Suchergebnisse - "Copeland, William"

PubPharm (20)

1

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

enthalten in: Human molecular genetics | 2015

von Young, M. | Humble, M. | DeBalsi, K. | +2

2

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

enthalten in: Human molecular genetics | 2015

von Young, M. | Humble, M. | DeBalsi, K. | +2

3

POLG2disease variants: analyses reveal a dominant negative heterodimer, altered mitochondrial localization and impaired respiratory capacity

enthalten in: Human molecular genetics | 2015

von Young, M. | Humble, M. | DeBalsi, K. | +2

4

Mutations in human DNA polymerase γ confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients

enthalten in: Human molecular genetics | 2013

von Sohl, C. | Kasiviswanathan, R. | Copeland, W. | +1

5

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

enthalten in: Human molecular genetics | 2013

von Humble, M. | Young, M. | Foley, J. | +3

6

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

enthalten in: Human molecular genetics | 2013

von Humble, M. | Young, M. | Foley, J. | +3

7

Biochemical analysis of human POLG2 variants associated with mitochondrial disease

enthalten in: Human molecular genetics | 2011

von Young, M. | Longley, M. | Li, F. | +3

8

Biochemical analysis of human POLG2 variants associated with mitochondrial disease

enthalten in: Human molecular genetics | 2011

von Young, M. | Longley, M. | Li, F. | +3

9

mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae

enthalten in: Human molecular genetics | 2010

von Stumpf, J. | Bailey, C. | Spell, D. | +3

10

mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae

enthalten in: Human molecular genetics | 2010

von Stumpf, J. | Bailey, C. | Spell, D. | +3