High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defect

Perspectives on Glycosylation and Its Congenital Disorders

(2018) Bobby G. Ng et al.   TRENDS IN GENETICS

Endoplasmic reticulum proteins SDF2 and SDF2L1 act as components of the BiP chaperone cycle to prevent protein aggregation

(2017) Tsutomu Fujimori et al.   GENES TO CELLS

Mutations in the X-linkedATP6AP2cause a glycosylation disorder with autophagic defects

(2017) Maria A. Rujano et al.   JOURNAL OF EXPERIMENTAL MEDICINE

What is new in CDG?

(2017) Jaak Jaeken et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Clinical, laboratory and molecular findings and long-term follow-up data in 96 French patients with PMM2-CDG (phosphomannomutase 2-congenital disorder of glycosylation) and review of the literature

(2017) Manuel Schiff et al.   JOURNAL OF MEDICAL GENETICS

Quantitative Profiling of N-linked Glycosylation Machinery in YeastSaccharomyces cerevisiae

(2017) Kristina Poljak et al.   MOLECULAR & CELLULAR PROTEOMICS

Neural Cell Adhesion Molecules of the Immunoglobulin Superfamily Regulate Synapse Formation, Maintenance, and Function

(2017) Vladimir Sytnyk et al.   TRENDS IN NEUROSCIENCES

SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features

(2016) Patricia G. Wheeler et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2

(2016) Barden Chan et al.   HUMAN MOLECULAR GENETICS

RAB43 facilitates cross-presentation of cell-associated antigens by CD8α + dendritic cells

(2016) Nicole M. Kretzer et al.   JOURNAL OF EXPERIMENTAL MEDICINE

Sensitivity of mass spectrometry analysis depends on the shape of the filtration unit used for filter aided sample preparation (FASP)

(2016) Joanna Lipecka et al.   PROTEOMICS

Mammalian cells lacking either the cotranslational or posttranslocational oligosaccharyltransferase complex display substrate-dependent defects in asparagine linked glycosylation

(2016) Natalia A. Cherepanova et al.   Scientific Reports

Neurological Aspects of Human Glycosylation Disorders

(2015) Hudson H. Freeze et al.   Annual Review of Neuroscience

Enhanced Aromatic Sequons Increase Oligosaccharyltransferase Glycosylation Efficiency and Glycan Homogeneity

(2015) Amber N. Murray et al.   CHEMISTRY & BIOLOGY

Solving Glycosylation Disorders: Fundamental Approaches Reveal Complicated Pathways

(2014) Hudson H. Freeze et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Adult phenotype and further phenotypic variability in SRD5A3-CDG

(2014) Bülent Kara et al.   BMC Medical Genetics

Mutation of Nogo-B Receptor, a Subunit of cis-Prenyltransferase, Causes a Congenital Disorder of Glycosylation

(2014) Eon Joo Park et al.   Cell Metabolism

The role of protein N-glycosylation in neural transmission

(2014) H. Scott et al.   GLYCOBIOLOGY

N-glycosylation deficiency reduces ICAM-1 induction and impairs inflammatory response

(2014) Ping He et al.   GLYCOBIOLOGY

Myelin Basic Protein Cleaves Cell Adhesion Molecule L1 and Promotes Neuritogenesis and Cell Survival

(2014) David Lutz et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Interaction of the Cell Adhesion Molecule CHL1 with Vitronectin, Integrins, and the Plasminogen Activator Inhibitor-2 Promotes CHL1-Induced Neurite Outgrowth and Neuronal Migration

(2014) J. Katic et al.   JOURNAL OF NEUROSCIENCE

Contactin-1 regulates myelination and nodal/paranodal domain organization in the central nervous system

(2014) G. Colakoglu et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Differential Labeling of Cell-surface and Internalized Proteins after Antibody Feeding of Live Cultured Neurons

(2014) Nissa L. Carrodus et al.   Jove-Journal of Visualized Experiments

AMPD2 Regulates GTP Synthesis and Is Mutated in a Potentially Treatable Neurodegenerative Brainstem Disorder

(2013) Naiara Akizu et al.   CELL

Consensus Paper: The Cerebellum's Role in Movement and Cognition

(2013) Leonard F. Koziol et al.   CEREBELLUM

Differentiation from human pluripotent stem cells of cortical neurons of the superficial layers amenable to psychiatric disease modeling and high-throughput drug screening

(2013) C Boissart et al.   Translational Psychiatry

Glial scaffold required for cerebellar granule cell migration is dependent on dystroglycan function as a receptor for basement membrane proteins

