Related references
Note: Only part of the references are listed.Misfolded BRICHOS SP-C mutant proteins induce apoptosis via caspase-4- and cytochrome c-related mechanisms
Surafel Mulugeta et al.
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY (2007)
Telomerase mutations in families with idiopathic pulmonary fibrosis
Mary Y. Armanios et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
Clinical and pathologic features of familial interstitial pneumonia
MP Steele et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2005)
A surfactant protein C precursor protein BRICHOS domain mutation causes endoplasmic reticulum stress, proteasome dysfunction, and caspase 3 activation
S Mulugeta et al.
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY (2005)
Human cytomegalovirus infection activates and regulates the unfolded protein response
JA Isler et al.
JOURNAL OF VIROLOGY (2005)
Constitutively active K-cyclin/cdk6 kinase in Kaposi sarcoma-associated herpesvirus-infected cells
R Van Dross et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2005)
Characterization of fibroblast-specific protein 1 in pulmonary fibrosis
WE Lawson et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2005)
Quantitative measurement of events in the mammalian unfolded protein response
J Shang
METHODS (2005)
The ER chaperone and signaling regulator GRP78/BiP as a monitor of endoplasmic reticulum stress
AS Lee
METHODS (2005)
BK and JC polyomaviruses are not associated with idiopathic pulmonary fibrosis
GW Procop et al.
JOURNAL OF CLINICAL MICROBIOLOGY (2005)
Herpes simplex virus 1 infection activates the endoplasmic reticulum resident kinase PERK and mediates eIF-2α dephosphorylation by the γ134.5 protein
GF Cheng et al.
JOURNAL OF VIROLOGY (2005)
Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF
WE Lawson et al.
THORAX (2004)
Mechanisms of pulmonary fibrosis
VJ Thannickal et al.
ANNUAL REVIEW OF MEDICINE (2004)
Herpesvirus DNA is consistently detected in lungs of patients with idiopathic pulmonary fibrosis
YW Tang et al.
JOURNAL OF CLINICAL MICROBIOLOGY (2003)
Mechanisms of disease: Hydrophobic surfactant proteins in lung function and disease
JA Whitsett et al.
NEW ENGLAND JOURNAL OF MEDICINE (2002)
Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred
AQ Thomas et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2002)
XBP1 mRNA is induced by ATF6 and spliced by IRE1 in response to ER stress to produce a highly active transcription factor
H Yoshida et al.
CELL (2001)
Medical progress: Idiopathic pulmonary fibrosis.
TJ Gross et al.
NEW ENGLAND JOURNAL OF MEDICINE (2001)
Feedback inhibition of the unfolded protein response by GADD34-mediated dephosphorylation of eIF2α
I Novoa et al.
JOURNAL OF CELL BIOLOGY (2001)
A mutation in the surfactant protein C gene associated with familial interstitial lung disease.
LM Nogee et al.
NEW ENGLAND JOURNAL OF MEDICINE (2001)
Involvement of Epstein-Barr virus latent membrane protein 1 in disease progression in patients with idiopathic pulmonary fibrosis
K Tsukamoto et al.
THORAX (2000)
Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response
A Bertolotti et al.
NATURE CELL BIOLOGY (2000)
Perk is essential for translational regulation and cell survival during the unfolded protein response
HP Harding et al.
MOLECULAR CELL (2000)
Caspase-12 mediates endoplasmic-reticulum-specific apoptosis and cytotoxicity by amyloid-β
T Nakagawa et al.
NATURE (2000)