Detalhe da pesquisa
1.
The pathogenic m.8993 T > G mutation in mitochondrial ATP6 gene prevents proton release from the subunit c-ring rotor of ATP synthase.
Hum Mol Genet
; 30(5): 381-392, 2021 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33600551
2.
The renal effects of droxidopa are maintained in propranolol treated cirrhotic rats.
Liver Int
; 35(2): 326-34, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24517276
3.
A yeast-based assay identifies drugs active against human mitochondrial disorders.
Proc Natl Acad Sci U S A
; 108(29): 11989-94, 2011 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-21715656
4.
Droxidopa, an oral norepinephrine precursor, improves hemodynamic and renal alterations of portal hypertensive rats.
Hepatology
; 56(5): 1849-60, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22610782
5.
Blockage of the afferent sensitive pathway prevents sympathetic atrophy and hemodynamic alterations in rat portal hypertension.
Liver Int
; 32(8): 1295-305, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22292477
6.
Consequences of the pathogenic T9176C mutation of human mitochondrial DNA on yeast mitochondrial ATP synthase.
Biochim Biophys Acta
; 1797(6-7): 1105-12, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20056103
7.
Atrophy of mesenteric sympathetic innervation may contribute to splanchnic vasodilation in rat portal hypertension.
Liver Int
; 30(4): 593-602, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19968782
8.
Inhibition of neuronal apoptosis and axonal regression ameliorates sympathetic atrophy and hemodynamic alterations in portal hypertensive rats.
PLoS One
; 9(1): e84374, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24400086
9.
Defining the pathogenesis of human mtDNA mutations using a yeast model: the case of T8851C.
Int J Biochem Cell Biol
; 45(1): 130-40, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22789932
10.
Physiopathology of splanchnic vasodilation in portal hypertension.
World J Hepatol
; 2(6): 208-20, 2010 Jun 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-21160999
11.
A yeast model of the neurogenic ataxia retinitis pigmentosa (NARP) T8993G mutation in the mitochondrial ATP synthase-6 gene.
J Biol Chem
; 282(47): 34039-47, 2007 Nov 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-17855363