Detalhe da pesquisa
1.
Loss of MYO5B expression deregulates late endosome size which hinders mitotic spindle orientation.
PLoS Biol
; 17(11): e3000531, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31682603
2.
A Molecular Mechanism Underlying Genotype-Specific Intrahepatic Cholestasis Resulting From MYO5B Mutations.
Hepatology
; 72(1): 213-229, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31750554
3.
Pluripotent stem cell-derived bile canaliculi-forming hepatocytes to study genetic liver diseases involving hepatocyte polarity.
J Hepatol
; 71(2): 344-356, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30965071
4.
MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update.
Hum Mutat
; 39(3): 333-344, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29266534
5.
Letter to the Editor: Liver Cell Models for Premature Termination Codon Readthrough Analyses.
Hepatology
; 74(3): 1711-1712, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33314224
6.
Identification of intestinal ion transport defects in microvillus inclusion disease.
Am J Physiol Gastrointest Liver Physiol
; 311(1): G142-55, 2016 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27229121
7.
Myosin Vb and Rab11a regulate phosphorylation of ezrin in enterocytes.
J Cell Sci
; 127(Pt 5): 1007-17, 2014 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24413175
8.
Unequal Effects of Myosin 5B Mutations in Liver and Intestine Determine the Clinical Presentation of Low-Gamma-Glutamyltransferase Cholestasis.
Hepatology
; 72(4): 1461-1468, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32583448
9.
Par1b induces asymmetric inheritance of plasma membrane domains via LGN-dependent mitotic spindle orientation in proliferating hepatocytes.
PLoS Biol
; 11(12): e1001739, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24358023
10.
Hepatitis C virus infection of cholangiocarcinoma cell lines.
J Gen Virol
; 96(Pt 6): 1380-1388, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25701818
11.
Uncovering the Relationship Between Genes and Phenotypes Beyond the Gut in Microvillus Inclusion Disease.
Cell Mol Gastroenterol Hepatol
; 17(6): 983-1005, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38307491
12.
RhoA downregulation in the murine intestinal epithelium results in chronic Wnt activation and increased tumorigenesis.
iScience
; 27(4): 109400, 2024 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38523777
13.
An overview and online registry of microvillus inclusion disease patients and their MYO5B mutations.
Hum Mutat
; 34(12): 1597-605, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24014347
14.
CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndrome.
Gastroenterology
; 142(3): 453-462.e3, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22155368
15.
Adenosine A2B receptor-mediated leukemia inhibitory factor release from astrocytes protects cortical neurons against excitotoxicity.
J Neuroinflammation
; 9: 198, 2012 Aug 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-22894638
16.
MYO5B mutations in patients with microvillus inclusion disease presenting with transient renal Fanconi syndrome.
J Pediatr Gastroenterol Nutr
; 54(4): 491-8, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22441677
17.
Fetal Bowel Abnormalities Suspected by Ultrasonography in Microvillus Inclusion Disease: Prevalence and Clinical Significance.
J Clin Med
; 11(15)2022 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-35893420
18.
Induction of Bile Canaliculi-Forming Hepatocytes from Human Pluripotent Stem Cells.
Methods Mol Biol
; 2544: 71-82, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36125710
19.
A Functional Relationship Between UNC45A and MYO5B Connects Two Rare Diseases With Shared Enteropathy.
Cell Mol Gastroenterol Hepatol
; 14(2): 295-310, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35421597
20.
Myosin Vb as a tumor suppressor gene in intestinal cancer.
Oncogene
; 41(49): 5279-5288, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36316444