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UnknownCorrection of a homoplasmic mitochondrial tRNA mutation in patient-derived iPSCs via a mitochondrial base editor.
Not available
S-EPMC10624837 | biostudies-literature
GenomicsHomo sapiens
Correction of homoplasmic mitochondrial tRNA mutation in patient-derived iPSCs via DdCBE
PRJNA921944 | ENA
UnknownA novel homoplasmic mutation in mtDNA with a single evolutionary origin as a risk factor for cardiomyopathy.
Not available
S-EPMC1287941 | biostudies-literature
UnknownOverexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation.
Not available
S-EPMC2396425 | biostudies-literature
UnknownThe Mitochondrial tRNAPhe 625G>A Mutation in Three Han Chinese Families With Cholecystolithiasis.
Not available
S-EPMC9198646 | biostudies-literature
UnknownMaternally Inherited Diabetes Mellitus Associated with a Novel m.15897G>A Mutation in Mitochondrial tRNAThr Gene.
Not available
S-EPMC7011485 | biostudies-literature
UnknownA Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction.
Not available
S-EPMC5076513 | biostudies-literature
UnknownNon-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases.
Not available
S-EPMC3565634 | biostudies-literature
UnknownNovel m.4268T>C mutation in the mitochondrial tRNAIle gene is associated with hearing loss in two Chinese families.
Not available
S-EPMC8727281 | biostudies-literature
UnknownA hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR).
Not available
S-EPMC5572913 | biostudies-literature
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