Detalhe da pesquisa
1.
How dietary advanced glycation end products could facilitate the occurrence of food allergy.
J Allergy Clin Immunol;
153(3): 742-758, 2024 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38042501
2.
Carnitine is a pharmacological allosteric chaperone of the human lysosomal α-glucosidase.
J Enzyme Inhib Med Chem;
36(1): 2068-2079, 2021 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34565280
3.
Pathogenesis of Mucopolysaccharidoses, an Update.
Int J Mol Sci;
21(7)2020 Apr 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32260444
4.
microRNAs as biomarkers in Pompe disease.
Genet Med;
21(3): 591-600, 2019 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29997386
5.
Postbiotic Preparation of Lacticaseibacillus rhamnosus GG against Diarrhea and Oxidative Stress Induced by Spike Protein of SARS-CoV-2 in Human Enterocytes.
Antioxidants (Basel);
12(10)2023 Oct 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37891957
6.
SARS-CoV-2 causes secretory diarrhea with an enterotoxin-like mechanism, which is reduced by diosmectite.
Heliyon;
8(8): e10246, 2022 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35996551
7.
Correction of oxidative stress enhances enzyme replacement therapy in Pompe disease.
EMBO Mol Med;
13(11): e14434, 2021 11 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34606154
8.
The pharmacological chaperone N-butyldeoxynojirimycin enhances enzyme replacement therapy in Pompe disease fibroblasts.
Mol Ther;
17(6): 964-71, 2009 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19293774
9.
Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases.
PLoS One;
15(5): e0233050, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32428018
10.
Satellite cells maintain regenerative capacity but fail to repair disease-associated muscle damage in mice with Pompe disease.
Acta Neuropathol Commun;
6(1): 119, 2018 11 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30404653
11.
AAV-mediated transcription factor EB (TFEB) gene delivery ameliorates muscle pathology and function in the murine model of Pompe Disease.
Sci Rep;
7(1): 15089, 2017 11 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29118420
12.
Wilson disease protein ATP7B utilizes lysosomal exocytosis to maintain copper homeostasis.
Dev Cell;
29(6): 686-700, 2014 Jun 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24909901
13.
Abnormal mannose-6-phosphate receptor trafficking impairs recombinant alpha-glucosidase uptake in Pompe disease fibroblasts.
Pathogenetics;
1(1): 6, 2008 Dec 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19046416