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Annals of Neurology
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November 26, 2002
Coenzyme Q-responsive Leigh's encephalopathy in two sisters
Lionel Van Maldergem, Frans Trijbels, Salvatore DiMauro, et al.
Journal of Child Neurology
|
December 7, 2000
G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome
A Shtilbans, S Shanske, S Goodman, et al.
American Journal of Human Genetics
|
May 1, 1996
Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A)
F M Santorelli, S C Mak, M El-Schahawi, et al.
Annals of Neurology
|
August 1, 1997
Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene
F M Santorelli, K Tanji, M Sano, et al.
Annals of Neurology
|
June 1, 1993
Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA
W D Graf, S M Sumi, M K Copass, et al.
Plos One
|
May 9, 2014
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck
Francesco Pallotti, Giorgio Binelli, Raffaella Fabbri, et al.
RSC Medicinal Chemistry
|
May 24, 2024
Live cell screening to identify RNA-binding small molecule inhibitors of the pre-let-7-Lin28 RNA-protein interaction
Sydney L Rosenblum, Dalia M Soueid, George Giambasu, et al.
Clinical Genetics
|
January 29, 2016
Cerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3
E Barca, O Musumeci, F Montagnese, et al.
Nature Communications
|
August 9, 2014
Diffraction using laser-driven broadband electron wave packets
Junliang Xu, Cosmin I Blaga, Kaikai Zhang, et al.
Biochemistry
|
November 14, 2014
Acetylation of Gly1 and Lys2 promotes aggregation of human γD-crystallin
Michael A DiMauro, Sandip K Nandi, Cibin T Raghavan, et al.
Page
of 95
Search research articles
Search
Showing results (631-640 of 942) with videos related to
Sort By:
Page
of 95
Annals of Neurology
|
November 26, 2002
Coenzyme Q-responsive Leigh's encephalopathy in two sisters
Lionel Van Maldergem, Frans Trijbels, Salvatore DiMauro, et al.
Journal of Child Neurology
|
December 7, 2000
G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome
A Shtilbans, S Shanske, S Goodman, et al.
American Journal of Human Genetics
|
May 1, 1996
Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A)
F M Santorelli, S C Mak, M El-Schahawi, et al.
Annals of Neurology
|
August 1, 1997
Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene
F M Santorelli, K Tanji, M Sano, et al.
Annals of Neurology
|
June 1, 1993
Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA
W D Graf, S M Sumi, M K Copass, et al.
Plos One
|
May 9, 2014
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck
Francesco Pallotti, Giorgio Binelli, Raffaella Fabbri, et al.
RSC Medicinal Chemistry
|
May 24, 2024
Live cell screening to identify RNA-binding small molecule inhibitors of the pre-let-7-Lin28 RNA-protein interaction
Sydney L Rosenblum, Dalia M Soueid, George Giambasu, et al.
Clinical Genetics
|
January 29, 2016
Cerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3
E Barca, O Musumeci, F Montagnese, et al.
Nature Communications
|
August 9, 2014
Diffraction using laser-driven broadband electron wave packets
Junliang Xu, Cosmin I Blaga, Kaikai Zhang, et al.
Biochemistry
|
November 14, 2014
Acetylation of Gly1 and Lys2 promotes aggregation of human γD-crystallin
Michael A DiMauro, Sandip K Nandi, Cibin T Raghavan, et al.
Page
of 95