Results 191 to 200 of about 12,888 (214)
Some of the next articles are maybe not open access.
Molecular and biochemical parasitology, 2019
Unequal usage of synonymous codons in the gene transcript for an amino acid is known as codon usage bias (CUB). It is a unique property of gene as well as genome. Mutation and natural selection are known to be the major factors that influence CUB.
Gulshana A, Mazumder +2 more
openaire +1 more source
Unequal usage of synonymous codons in the gene transcript for an amino acid is known as codon usage bias (CUB). It is a unique property of gene as well as genome. Mutation and natural selection are known to be the major factors that influence CUB.
Gulshana A, Mazumder +2 more
openaire +1 more source
Mitochondrion, 2019
Elevations of specific acylcarnitines in blood reflect carboxylase deficiencies, and have utility in newborn screening for life-threatening organic acidemias and other inherited metabolic diseases. In this report, we describe a newly-identified association of biochemical features of multiple carboxylase deficiency in individuals harboring mitochondrial
Austin A. Larson +17 more
openaire +2 more sources
Elevations of specific acylcarnitines in blood reflect carboxylase deficiencies, and have utility in newborn screening for life-threatening organic acidemias and other inherited metabolic diseases. In this report, we describe a newly-identified association of biochemical features of multiple carboxylase deficiency in individuals harboring mitochondrial
Austin A. Larson +17 more
openaire +2 more sources
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations
Neurology, 2013To report that homoplasmic deleterious mutations in the mitochondrial DNA MT-ATP6/8 genes may be responsible for acute episodes of limb weakness mimicking periodic paralysis due to channelopathies and dramatically responding to acetazolamide.Mitochondrial DNA sequencing and restriction PCR, oxidative phosphorylation functional assays, reactive oxygen ...
Karine, Auré +16 more
openaire +2 more sources
The wheat mitochondrial rps13 gene: RNA editing and co-transcription with the atp6 gene
Current Genetics, 1997Northern analyses and reverse transcription-polymerase chain-reaction (RT-PCR) experiments, followed by PCR amplification product sequencing, were performed on total mitochondrial (mt) RNAs from wheat seedlings and tissue cultures. It was shown that the rps13 gene, which encodes ribosomal protein S13, and the atp6 gene, which encodes subunit 6 of the ...
A, Takvorian +4 more
openaire +2 more sources
Unlocking atp6 gene variation in Allium species
2023Yeswanth Mahidar Gowd +4 more
openaire +1 more source
A MT-ATP6 Mutation Causes a Slowly Progressive Myeloneuropathy
Journal of Neuromuscular Diseases, 2019Tanya, Bardakjian, Steven S, Scherer
openaire +3 more sources
Allelic variability and transferability of atp6 gene among Allium species
Genetic Resources and Crop Evolution, 2022Talamarla Yeswanth Mahidar Gowd +5 more
openaire +1 more source
Genotype-phenotype analysis of MT-ATP6-associated Leigh syndrome
Acta Neurologica Scandinavica, 2022Ji-Hoon Na, Young Mok Lee
exaly

