Related references
Note: Only part of the references are listed.Protter: interactive protein feature visualization and integration with experimental proteomic data
Ulrich Omasits et al.
BIOINFORMATICS (2014)
Human pathology in NCL
Glenn W. Anderson et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2013)
Neuronal Ceroid Lipofuscinosis: Impact of Recent Genetic Advances and Expansion of the Clinicopathologic Spectrum
Susan L. Cotman et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2013)
Large-Scale Phenotyping of an Accurate Genetic Mouse Model of JNCL Identifies Novel Early Pathology Outside the Central Nervous System
John F. Staropoli et al.
PLOS ONE (2012)
Analysis of Potential Biomarkers and Modifier Genes Affecting the Clinical Course of CLN3 Disease
Anne-Helene Lebrun et al.
MOLECULAR MEDICINE (2011)
Cardiac involvement in juvenile neuronal ceroid lipofuscinosis (Batten disease)
J. R. Ostergaard et al.
NEUROLOGY (2011)
Distinct Early Molecular Responses to Mutations Causing vLINCL and JNCL Presage ATP Synthase Subunit C Accumulation in Cerebellar Cells
Yi Cao et al.
PLOS ONE (2011)
Neuronal ceroid lipofuscinoses
Anu Jalanko et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2009)
Towards understanding the neuronal ceroid lipofuscinoses
Alfried Kohlschuetter et al.
BRAIN & DEVELOPMENT (2009)
TOPCONS: consensus prediction of membrane protein topology
Andreas Bernsel et al.
NUCLEIC ACIDS RESEARCH (2009)
The transmembrane topology of Batten disease protein CLN3 determined by consensus computational prediction constrained by experimental data
Timothy Nugent et al.
FEBS LETTERS (2008)
A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis
Claudia Kitzmueller et al.
HUMAN MOLECULAR GENETICS (2008)
Molecular code for transmembrane-helix recognition by the Sec61 translocon
Tara Hessa et al.
NATURE (2007)
α-synuclein and its disease-related mutants interact differentially with the microtubule protein tau and associate with the actin cytoskeleton
Alessandro Esposito et al.
NEUROBIOLOGY OF DISEASE (2007)
ZPRED:: Predicting the distance to the membrane center for residues in α-helical membrane proteins
Erik Granseth et al.
BIOINFORMATICS (2006)
Saccharomyces cerevisiae lacking Btn1p modulate vacuolar ATPase activity to regulate pH imbalance in the vacuole
S Padilla-López et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
CellProfiler: image analysis software for identifying and quantifying cell phenotypes
Anne E. Carpenter et al.
GENOME BIOLOGY (2006)
CLN3, the protein associated with batten disease: Structure, function and localization
SN Phillips et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2005)
Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses
SE Mole et al.
NEUROGENETICS (2005)
Two motifs target Batten disease protein CLN3 to lysosomes in transfected nonneuronal and neuronal cells
A Kyttälä et al.
MOLECULAR BIOLOGY OF THE CELL (2004)
A faster way to make GFP-based biosensors: Two new transposons for creating multicolored libraries of fluorescent fusion proteins
DL Sheridan et al.
BMC BIOTECHNOLOGY (2004)
Membrane trafficking and mitochondrial abnormalities precede subunit c deposition in a cerebellar cell model of juvenile neuronal ceroid lipofuscinosis
E Fossale et al.
BMC NEUROSCIENCE (2004)
Current state of clinical and morphological features in human NCL
HH Goebel et al.
BRAIN PATHOLOGY (2004)
A role in vacuolar arginine transport for yeast Btn1p and for human CLN3, the protein defective in Batten disease
Y Kim et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Characterization of Cln3p, the gene product responsible for juvenile neuronal ceroid lipofuscinosis, as a lysosomal integral membrane glycoprotein
J Ezaki et al.
JOURNAL OF NEUROCHEMISTRY (2003)
Membrane topology of CLN3, the protein underlying Batten disease
QW Mao et al.
FEBS LETTERS (2003)
Cln3Δex7/8 knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth
SL Cotman et al.
HUMAN MOLECULAR GENETICS (2002)
A new way to rapidly create functional, fluorescent fusion proteins: random insertion of GFP with an in vitro transposition reaction
Douglas L. Sheridan et al.
BMC NEUROSCIENCE (2002)
Elevated lysosomal pH in neuronal ceroid lipofuscinoses (NCLs)
JM Holopainen et al.
EUROPEAN JOURNAL OF BIOCHEMISTRY (2001)