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1. ANGEL2 phosphatase activity is required for non-canonical mitochondrial RNA processing.

2. Pathogenic SLC25A26 variants impair SAH transport activity causing mitochondrial disease.

3. Severe congenital lactic acidosis and hypertrophic cardiomyopathy caused by an intronic variant in NDUFB7.

4. Case Report: A Novel Mutation in the Mitochondrial MT-ND5 Gene Is Associated With Leber Hereditary Optic Neuropathy (LHON).

5. Novel Mutation m.10372A>G in MT-ND3 Causing Sensorimotor Axonal Polyneuropathy.

6. Quantitative Proteomics in Drosophila with Holidic Stable-Isotope Labeling of Amino Acids in Fruit Flies (SILAF).

7. FBXL4 deficiency increases mitochondrial removal by autophagy.

8. C6orf203 is an RNA-binding protein involved in mitochondrial protein synthesis.

9. Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivo.

10. TEFM regulates both transcription elongation and RNA processing in mitochondria.

11. SQSTM1/p62-Directed Metabolic Reprogramming Is Essential for Normal Neurodifferentiation.

12. A multi-systemic mitochondrial disorder due to a dominant p.Y955H disease variant in DNA polymerase gamma.

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