Matthew J. Young

发表

Biochemical analysis of human POLG2 variants associated with mitochondrial disease.

L. Wong, R. Kasiviswanathan, W. Copeland, 2011, Human molecular genetics.

Polg2 is essential for mammalian embryogenesis and is required for mtDNA maintenance.

J. Foley, A. Pandiri, W. Copeland, 2013, Human molecular genetics.

Suppression of p65 phosphorylation coincides with inhibition of IκBα polyubiquitination and degradation

N. Colburn, Mohammed Haseebuddin, Matthew J. Young, 2005 .

Suppression of p65 phosphorylation coincides with inhibition of IkappaBalpha polyubiquitination and degradation.

N. Colburn, Mohammed Haseebuddin, Matthew J. Young, 2005, Molecular carcinogenesis.

Off-Target Effects of Drugs that Disrupt Human Mitochondrial DNA Maintenance

Matthew J. Young, 2017, Front. Mol. Biosci..

A p.R369G POLG2 mutation associated with adPEO and multiple mtDNA deletions causes decreased affinity between polymerase γ subunits.

Robert W. Taylor, D. Turnbull, W. Copeland, 2012, Mitochondrion.

Observation on the ultrastructure morphology of HeLa cells treated with ethanol: Statistical analysis

S. Yao, M. Yoshimura, Matthew J. Young, 2016, Ultrastructural pathology.

POLG2 disease variants: analyses reveal a dominant negative heterodimer, altered mitochondrial localization and impaired respiratory capacity.

Kathie Y Sun, K. DeBalsi, W. Copeland, 2015, Human molecular genetics.

Purification and functional characterization of human mitochondrial DNA polymerase gamma harboring disease mutations.

R. Kasiviswanathan, W. Copeland, M. Longley, 2010, Methods.