The biochemical and morphological characteristics of porcine cerebrospinal lipodystrophy in different stages of development were ascertained and were compared to corresponding characteristics of the human GM₂-gangliosidoses. The study was divided into 2 separate experiments. In the 1st experiment 11 control (normal and carrier) and 14 affected Yorkshire pigs were used to investigate the pathogenesis of the fundamental cellular lesion by evaluating the progression of the basic biochemical (enzyme and ganglioside assays) and morphological (neuronal and glial) changes in the central nervous system. Tissues were collected from pigs killed at 1 day (newborn or stillborn) to 175 days of age. The purpose of the 2nd experiment was to evaluate the e...
The definitive version is available at www.blackwell-synergy.comAlpha-mannosidosis is an inherited m...
This study reports the occurrence of the lysosomal storage disease GM2 gangliosidosis (Sandhoff dise...
β-N-acetylhexosaminidase B, or just β-hexosaminidase, is an enzyme responsible for the degradation o...
The biochemical and morphological characteristics of porcine cerebrospinal lipodystrophy in differen...
Gangliosidoses are inherited lysosomal storage disorders caused by reduced or absent activity of eit...
GMl-gangliosidosis is an inherited disease quite distinct from Tay-Sachs and Hurler's diseases. It e...
Abstract. Ganglioside storage diseases are inherited defects of lysosomal hydrolases that result in ...
Cytidine monophosphate-Nacetylneuraminic acid (Neu5Ac) hydroxylase (CMAH) and glycoprotein, alpha1, ...
Le patologie da accumulo lisosomiale (LSDs) sono un gruppo eterogeneo di rare, progressive, letali, ...
Abstract Gangliosidoses are inherited lysosomal storage disorders caused by reduced or absent activ...
Specific-pathogen-free (SPF) swine were given orally 15 mg/kg of chloroquine daily; 8 were sacrifice...
Gangliosidosis are inherited lysosomal storage disorders caused by defective activity of a lysosomal...
Alpha-mannosidosis is a lysosomal storage disorder resulting from deficient activity of lysosomal al...
Pathomorphological study of the neonatal period piglets of ontogenesis from the pig breeding complex...
Studies in recent years have demonstrated that ganglioside storage disease is characterized not only...
The definitive version is available at www.blackwell-synergy.comAlpha-mannosidosis is an inherited m...
This study reports the occurrence of the lysosomal storage disease GM2 gangliosidosis (Sandhoff dise...
β-N-acetylhexosaminidase B, or just β-hexosaminidase, is an enzyme responsible for the degradation o...
The biochemical and morphological characteristics of porcine cerebrospinal lipodystrophy in differen...
Gangliosidoses are inherited lysosomal storage disorders caused by reduced or absent activity of eit...
GMl-gangliosidosis is an inherited disease quite distinct from Tay-Sachs and Hurler's diseases. It e...
Abstract. Ganglioside storage diseases are inherited defects of lysosomal hydrolases that result in ...
Cytidine monophosphate-Nacetylneuraminic acid (Neu5Ac) hydroxylase (CMAH) and glycoprotein, alpha1, ...
Le patologie da accumulo lisosomiale (LSDs) sono un gruppo eterogeneo di rare, progressive, letali, ...
Abstract Gangliosidoses are inherited lysosomal storage disorders caused by reduced or absent activ...
Specific-pathogen-free (SPF) swine were given orally 15 mg/kg of chloroquine daily; 8 were sacrifice...
Gangliosidosis are inherited lysosomal storage disorders caused by defective activity of a lysosomal...
Alpha-mannosidosis is a lysosomal storage disorder resulting from deficient activity of lysosomal al...
Pathomorphological study of the neonatal period piglets of ontogenesis from the pig breeding complex...
Studies in recent years have demonstrated that ganglioside storage disease is characterized not only...
The definitive version is available at www.blackwell-synergy.comAlpha-mannosidosis is an inherited m...
This study reports the occurrence of the lysosomal storage disease GM2 gangliosidosis (Sandhoff dise...
β-N-acetylhexosaminidase B, or just β-hexosaminidase, is an enzyme responsible for the degradation o...