Detalhe da pesquisa
1.
Subcellular origin of mitochondrial DNA deletions in human skeletal muscle.
Ann Neurol
; 84(2): 289-301, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30014514
2.
Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis.
Nucleic Acids Res
; 44(11): 5313-29, 2016 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27131788
3.
Polyfunctional response by ImmTAC (IMCgp100) redirected CD8+ and CD4+ T cells.
Immunology
; 152(3): 425-438, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28640942
4.
Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.
Ann Neurol
; 79(3): 366-78, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26605748
5.
The ageing neuromuscular system and sarcopenia: a mitochondrial perspective.
J Physiol
; 594(16): 4499-512, 2016 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26921061
6.
Mitochondrial and inflammatory changes in sporadic inclusion body myositis.
Neuropathol Appl Neurobiol
; 41(3): 288-303, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24750247
7.
Characterization of covalent inhibitors that disrupt the interaction between the tandem SH2 domains of SYK and FCER1G phospho-ITAM.
PLoS One
; 19(2): e0293548, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38359047
8.
Recent advances in the structural biology of tyrosine kinases.
Curr Opin Struct Biol
; 82: 102665, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37562149
9.
Characterization of covalent inhibitors that disrupt the interaction between the tandem SH2 domains of SYK and FCER1G phospho-ITAM.
bioRxiv
; 2023 Jul 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37547005
10.
T cell-mediated biliary epithelial-to-mesenchymal transition in liver allograft rejection.
Liver Transpl
; 16(5): 567-76, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20440766
11.
Epithelial-mesenchymal transition contributes to portal tract fibrogenesis during human chronic liver disease.
Lab Invest
; 88(2): 112-23, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18059363
12.
Skeletal muscle mitochondrial oxidative phosphorylation function in idiopathic pulmonary arterial hypertension: in vivo and in vitro study.
Pulm Circ
; 8(2): 2045894018768290, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29799315
13.
Preferential amplification of a human mitochondrial DNA deletion in vitro and in vivo.
Sci Rep
; 8(1): 1799, 2018 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-29379065
14.
An approved in vitro approach to preclinical safety and efficacy evaluation of engineered T cell receptor anti-CD3 bispecific (ImmTAC) molecules.
PLoS One
; 13(10): e0205491, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30321203
15.
Dysferlin mutations and mitochondrial dysfunction.
Neuromuscul Disord
; 26(11): 782-788, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27666772
16.
Mitochondrial dysfunction in myofibrillar myopathy.
Neuromuscul Disord
; 26(10): 691-701, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27618136
17.
Triplex real-time PCR--an improved method to detect a wide spectrum of mitochondrial DNA deletions in single cells.
Sci Rep
; 5: 9906, 2015 May 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25989140
18.
A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis.
Sci Rep
; 5: 15037, 2015 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26469001
19.
Respiratory chain deficiency in aged spinal motor neurons.
Neurobiol Aging
; 35(10): 2230-8, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24684792
20.
Quantitative quadruple-label immunofluorescence of mitochondrial and cytoplasmic proteins in single neurons from human midbrain tissue.
J Neurosci Methods
; 232: 143-9, 2014 Jul 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-24880043