Mutations in genes critical for proper intra-Golgi transport can cause human syndromes due to defects in glycosylation of proteins. Here, the authors identify a human variant of Syntaxin-5 that causes fatal multisystem disease and mislocalization of glycosyltransferases due to altered Golgi transport
Almost 50 inborn errors of metabolism have been described due to congenital defects in N-linked glyc...
Protein glycosylation is a complex process that depends not only on the activities of several enzyme...
Biochemical analysis and whole-exome sequencing identified mutations in the Golgi-localized UDP-gala...
The SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) protein syntaxin-5...
Loss-of-function of the glucose-6-phosphate transporter is caused by biallelic mutations in SLC37A4 ...
Glycosylation is an important post-translational modification for both intracellular and secreted pr...
The conserved oligomeric Golgi (COG) complex is a hetero-octameric complex that regulates intraGolgi...
Deficiency of subunit 6 of the conserved oligomeric Golgi (COG6) complex causes a new combined N- an...
Glycosylation is a ubiquitous modification of lipids and proteins. Despite the essential contributio...
The conserved oligomeric Golgi (COG) complex is a tethering factor composed of eight subunits that i...
Congenital disorders of glycosylation (CDG) are a heterogeneous and rapidly growing group of disease...
Processing of the glycan structures on glycoproteins by different glycosylation enzymes depends on, ...
Hansske B, Thiel C, Lübke T, et al. Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galacto...
Almost 50 inborn errors of metabolism have been described due to congenital defects in N-linked glyc...
Protein glycosylation is a complex process that depends not only on the activities of several enzyme...
Biochemical analysis and whole-exome sequencing identified mutations in the Golgi-localized UDP-gala...
The SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) protein syntaxin-5...
Loss-of-function of the glucose-6-phosphate transporter is caused by biallelic mutations in SLC37A4 ...
Glycosylation is an important post-translational modification for both intracellular and secreted pr...
The conserved oligomeric Golgi (COG) complex is a hetero-octameric complex that regulates intraGolgi...
Deficiency of subunit 6 of the conserved oligomeric Golgi (COG6) complex causes a new combined N- an...
Glycosylation is a ubiquitous modification of lipids and proteins. Despite the essential contributio...
The conserved oligomeric Golgi (COG) complex is a tethering factor composed of eight subunits that i...
Congenital disorders of glycosylation (CDG) are a heterogeneous and rapidly growing group of disease...
Processing of the glycan structures on glycoproteins by different glycosylation enzymes depends on, ...
Hansske B, Thiel C, Lübke T, et al. Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galacto...
Almost 50 inborn errors of metabolism have been described due to congenital defects in N-linked glyc...
Protein glycosylation is a complex process that depends not only on the activities of several enzyme...
Biochemical analysis and whole-exome sequencing identified mutations in the Golgi-localized UDP-gala...