Abstractβ-1,3-galactosyltransferase-1 (β3GalT-1) is the key enzyme to form the type 1 chain structure. Northern blot analysis indicated that β3GalT-1 was expressed predominantly in the brain. In the present study, it was revealed that the gene expression of β3GalT-1 in mouse brain was developmentally decreased. High expression levels of β3GalT-1 were found in cerebral cortex and hippocampus in both newborn and adult mice, while in cerebellum, the expression levels decreased markedly during development. In situ hybridization revealed that the absence of expression in cerebellar granual cell layers contributed to the main loss of β3GalT-1 expression in adult mouse cerebellum. Moreover, the decreased levels of β3GalT-1could affect the synthesi...
AbstractA hemizygous deletion ofLIS1,the gene encoding αLis1protein, causes Miller–Dieker syndrome (...
AbstractChanges in the relative abundance of the G protein α subunits were observed during early mou...
The enzyme glucocerebrosidase (GBA) hydrolyses glucosylceramide (GlcCer) in lysosomes. Markedly redu...
The distinction between the different classes of glycolipids is conditioned by the action of specifi...
Background. α1,3-galactosyltransferase (α1,3GT) is an enzyme that produces carbohydrate chains terme...
The enzyme glucocerebrosidase (GBA) hydrolyses glucosylceramide (GlcCer) in lysosomes. Markedly redu...
AbstractMucopolysaccharidosis I (MPS I) is a congenital disorder caused by the deficiency of α-l-idu...
Human and mouse cDNAs encoding a new beta-1,3-N-acetylglucosaminyltransferase (beta3GnT) have been i...
Juvenile neuronal ceroid lipofuscinosis (JNCL) is caused by mutations in the CLN3 gene. Most JNCL pa...
AbstractDespite much attention, the function of oligosaccharide chains on glycoproteins and glycolip...
Juvenile neuronal ceroid lipofuscinosis (JNCL) is caused by mutations in the CLN3 gene. Most JNCL pa...
AbstractUDP-Gal:GA2/GM2/GD2/GT2 galactosyltransferase (Gal-T2) transfers galactose to the terminal N...
GM1-gangliosidosis is a lysosomal disease resulting from a deficiency in the hydrolase β-galactosida...
Based on the detection of expressed sequence tags that are similar to known galactosyltransferase se...
Galactosylceramide ("galactocerebroside"; GalC) is a major glycolipid in the myelin sheath of the CN...
AbstractA hemizygous deletion ofLIS1,the gene encoding αLis1protein, causes Miller–Dieker syndrome (...
AbstractChanges in the relative abundance of the G protein α subunits were observed during early mou...
The enzyme glucocerebrosidase (GBA) hydrolyses glucosylceramide (GlcCer) in lysosomes. Markedly redu...
The distinction between the different classes of glycolipids is conditioned by the action of specifi...
Background. α1,3-galactosyltransferase (α1,3GT) is an enzyme that produces carbohydrate chains terme...
The enzyme glucocerebrosidase (GBA) hydrolyses glucosylceramide (GlcCer) in lysosomes. Markedly redu...
AbstractMucopolysaccharidosis I (MPS I) is a congenital disorder caused by the deficiency of α-l-idu...
Human and mouse cDNAs encoding a new beta-1,3-N-acetylglucosaminyltransferase (beta3GnT) have been i...
Juvenile neuronal ceroid lipofuscinosis (JNCL) is caused by mutations in the CLN3 gene. Most JNCL pa...
AbstractDespite much attention, the function of oligosaccharide chains on glycoproteins and glycolip...
Juvenile neuronal ceroid lipofuscinosis (JNCL) is caused by mutations in the CLN3 gene. Most JNCL pa...
AbstractUDP-Gal:GA2/GM2/GD2/GT2 galactosyltransferase (Gal-T2) transfers galactose to the terminal N...
GM1-gangliosidosis is a lysosomal disease resulting from a deficiency in the hydrolase β-galactosida...
Based on the detection of expressed sequence tags that are similar to known galactosyltransferase se...
Galactosylceramide ("galactocerebroside"; GalC) is a major glycolipid in the myelin sheath of the CN...
AbstractA hemizygous deletion ofLIS1,the gene encoding αLis1protein, causes Miller–Dieker syndrome (...
AbstractChanges in the relative abundance of the G protein α subunits were observed during early mou...
The enzyme glucocerebrosidase (GBA) hydrolyses glucosylceramide (GlcCer) in lysosomes. Markedly redu...