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7. List of Contributors

16. Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration

18. A Model-Based Strategy on COVID-19 Vaccine Roll-out in the Philippines

24. The isolated carboxy‐terminal domain of human mitochondrial leucyl‐tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells

26. RCC1L (WBSCR16) isoforms coordinate mitochondrial ribosome assembly through their interaction with GTPases

27. Correction to ‘DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion’

29. DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion (vol 49, pg 5230, 2021)

30. DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion

34. MPV17L2 is required for ribosome assembly in mitochondria

35. DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion

43. Biased incorporation of ribonucleotides on the mitochondrial L-strand accounts for apparent strand-asymmetric DNA replication

47. In vivo and in vitro mechanistic characterization of a clinically relevant PolγA mutation

49. Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features

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