Search research articles
Contact Us
Filters
Showing results (31-40 of 59) with videos related to
Page
of 6
Sort By:
Human Molecular Genetics
|
March 1, 1997
Molecular phenotype of a human lymphoblastoid cell-line homoplasmic for the np 7445 deafness-associated mitochondrial mutation
F M Reid, A Rovio, I J Holt, et al.
Journal of Molecular Biology
|
July 20, 1988
Nucleotide sequence and gene organization of sea urchin mitochondrial DNA
H T Jacobs, D J Elliott, V B Math, et al.
Human Molecular Genetics
|
November 18, 1998
Mitochondrial tRNALeu isoforms in lung carcinoma cybrid cells containing the np 3243 mtDNA mutation
A El Meziane, S K Lehtinen, I J Holt, et al.
Clinical Otolaryngology and Allied Sciences
|
August 1, 1994
Bilateral sensorineural hearing loss in members of a maternal lineage with mitochondrial point mutation
G A Vernham, F M Reid, P A Rundle, et al.
FEBS Letters
|
September 21, 2000
The mitochondrial inner membrane AAA metalloprotease family in metazoans
M K Juhola, Z H Shah, L A Grivell, et al.
EMBO Reports
|
November 20, 2001
Prominent mitochondrial DNA recombination intermediates in human heart muscle
O A Kajander, P J Karhunen, I J Holt, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 3, 1995
Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes
D R Dunbar, P A Moonie, H T Jacobs, et al.
Gene
|
January 20, 1998
Metazoan nuclear genes for mitoribosomal protein S12
Z H Shah, K M O'Dell, S C Miller, et al.
Current Genetics
|
March 1, 1989
Conserved tRNA gene cluster in starfish mitochondrial DNA
H T Jacobs, S Asakawa, T Araki, et al.
Nature Medicine
|
September 2, 1999
The dangers of extended PCR in the clinic
O A Kajander, J Poulton, J N Spelbrink, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 59) with videos related to
Sort By:
Page
of 6
Human Molecular Genetics
|
March 1, 1997
Molecular phenotype of a human lymphoblastoid cell-line homoplasmic for the np 7445 deafness-associated mitochondrial mutation
F M Reid, A Rovio, I J Holt, et al.
Journal of Molecular Biology
|
July 20, 1988
Nucleotide sequence and gene organization of sea urchin mitochondrial DNA
H T Jacobs, D J Elliott, V B Math, et al.
Human Molecular Genetics
|
November 18, 1998
Mitochondrial tRNALeu isoforms in lung carcinoma cybrid cells containing the np 3243 mtDNA mutation
A El Meziane, S K Lehtinen, I J Holt, et al.
Clinical Otolaryngology and Allied Sciences
|
August 1, 1994
Bilateral sensorineural hearing loss in members of a maternal lineage with mitochondrial point mutation
G A Vernham, F M Reid, P A Rundle, et al.
FEBS Letters
|
September 21, 2000
The mitochondrial inner membrane AAA metalloprotease family in metazoans
M K Juhola, Z H Shah, L A Grivell, et al.
EMBO Reports
|
November 20, 2001
Prominent mitochondrial DNA recombination intermediates in human heart muscle
O A Kajander, P J Karhunen, I J Holt, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 3, 1995
Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes
D R Dunbar, P A Moonie, H T Jacobs, et al.
Gene
|
January 20, 1998
Metazoan nuclear genes for mitoribosomal protein S12
Z H Shah, K M O'Dell, S C Miller, et al.
Current Genetics
|
March 1, 1989
Conserved tRNA gene cluster in starfish mitochondrial DNA
H T Jacobs, S Asakawa, T Araki, et al.
Nature Medicine
|
September 2, 1999
The dangers of extended PCR in the clinic
O A Kajander, J Poulton, J N Spelbrink, et al.
Page
of 6