 Cleaves the Carboxyl Termini of Three Human Atg8 Homologues and Delipidates Microtubule-associated Protein Light Chain 3- and GABAA Receptor-associated Protein-Phospholipid Conjugates

Excess Peroxisomes Are Degraded by Autophagic Machinery in Mammals

PARK2/Parkin-mediated mitochondrial clearance contributes to proteasome activation during slow-twitch muscle atrophy via NFE2L1 nuclear translocation

Interleukin-11 links oxidative stress and compensatory proliferation

Ferulic Acid Induces Mammalian Target of Rapamycin Inactivation in Cultured Mammalian Cells

Differences in expression patterns of cathepsin C/dipeptidyl peptidase I in normal, pathological and aged mouse central nervous system

Metabolic contribution of hepatic autophagic proteolysis: Old wine in new bottles

A treadmill exercise reactivates the signaling of the mammalian target of rapamycin (mTor) in the skeletal muscles of starved mice

Peroxisome degradation in mammals

The Intracellular Location and Function Of Proteins Of Neuronal Ceroid Lipofuscinoses

CLC‐3 deficiency leads to phenotypes similar to human neuronal ceroid lipofuscinosis

A Lysosomal Proteinase, the Late Infantile Neuronal Ceroid Lipofuscinosis Gene (CLN2) Product, Is Essential for Degradation of a Hydrophobic Protein, the Subunit c of ATP Synthase

Tripeptidyl Peptidase I, the Late Infantile Neuronal Ceroid Lipofuscinosis Gene Product, Initiates the Lysosomal Degradation of Subunit c of ATP Synthase

FAM83B is a novel biomarker for diagnosis and prognosis of lung squamous cell carcinoma

Establishment and Characterization of a Novel Human Clear-cell Sarcoma of Soft-tissue Cell Line, RSAR001, Derived from Pleural Effusion of a Patient with Pleural Dissemination

A novel gene expression scoring system for accurate diagnosis of basaloid squamous cell carcinoma of the esophagus

Clinical and therapeutic impact of family with sequence similarity 83, member B in EGFR gene wild type-lung adenocarcinoma

Abstract 422: Functional analysis of family with sequence similarity 83, member B in lung adenocarcinoma

Specific Delay in the Degradation of Mitochondrial ATP Synthase Subunit c in Late Infantile Neuronal Ceroid Lipofuscinosis Is Derived from Cellular Proteolytic Dysfunction Rather than Structural Alteration of Subunit c

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