gm1 gangliosidosis Pages on BioPortfolio:

BioPortfolio - Gangliosidosis Gm1
Gangliosidosis Gm1 - BioPortfolio - Indepth. ... GM1 gangliosidosis is an autosomal recessive disorder caused by the... 13th September, 2008 ...
http://www.bioportfolio.com/indepth/Gangliosidosis_Gm1.html...

BioPortfolio - Neurons
GM1-gangliosidosis is a lysosomal storage disease (LSD) caused by an... 27th September, 2008, [1] 1Department of Neurology, Molecular Neurogenetics Unit, ...
http://www.bioportfolio.com/indepth/Neurons.html...

BioPortfolio.com - BioWeb ETHAMBUTOL ETHAMBUTOL HYDROCHLORIDE ...
TRENDS in Cell Biology GM1 gangliosidosis TayTH Sachs and Sandhoff disease Sandhoff disease Fabry disease Gaucher disease Metachromatic leukodystrophy ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?DB=se...

BioPortfolio's Genetic Abnormality Conditions Specilized Searches
Gangliosidoses · Gangliosidosis GM1 · Gaucher · Genes Gene Therapy · Genetic Brain Disorders · Genetic Inborn · Genetic X-Linked · Genetic Disorders ...
http://www.bioportfolio.com/biotechnology/genetic_ab.html...

BioPortfolio.com - BioWeb Tay-Sachs Disease Search
... Tay- Sachs Hexosaminidase A GM2 ganglioside Sandhoff Hexosaminidases A and B GM2 ganglioside GM1 gangliosidosis b- Galactosidase GM1. ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio's Brain and Nervous Diseases Specialized Searches
Gangliosidosis GM1 · Gaucher Disease · Genetic Brain Disorders · Glycogen Storage Disease Type II · Guillain-Barre · Hallucinations · Head Brain Injuries
...
http://www.bioportfolio.com/biotechnology/brain.html...

BioPortfolio.com - BioWeb Gaucher Disease Search
... are: Gaucher types 1, 2 and 3, Fabry, TayTH Sachs, Sandhoff and GM2 gangliosidosis ... A and B GM2 ganglioside GM1 gangliosidosis b- Galactosidase
GM1. ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio - the biotechnology, pharmaceutical, life science and ...
BioPortfolio the comprehensive website for data, information, search engine and services on biotechnology, pharmaceutical and healthcare research, ...
http://www.bioportfolio.com/...

BioPortfolio's Metabolic and Nutritional Specialized Searches
Gangliosidosis GM1 · Gaucher Disease · Glucose Intolerance · Glucosephosphate Dehydrogenase Deficiency · Glycogen Storage Disease Type II ...
http://www.bioportfolio.co.uk/web/metabolic.shtml...

Results from other life science and pharmaceutical sites:

OMIM - GM1-GANGLIOSIDOSIS, TYPE I
MIM #230500 · Text · Description · Clinical Features · Other Features · Biochemical Features · Molecular Genetics · Genotype/Phenotype Correlations ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230500...

Genetic heterogeneity in GM1-gangliosidosis
GM1-GANGLIOSIDOSIS is an inherited lysosomal storage disease which is due to a deficiency of the acid hydrolase GM1- beta -galactosidase1. ...
http://www.nature.com/nature/journal/v257/n5521/abs/257060a0...

OMIM - GM1-GANGLIOSIDOSIS, TYPE III
MIM #230650 · Text · Description · Clinical Features · Biochemical Features · Molecular Genetics · See Also · References · Contributors · Creation Date ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230650...

GM1 gangliosidosis (type 1) in a cat.
Feline GM1 gangliosidosis: characterization of the residual liver acid beta- galactosidase. Am J Hum Genet. 1978 Sep;30(5):505–515. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=11...

OMIM - GM1-GANGLIOSIDOSIS, TYPE II
MIM #230600 · Text · See Also · References · Contributors · Creation Date · Edit History · Clinical Synopsis ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230600...

Human beta-galactosidase gene mutations in GM1-gangliosidosis: a ...
Molecular analysis of the human beta-galactosidase gene revealed six different mutations in 10 of 11 Japanese GM1-gangliosidosis patients. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=16...

GM1 gangliosidosis: review of clinical, molecular,...[Mol Genet ...
GM(1) gangliosidosis is a lysosomal storage disorder due to deficiency of the beta-galactosidase enzyme. This deficiency results in accumulation of GM(1) ...
http://www.ncbi.nlm.nih.gov/pubmed/18524657...

Dog GM1 gangliosidosis: characterization of the residual liver ...
The residual liver acid beta-galactosidase activity from the first documented case of GM1 gangliosidosis in dogs was partially purified and characterized ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=16...

Gangliosidoses Information Page: National Institute of ...
The GM1 gangliosidoses are caused by a deficiency of beta-galactosidase. Symptoms of early infantile GM1 (the most severe subtype, with onset shortly
after ...
http://www.ninds.nih.gov/disorders/gangliosidoses/Gangliosid...

Prenatal diagnosis of GM1 gangliosidosis by detection of ...
Prenatal diagnosis of infantile GM1 gangliosidosis was accomplished by analyzing the galactosyl-oligosaccharides accumulating in amniotic fluid with ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=16...

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