Related references
Note: Only part of the references are listed.DNAJB1 destabilizes PDCD5 to suppress p53-mediated apoptosis
Xiandan Cui et al.
CANCER LETTERS (2015)
Functional Analysis of FOXE3 Mutations Causing Dominant and Recessive Ocular Anterior Segment Disease
Lily Islam et al.
HUMAN MUTATION (2015)
Transcriptome Profiling of Developing Murine Lens Through RNA Sequencing
Shahid Y. Khan et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2015)
DNAJB1 stabilizes MDM2 and contributes to cancer cell proliferation in a p53-dependent manner
Min Qi et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS (2014)
WIPI2 Links LC3 Conjugation with PI3P, Autophagosome Formation, and Pathogen Clearance by Recruiting Atg12-5-16L1
Hannah C. Dooley et al.
MOLECULAR CELL (2014)
Detection of a Recurrent DNAJB1-PRKACA Chimeric Transcript in Fibrolamellar Hepatocellular Carcinoma
Joshua N. Honeyman et al.
SCIENCE (2014)
Increased Expression of Endoplasmic Reticulum Stress and Unfolded Protein Response Genes in Peripheral Blood Mononuclear Cells From Patients With Limited Cutaneous Systemic Sclerosis and Pulmonary Arterial Hypertension
Stefania Lenna et al.
ARTHRITIS AND RHEUMATISM (2013)
TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
Daehwan Kim et al.
GENOME BIOLOGY (2013)
Growth inhibition of human lens epithelial cells by short hairpin RNA in transcription factor forkhead box E3 (FOXE3)
Ye Wang et al.
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY (2012)
Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts
Jianjun Chen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Peters Anomaly: Review of the Literature
Ramanath Bhandari et al.
CORNEA (2011)
A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly
Lance Doucette et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
Mammalian Atg18 (WIPI2) localizes to omegasome-anchored phagophores and positively regulates LC3 lipidation
Hannah E. J. Polson et al.
AUTOPHAGY (2010)
Network organization of the human autophagy system
Christian Behrends et al.
NATURE (2010)
Differential expression analysis for sequence count data
Simon Anders et al.
GENOME BIOLOGY (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Universal sample preparation method for proteome analysis
Jacek R. Wisniewski et al.
NATURE METHODS (2009)
Persistent FoxE3 expression blocks cytoskeletal remodeling and organelle degradation during lens fiber differentiation
Henrik Landgren et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2008)
Mapping and quantifying mammalian transcriptomes by RNA-Seq
Ali Mortazavi et al.
NATURE METHODS (2008)
Molecular and developmental mechanisms of anterior segment dysgenesis
J. C. Sowden
EYE (2007)
Classical nuclear localization signals:: Definition, function, and interaction with importin α
Allison Lange et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans
Sophie Valleix et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Severe defects in proliferation and differentiation of lens cells in Foxe3 null mice
O Medina-Martinez et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
Prenatal sonographic findings in Peters-plus syndrome
G Boog et al.
ULTRASOUND IN OBSTETRICS & GYNECOLOGY (2005)
Anterior segment dysgenesis and the developmental glaucomas are complex traits
DB Gould et al.
HUMAN MOLECULAR GENETICS (2002)
Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method
KJ Livak et al.
METHODS (2001)
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye
DY Nishimura et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Ocular and systemic features of Peters' anomaly
H Ozeki et al.
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY (2000)