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Trehalase

An enzyme that catalyzes the conversion of alpha,alpha-trehalose and water to D-glucose. EC 3.2.1.28.
Also Known As:
alpha,alpha-Trehalose glucohydrolase
Networked: 101 relevant articles (1 outcomes, 11 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Chen, Wan-Ling: 3 articles (01/2020 - 05/2015)
2. Lee-Chen, Guey-Jen: 3 articles (01/2020 - 05/2015)
3. Lin, Chih-Hsin: 3 articles (01/2020 - 05/2015)
4. Wu, Yih-Ru: 3 articles (01/2020 - 05/2015)
5. Chao, Chih-Ying: 2 articles (01/2020 - 01/2016)
6. Tang, Bin: 2 articles (07/2017 - 01/2016)
7. Chen, Chiung-Mei: 2 articles (01/2016 - 05/2015)
8. Hsu, Kai-Cheng: 2 articles (01/2016 - 05/2015)
9. Lee, Guan-Chiun: 2 articles (01/2016 - 05/2015)
10. Yang, Jinn-Moon: 2 articles (01/2016 - 05/2015)

Related Diseases

1. Inflammatory Bowel Diseases (Inflammatory Bowel Disease)
2. Crohn Disease (Crohn's Disease)
3. Ulcerative Colitis
4. Infections
5. Spinocerebellar Ataxias (Spinocerebellar Ataxia)
01/01/2016 - "In this study, two trehalase analogs, lactulose and melibiose, were examined for their potentials in spinocerebellar ataxia treatment. "
01/01/2020 - "Its trehalase-indigestible analogs, lactulose and melibiose, also demonstrated potentials to reduce abnormal protein aggregation in spinocerebellar ataxia cell models. "
01/01/2019 - "Abbreviations: ALS: amyotrophic lateral sclerosis; AR: androgen receptor; ATG: autophagy related; AV: autophagic vacuole; BAG3: BCL2-associated athanogene 3; BECN1: beclin 1, autophagy related; CASA: chaperone-assisted selective autophagy; CTSB: cathepsin b; DAPI: 4',6-diamidino-2-phenylindole; DMEM: Dulbecco's modified Eagle's medium; EGFP: enhanced green fluorescent protein; fALS, familial amyotrophic lateral sclerosis; FRA: filter retardation assay; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GLA: galactosidase, alpha; HD: Huntington disease; hIPSCs: human induced pluripotent stem cells; HSPA8: heat shock protein A8; HSPB8: heat shock protein B8; IF: immunofluorescence analysis; LAMP1: lysosomal-associated membrane protein 1; LAMP2A: lysosomal-associated membrane protein 2A; LGALS3: lectin, galactose binding, soluble 3; LLOMe: L-leucyl-L-leucine methyl ester; LMP: lysosomal membrane permeabilization; Lys: lysosomes; MAP1LC3B: microtubule-associated protein 1 light chain 3 beta; MCOLN1: mucolipin 1; mRNA: messenger RNA; MTOR: mechanistic target of rapamycin kinase; NDs: neurodegenerative diseases; NSC34: neuroblastoma x spinal cord 34; PBS: phosphate-buffered saline; PD: Parkinson disease; polyQ: polyglutamine; PPARGC1A: peroxisome proliferative activated receptor, gamma, coactivator 1 alpha; PPP3CB: protein phosphatase 3, catalytic subunit, beta isoform; RT-qPCR: real-time quantitative polymerase chain reaction; SBMA: spinal and bulbar muscular atrophy; SCAs: spinocerebellar ataxias; siRNA: small interfering RNA; SLC2A8: solute carrier family 2, (facilitated glucose transporter), member 8; smNPCs: small molecules neural progenitors cells; SOD1: superoxide dismutase 1; SQSTM1/p62: sequestosome 1; STED: stimulated emission depletion; STUB1: STIP1 homology and U-box containing protein 1; TARDBP/TDP-43: TAR DNA binding protein; TFEB: transcription factor EB; TPP1: tripeptidyl peptidase I; TREH: trehalase (brush-border membrane glycoprotein); WB: western blotting; ZKSCAN3: zinc finger with KRAB and SCAN domains 3."

Related Drugs and Biologics

1. Sucrase (Sucrose alpha-D-Glucohydrolase)
2. Lactase
3. Disaccharidases
4. Enzymes
5. Proteins (Proteins, Gene)
6. Trehalose
7. gamma-Glutamyltransferase (gamma-Glutamyl Transpeptidase)
8. Hydrolases
9. Muramidase (Lysozyme)
10. Melibiose

Related Therapies and Procedures

1. Aftercare (After-Treatment)