4-methylumbelliferyl-6-sulfo-2-acetamido-2-deoxy-beta-glucopyranoside and Gangliosidosis, GM1

4-methylumbelliferyl-6-sulfo-2-acetamido-2-deoxy-beta-glucopyranoside has been researched along with Gangliosidosis, GM1 in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Cao, Z; Petroulakis, E; Salo, T; Triggs-Raine, B	1

Other Studies

1 other study(ies) available for 4-methylumbelliferyl-6-sulfo-2-acetamido-2-deoxy-beta-glucopyranoside and Gangliosidosis, GM1

Article	Year
Benign HEXA mutations, C739T(R247W) and C745T(R249W), cause beta-hexosaminidase A pseudodeficiency by reducing the alpha-subunit protein levels. The Journal of biological chemistry, 1997, Jun-06, Volume: 272, Issue:23 Topics: Adult; Age of Onset; Animals; beta-N-Acetylhexosaminidases; Child; COS Cells; Gangliosidosis, GM1; Hexosaminidase A; Humans; Hymecromone; Infant; Isoenzymes; Kinetics; Macromolecular Substances; Point Mutation; Recombinant Proteins; Transfection	1997

Article

Year

Benign HEXA mutations, C739T(R247W) and C745T(R249W), cause beta-hexosaminidase A pseudodeficiency by reducing the alpha-subunit protein levels.

The Journal of biological chemistry, 1997, Jun-06, Volume: 272, Issue:23

Topics: Adult; Age of Onset; Animals; beta-N-Acetylhexosaminidases; Child; COS Cells; Gangliosidosis, GM1; Hexosaminidase A; Humans; Hymecromone; Infant; Isoenzymes; Kinetics; Macromolecular Substances; Point Mutation; Recombinant Proteins; Transfection

1997