(Q50776761)

English

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

scientific article published on 11 December 2011

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

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

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

1 reference

based on heuristic

inferred from title

congenital disorder

1 reference

based on heuristic

inferred from title

congenital disorder

1 reference

based on heuristic

inferred from title

author name string

Anette Schneider

1

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

Christian Thiel

2

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

Jan Rindermann

3

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

Charles DeRossi

4

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

Diana Popovici

5

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

Georg F Hoffmann

6

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

Hermann-Josef Gröne

7

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

Christian Körner

8

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

language of work or name

0 references

publication date

11 December 2011

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

Nature Medicine

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

18

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

1

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

71-73

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

Fetal nutrition and adult disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The X-ray crystal structures of human alpha-phosphomannomutase 1 reveal the structural basis of congenital disorder of glycosylation type 1a

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1A.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical spectrum of phosphomannomutase 2 deficiency (CDG-Ia).

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Continuous mannose infusion in carbohydrate-deficient glycoprotein syndrome type I

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mannose supplementation in carbohydrate-deficient glycoprotein syndrome type I and phosphomannomutase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mannose corrects altered N-glycosylation in carbohydrate-deficient glycoprotein syndrome fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carbohydrate-deficient glycoprotein syndrome type 1A: expression and characterisation of wild type and mutant PMM2 in E. coli

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carbohydrate-deficient glycoprotein syndrome type 1: correction of the glycosylation defect by deprivation of glucose or supplementation of mannose

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/22157680

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/NM.2548

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22157680

ResearchGate publication ID

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