Search details
1.
Minimizing the damage: repair pathways keep mitochondrial DNA intact.
Nat Rev Mol Cell Biol
; 13(10): 659-71, 2012 Oct.
Article
in English
| MEDLINE | ID: mdl-22992591
2.
A model-based strategy for the COVID-19 vaccine roll-out in the Philippines.
J Theor Biol
; 573: 111596, 2023 09 21.
Article
in English
| MEDLINE | ID: mdl-37597691
3.
DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion.
Nucleic Acids Res
; 49(9): 5230-5248, 2021 05 21.
Article
in English
| MEDLINE | ID: mdl-33956154
4.
RCC1L (WBSCR16) isoforms coordinate mitochondrial ribosome assembly through their interaction with GTPases.
PLoS Genet
; 16(7): e1008923, 2020 07.
Article
in English
| MEDLINE | ID: mdl-32735630
5.
Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features.
J Med Genet
; 58(3): 155-167, 2021 03.
Article
in English
| MEDLINE | ID: mdl-32439808
6.
RNase H1 directs origin-specific initiation of DNA replication in human mitochondria.
PLoS Genet
; 15(1): e1007781, 2019 01.
Article
in English
| MEDLINE | ID: mdl-30605451
7.
PrimPol, an archaic primase/polymerase operating in human cells.
Mol Cell
; 52(4): 541-53, 2013 Nov 21.
Article
in English
| MEDLINE | ID: mdl-24207056
8.
Mitochondrial maintenance under oxidative stress depends on mitochondrially localised α-OGG1.
J Cell Sci
; 131(12)2018 06 25.
Article
in English
| MEDLINE | ID: mdl-29848661
9.
Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement.
Mol Genet Metab
; 129(1): 26-34, 2020 01.
Article
in English
| MEDLINE | ID: mdl-31787496
10.
A two-nuclease pathway involving RNase H1 is required for primer removal at human mitochondrial OriL.
Nucleic Acids Res
; 46(18): 9471-9483, 2018 10 12.
Article
in English
| MEDLINE | ID: mdl-30102370
11.
Transcript availability dictates the balance between strand-asynchronous and strand-coupled mitochondrial DNA replication.
Nucleic Acids Res
; 46(20): 10771-10781, 2018 11 16.
Article
in English
| MEDLINE | ID: mdl-30239839
12.
RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy.
Am J Hum Genet
; 97(1): 186-93, 2015 Jul 02.
Article
in English
| MEDLINE | ID: mdl-26094573
13.
Compound heterozygous missense and deep intronic variants in NDUFAF6 unraveled by exome sequencing and mRNA analysis.
J Hum Genet
; 63(5): 563-568, 2018 May.
Article
in English
| MEDLINE | ID: mdl-29531337
14.
Mathematical model and intervention strategies for mitigating tuberculosis in the Philippines.
J Theor Biol
; 443: 100-112, 2018 04 14.
Article
in English
| MEDLINE | ID: mdl-29407656
15.
A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy.
J Med Genet
; 54(12): 815-824, 2017 12.
Article
in English
| MEDLINE | ID: mdl-29079705
16.
Correction to 'DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion'.
Nucleic Acids Res
; 49(18): 10803, 2021 Oct 11.
Article
in English
| MEDLINE | ID: mdl-34520541
17.
Foxg1 localizes to mitochondria and coordinates cell differentiation and bioenergetics.
Proc Natl Acad Sci U S A
; 112(45): 13910-5, 2015 Nov 10.
Article
in English
| MEDLINE | ID: mdl-26508630
18.
New genes and pathomechanisms in mitochondrial disorders unraveled by NGS technologies.
Biochim Biophys Acta
; 1857(8): 1326-1335, 2016 Aug.
Article
in English
| MEDLINE | ID: mdl-26968897
19.
COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency.
J Med Genet
; 53(12): 846-849, 2016 12.
Article
in English
| MEDLINE | ID: mdl-27683825
20.
The Role of DNA Repair in Maintaining Mitochondrial DNA Stability.
Adv Exp Med Biol
; 1038: 85-105, 2017.
Article
in English
| MEDLINE | ID: mdl-29178071