Related references
Note: Only part of the references are listed.Chaperone functions of the E3 ubiquitin ligase CHIP
Meredith F. N. Rosser et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis
Maxence V. Nachury et al.
CELL (2007)
Two families of chaperonin: Physiology and mechanism
Arthur L. Horwich et al.
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY (2007)
Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome
Corinne Stoetzel et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
The chaperonin TRiC controls polyglutamine aggregation and toxicity through subunit-specific interactions
Stephen Tam et al.
NATURE CELL BIOLOGY (2006)
Cytosolic chaperonin prevents polyglutamine toxicity with altering the aggregation state
Akira Kitamura et al.
NATURE CELL BIOLOGY (2006)
Chaperonin TRiC promotes the assembly of polyQ expansion proteins into nontoxic oligomers
Christian Behrends et al.
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Sequential quality-control checkpoints triage misfolded cystic fibrosis transmembrane conductance regulator
J. Michael Younger et al.
CELL (2006)
Cytosolic chaperonin protects folding intermediates of Gß from aggregation by recognizing hydrophobic ß-strands
S Kubota et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus
C Stoetzel et al.
NATURE GENETICS (2006)
Homozygosity mapping with SNP arrays identifies TRIM32 an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)
AP Chiang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Engineering of a monomeric green-to-red photoactivatable fluorescent protein induced by blue light
NG Gurskaya et al.
NATURE BIOTECHNOLOGY (2006)
CHIP-mediated stress recovery by sequential ubiquitination of substrates and Hsp70
SB Qian et al.
NATURE (2006)
Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function
HJ Yen et al.
HUMAN MOLECULAR GENETICS (2006)
Dissection of epistasis in oligogenic Bardet-Biedl syndrome
JL Badano et al.
NATURE (2006)
14-3-3η is a novel regulator of parkin ubiquitin ligase
S Sato et al.
EMBO JOURNAL (2006)
Bardet-Biedl syndrome: an emerging pathomechanism of intracellular transport
O. E. Blacque et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2006)
Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene
DY Nishimura et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Functional coordination of intraflagellar transport motors
GS Ou et al.
NATURE (2005)
Lifting the lid on Pandora's box: the Bardet-Biedl syndrome
PL Beales
CURRENT OPINION IN GENETICS & DEVELOPMENT (2005)
Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome
MA Fath et al.
HUMAN MOLECULAR GENETICS (2005)
The biological and chemical basis for tissue-selective amyloid disease
Y Sekijima et al.
CELL (2005)
The centrosome in human genetic disease
JL Badano et al.
NATURE REVIEWS GENETICS (2005)
MKKS/BBS6, a divergent chaperonin-like protein linked to the obesity disorder Bardet-Biedl syndrome, is a novel centrosomal component required for cytokinesis
JC Kim et al.
JOURNAL OF CELL SCIENCE (2005)
Global impairment of the ubiquitin-proteasome system by nuclear or cytoplasmic protein aggregates precedes inclusion body formation
EJ Bennett et al.
MOLECULAR CELL (2005)
The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression
JC Kim et al.
NATURE GENETICS (2004)
Establishing a connection between cilia and Bardet-Biedl Syndrome
K Mykytyn et al.
TRENDS IN MOLECULAR MEDICINE (2004)
Roles of molecular chaperones in protein misfolding diseases
JM Barral et al.
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2004)
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse
HM Kulaga et al.
NATURE GENETICS (2004)
Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)
AP Chiang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
A foldable CFTRΔF508 biogenic intermediate accumulates upon inhibition of the Hsc70-CHIP E3 ubiquitin ligase
JM Younger et al.
JOURNAL OF CELL BIOLOGY (2004)
Ligand-dependent switching of ubiquitin-proteasome pathways for estrogen receptor
Y Tateishi et al.
EMBO JOURNAL (2004)
Cellular toxicity of polyglutamine expansion proteins: Mechanism of transcription factor deactivation
G Schaffar et al.
MOLECULAR CELL (2004)
Loss of C-elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport
OE Blacque et al.
GENES & DEVELOPMENT (2004)
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin
DY Nishimura et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly
K Mykytyn et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Mechanism of the eukaryotic chaperonin: protein folding in the chamber of secrets
C Spiess et al.
TRENDS IN CELL BIOLOGY (2004)
Inefficient degradation of truncated polyglutamine proteins by the proteasome
CI Holmberg et al.
EMBO JOURNAL (2004)
Pathways of chaperone-mediated protein folding in the cytosol
JC Young et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2004)
Comparative and basal genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene
JB Li et al.
CELL (2004)
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
SJ Ansley et al.
NATURE (2003)
The ubiquitin proteasome system in neurodegenerative diseases: Sometimes the chicken, sometimes the egg
A Ciechanover et al.
NEURON (2003)
Overexpression of the cochaperone CHIP enhances Hsp70-dependent folding activity in mammalian cells
HH Kampinga et al.
MOLECULAR AND CELLULAR BIOLOGY (2003)
Closing the folding chamber of the eukaryotic chaperonin requires the transition state of ATP hydrolysis
AS Meyer et al.
CELL (2003)
Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2
JL Badano et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
C-terminal Hsp-interacting protein slows androgen receptor synthesis and reduces its rate of degradation
CP Cardozo et al.
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS (2003)
Polyglutamine protein aggregates are dynamic
S Kim et al.
NATURE CELL BIOLOGY (2002)
A photoactivatable GFP for selective photolabeling of proteins and cells
GH Patterson et al.
SCIENCE (2002)
Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients
AM Slavotinek et al.
HUMAN GENETICS (2002)
CHIP is a chaperone-dependent E3 ligase that ubiquitylates unfolded protein
S Murata et al.
EMBO REPORTS (2001)
Studying protein dynamics in living cells
J Lippincott-Schwartz et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2001)
Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci
PL Beales et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
The Hsc70 co-chaperone CHIP targets immature CFTR for proteasomal degradation
GC Meacham et al.
NATURE CELL BIOLOGY (2001)
The co-chaperone CHIP regulates protein triage decisions mediated by heat-shock proteins
P Connell et al.
NATURE CELL BIOLOGY (2001)
Aggresomes, inclusion bodies and protein aggregation
RR Kopito
TRENDS IN CELL BIOLOGY (2000)
Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome
DL Stone et al.
NATURE GENETICS (2000)
Dynamics and retention of misfolded proteins in native ER membranes
S Nehls et al.
NATURE CELL BIOLOGY (2000)
Mutations in MKKS cause Bardet-Biedl syndrome
AM Slavotinek et al.
NATURE GENETICS (2000)
Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome
N Katsanis et al.
NATURE GENETICS (2000)