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- 2018
-
Mark
Three unreported cases of TMEM199-CDG, a rare genetic liver disease with abnormal glycosylation
(
- Contribution to journal › Article
- 2014
-
Mark
Dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects.
(
- Contribution to journal › Article
- 2011
-
Mark
A novel treatment approach for paediatric Gorham-Stout syndrome with chylothorax
(
- Contribution to journal › Article
- 2010
-
Mark
Neonatal invasiv grupp B-streptokockinfektion. Förhastat av Socialstyrelsen att avfärda allmän screening.
(
- Contribution to journal › Article
- 2006
-
Mark
The congenital disorders of glycosylation: a multifaceted group of syndromes.
(
- Contribution to journal › Article
- 2005
-
Mark
Regulation of the chondroitin/dermatan fine structure by transforming growth factor-beta 1 through effects on polymer-modifying enzymes
(
- Contribution to journal › Article
- 2004
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Mark
The human antimicrobial peptide LL-37 transfers extracellular DNA plasmid to the nuclear compartment of mammalian cells via lipid rafts and proteoglycan-dependent endocytosis
(
- Contribution to journal › Article
- 2003
-
Mark
Initiation of the decorin glycosaminoglycan chain in the endoplasmic reticulum-Golgi intermediate compartment
(
- Contribution to journal › Article
- 2002
-
Mark
Proteoglycan production in disomic and trisomy 7-carrying human synovial cells.
(
- Contribution to journal › Article
- 2001
-
Mark
Expression of a functional proteinase inhibitor capable of accepting xylose: bikunin
(
- Contribution to journal › Article