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1. Mitochondrial tRNA variants in 811 Chinese probands with Leber's hereditary optic neuropathy.

2. Mitochondrial tRNA mutations in 887 Chinese subjects with hearing loss.

3. Molecular dynamics simulations on apo ADP/ATP carrier shed new lights on the featured motif of the mitochondrial carriers.

4. A deafness-associated mitochondrial DNA mutation altered the tRNA Ser(UCN) metabolism and mitochondrial function.

5. Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNA Thr in eight Chinese pedigrees.

6. Late onset nonsyndromic hearing loss in a Dongxiang Chinese family is associated with the 593T>C variant in the mitochondrial tRNA Phe gene.

7. Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertension.

8. Mitochondrial tRNA(Ser(UCN)) variants in 2651 Han Chinese subjects with hearing loss.

9. Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene.

10. Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families.

11. Loss of MED1 triggers mitochondrial biogenesis in C2C12 cells.

12. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families.

13. Mitochondrial tRNA mutations associated with deafness.

14. The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation.

15. Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity.

16. Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss.

17. Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.

18. Mutation in MTO1 involved in tRNA modification impairs mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae.

19. Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.

20. Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family.

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