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Proceedings of the National Academy of Sciences of the United States of America
|
January 20, 1999
A beta-1,3-N-acetylglucosaminyltransferase with poly-N-acetyllactosamine synthase activity is structurally related to beta-1,3-galactosyltransferases
D Zhou, A Dinter, R Gutiérrez Gallego, et al.
Free Radical Research
|
August 1, 1996
TNF alpha alters mitochondrial membrane potential in L929 but not in TNF alpha-resistant L929.12 cells: relationship with the expression of stress proteins, annexin 1 and superoxide dismutase activity
B S Polla, M R Jacquier-Sarlin, S Kantengwa, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2009
RFT1-CDG: deafness as a novel feature of congenital disorders of glycosylation
J Jaeken, W Vleugels, L Régal, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Congenital disorder of glycosylation (CDG) Ig: report on a patient and review of the literature
M Di Rocco, T Hennet, C E Grubenmann, et al.
Human Genetics
|
July 29, 2000
Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic
T Imbach, S Grünewald, B Schenk, et al.
Journal of Medical Genetics
|
July 6, 2004
Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)
E Schollen, C G Frank, L Keldermans, et al.
The Journal of Clinical Investigation
|
January 22, 2000
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie
T Imbach, B Schenk, E Schollen, et al.
Journal of Inherited Metabolic Disease
|
January 27, 2005
Congenital disorder of glycosylation (CDG) type Ie. A new patient
M T García-Silva, G Matthijs, E Schollen, et al.
The Journal of Clinical Investigation
|
December 26, 2001
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If
B Schenk, T Imbach, C G Frank, et al.
Annals of Neurology
|
June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesis
S Grünewald, T Imbach, K Huijben, et al.
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Search research articles
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Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Proceedings of the National Academy of Sciences of the United States of America
|
January 20, 1999
A beta-1,3-N-acetylglucosaminyltransferase with poly-N-acetyllactosamine synthase activity is structurally related to beta-1,3-galactosyltransferases
D Zhou, A Dinter, R Gutiérrez Gallego, et al.
Free Radical Research
|
August 1, 1996
TNF alpha alters mitochondrial membrane potential in L929 but not in TNF alpha-resistant L929.12 cells: relationship with the expression of stress proteins, annexin 1 and superoxide dismutase activity
B S Polla, M R Jacquier-Sarlin, S Kantengwa, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2009
RFT1-CDG: deafness as a novel feature of congenital disorders of glycosylation
J Jaeken, W Vleugels, L Régal, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Congenital disorder of glycosylation (CDG) Ig: report on a patient and review of the literature
M Di Rocco, T Hennet, C E Grubenmann, et al.
Human Genetics
|
July 29, 2000
Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic
T Imbach, S Grünewald, B Schenk, et al.
Journal of Medical Genetics
|
July 6, 2004
Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)
E Schollen, C G Frank, L Keldermans, et al.
The Journal of Clinical Investigation
|
January 22, 2000
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie
T Imbach, B Schenk, E Schollen, et al.
Journal of Inherited Metabolic Disease
|
January 27, 2005
Congenital disorder of glycosylation (CDG) type Ie. A new patient
M T García-Silva, G Matthijs, E Schollen, et al.
The Journal of Clinical Investigation
|
December 26, 2001
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If
B Schenk, T Imbach, C G Frank, et al.
Annals of Neurology
|
June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesis
S Grünewald, T Imbach, K Huijben, et al.
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of 4