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1.
YbeY is required for ribosome small subunit assembly and tRNA processing in human mitochondria.
Nucleic Acids Res
; 49(10): 5798-5812, 2021 06 04.
Article
in English
| MEDLINE | ID: mdl-34037799
2.
Regulation of Mammalian Mitochondrial Gene Expression: Recent Advances.
Trends Biochem Sci
; 42(8): 625-639, 2017 08.
Article
in English
| MEDLINE | ID: mdl-28285835
3.
Variants in PUS7 Cause Intellectual Disability with Speech Delay, Microcephaly, Short Stature, and Aggressive Behavior.
Am J Hum Genet
; 103(6): 1045-1052, 2018 12 06.
Article
in English
| MEDLINE | ID: mdl-30526862
4.
METTL15 introduces N4-methylcytidine into human mitochondrial 12S rRNA and is required for mitoribosome biogenesis.
Nucleic Acids Res
; 47(19): 10267-10281, 2019 11 04.
Article
in English
| MEDLINE | ID: mdl-31665743
5.
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies.
Am J Hum Genet
; 101(4): 525-538, 2017 Oct 05.
Article
in English
| MEDLINE | ID: mdl-28942965
6.
Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing.
Hum Mutat
; 40(10): 1731-1748, 2019 10.
Article
in English
| MEDLINE | ID: mdl-31045291
7.
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome.
Hum Mol Genet
; 26(21): 4257-4266, 2017 11 01.
Article
in English
| MEDLINE | ID: mdl-28973171
8.
The Pseudouridine Synthase RPUSD4 Is an Essential Component of Mitochondrial RNA Granules.
J Biol Chem
; 292(11): 4519-4532, 2017 03 17.
Article
in English
| MEDLINE | ID: mdl-28082677
9.
Near-complete elimination of mutant mtDNA by iterative or dynamic dose-controlled treatment with mtZFNs.
Nucleic Acids Res
; 44(16): 7804-16, 2016 09 19.
Article
in English
| MEDLINE | ID: mdl-27466392
10.
Protocol to study human mitochondrial ribosome using quantitative density gradient analysis by mass spectrometry and complexome profiling analysis.
STAR Protoc
; 4(4): 102605, 2023 Dec 15.
Article
in English
| MEDLINE | ID: mdl-37976156
11.
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.
Nat Commun
; 14(1): 1009, 2023 02 23.
Article
in English
| MEDLINE | ID: mdl-36823193
12.
A late-stage assembly checkpoint of the human mitochondrial ribosome large subunit.
Nat Commun
; 13(1): 929, 2022 02 17.
Article
in English
| MEDLINE | ID: mdl-35177605
13.
Quantitative density gradient analysis by mass spectrometry (qDGMS) and complexome profiling analysis (ComPrAn) R package for the study of macromolecular complexes.
Biochim Biophys Acta Bioenerg
; 1862(6): 148399, 2021 06 01.
Article
in English
| MEDLINE | ID: mdl-33592209
14.
Cardiac mitochondrial function depends on BUD23 mediated ribosome programming.
Elife
; 92020 01 15.
Article
in English
| MEDLINE | ID: mdl-31939735
15.
The mammalian mitochondrial epitranscriptome.
Biochim Biophys Acta Gene Regul Mech
; 1862(3): 429-446, 2019 03.
Article
in English
| MEDLINE | ID: mdl-30529456
16.
Linear mitochondrial DNA is rapidly degraded by components of the replication machinery.
Nat Commun
; 9(1): 1727, 2018 04 30.
Article
in English
| MEDLINE | ID: mdl-29712893
17.
Genome editing in mitochondria corrects a pathogenic mtDNA mutation in vivo.
Nat Med
; 24(11): 1691-1695, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30250142
18.
Pathogenic variants in glutamyl-tRNAGln amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder.
Nat Commun
; 9(1): 4065, 2018 10 03.
Article
in English
| MEDLINE | ID: mdl-30283131
19.
Maturation of selected human mitochondrial tRNAs requires deadenylation.
Elife
; 62017 07 26.
Article
in English
| MEDLINE | ID: mdl-28745585
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