(2013) Huy Nguyen et al.   Acta Neuropathologica Communications

Homophilic interaction of the L1 family of cell adhesion molecules

(2012) Chun Hua Wei et al.   EXPERIMENTAL AND MOLECULAR MEDICINE

Regulation of dolichol-linked glycosylation

(2012) Michael Welti   GLYCOCONJUGATE JOURNAL

Identification of Intercellular Cell Adhesion Molecule 1 (ICAM-1) as a Hypoglycosylation Marker in Congenital Disorders of Glycosylation Cells

(2012) Ping He et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The role of cell adhesion molecules for navigating axons: Density matters

(2012) G.E. Pollerberg et al.   MECHANISMS OF DEVELOPMENT

A zebrafish model of PMM2-CDG reveals altered neurogenesis and a substrate-accumulation mechanism for N-linked glycosylation deficiency

(2012) Abigail Cline et al.   MOLECULAR BIOLOGY OF THE CELL

Mapping N-Glycosylation Sites across Seven Evolutionarily Distant Species Reveals a Divergent Substrate Proteome Despite a Common Core Machinery

(2012) Dorota F. Zielinska et al.   MOLECULAR CELL

L1CAM

(2012) Helena Kiefel et al.   Cell Adhesion & Migration

F3/contactin and TAG1 play antagonistic roles in the regulation of sonic hedgehog-induced cerebellar granule neuron progenitor proliferation

(2011) D. Xenaki et al.   DEVELOPMENT

From glycosylation disorders to dolichol biosynthesis defects: a new class of metabolic diseases

(2011) Vincent Cantagrel et al.   JOURNAL OF INHERITED METABOLIC DISEASE

NrCAM Deletion Causes Topographic Mistargeting of Thalamocortical Axons to the Visual Cortex and Disrupts Visual Acuity

(2011) G. P. Demyanenko et al.   JOURNAL OF NEUROSCIENCE

Life with too much polyprenol: polyprenol reductase deficiency

(2011) J.E.H. Gründahl et al.   MOLECULAR GENETICS AND METABOLISM

A novel cerebello-ocular syndrome with abnormal glycosylation due to abnormalities in dolichol metabolism

(2010) Eva Morava et al.   BRAIN

Precision Mapping of an In Vivo N-Glycoproteome Reveals Rigid Topological and Sequence Constraints

(2010) Dorota F. Zielinska et al.   CELL

SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder

(2010) Vincent Cantagrel et al.   CELL

“CRASH”ing with the worm: Insights into L1CAM functions and mechanisms

(2010) Lihsia Chen et al.   DEVELOPMENTAL DYNAMICS

Improvement of Dolichol-linked Oligosaccharide Biosynthesis by the Squalene Synthase Inhibitor Zaragozic Acid

(2010) Micha A. Haeuptle et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Neural circuit formation in the cerebellum is controlled by cell adhesion molecules of the Contactin family

(2010) Esther T. Stoeckli   Cell Adhesion & Migration

Metabolism, Cell Surface Organization, and Disease

(2009) James W. Dennis et al.   CELL

Alteration of the unfolded protein response modifies neurodegeneration in a mouse model of Marinesco–Sjögren syndrome

(2009) Lihong Zhao et al.   HUMAN MOLECULAR GENETICS

A new mouse model for the trisomy of the Abcg1–U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome

(2009) Patricia Lopes Pereira et al.   HUMAN MOLECULAR GENETICS

Lewisx and  2,3-Sialyl Glycans and Their Receptors TAG-1, Contactin, and L1 Mediate CD24-Dependent Neurite Outgrowth

(2009) A. Lieberoth et al.   JOURNAL OF NEUROSCIENCE

Universal sample preparation method for proteome analysis

(2009) Jacek R Wiśniewski et al.   NATURE METHODS

IgCAMs redundantly control axon navigation in Caenorhabditis elegans

(2009) Valentin Schwarz et al.   Neural Development

Isolation and Culture of Post-Natal Mouse Cerebellar Granule Neuron Progenitor Cells and Neurons

(2009) Hae Young Lee et al.   Jove-Journal of Visualized Experiments

Congenital disorder of glycosylation Ia: New differentially expressed proteins identified by 2-DE

(2008) Eva Richard et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Ophthalmological abnormalities in children with congenital disorders of glycosylation type I

(2008) E Morava et al.   BRITISH JOURNAL OF OPHTHALMOLOGY