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1. Clinical, neuroradiological, and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder

2. Cellular allostatic load is linked to increased energy expenditure and accelerated biological aging

3. Cardiac Outcomes in Adults With Mitochondrial Diseases

4. Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disorders

6. The cytokine profile of follicular fluid changes during ovarian ageing

7. Metabolomics reveals highly regional specificity of cerebral sexual dimorphism in mice

9. Warburg-like effect is a hallmark of complex I assembly defects

10. eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing data

11. Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion

14. Study of mitochondrial function in placental insufficiency

15. The accumulation of assembly intermediates of the mitochondrial complex I matrix arm is reduced by limiting glucose uptake in a neuronal-like model of MELAS syndrome

17. Placental Multi-Omics Data-Mining in Intrauterine Growth Restriction

18. International Workshop

20. The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model

21. Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy

22. Ketogenic Diet alleviates mitochondrial dysfunction in MELAS syndrome by restoring complex I assembly and activity

24. OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology

25. Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome

26. Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency

28. Mitochondrial Disease Sequence Data Resource (MSeqDR): A global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities

29. Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

31. Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells

33. Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELAS

35. Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome

36. Mitochondrial dysfunction and pathophysiology of Charcot–Marie–Tooth disease involving GDAP1 mutations

37. Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation

38. Yeast models of ATPase-based diseases

41. Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity

43. OPA1-associated disorders: Phenotypes and pathophysiology

44. A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b gene

49. 76 Biochemical study of complex i deficient patient cell lines

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