Detalhe da pesquisa
1.
Apoptotic stress causes mtDNA release during senescence and drives the SASP.
Nature
; 622(7983): 627-636, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37821702
2.
Author Correction: Apoptotic stress causes mtDNA release during senescence and drives the SASP.
Nature
; 625(7995): E15, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38168624
3.
Mitochondrial DNA Mutations and Ageing.
Subcell Biochem
; 102: 77-98, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36600130
4.
Length-independent telomere damage drives post-mitotic cardiomyocyte senescence.
EMBO J
; 38(5)2019 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30737259
5.
Aberrant mitochondrial function in ageing and cancer.
Biogerontology
; 21(4): 445-459, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31802313
6.
A novel histochemistry assay to assess and quantify focal cytochrome c oxidase deficiency.
J Pathol
; 245(3): 311-323, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29660116
7.
Inherited pathogenic mitochondrial DNA mutations and gastrointestinal stem cell populations.
J Pathol
; 246(4): 427-432, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30146801
8.
Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageing.
PLoS Genet
; 10(9): e1004620, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25232829
9.
The role of the mitochondrial ribosome in human disease: searching for mutations in 12S mitochondrial rRNA with high disruptive potential.
Hum Mol Genet
; 23(4): 949-67, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24092330
10.
Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expression.
Clin Sci (Lond)
; 128(12): 895-904, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25626417
11.
Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutations.
PLoS Genet
; 8(11): e1003082, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23166522
12.
Mitochondrial DNA and disease.
J Pathol
; 226(2): 274-86, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21989606
13.
In situ lineage tracking of human prostatic epithelial stem cell fate reveals a common clonal origin for basal and luminal cells.
J Pathol
; 225(2): 181-8, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21898876
14.
Mitochondrial DNA mutations in ageing and cancer.
Mol Oncol
; 16(18): 3276-3294, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35842901
15.
Automated quantitative high-throughput multiplex immunofluorescence pipeline to evaluate OXPHOS defects in formalin-fixed human prostate tissue.
Sci Rep
; 12(1): 6660, 2022 04 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35459777
16.
Mitochondrial complex I subunit deficiency promotes pancreatic α-cell proliferation.
Mol Metab
; 60: 101489, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35390502
17.
Age-associated mitochondrial complex I deficiency is linked to increased stem cell proliferation rates in the mouse colon.
Aging Cell
; 20(3): e13321, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33626245
18.
Mitochondrial DNA mutations and ageing.
Biochim Biophys Acta
; 1790(10): 1015-20, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19409965
19.
Locating the stem cell niche and tracing hepatocyte lineages in human liver.
Hepatology
; 49(5): 1655-63, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19309719
20.
A methodological approach to tracing cell lineage in human epithelial tissues.
Stem Cells
; 27(6): 1410-20, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19489031