4-methylumbelliferyl-6-sulfo-2-acetamido-2-deoxy-beta-glucopyranoside has been researched along with Tay-Sachs Disease in 11 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 6 (54.55) | 18.7374 |
1990's | 4 (36.36) | 18.2507 |
2000's | 1 (9.09) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Guetta, E; Peleg, L | 1 |
Inui, K; Wenger, DA | 1 |
Bayleran, J; Hechtman, P; Saray, W | 1 |
Jendoubi, M; Lacorazza, HD | 1 |
Goldman, B; Peleg, L | 1 |
Bobrow, M; Ellis, IH; Fensom, AH; Landels, EC | 1 |
Archibald, A; Callahan, JW; Clarke, JT; Shuman, C; Skomorowski, MA | 1 |
Grebner, EE; Wenger, DA | 1 |
Besley, GT; Broadhead, DM; Young, JA | 1 |
Charrow, J; Inui, K; Wenger, DA | 1 |
Furukawa, M; Inui, K; Okada, S; Suehara, N; Tanizawa, O; Wenger, DA; Yabuuchi, H; Yutaka, Y | 1 |
11 other study(ies) available for 4-methylumbelliferyl-6-sulfo-2-acetamido-2-deoxy-beta-glucopyranoside and Tay-Sachs Disease
Article | Year |
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Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
Topics: Acetylglucosamine; Amniocentesis; Amniotic Fluid; beta-Hexosaminidase alpha Chain; Biological Assay; Chorionic Villi; Chorionic Villi Sampling; DNA Mutational Analysis; Female; Fetal Blood; Gene Expression Regulation, Developmental; Genetic Testing; Humans; Hymecromone; Mutation; Polymerase Chain Reaction; Predictive Value of Tests; Pregnancy; Prenatal Diagnosis; Reproducibility of Results; Substrate Specificity; Tay-Sachs Disease; Time Factors | 2008 |
Usefulness of 4-methylumbelliferyl-6-sulfo-2-acetamido-2-deoxy-beta-D-glucopyrano sid e for the diagnosis of GM2 gangliosidoses in leukocytes.
Topics: Acetylglucosaminidase; beta-N-Acetylhexosaminidases; Female; Genetic Carrier Screening; Hexosaminidase A; Hexosaminidases; Humans; Hymecromone; Leukocytes; Male; Sandhoff Disease; Substrate Specificity; Tay-Sachs Disease; Umbelliferones | 1984 |
Synthesis of 4-methylumbelliferyl-beta-D-N-acetylglucosamine-6-sulfate and its use in classification of GM2 gangliosidosis genotypes.
Topics: beta-N-Acetylhexosaminidases; Cell Line; Drug Stability; Fibroblasts; Gangliosidoses; Genetic Carrier Screening; Genotype; Hexosaminidase A; Hexosaminidase B; Hexosaminidases; Homozygote; Hot Temperature; Humans; Hymecromone; Kinetics; Liver; Substrate Specificity; Tay-Sachs Disease; Umbelliferones | 1984 |
In situ assessment of beta-hexosaminidase activity.
Topics: Acetylglucosamine; beta-N-Acetylhexosaminidases; Cells, Cultured; Fibroblasts; Glucuronates; Histocytochemistry; Humans; Hymecromone; Isoenzymes; Mutation; Naphthols; Sandhoff Disease; Spectrometry, Fluorescence; Tay-Sachs Disease | 1995 |
Detection of Tay-Sachs disease carriers among individuals with thermolabile hexosaminidase B.
Topics: Acetylglucosamine; beta-N-Acetylhexosaminidases; Chromatography, Ion Exchange; Enzyme Stability; Genetic Carrier Screening; Genetic Testing; Genotype; Hexosaminidase A; Hexosaminidase B; Hot Temperature; Humans; Hymecromone; Jews; Substrate Specificity; Tay-Sachs Disease | 1994 |
Tay-Sachs disease heterozygote detection: use of a centrifugal analyser for automation of hexosaminidase assays with two different artificial substrates.
Topics: Acetylglucosamine; Automation; beta-N-Acetylhexosaminidases; Cell Separation; Centrifugation; Female; Flow Cytometry; Genetic Carrier Screening; Genetic Testing; Glucosamine; Hexosaminidase A; Hot Temperature; Humans; Hymecromone; Leukocytes; Pregnancy; Prenatal Diagnosis; Tay-Sachs Disease | 1991 |
First trimester prenatal diagnosis of Tay-Sachs disease using the sulfated synthetic substrate for hexosaminidase A.
Topics: beta-N-Acetylhexosaminidases; Cells, Cultured; Chorionic Villi; Female; Hexosaminidase A; Humans; Hymecromone; Pregnancy; Pregnancy Trimester, First; Prenatal Diagnosis; Risk Factors; Substrate Specificity; Tay-Sachs Disease | 1990 |
Use of 4-methylumbelliferyl-6-sulpho-2-acetamido-2-deoxy-beta- D-glucopyranoside for prenatal diagnosis of Tay-Sachs disease using chorionic villi.
Topics: beta-N-Acetylhexosaminidases; Chorionic Villi; Female; Hexosaminidase A; Humans; Hymecromone; Pregnancy; Prenatal Diagnosis; Tay-Sachs Disease; Umbelliferones | 1987 |
GM2-gangliosidosis variant with altered substrate specificity: evidence for alpha-locus genetic compound.
Topics: beta-N-Acetylhexosaminidases; Humans; Hymecromone; Infant; Male; Substrate Specificity; Tay-Sachs Disease | 1987 |
Late onset GM2 gangliosidosis: an alpha-locus genetic compound with near normal hexosaminidase activity.
Topics: Acetylglucosamine; Alleles; beta-N-Acetylhexosaminidases; Child, Preschool; Female; Glucosamine; Heterozygote; Hexosaminidase A; Hexosaminidases; Humans; Hymecromone; Mutation; Pedigree; Substrate Specificity; Tay-Sachs Disease | 1985 |
Prenatal diagnosis of GM2 gangliosidoses using a fluorogenic sulfated substrate.
Topics: Amniotic Fluid; Female; Hexosaminidases; Humans; Hymecromone; Pregnancy; Prenatal Diagnosis; Sandhoff Disease; Tay-Sachs Disease; Umbelliferones | 1986 |