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Gert Matthijs

Showing results (51-60 of 199) with videos related to

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Diabetes|November 25, 2003
A mammalian protein homologous to fructosamine-3-kinase is a ketosamine-3-kinase acting on psicosamines and ribulosamines but not on fructosaminesFrançois Collard, Ghislain Delpierre, Vincent Stroobant, et al.
Molecular and Cellular Biology|July 19, 2006
Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethalityChristian Thiel, Torben Lübke, Gert Matthijs, et al.
American Journal of Respiratory and Critical Care Medicine|February 26, 2008
A new missense mutation in the CASR gene in familial interstitial lung disease with hypocalciuric hypercalcemia and defective granulocyte functionMaurits Demedts, Willy Lissens, Wim Wuyts, et al.
Glycobiology|March 11, 2003
Increased fucosylation and reduced branching of serum glycoprotein N-glycans in all known subtypes of congenital disorder of glycosylation INico Callewaert, Els Schollen, Annelies Vanhecke, et al.
Genetic Testing|June 25, 2003
Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5AAimée Paulussen, Gert Matthijs, Marc Gewillig, et al.
Glycoconjugate Journal|September 18, 2012
Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDGGert Matthijs, Daisy Rymen, María Beatriz Bistué Millón, et al.
Chemical Communications (Cambridge, England)|October 25, 2013
Alkynyl monosaccharide analogues as a tool for evaluating Golgi glycosylation efficiency: application to Congenital Disorders of Glycosylation (CDG)Jorick Vanbeselaere, Dorothée Vicogne, Gert Matthijs, et al.
Molecular Genetics and Metabolism|July 30, 2013
Dolichol kinase deficiency (DOLK-CDG) with a purely neurological presentation caused by a novel mutationAnders Helander, Tommy Stödberg, Jaak Jaeken, et al.
Trends in Biotechnology|July 8, 2011
Patent pools and clearinghouses in the life sciencesEsther van Zimmeren, Sven Vanneste, Gert Matthijs, et al.
Orphanet Journal of Rare Diseases|April 20, 2010
A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a case reportMohammed Al-Owain, Sarar Mohamed, Namik Kaya, et al.
Pageof 20

Showing results (51-60 of 199) with videos related to

Sort By:
Pageof 20
Diabetes|November 25, 2003
A mammalian protein homologous to fructosamine-3-kinase is a ketosamine-3-kinase acting on psicosamines and ribulosamines but not on fructosaminesFrançois Collard, Ghislain Delpierre, Vincent Stroobant, et al.
Molecular and Cellular Biology|July 19, 2006
Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethalityChristian Thiel, Torben Lübke, Gert Matthijs, et al.
American Journal of Respiratory and Critical Care Medicine|February 26, 2008
A new missense mutation in the CASR gene in familial interstitial lung disease with hypocalciuric hypercalcemia and defective granulocyte functionMaurits Demedts, Willy Lissens, Wim Wuyts, et al.
Glycobiology|March 11, 2003
Increased fucosylation and reduced branching of serum glycoprotein N-glycans in all known subtypes of congenital disorder of glycosylation INico Callewaert, Els Schollen, Annelies Vanhecke, et al.
Genetic Testing|June 25, 2003
Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5AAimée Paulussen, Gert Matthijs, Marc Gewillig, et al.
Glycoconjugate Journal|September 18, 2012
Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDGGert Matthijs, Daisy Rymen, María Beatriz Bistué Millón, et al.
Chemical Communications (Cambridge, England)|October 25, 2013
Alkynyl monosaccharide analogues as a tool for evaluating Golgi glycosylation efficiency: application to Congenital Disorders of Glycosylation (CDG)Jorick Vanbeselaere, Dorothée Vicogne, Gert Matthijs, et al.
Molecular Genetics and Metabolism|July 30, 2013
Dolichol kinase deficiency (DOLK-CDG) with a purely neurological presentation caused by a novel mutationAnders Helander, Tommy Stödberg, Jaak Jaeken, et al.
Trends in Biotechnology|July 8, 2011
Patent pools and clearinghouses in the life sciencesEsther van Zimmeren, Sven Vanneste, Gert Matthijs, et al.
Orphanet Journal of Rare Diseases|April 20, 2010
A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a case reportMohammed Al-Owain, Sarar Mohamed, Namik Kaya, et al.
Pageof 20