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The Journal of Clinical Investigation
|
December 1, 1993
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
C T Moraes, F Ciacci, E Bonilla, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
September 1, 1994
Sequencing of heparan sulfate proteoglycans: identification of variable and constant oligosaccharide regions in eight heparan sulfate proteoglycans of different origins
I L Tersariol, T M Ferreira, M G Medeiros, et al.
Revue Neurologique
|
January 1, 1991
Mitochondrial encephalomyopathies: biochemical approach
S Dimauro, C T Moraes, S Shanske, et al.
Cloning
|
October 13, 2005
Cloning of an endangered species (Bos gaurus) using interspecies nuclear transfer
R P Lanza, J B Cibelli, F Diaz, et al.
Neurology
|
January 1, 1992
Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA
H J Tritschler, F Andreetta, C T Moraes, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 14, 1999
Sequence analysis of the diabetes-protective human leukocyte antigen-DQB1*0602 allele in unaffected, islet cell antibody-positive first degree relatives and in rare patients with type 1 diabetes
A Pugliese, E Kawasaki, M Zeller, et al.
Neurology
|
October 23, 2002
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA
M Mancuso, L Salviati, S Sacconi, et al.
Nature Communications
|
July 23, 2020
Mitochondrial respiration controls neoangiogenesis during wound healing and tumour growth
L M Schiffmann, J P Werthenbach, F Heintges-Kleinhofer, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 88) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 88 results.
The Journal of Clinical Investigation
|
December 1, 1993
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
C T Moraes, F Ciacci, E Bonilla, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
September 1, 1994
Sequencing of heparan sulfate proteoglycans: identification of variable and constant oligosaccharide regions in eight heparan sulfate proteoglycans of different origins
I L Tersariol, T M Ferreira, M G Medeiros, et al.
Revue Neurologique
|
January 1, 1991
Mitochondrial encephalomyopathies: biochemical approach
S Dimauro, C T Moraes, S Shanske, et al.
Cloning
|
October 13, 2005
Cloning of an endangered species (Bos gaurus) using interspecies nuclear transfer
R P Lanza, J B Cibelli, F Diaz, et al.
Neurology
|
January 1, 1992
Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA
H J Tritschler, F Andreetta, C T Moraes, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 14, 1999
Sequence analysis of the diabetes-protective human leukocyte antigen-DQB1*0602 allele in unaffected, islet cell antibody-positive first degree relatives and in rare patients with type 1 diabetes
A Pugliese, E Kawasaki, M Zeller, et al.
Neurology
|
October 23, 2002
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA
M Mancuso, L Salviati, S Sacconi, et al.
Nature Communications
|
July 23, 2020
Mitochondrial respiration controls neoangiogenesis during wound healing and tumour growth
L M Schiffmann, J P Werthenbach, F Heintges-Kleinhofer, et al.
Page
of 9