Page last updated: 2024-08-17

adenosine diphosphate and Lysosomal Enzyme Disorders

adenosine diphosphate has been researched along with Lysosomal Enzyme Disorders in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bonten, E; d'Azzo, A; Rottier, RJ	1
Hashizume, Y; Itoh, K; Oyanagi, K; Sakuraba, H; Sato, T; Shimmoto, M; Takahashi, H	1

Other Studies

2 other study(ies) available for adenosine diphosphate and Lysosomal Enzyme Disorders

Article	Year
A point mutation in the neu-1 locus causes the neuraminidase defect in the SM/J mouse. Human molecular genetics, 1998, Volume: 7, Issue:2 Topics: Adenosine Diphosphate; Amino Acid Sequence; Animals; COS Cells; Disease Models, Animal; DNA Mutational Analysis; DNA, Complementary; Dwarfism; Fibroblasts; Genes; Genotype; Glycosylation; Immunologic Deficiency Syndromes; Lysosomal Storage Diseases; Lysosomes; Macromolecular Substances; Mice; Mice, Inbred BALB C; Mice, Inbred Strains; Mice, Mutant Strains; Molecular Sequence Data; Neuraminidase; Phenotype; Point Mutation; Protein Processing, Post-Translational; Recombinant Fusion Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Transfection	1998
Endothelin-1 in the brain of patients with galactosialidosis: its abnormal increase and distribution pattern. Annals of neurology, 2000, Volume: 47, Issue:1 Topics: Adenosine Diphosphate; Adolescent; Adult; beta-Galactosidase; Brain; Child; Child, Preschool; Endothelin-1; Humans; Immunohistochemistry; Lysosomal Storage Diseases; Male	2000

Article

Year

A point mutation in the neu-1 locus causes the neuraminidase defect in the SM/J mouse.

Human molecular genetics, 1998, Volume: 7, Issue:2

Topics: Adenosine Diphosphate; Amino Acid Sequence; Animals; COS Cells; Disease Models, Animal; DNA Mutational Analysis; DNA, Complementary; Dwarfism; Fibroblasts; Genes; Genotype; Glycosylation; Immunologic Deficiency Syndromes; Lysosomal Storage Diseases; Lysosomes; Macromolecular Substances; Mice; Mice, Inbred BALB C; Mice, Inbred Strains; Mice, Mutant Strains; Molecular Sequence Data; Neuraminidase; Phenotype; Point Mutation; Protein Processing, Post-Translational; Recombinant Fusion Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Transfection

1998

Endothelin-1 in the brain of patients with galactosialidosis: its abnormal increase and distribution pattern.

Annals of neurology, 2000, Volume: 47, Issue:1

Topics: Adenosine Diphosphate; Adolescent; Adult; beta-Galactosidase; Brain; Child; Child, Preschool; Endothelin-1; Humans; Immunohistochemistry; Lysosomal Storage Diseases; Male

2000