(Q73693678)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12872840%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Abnormal lysosomal inclusions in liver hepatocytes but not in fibroblasts in congenital disorders of glycosylation (CDG) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12872840%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

S Grünewald

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12872840%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

R De Vos

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12872840%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

J Jaeken

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12872840%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 January 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12872840%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

6 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12872840%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

26

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12872840%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12872840%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

49-54

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12872840%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1023/a:1024023429680

6 November 2019

exact match

0 references

cites work

Carbohydrate-deficient glycoprotein syndrome type II

1 reference

12 December 2020

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

1 reference

12 December 2020

Screening for "prelysosomal disorders": carbohydrate-deficient glycoprotein syndromes

1 reference

12 December 2020

β-Hexosaminidase, α-d-mannosidase, and β-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I

1 reference

12 December 2020

Abnormal surface expression of sialoglycans on B lymphocyte cell lines from patients with carbohydrate deficient glycoprotein syndrome I A (CDGS I A).

1 reference

12 December 2020

Carbohydrate-deficient glycoprotein syndromes: inborn errors of protein glycosylation

1 reference

12 December 2020

Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.

1 reference

12 December 2020

Defect in N-glycosylation of proteins is tissue-dependent in Congenital Disorders of Glycosylation Ia

1 reference

12 December 2020

Congenital disorders of glycosylation

1 reference

12 December 2020

Increased expression of beta-hexosaminidase alpha chain in cultured skin fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome type I.

1 reference

12 December 2020

Carbohydrate-deficient glycoprotein syndrome (CDGS)--glycosylation, folding and intracellular transport of newly synthesized glycoproteins

1 reference

12 December 2020

Lysosomal enzyme activities in serum and leukocytes from patients with carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase deficiency)

1 reference

12 December 2020

Carbohydrate deficient glycoprotein syndrome type II: a deficiency in Golgi localised N-acetyl-glucosaminyltransferase II.

1 reference

12 December 2020