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4-methylumbelliferyl-galactopyranoside and alpha-Galactosidase A Deficiency

4-methylumbelliferyl-galactopyranoside has been researched along with alpha-Galactosidase A Deficiency in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chiba, Y; Fukushige, T; Itoh, K; Jigami, Y; Kanekura, T; Kawashima, I; Kuroda, M; Ohashi, T; Ohno, K; Sakuraba, H; Sugawara, K; Suzuki, T; Tajima, Y; Togawa, T; Tsukimura, T1
Donaldson, ML; Mayes, JS; Scheerer, JB; Sifers, RN1

Other Studies

2 other study(ies) available for 4-methylumbelliferyl-galactopyranoside and alpha-Galactosidase A Deficiency

ArticleYear
Use of a modified alpha-N-acetylgalactosaminidase in the development of enzyme replacement therapy for Fabry disease.
    American journal of human genetics, 2009, Volume: 85, Issue:5

    Topics: alpha-N-Acetylgalactosaminidase; Amino Acid Substitution; Animals; Binding Sites; Catalysis; Cells, Cultured; CHO Cells; Cricetinae; Cricetulus; Culture Media, Conditioned; Disease Models, Animal; DNA, Complementary; Drug Stability; Enzyme Replacement Therapy; Fabry Disease; Fibroblasts; Fluorescent Dyes; Galactosides; Genetic Vectors; Humans; Hydrogen-Ion Concentration; Hymecromone; Immunohistochemistry; Kidney; Liver; Mice; Mice, Knockout; Models, Molecular; Molecular Weight; Myocardium; Recombinant Proteins; Retroviridae; Transfection; Trihexosylceramides

2009
Differential assay for lysosomal alpha-galactosidases in human tissues and its application to Fabry's disease.
    Clinica chimica acta; international journal of clinical chemistry, 1981, May-05, Volume: 112, Issue:2

    Topics: Acetylgalactosamine; Adult; alpha-Galactosidase; alpha-N-Acetylgalactosaminidase; Cells, Cultured; Fabry Disease; Female; Fibroblasts; Galactosidases; Galactosides; Genetic Carrier Screening; Hexosaminidases; Humans; Hymecromone; Lysosomes; Male

1981