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Issues in Mental Health Nursing
|
January 14, 2000
Research priorities in mental health nursing
L Pullen, I Tuck, D C Wallace
Proceedings of the National Academy of Sciences of the United States of America
|
August 30, 1994
Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio
I Trounce, S Neill, D C Wallace
Nature
|
September 17, 1987
Conformational mutations in human mitochondrial DNA
G Singh, N Neckelmann, D C Wallace
The New England Journal of Medicine
|
May 18, 1989
A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy
G Singh, M T Lott, D C Wallace
American Journal of Physical Anthropology
|
October 1, 1985
Dramatic founder effects in Amerindian mitochondrial DNAs
D C Wallace, K Garrison, W C Knowler
Nucleic Acids Research
|
November 11, 1981
Different nucleotide changes in the large rRNA gene of the mitochondrial DNA confer chloramphenicol resistance on two human cell lines
H Blanc, C W Adams, D C Wallace
The Journal of Biological Chemistry
|
November 25, 1990
OXBOX, a positive transcriptional element of the heart-skeletal muscle ADP/ATP translocator gene
K Li, J A Hodge, D C Wallace
American Journal of Human Genetics
|
February 1, 1997
Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage
M D Brown, F Sun, D C Wallace
Mutation Research
|
September 16, 1999
Mouse models of mitochondrial disease, oxidative stress, and senescence
S Melov, P E Coskun, D C Wallace
Somatic Cell Genetics
|
July 1, 1980
Characterization of mitochondrial DNA in chloramphenicol-resistant interspecific hybrids and a cybrid
R E Giles, I Stroynowski, D C Wallace
Page
of 26
Search research articles
Search
Showing results (71-80 of 258) with videos related to
Sort By:
Page
of 26
Issues in Mental Health Nursing
|
January 14, 2000
Research priorities in mental health nursing
L Pullen, I Tuck, D C Wallace
Proceedings of the National Academy of Sciences of the United States of America
|
August 30, 1994
Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio
I Trounce, S Neill, D C Wallace
Nature
|
September 17, 1987
Conformational mutations in human mitochondrial DNA
G Singh, N Neckelmann, D C Wallace
The New England Journal of Medicine
|
May 18, 1989
A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy
G Singh, M T Lott, D C Wallace
American Journal of Physical Anthropology
|
October 1, 1985
Dramatic founder effects in Amerindian mitochondrial DNAs
D C Wallace, K Garrison, W C Knowler
Nucleic Acids Research
|
November 11, 1981
Different nucleotide changes in the large rRNA gene of the mitochondrial DNA confer chloramphenicol resistance on two human cell lines
H Blanc, C W Adams, D C Wallace
The Journal of Biological Chemistry
|
November 25, 1990
OXBOX, a positive transcriptional element of the heart-skeletal muscle ADP/ATP translocator gene
K Li, J A Hodge, D C Wallace
American Journal of Human Genetics
|
February 1, 1997
Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage
M D Brown, F Sun, D C Wallace
Mutation Research
|
September 16, 1999
Mouse models of mitochondrial disease, oxidative stress, and senescence
S Melov, P E Coskun, D C Wallace
Somatic Cell Genetics
|
July 1, 1980
Characterization of mitochondrial DNA in chloramphenicol-resistant interspecific hybrids and a cybrid
R E Giles, I Stroynowski, D C Wallace
Page
of 26