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Ablation of Mouse Phosphomannose Isomerase (Mpi) Causes Mannose 6-Phosphate Accumulation, Toxicity, and Embryonic Lethality

The Journal of biological chemistry, 2006-03, Vol.281 (9), p.5916-5927

2006

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Two Proteins Modulating Transendothelial Migration of Leukocytes Recognize Novel Carboxylated Glycans on Endothelial Cells

The Journal of immunology (1950), 2001-04, Vol.166 (7), p.4678-4688

2001

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Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)

The Journal of clinical investigation, 2000-01, Vol.105 (2), p.191-198

2000

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Functional Differences in Yeast Protein Disulfide Isomerases

The Journal of cell biology, 2001-02, Vol.152 (3), p.553-562

2001

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Bifidobacterium breve Bif195 Protects Against Small-Intestinal Damage Caused by Acetylsalicylic Acid in Healthy Volunteers

Gastroenterology (New York, N.Y. 1943), 2019-09, Vol.157 (3), p.637-646.e4

2019

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Bifidobacteriumbreve Bif195 Protects Against Small-Intestinal Damage Caused by Acetylsalicylic Acid in Healthy Volunteers

Gastroenterology (New York, N.Y. 1943), 2019-09, Vol.157 (3), p.637-646.e4

2019

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Congenital disorders of glycosylation: have you encountered them?

Genetics in medicine, 2000-11, Vol.2 (6), p.329-337

2000

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Multiple Pathways for Vacuolar Sorting of Yeast Proteinase A (∗)

The Journal of biological chemistry, 1996-05, Vol.271 (20), p.11865-11870

1996

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Functional properties of the two redox-active sites in yeast protein disulphide isomerase in Vitro and in Vivo 1 1Edited by G. Von Heijne

Journal of molecular biology, 1999-03, Vol.286 (4), p.1229-1239

1999

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Reduced Heparan Sulfate Accumulation in Enterocytes Contributes to Protein-Losing Enteropathy in a Congenital Disorder of Glycosylation

The American journal of pathology, 2000-12, Vol.157 (6), p.1917-1925

2000

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Time limits for gastrointestinal decontamination in poisoning

Ugeskrift for læger, 2009-02, Vol.171 (9), p.718

2009

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Balancing N-linked glycosylation to avoid disease

Biochimie, 2001-08, Vol.83 (8), p.791-799

2001

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Congenital disorder of glycosylation (CDG)-Ih patient with a severe hepato-intestinal phenotype and evolving central nervous system pathology

The Journal of pediatrics, 2005-12, Vol.147 (6), p.847-850

2005

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A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation la (CDG-Ia) caused by phosphomannomutase deficiency

Human molecular genetics, 2002-03, Vol.11 (5), p.599-604

2002

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A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency

Human molecular genetics, 2002-03, Vol.11 (5), p.599-604

2002

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Genetic and Metabolic Analysis of the First Adult with Congenital Disorder of Glycosylation Type Ib: Long-Term Outcome and Effects of Mannose Supplementation

Molecular genetics and metabolism, 2001-05, Vol.73 (1), p.77-85

2001

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Functional significance of PMM2 mutations in mildly affected patients with congenital disorders of glycosylation Ia

Genetics in medicine, 2001-11, Vol.3 (6), p.393-398

2001

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Identification of a frequent variant inALG6, the cause of Congenital Disorder of Glycosylation-Ic

Human mutation, 2003-11, Vol.22 (5), p.420-421

2003

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Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic

Human mutation, 2003-11, Vol.22 (5), p.420-421

2003

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Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins

The Journal of pediatrics, 2002-11, Vol.141 (5), p.695-700

2002

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Functional properties of the two redox-active sites in yeast protein disulphide isomerase in vitro and in vivo

Journal of molecular biology, 1999-03, Vol.286 (4), p.1229-1239

1999

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Analysis of Multiple Mutations in the hALG6 Gene in a Patient with Congenital Disorder of Glycosylation Ic

Molecular genetics and metabolism, 2000-07, Vol.70 (3), p.219-223

2000

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Functional Analysis of Novel Mutations in a Congenital Disorder of Glycosylation Ia Patient with Mixed Asian Ancestry

Molecular genetics and metabolism, 2001-05, Vol.73 (1), p.71-76

2001

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Molecular cloning, gene organization, and expression of mouse Mpi encoding phosphomannose isomerase

Glycobiology (Oxford), 2002-07, Vol.12 (7), p.435-442

2002

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Preparation of fluorescence quenched libraries containing interchain disulphide bonds for studies of protein disulphide isomerases

Journal of peptide science, 1998-04, Vol.4 (2), p.128-137

1998

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Ablation of Mouse Phosphomannose Isomerase (Mpi) Causes Mannose 6-Phosphate Accumulation, Toxicity, and Embryonic Lethality

Two Proteins Modulating Transendothelial Migration of Leukocytes Recognize Novel Carboxylated Glycans on Endothelial Cells

Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)

Functional Differences in Yeast Protein Disulfide Isomerases

Bifidobacterium breve Bif195 Protects Against Small-Intestinal Damage Caused by Acetylsalicylic Acid in Healthy Volunteers

Bifidobacteriumbreve Bif195 Protects Against Small-Intestinal Damage Caused by Acetylsalicylic Acid in Healthy Volunteers

Congenital disorders of glycosylation: have you encountered them?

Multiple Pathways for Vacuolar Sorting of Yeast Proteinase A (∗)

Functional properties of the two redox-active sites in yeast protein disulphide isomerase in Vitro and in Vivo 1 1Edited by G. Von Heijne

Reduced Heparan Sulfate Accumulation in Enterocytes Contributes to Protein-Losing Enteropathy in a Congenital Disorder of Glycosylation

Time limits for gastrointestinal decontamination in poisoning

Balancing N-linked glycosylation to avoid disease

Congenital disorder of glycosylation (CDG)-Ih patient with a severe hepato-intestinal phenotype and evolving central nervous system pathology

A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation la (CDG-Ia) caused by phosphomannomutase deficiency

A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency

Genetic and Metabolic Analysis of the First Adult with Congenital Disorder of Glycosylation Type Ib: Long-Term Outcome and Effects of Mannose Supplementation

Functional significance of PMM2 mutations in mildly affected patients with congenital disorders of glycosylation Ia

Identification of a frequent variant inALG6, the cause of Congenital Disorder of Glycosylation-Ic

Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic

Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins

Functional properties of the two redox-active sites in yeast protein disulphide isomerase in vitro and in vivo

Analysis of Multiple Mutations in the hALG6 Gene in a Patient with Congenital Disorder of Glycosylation Ic

Functional Analysis of Novel Mutations in a Congenital Disorder of Glycosylation Ia Patient with Mixed Asian Ancestry

Molecular cloning, gene organization, and expression of mouse Mpi encoding phosphomannose isomerase

Preparation of fluorescence quenched libraries containing interchain disulphide bonds for studies of protein disulphide isomerases

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