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glucose, (beta-d)-isomer and Glycogen Storage Disease Type II

glucose, (beta-d)-isomer has been researched along with Glycogen Storage Disease Type II in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19905 (55.56)18.7374
1990's1 (11.11)18.2507
2000's1 (11.11)29.6817
2010's1 (11.11)24.3611
2020's1 (11.11)2.80

Authors

AuthorsStudies
Alila-Fersi, O; Aloulou, H; Belguith, N; Chabchoub, I; Fakhfakh, F; Hachicha, M; Kammoun, H; Keskes, L; Mahfoudh, N; Werteni, I1
Austin, CP; Goldin, E; Griffiths, GL; Liu, K; Motabar, O; Shi, ZD; Sidransky, E; Southall, N; Zheng, W1
Chiang, SC; Chien, YH; Hsu, LW; Hwu, WL; Lee, NC1
Anson, DS; Fuller, M; Hopwood, JJ; Reuser, AJ; Van der Ploeg, A1
Butterworth, J; Droadhead, DM1
Brouwer-Kelder, B; Donker-Koopman, WE; Hamers, MN; Loonen, C; Schram, AW; Tager, JM1
Broadhead, DM; Butterworth, J1
Ishiura, S; Sugita, H; Usuki, F1
Blitzer, MG; Dunn, DW; Shapira, E; Temple, JK1

Other Studies

9 other study(ies) available for glucose, (beta-d)-isomer and Glycogen Storage Disease Type II

ArticleYear
Mutations in GAA Gene in Tunisian Families with Infantile Onset Pompe Disease: Novel Mutation and Structural Modeling Investigations.
    Journal of molecular neuroscience : MN, 2020, Volume: 70, Issue:7

    Topics: alpha-Glucosidases; Catalytic Domain; Female; Glucosides; Glycogen Storage Disease Type II; Humans; Hymecromone; Infant; Male; Molecular Docking Simulation; Mutation; Protein Binding

2020
A new resorufin-based alpha-glucosidase assay for high-throughput screening.
    Analytical biochemistry, 2009, Jul-01, Volume: 390, Issue:1

    Topics: alpha-Glucosidases; Benzoxazines; Fluorescent Dyes; Glucosides; Glycogen Storage Disease Type II; Humans; Kinetics; Mutation; Oxazines; Spectrometry, Fluorescence

2009
Algorithm for Pompe disease newborn screening: results from the Taiwan screening program.
    Molecular genetics and metabolism, 2012, Volume: 106, Issue:3

    Topics: Algorithms; alpha-Galactosidase; alpha-Glucosidases; Base Sequence; Glucosides; Glycogen Storage Disease Type II; Humans; Hymecromone; Infant, Newborn; Molecular Sequence Data; Neonatal Screening; Reproducibility of Results; Taiwan

2012
Isolation and characterisation of a recombinant, precursor form of lysosomal acid alpha-glucosidase.
    European journal of biochemistry, 1995, Dec-15, Volume: 234, Issue:3

    Topics: alpha-Glucosidases; Amino Acid Sequence; Animals; Cells, Cultured; CHO Cells; Cricetinae; Endocytosis; Enzyme Precursors; Glucan 1,4-alpha-Glucosidase; Glucosides; Glycogen; Glycogen Storage Disease Type II; Humans; Hydrogen-Ion Concentration; Hymecromone; Lysosomes; Mannosephosphates; Molecular Sequence Data; Muscle, Skeletal; Peptide Elongation Factor 1; Peptide Elongation Factors; Protein Processing, Post-Translational; Recombinant Proteins; Sequence Analysis

1995
Diagnosis of Pompe's disease in cultured skin fibroblasts and primary amniotic fluid cells using 4-methylumbelliferyl-alpha-D-glucopyranoside as substrate.
    Clinica chimica acta; international journal of clinical chemistry, 1977, Jul-15, Volume: 78, Issue:2

    Topics: Amniotic Fluid; Cells, Cultured; Drug Stability; Female; Fibroblasts; Glucosidases; Glucosides; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Hydrogen-Ion Concentration; Hymecromone; Kinetics; Pregnancy; Prenatal Diagnosis; Skin

1977
Use of immobilized antibodies in investigating acid alpha-glucosidase in urine in relation to Pompe's disease.
    Biochimica et biophysica acta, 1979, Apr-12, Volume: 567, Issue:2

    Topics: alpha-Glucosidases; Glucosidases; Glucosides; Glycogen Storage Disease; Glycogen Storage Disease Type II; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Immunoenzyme Techniques; Kinetics; Liver

1979
Pompe's disease: diagnosis in kidney and leucocytes using 4-methylumbelliferyl-alpha-D-glucopyranoside.
    Clinical genetics, 1978, Volume: 13, Issue:6

    Topics: alpha-Glucosidases; Glucosides; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Hymecromone; Kidney; Leukocytes; Umbelliferones

1978
Isolation and characterization of three alpha-glucosidases from the Japanese quail.
    Journal of biochemistry, 1986, Volume: 99, Issue:3

    Topics: Age Factors; alpha-Glucosidases; Animals; Chromatography, Affinity; Chromatography, DEAE-Cellulose; Coturnix; Glucosidases; Glucosides; Glycogen Storage Disease Type II; Glycoside Hydrolase Inhibitors; Hydrogen-Ion Concentration; Hymecromone; Molecular Weight; Muscles; Substrate Specificity

1986
The "muscular variant" of Pompe disease: clinical, biochemical and histologic characteristics.
    American journal of medical genetics, 1985, Volume: 21, Issue:3

    Topics: alpha-Glucosidases; Child, Preschool; Fibroblasts; Genes, Recessive; Genetic Variation; Glucosides; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Hymecromone; Leukocytes; Male; Muscles; Muscular Diseases; Respiratory Insufficiency

1985