Related references
Note: Only part of the references are listed.Inhibition of Proteasome Activity Induces Formation of Alternative Proteasome Complexes
Vanessa Welk et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2016)
Identification of novel polyglutamine-expanded aggregation species in spinal and bulbar muscular atrophy
Tamar R. Berger et al.
BRAIN RESEARCH (2015)
Proteasome-mediated Proteolysis of the Polyglutamine-expanded Androgen Receptor Is a Late Event in Spinal and Bulbar Muscular Atrophy (SBMA) Pathogenesis
Erin M. Heine et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2015)
Preventing the Androgen Receptor N/C Interaction Delays Disease Onset in a Mouse Model of SBMA
Lori Zboray et al.
CELL REPORTS (2015)
Chk2 and REGγ-dependent DBC1 regulation in DNA damage induced apoptosis
Martina Magni et al.
NUCLEIC ACIDS RESEARCH (2014)
The REGγ Proteasome Regulates Hepatic Lipid Metabolism through Inhibition of Autophagy
Shuxian Dong et al.
CELL METABOLISM (2013)
SIRT1 Modulates Aggregation and Toxicity through Deacetylation of the Androgen Receptor in Cell Models of SBMA
Heather L. Montie et al.
JOURNAL OF NEUROSCIENCE (2011)
REGγ proteasome mediates degradation of the ubiquitin ligase Smurf1
Jing Nie et al.
FEBS LETTERS (2010)
An Interdomain Interaction of the Androgen Receptor Is Required for Its Aggregation and Toxicity in Spinal and Bulbar Muscular Atrophy
Christopher R. Orr et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Native Functions of the Androgen Receptor Are Essential to Pathogenesis in a Drosophila Model of Spinobulbar Muscular Atrophy
Natalia B. Nedelsky et al.
NEURON (2010)
Autophagy and access Understanding the role of androgen receptor subcellular localization in SBMA
Heather L. Montie et al.
AUTOPHAGY (2009)
Cytoplasmic retention of polyglutamine-expanded androgen receptor ameliorates disease via autophagy in a mouse model of spinal and bulbar muscular atrophy
Heather L. Montie et al.
HUMAN MOLECULAR GENETICS (2009)
FOXO3a Is Broadly Neuroprotective In Vitro and In Vivo against Insults Implicated in Motor Neuron Diseases
Jelena Mojsilovic-Petrovic et al.
JOURNAL OF NEUROSCIENCE (2009)
The SR protein family
Peter J. Shepard et al.
GENOME BIOLOGY (2009)
E2F1 controls alternative splicing pattern of genes involved in apoptosis through upregulation of the splicing factor SC35
G. Merdzhanova et al.
CELL DEATH AND DIFFERENTIATION (2008)
Proteasome activator PA28γ regulates p53 by enhancing its MDM2-mediated degradation
Zhuo Zhang et al.
EMBO JOURNAL (2008)
CHIP deletion reveals functional redundancy of E3 ligases in promoting degradation of both signaling proteins and expanded glutamine proteins
Yoshihiro Morishima et al.
HUMAN MOLECULAR GENETICS (2008)
A novel role for PA28γ-proteasome in nuclear speckle organization and SR protein trafficking
Veronique Baldin et al.
MOLECULAR BIOLOGY OF THE CELL (2008)
Ubiquitin-independent degradation of cell-cycle inhibitors by the REGγ proteasome
Xueyan Chen et al.
MOLECULAR CELL (2007)
Ubiquitin- and ATP-independent proteolytic turnover of p21 by the REGγ-proteasome pathway
Xiaotao Li et al.
MOLECULAR CELL (2007)
Proteasome Activator Enhances Survival of Huntington's Disease Neuronal Model Cells
Hyemyung Seo et al.
PLOS ONE (2007)
Soluble androgen receptor oligomers underlie pathology in a mouse model of spinobulbar muscular atrophy
Mei Li et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
UV-induced fragmentation of Cajal bodies
Mario Cioce et al.
JOURNAL OF CELL BIOLOGY (2006)
Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington's disease mice:: exclusion of proteasome activator REGγ as a therapeutic target (vol 15, pg 33, 2006)
JS Bett et al.
HUMAN MOLECULAR GENETICS (2006)
The SRC-3/AIB1 coactivator is degraded 14 in a ubiquitin- and ATP-independent manner by the REGγ proteasome
XT Li et al.
CELL (2006)
Immune defects in 28-kDa proteasome activator γ-deficient mice
LF Barton et al.
JOURNAL OF IMMUNOLOGY (2004)
Castration restores function and neurofilament alterations of aged symptomatic males in a transgenic mouse model of spinal and bulbar muscular atrophy
ES Chevalier-Larsen et al.
JOURNAL OF NEUROSCIENCE (2004)
Ubiquitin-independent proteolytic functions of the proteasome
M Orlowski et al.
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS (2003)
Ligand promotes intranuclear inclusions in a novel cell model of spinal and bulbar muscular atrophy
JL Walcott et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy
M Katsuno et al.
NEURON (2002)
Androgen-dependent neurodegeneration by polyglutamine-expanded human androgen receptor in Drosophila
K Takeyama et al.
NEURON (2002)
Phosphorylation-dependent ubiquitylation and degradation of androgen receptor by Akt require Mdm2 E3 ligase
HK Lin et al.
EMBO JOURNAL (2002)
Molecular chaperones enhance the degradation of expanded polyglutamine repeat androgen receptor in a cellular model of spinal and bulbar muscular atrophy
CK Bailey et al.
HUMAN MOLECULAR GENETICS (2002)
Lysine 188 substitutions convert the pattern of proteasome activation by REGγ to that of REGs α and β
J Li et al.
EMBO JOURNAL (2001)
Identification of a novel phosphorylation site in human androgen receptor by mass spectrometry
ZX Zhu et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2001)
Expression of expanded repeat androgen receptor produces neurologic disease in transgenic mice
A Abel et al.
HUMAN MOLECULAR GENETICS (2001)
Hybrid proteasomes -: Induction by interferon-γ and contribution to ATP-dependent proteolysis
N Tanahashi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Share Paper
