Related references
Note: Only part of the references are listed.The endoplasmic reticulum-mitochondria connection: One touch, multiple functions
Saverio Marchi et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2014)
C19orf12 mutation leads to a pallido-pyramidal syndrome
Michael C. Kruer et al.
GENE (2014)
Impairment of Drosophila Orthologs of the Human Orphan Protein C19orf12 Induces Bang Sensitivity and Neurodegeneration
Arcangela Iuso et al.
PLOS ONE (2014)
The structure and regulation of magnesium selective ion channels
Jian Payandeh et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2013)
Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in C19orf12
Guida Landoure et al.
HUMAN MUTATION (2013)
Autophagosomes form at ER-mitochondria contact sites
Maho Hamasaki et al.
NATURE (2013)
Subcellular calcium measurements in mammalian cells using jellyfish photoprotein aequorin-based probes
Massimo Bonora et al.
NATURE PROTOCOLS (2013)
Iron metabolism in the CNS: implications for neurodegenerative diseases
Tracey A. Rouault
NATURE REVIEWS NEUROSCIENCE (2013)
Review: Membrane-associated misfolded protein propagation in natural transmissible spongiform encephalopathies (TSEs), synthetic prion diseases and Alzheimer's disease
M. Jeffrey
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2013)
Substitution p.A350V in Na+/Mg2+ Exchanger SLC41A1, Potentially Associated with Parkinson's Disease, Is a Gain-of-Function Mutation
Martin Kolisek et al.
PLOS ONE (2013)
Guidelines for the use and interpretation of assays for monitoring autophagy
Daniel J. Klionsky et al.
AUTOPHAGY (2012)
Spatial distribution of cytoplasmic domains of the Mg2+-transporter MgtE, in a solution lacking Mg2+, revealed by paramagnetic relaxation enhancement
Shunsuke Imai et al.
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS (2012)
An international registry for neurodegeneration with brain iron accumulation
Bernadette Kalman et al.
ORPHANET JOURNAL OF RARE DISEASES (2012)
C19orf12 and FA2H Mutations Are Rare in Italian Patients With Neurodegeneration With Brain Iron Accumulation
Celeste Panteghini et al.
SEMINARS IN PEDIATRIC NEUROLOGY (2012)
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
Monika B. Hartig et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Calcium signaling around Mitochondria Associated Membranes (MAMs)
Simone Patergnani et al.
CELL COMMUNICATION AND SIGNALING (2011)
Is Alzheimer's Disease a Disorder of Mitochondria-Associated Membranes?
Eric A. Schon et al.
JOURNAL OF ALZHEIMERS DISEASE (2010)
Isolation of mitochondria for biogenetical studies: An update
Erika Fernandez-Vizarra et al.
MITOCHONDRION (2010)
Enhancement of Learning and Memory by Elevating Brain Magnesium
Inna Slutsky et al.
NEURON (2010)
Mg2+-dependent gating of bacterial MgtE channel underlies Mg2+ homeostasis
Motoyuki Hattori et al.
EMBO JOURNAL (2009)
Isolation of mitochondria-associated membranes and mitochondria from animal tissues and cells
Mariusz R. Wieckowski et al.
NATURE PROTOCOLS (2009)
Magnesium homeostasis and aging
Mario Barbagallo et al.
MAGNESIUM RESEARCH (2009)
Validation of protein models by a neural network approach
Paolo Mereghetti et al.
BMC BIOINFORMATICS (2008)
The neurological presentation of ceruloplasmin gene mutations
Alisdair McNeill et al.
EUROPEAN NEUROLOGY (2008)
Crystal structure of the MgtE Mg2+ transporter
Motoyuki Hattori et al.
NATURE (2007)
LC3, an autophagosome marker, can be incorporated into protein aggregates independent of autophagy
Akiko Kuma et al.
AUTOPHAGY (2007)
Improving the accuracy of transmembrane protein topology prediction using evolutionary information
David T. Jones
BIOINFORMATICS (2007)
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation
Patrick F. Chinnery et al.
BRAIN (2007)
A guided tour into subcellular colocalization analysis in light microscopy
S. Bolte et al.
JOURNAL OF MICROSCOPY (2006)
Magnesium transporters: Properties, regulation and structure
Michael E. Maguire
FRONTIERS IN BIOSCIENCE-LANDMARK (2006)
CellProfiler: image analysis software for identifying and quantifying cell phenotypes
Anne E. Carpenter et al.
GENOME BIOLOGY (2006)
Transmembrane glycine zippers: Physiological and pathological roles in membrane proteins
S Kim et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
The HHpred interactive server for protein homology detection and structure prediction
J Söding et al.
NUCLEIC ACIDS RESEARCH (2005)
The FoldX web server: an online force field
J Schymkowitz et al.
NUCLEIC ACIDS RESEARCH (2005)
Magnesium deficiency impairs fear conditioning in mice
ME Bardgett et al.
BRAIN RESEARCH (2005)
Ethylmalonic encephalopathy is caused by mutations in ETHE1, a gene encoding a mitochondrial matrix protein
V Tiranti et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Enhancement of synaptic plasticity through chronically reduced Ca2+ flux during uncorrelated activity
I Slutsky et al.
NEURON (2004)
The endoplasmic reticulum: a multifunctional signaling organelle
MJ Berridge
CELL CALCIUM (2002)
Predicting changes in the stability of proteins and protein complexes: A study of more than 1000 mutations
R Guerois et al.
JOURNAL OF MOLECULAR BIOLOGY (2002)
The PSIPRED protein structure prediction server
LJ McGuffin et al.
BIOINFORMATICS (2000)
Share Paper
