Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder
Authors
Keywords
-
Journal
BRAIN
Volume 138, Issue 9, Pages 2521-2536
Publisher
Oxford University Press (OUP)
Online
2015-07-16
DOI
10.1093/brain/awv204
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- A de novo TUBB4A mutation in a patient with hypomyelination mimicking Pelizaeus–Merzbacher disease
- (2015) Keiko Shimojima et al. BRAIN & DEVELOPMENT
- Hypomyelinating leukodystrophies: Translational research progress and prospects
- (2014) Petra J. W. Pouwels et al. ANNALS OF NEUROLOGY
- Accurate Proteome-wide Label-free Quantification by Delayed Normalization and Maximal Peptide Ratio Extraction, Termed MaxLFQ
- (2014) Jürgen Cox et al. MOLECULAR & CELLULAR PROTEOMICS
- Expanding the phenotypic spectrum of TUBB4A-associated hypomyelinating leukoencephalopathies
- (2014) S. Miyatake et al. NEUROLOGY
- Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders
- (2014) G. Novarino et al. SCIENCE
- Myelin-specific proteins: A structurally diverse group of membrane-interacting molecules
- (2013) Huijong Han et al. BIOFACTORS
- Pelizaeus-Merzbacher Disease, Pelizaeus-Merzbacher-Like Disease 1, and Related Hypomyelinating Disorders
- (2012) Grace Hobson et al. SEMINARS IN NEUROLOGY
- Andromeda: A Peptide Search Engine Integrated into the MaxQuant Environment
- (2011) Jürgen Cox et al. JOURNAL OF PROTEOME RESEARCH
- SMART 7: recent updates to the protein domain annotation resource
- (2011) I. Letunic et al. NUCLEIC ACIDS RESEARCH
- Pelizaeus-Merzbacher-like Disease Caused by AIMP1/p43 Homozygous Mutation
- (2010) Miora Feinstein et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The Cavβ subunit prevents RFP2-mediated ubiquitination and proteasomal degradation of L-type channels
- (2010) Christophe Altier et al. NATURE NEUROSCIENCE
- I-TASSER: a unified platform for automated protein structure and function prediction
- (2010) Ambrish Roy et al. Nature Protocols
- Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects
- (2009) Catherine Vaurs-Barrière et al. ANNALS OF NEUROLOGY
- Axonal Protective Effects of the Myelin-Associated Glycoprotein
- (2009) T. Nguyen et al. JOURNAL OF NEUROSCIENCE
- HomozygosityMapper--an interactive approach to homozygosity mapping
- (2009) D. Seelow et al. NUCLEIC ACIDS RESEARCH
- Mitochondrial Hsp60 Chaperonopathy Causes an Autosomal-Recessive Neurodegenerative Disorder Linked to Brain Hypomyelination and Leukodystrophy
- (2008) Daniella Magen et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Classification of Childhood White Matter Disorders Using Proton MR Spectroscopic Imaging
- (2008) A. Bizzi et al. AMERICAN JOURNAL OF NEURORADIOLOGY
- Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations
- (2008) Jennifer L. Orthmann-Murphy et al. BRAIN
- Coordinated Lipid Transfer between the Endoplasmic Reticulum and the Golgi Complex Requires the VAP Proteins and Is Essential for Golgi-mediated Transport
- (2008) Diego Peretti et al. MOLECULAR BIOLOGY OF THE CELL
- OS-9 and GRP94 deliver mutant α1-antitrypsin to the Hrd1–SEL1L ubiquitin ligase complex for ERAD
- (2008) John C. Christianson et al. NATURE CELL BIOLOGY
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now