Understanding human glycosylation disorders: biochemistry leads the charge (Q36666135)

15 August 2017

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title

Understanding human glycosylation disorders: biochemistry leads the charge (English)

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15 August 2017

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Hudson H Freeze

1

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language of work or name

English

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publication date

17 January 2013

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15 August 2017

10

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Journal of Biological Chemistry

inferred from page(s)

published in

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15 August 2017

288

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15 August 2017

6936-6945

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15 August 2017

10

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Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDG.

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1 reference

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Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome

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

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1 reference

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A zebrafish model of congenital disorders of glycosylation with phosphomannose isomerase deficiency reveals an early opportunity for corrective mannose supplementation

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Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates

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1 reference

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TMEM165 deficiency causes a congenital disorder of glycosylation

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1 reference

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Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation

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Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

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ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

30 September 2017

1 reference

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Neurology of inherited glycosylation disorders

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Isoprenoid biosynthesis in bacterial pathogens

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Mutations in the glycosylphosphatidylinositol gene PIGL cause CHIME syndrome

30 September 2017

1 reference

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Diseases of glycosylation beyond classical congenital disorders of glycosylation

30 September 2017

1 reference

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The phenotype of a germline mutation in PIGA: the gene somatically mutated in paroxysmal nocturnal hemoglobinuria

30 September 2017

1 reference

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DDOST mutations identified by whole-exome sequencing are implicated in congenital disorders of glycosylation

30 September 2017

1 reference

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Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE

30 September 2017

1 reference

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Innovative therapy for Classic Galactosemia - tale of two HTS.

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1 reference

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N-Acetylglucosamine Inhibits T-helper 1 (Th1)/T-helper 17 (Th17) Cell Responses and Treats Experimental Autoimmune Encephalomyelitis

30 September 2017

1 reference

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Mammalian O-mannosylation: unsolved questions of structure/function

30 September 2017

1 reference

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ST3GAL3 mutations impair the development of higher cognitive functions.

30 September 2017

1 reference

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Muscular dystrophies due to glycosylation defects: diagnosis and therapeutic strategies

30 September 2017

1 reference

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Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability.

30 September 2017

1 reference

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Mannose-6-phosphate regulates destruction of lipid-linked oligosaccharides

30 September 2017

1 reference

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Paroxysmal nocturnal hemoglobinuria from bench to bedside

30 September 2017

1 reference

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Nogo-B receptor is necessary for cellular dolichol biosynthesis and protein N-glycosylation

30 September 2017

1 reference

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Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN.

30 September 2017

1 reference

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A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®).

30 September 2017

1 reference

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30 September 2017

1 reference

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G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction

30 September 2017

1 reference

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

30 September 2017

1 reference

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The impact of mass spectrometry in the diagnosis of congenital disorders of glycosylation

30 September 2017

1 reference

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Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect

30 September 2017

1 reference

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Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa

30 September 2017

1 reference

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A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi Jews

30 September 2017

1 reference

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Transgenic overexpression of LARGE induces α-dystroglycan hyperglycosylation in skeletal and cardiac muscle

30 September 2017

1 reference

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Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder

30 September 2017

1 reference

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Metabolic manipulation of glycosylation disorders in humans and animal models

30 September 2017

1 reference

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A method and server for predicting damaging missense mutations

30 September 2017

1 reference

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O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.

30 September 2017

1 reference

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Detection of nonneutral substitution rates on mammalian phylogenies

30 September 2017

1 reference

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CDG nomenclature: time for a change!

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Muscular dystrophies due to glycosylation defects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

The congenital disorders of glycosylation: a multifaceted group of syndromes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Ablation of mouse phosphomannose isomerase (Mpi) causes mannose 6-phosphate accumulation, toxicity, and embryonic lethality

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

DPM1, the catalytic subunit of dolichol-phosphate mannose synthase, is tethered to and stabilized on the endoplasmic reticulum membrane by DPM3

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Analysis of glycosylation in CDG-Ia fibroblasts by fluorophore-assisted carbohydrate electrophoresis: implications for extracellular glucose and intracellular mannose 6-phosphate

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

PIG-M transfers the first mannose to glycosylphosphatidylinositol on the lumenal side of the ER.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

RPTPζ/phosphacan is abnormally glycosylated in a model of muscle-eye-brain disease lacking functional POMGnT1

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Mechanism for release of alkaline phosphatase caused by glycosylphosphatidylinositol deficiency in patients with hyperphosphatasia mental retardation syndrome

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

SRD5A3: A surprising role in glycosylation

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Detection of hypo-N-glycosylation using mass spectrometry of transferrin

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Diagnostic exome sequencing in persons with severe intellectual disability

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

A novel congenital disorder of glycosylation type without central nervous system involvement caused by mutations in the phosphoglucomutase 1 gene.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Unfolded protein response.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Successful prenatal mannose treatment for congenital disorder of glycosylation-Ia in mice.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

COG8 deficiency causes new congenital disorder of glycosylation type IIh.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiency

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG. First International Workshop on CDGS.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591604

20 September 2018

1 reference

12 December 2020

Extension of lipid-linked oligosaccharides is a high-priority aspect of the unfolded protein response: endoplasmic reticulum stress in Type I congenital disorder of glycosylation fibroblasts

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Elevated Carbohydrate-Deficient Transferrin (CDT) and Its Normalization on Dietary Treatment as a Useful Biochemical Test for Hereditary Fructose Intolerance and Galactosemia

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DPAGT1-CDG: report of a patient with fetal hypokinesia phenotype

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Diagnostic exome sequencing--are we there yet?

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Targeted therapy for inherited GPI deficiency

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12 December 2020

Identifiers

DOI

10.1074/JBC.R112.429274

1 reference

15 August 2017

1 reference

15 August 2017

1 reference

PMCID

3591604