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Humans with pulmonary arterial hypertension display a global hypermethylation signature that worsens in patients who have a mutation in the gene encoding the methylation eraser, Tet methylcytosine dioxygenase 2 (TET2)

This substantiates the evidence that the spared white matter holds the key to the functional motor recovery of the hind limbs after SCI and is closely correlated with the functional restoration of the paralyzed hind limbs [50,51,52]

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These two residues are part of the oxyanion hole

Glutaric aciduria type 1: Insights into diagnosis and neurogenetic outcomes

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