Detalhe da pesquisa
1.
Disrupted glucose homeostasis and skeletal-muscle-specific glucose uptake in an exocyst knockout mouse model.
J Biol Chem
; 296: 100482, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33647317
2.
Primary cilia and the exocyst are linked to urinary extracellular vesicle production and content.
J Biol Chem
; 294(50): 19099-19110, 2019 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31694916
3.
The exocyst complex regulates insulin-stimulated glucose uptake of skeletal muscle cells.
Am J Physiol Endocrinol Metab
; 317(6): E957-E972, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31593505
4.
The exocyst gene Sec10 regulates renal epithelial monolayer homeostasis and apoptotic sensitivity.
Am J Physiol Cell Physiol
; 309(3): C190-201, 2015 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26040895
5.
Exocyst Sec10 protects renal tubule cells from injury by EGFR/MAPK activation and effects on endocytosis.
Am J Physiol Renal Physiol
; 307(12): F1334-41, 2014 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25298525
6.
Rett networked database: an integrated clinical and genetic network of Rett syndrome databases.
Hum Mutat
; 33(7): 1031-6, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22415763
7.
The Exocyst Is Required for CD36 Fatty Acid Translocase Trafficking and Free Fatty Acid Uptake in Skeletal Muscle Cells.
Cells
; 11(15)2022 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35954283
8.
Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
J Hum Genet
; 56(3): 183-7, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21160487
9.
Interaction between CTLA4 gene and IBD5 locus in Hungarian Crohn's disease patients.
Int J Colorectal Dis
; 26(9): 1119-25, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21519805
10.
[Molecular genetic diagnosis of neurofibromatosis type I]. / Az 1-es típusú neurofibromatosis molekuláris genetikai diagnosztikája.
Orv Hetil
; 152(11): 415-9, 2011 Mar 13.
Artigo
em Húngaro
| MEDLINE | ID: mdl-21362601
11.
[Unusual clinical manifestations of type 1 neurofibromatosis]. / Az 1-es típusú neurofibromatosis ritka megjelenésu, tanulságos esetei.
Orv Hetil
; 152(49): 1965-70, 2011 Dec 04.
Artigo
em Húngaro
| MEDLINE | ID: mdl-22106164
12.
GCKR gene functional variants in type 2 diabetes and metabolic syndrome: do the rare variants associate with increased carotid intima-media thickness?
Cardiovasc Diabetol
; 9: 79, 2010 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-21114848
13.
Interethnic differences of CYP2C9 alleles in healthy Hungarian and Roma population samples: relationship to worldwide allelic frequencies.
Blood Cells Mol Dis
; 43(3): 239-42, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19541511
14.
Regulation of Cell Polarity by Exocyst-Mediated Trafficking.
Cold Spring Harb Perspect Biol
; 10(3)2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28264817
15.
Fibroproliferative response to urothelial failure obliterates the ureter lumen in a mouse model of prenatal congenital obstructive nephropathy.
Sci Rep
; 6: 31137, 2016 08 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27511831
16.
Arl13b and the exocyst interact synergistically in ciliogenesis.
Mol Biol Cell
; 27(2): 308-20, 2016 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26582389
17.
Urothelial Defects from Targeted Inactivation of Exocyst Sec10 in Mice Cause Ureteropelvic Junction Obstructions.
PLoS One
; 10(6): e0129346, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26046524
18.
Association of myasthenia gravis with polymorphisms in the gene of histamine N-methyltransferase.
Hum Immunol
; 74(12): 1701-4, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23932992
19.
Haplotype analysis of the apolipoprotein A5 gene in obese pediatric patients.
Int J Pediatr Obes
; 6(2-2): e318-25, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20883102
20.
Triglyceride level-influencing functional variants of the ANGPTL3, CILP2, and TRIB1 loci in ischemic stroke.
Neuromolecular Med
; 13(3): 179-86, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21691831