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Maria Falkenberg

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EMBO Molecular Medicine|April 4, 2023

Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stabilityDirenis Erdinc, Alejandro Rodríguez-Luis, Mahmoud R Fassad, et al.

Nature Communications|February 19, 2021

POLRMT mutations impair mitochondrial transcription causing neurological diseaseMonika Oláhová, Bradley Peter, Zsolt Szilagyi, et al.

The Journal of Clinical Investigation|September 25, 2019

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorderValentina Del Dotto, Farid Ullah, Ivano Di Meo, et al.

Nature Communications|June 18, 2020

Recurrent horizontal transfer identifies mitochondrial positive selection in a transmissible cancerAndrea Strakova, Thomas J Nicholls, Adrian Baez-Ortega, et al.

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Search research articles

Showing results (101-110 of 104) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 104 results.

EMBO Molecular Medicine|April 4, 2023

Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stabilityDirenis Erdinc, Alejandro Rodríguez-Luis, Mahmoud R Fassad, et al.

Nature Communications|February 19, 2021

POLRMT mutations impair mitochondrial transcription causing neurological diseaseMonika Oláhová, Bradley Peter, Zsolt Szilagyi, et al.

The Journal of Clinical Investigation|September 25, 2019

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorderValentina Del Dotto, Farid Ullah, Ivano Di Meo, et al.

Nature Communications|June 18, 2020

Recurrent horizontal transfer identifies mitochondrial positive selection in a transmissible cancerAndrea Strakova, Thomas J Nicholls, Adrian Baez-Ortega, et al.

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