Detalhe da pesquisa
1.
Microscopy-based phenotypic monitoring of MDA-MB-231 spheroids allows the evaluation of phenotype-directed therapy.
Exp Cell Res
; 425(2): 113527, 2023 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-36889574
2.
LYST deficiency impairs autophagic lysosome reformation in neurons and alters lysosome number and size.
Cell Mol Life Sci
; 80(2): 53, 2023 Jan 28.
Artigo
Inglês
| MEDLINE | ID: mdl-36707427
3.
Reduction of glutamate neurotoxicity: A novel therapeutic approach for Niemann-Pick disease, type C1.
Mol Genet Metab
; 134(4): 330-336, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34802899
4.
Microglia activation in Niemann-Pick disease, type C1 is amendable to therapeutic intervention.
Hum Mol Genet
; 27(12): 2076-2089, 2018 06 15.
Artigo
Inglês
| MEDLINE | ID: mdl-29617956
5.
Toll-like receptor mediated lysozyme expression in Niemann-pick disease, type C1.
Mol Genet Metab
; 131(3): 364-366, 2020 11.
Artigo
Inglês
| MEDLINE | ID: mdl-33129690
6.
Maternal immune activation modifies the course of Niemann-pick disease, type C1 in a gender specific manner.
Mol Genet Metab
; 129(2): 165-170, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31668555
7.
Single Cell Transcriptome Analysis of Niemann-Pick Disease, Type C1 Cerebella.
Int J Mol Sci
; 21(15)2020 Jul 28.
Artigo
Inglês
| MEDLINE | ID: mdl-32731618
8.
Unique molecular signature in mucolipidosis type IV microglia.
J Neuroinflammation
; 16(1): 276, 2019 Dec 28.
Artigo
Inglês
| MEDLINE | ID: mdl-31883529
9.
Evaluation of age of death in Niemann-Pick disease, type C: Utility of disease support group websites to understand natural history.
Mol Genet Metab
; 126(4): 466-469, 2019 04.
Artigo
Inglês
| MEDLINE | ID: mdl-30850267
10.
Correction: LYST deficiency impairs autophagic lysosome reformation in neurons and alters lysosome number and size.
Cell Mol Life Sci
; 80(3): 81, 2023 Mar 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36869920
11.
Identification of Novel Pathways Associated with Patterned Cerebellar Purkinje Neuron Degeneration in Niemann-Pick Disease, Type C1.
Int J Mol Sci
; 21(1)2019 Dec 31.
Artigo
Inglês
| MEDLINE | ID: mdl-31906248
12.
Differential Proteomics Reveals miR-155 as a Novel Indicator of Liver and Spleen Pathology in the Symptomatic Niemann-Pick Disease, Type C1 Mouse Model.
Molecules
; 24(5)2019 Mar 12.
Artigo
Inglês
| MEDLINE | ID: mdl-30870990
13.
FTY720/fingolimod increases NPC1 and NPC2 expression and reduces cholesterol and sphingolipid accumulation in Niemann-Pick type C mutant fibroblasts.
FASEB J
; 31(4): 1719-1730, 2017 04.
Artigo
Inglês
| MEDLINE | ID: mdl-28082351
14.
Gastrointestinal Tract Pathology in a BALB/c Niemann-Pick Disease Type C1 Null Mouse Model.
Dig Dis Sci
; 63(4): 870-880, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29357083
15.
Small-molecule inhibitors prevent the genotoxic and protumoural effects induced by colibactin-producing bacteria.
Gut
; 65(2): 278-85, 2016 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-25588406
16.
High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data sets.
Genet Med
; 18(1): 41-8, 2016 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-25764212
17.
Altered cerebrospinal fluid proteins in Smith-Lemli-Opitz syndrome patients.
Am J Med Genet A
; 170(8): 2060-2068, 2016 08.
Artigo
Inglês
| MEDLINE | ID: mdl-27148958
18.
Bacterial genotoxin colibactin promotes colon tumour growth by inducing a senescence-associated secretory phenotype.
Gut
; 63(12): 1932-42, 2014 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24658599
19.
Colibactin-producing Escherichia coli enhance resistance to chemotherapeutic drugs by promoting epithelial to mesenchymal transition and cancer stem cell emergence.
Gut Microbes
; 16(1): 2310215, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-38374654
20.
Chromosome-mediated OXA-48 carbapenemase in highly virulent Escherichia coli.
J Antimicrob Chemother
; 68(7): 1558-61, 2013 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-23447140