"beta-Galactosidase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A group of enzymes that catalyzes the hydrolysis of terminal, non-reducing beta-D-galactose residues in beta-galactosides. Deficiency of beta-Galactosidase A1 may cause GANGLIOSIDOSIS, GM1.
| Descriptor ID |
D001616
|
| MeSH Number(s) |
D08.811.277.450.410.100
|
| Concept/Terms |
beta-Galactosidase- beta-Galactosidase
- beta Galactosidase
- beta-Galactosidases
- beta Galactosidases
- lac Z Protein
- Protein, lac Z
- Lactases
- beta-D-Galactosidase
- beta D Galactosidase
|
Below are MeSH descriptors whose meaning is more general than "beta-Galactosidase".
Below are MeSH descriptors whose meaning is more specific than "beta-Galactosidase".
This graph shows the total number of publications written about "beta-Galactosidase" by people in this website by year, and whether "beta-Galactosidase" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 1 | 8 | 9 |
| 1995 | 2 | 10 | 12 |
| 1996 | 4 | 6 | 10 |
| 1997 | 2 | 22 | 24 |
| 1998 | 3 | 10 | 13 |
| 1999 | 1 | 8 | 9 |
| 2000 | 1 | 5 | 6 |
| 2001 | 1 | 14 | 15 |
| 2002 | 2 | 9 | 11 |
| 2003 | 0 | 10 | 10 |
| 2004 | 1 | 5 | 6 |
| 2005 | 1 | 4 | 5 |
| 2006 | 1 | 5 | 6 |
| 2007 | 0 | 8 | 8 |
| 2008 | 2 | 0 | 2 |
| 2009 | 0 | 4 | 4 |
| 2010 | 0 | 6 | 6 |
| 2011 | 1 | 4 | 5 |
| 2012 | 1 | 4 | 5 |
| 2014 | 0 | 3 | 3 |
| 2015 | 0 | 2 | 2 |
| 2018 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "beta-Galactosidase" by people in Profiles.
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Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patients. Mol Genet Metab. 2023 02; 138(2):107508.
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Intermittent enzyme replacement therapy with recombinant human ?-galactosidase prevents neuraminidase 1 deficiency J Biol Chem. 2020 09 25; 295(39):13556-13569.
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Detecting Protein-Protein Interaction Based on Protein Fragment Complementation Assay. Curr Protein Pept Sci. 2020; 21(6):598-610.
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Protein modeling and clinical description of a novel in-frame GLB1 deletion causing GM1 gangliosidosis type II. Mol Genet Genomic Med. 2018 11; 6(6):1229-1235.
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The evolutionary impact of intragenic FliA promoters in proteobacteria. Mol Microbiol. 2018 05; 108(4):361-378.
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Smooth Muscle Cells Derived From Second Heart Field and Cardiac Neural Crest Reside in Spatially Distinct Domains in the Media of the Ascending Aorta-Brief Report. Arterioscler Thromb Vasc Biol. 2017 09; 37(9):1722-1726.
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DksA involvement in transcription fidelity buffers stochastic epigenetic change. Nucleic Acids Res. 2015 Dec 02; 43(21):10190-9.
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The Drosophila melanogaster Mutants apblot and apXasta Affect an Essential apterous Wing Enhancer. G3 (Bethesda). 2015 Apr 02; 5(6):1129-43.
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Conditional deletion of the relaxin receptor gene in cells of smooth muscle lineage affects lower reproductive tract in pregnant mice. Biol Reprod. 2015 Apr; 92(4):91.
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Removal of 8-oxo-GTP by MutT hydrolase is not a major contributor to transcriptional fidelity. Nucleic Acids Res. 2014 Oct 29; 42(19):12015-26.