Modeling Congenital Disorders of N-Linked Glycoprotein Glycosylation in Drosophila melanogaster
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Modeling Congenital Disorders of N-Linked Glycoprotein Glycosylation in Drosophila melanogaster
Authors
Keywords
-
Journal
Frontiers in Genetics
Volume 9, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2018-10-02
DOI
10.3389/fgene.2018.00436
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- COG7 deficiency inDrosophilagenerates multifaceted developmental, behavioral and protein glycosylation phenotypes
- (2017) Anna Frappaolo et al. JOURNAL OF CELL SCIENCE
- Mutations in the X-linkedATP6AP2cause a glycosylation disorder with autophagic defects
- (2017) Maria A. Rujano et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Rab1 interacts with GOLPH3 and controls Golgi structure and contractile ring constriction during cytokinesis inDrosophila melanogaster
- (2017) Stefano Sechi et al. Open Biology
- Modeling congenital disease and inborn errors of development inDrosophila melanogaster
- (2016) Matthew J. Moulton et al. Disease Models & Mechanisms
- Synaptic roles for phosphomannomutase type 2 in a newDrosophilacongenital disorder of glycosylation disease model
- (2016) William M. Parkinson et al. Disease Models & Mechanisms
- Acute and long-term outcomes in aDrosophila melanogastermodel of classic galactosemia occur independently of galactose-1-phosphate accumulation
- (2016) Jennifer M. I. Daenzer et al. Disease Models & Mechanisms
- Coordinated movement, neuromuscular synaptogenesis and trans-synaptic signaling defects inDrosophilagalactosemia models
- (2016) Patricia P. Jumbo-Lucioni et al. HUMAN MOLECULAR GENETICS
- The role of acroblast formation duringDrosophilaspermatogenesis
- (2016) Karolina Fári et al. Biology Open
- Neurological Aspects of Human Glycosylation Disorders
- (2015) Hudson H. Freeze et al. Annual Review of Neuroscience
- Symbol Nomenclature for Graphical Representations of Glycans
- (2015) Ajit Varki et al. GLYCOBIOLOGY
- Autophagosome–lysosome fusion is independent of V-ATPase-mediated acidification
- (2015) Caroline Mauvezin et al. Nature Communications
- Defects in the COG complex and COG-related trafficking regulators affect neuronal Golgi function
- (2015) Leslie K. Climer et al. Frontiers in Neuroscience
- Solving Glycosylation Disorders: Fundamental Approaches Reveal Complicated Pathways
- (2014) Hudson H. Freeze et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations inCOG2encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylation
- (2014) H. Kodera et al. CLINICAL GENETICS
- Two Protein N-Acetylgalactosaminyl Transferases Regulate Synaptic Plasticity by Activity-Dependent Regulation of Integrin Signaling
- (2014) N. Dani et al. JOURNAL OF NEUROSCIENCE
- Congenital Disorders of Glycosylation with Emphasis on Cerebellar Involvement
- (2014) Rita Barone et al. SEMINARS IN NEUROLOGY
- The Golgi puppet master: COG complex at center stage of membrane trafficking interactions
- (2013) Rose Willett et al. HISTOCHEMISTRY AND CELL BIOLOGY
- Tethering the assembly of SNARE complexes
- (2013) WanJin Hong et al. TRENDS IN CELL BIOLOGY
- The conserved oligomeric Golgi complex is required for fucosylation of N-glycans in Caenorhabditis elegans
- (2012) Weston B Struwe et al. GLYCOBIOLOGY
- The N’s and O’s of Drosophila glycoprotein glycobiology
- (2012) Toshihiko Katoh et al. GLYCOCONJUGATE JOURNAL
- Molecular Insights into Vesicle Tethering at the Golgi by the Conserved Oligomeric Golgi (COG) Complex and the Golgin TATA Element Modulatory Factor (TMF)
- (2012) Victoria J. Miller et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- TheDrosophilaNeurally Altered Carbohydrate Mutant Has a Defective Golgi GDP-fucose Transporter
- (2012) Christoph Geisler et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Mutations inCog7affect Golgi structure, meiotic cytokinesis and sperm development duringDrosophilaspermatogenesis
- (2012) Giorgio Belloni et al. JOURNAL OF CELL SCIENCE
- Vertebrate protein glycosylation: diversity, synthesis and function
- (2012) Kelley W. Moremen et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Re‘COG’nition at the Golgi
- (2012) Victoria J. Miller et al. TRAFFIC
- Mechanisms and principles of N-linked protein glycosylation
- (2011) Flavio Schwarz et al. CURRENT OPINION IN STRUCTURAL BIOLOGY
- Sugar-free frosting, a homolog of SAD kinase, drives neural-specific glycan expression in the Drosophila embryo
- (2011) S. Baas et al. DEVELOPMENT
- Fragile X mental retardation protein is required for programmed cell death and clearance of developmentally-transient peptidergic neurons
- (2011) Cheryl L. Gatto et al. DEVELOPMENTAL BIOLOGY
- Golgi Glycosylation
- (2011) P. Stanley Cold Spring Harbor Perspectives in Biology
- Golgi Glycosylation and Human Inherited Diseases
- (2011) H. H. Freeze et al. Cold Spring Harbor Perspectives in Biology
- Proteome-wide post-translational modification statistics: frequency analysis and curation of the swiss-prot database
- (2011) George A. Khoury et al. Scientific Reports
- Precision Mapping of an In Vivo N-Glycoproteome Reveals Rigid Topological and Sequence Constraints
- (2010) Dorota F. Zielinska et al. CELL
- The vacuolar ATPase is required for physiological as well as pathological activation of the Notch receptor
- (2010) T. Vaccari et al. DEVELOPMENT
- Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation
- (2010) J. Lubbehusen et al. HUMAN MOLECULAR GENETICS
- Sialyltransferase Regulates Nervous System Function in Drosophila
- (2010) E. Repnikova et al. JOURNAL OF NEUROSCIENCE
- The clinical spectrum of phosphomannomutase 2 deficiency (CDG-Ia)
- (2009) Stephanie Grünewald BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- Towards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients
- (2009) Hudson H. Freeze BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- A new mutation in COG7 extends the spectrum of COG subunit deficiencies
- (2009) Renate Zeevaert et al. European Journal of Medical Genetics
- Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation
- (2009) P. Paesold-Burda et al. HUMAN MOLECULAR GENETICS
- Golgi function and dysfunction in the first COG4-deficient CDG type II patient
- (2009) Ellen Reynders et al. HUMAN MOLECULAR GENETICS
- Leukocyte trafficking in a mouse model for leukocyte adhesion deficiency II/congenital disorder of glycosylation IIc
- (2008) S. Yakubenia et al. BLOOD
- Structure of the Oligosaccharyl Transferase Complex at 12 Å Resolution
- (2008) Hua Li et al. STRUCTURE
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started