342 results on '"Nakada, Kazuto"'
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2. Author Response: Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment
3. Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment
4. Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment
5. Author Response: Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment
6. A high mutation load of m.14597A>G in MT-ND6 causes Leigh syndrome
7. Gene Therapy for Progeny of Mito-Mice Carrying Pathogenic mtDNA by Nuclear Transplantation
8. Rare Creation of Recombinant mtDNA Haplotypes in Mammalian Tissues
9. A novel mutation in TAZ causes mitochondrial respiratory chain disorder without cardiomyopathy
10. Pearson syndrome-like anemia induced by accumulation of mutant mtDNA and anemia with imbalanced white blood cell lineages induced by Drp1 deletion in a murine model
11. Transmitochondrial mice as models for primary prevention of diseases caused by mutation in the tRNALys gene
12. Aberrant RNA processing contributes to the pathogenesis of mitochondrial diseases in trans-mitochondrial mouse model carrying mitochondrial tRNALeu(UUR) with a pathogenic A2748G mutation
13. TFB2M and POLRMT are essential for mammalian mitochondrial DNA replication
14. Specific mitochondrial DNA mutation in mice regulates diabetes and lymphoma development
15. ROS-Generating Mitochondrial DNA Mutations Can Regulate Tumor Cell Metastasis
16. TFB2M and POLRMT are essential for mammalian mitochondrial DNA replication
17. Mitochondrial DNA deletion-dependent podocyte injuries in Mito-miceΔ, a murine model of mitochondrial disease
18. Mitochondria-Related Male Infertility
19. Mitochondrial DNA mutations are involved in the acquisition of cisplatin resistance in human lung cancer A549 cells
20. Comprehensive application of an mtDsRed2-Tg mouse strain for mitochondrial imaging
21. Attempts to understand the mechanisms of mitochondrial diseases: The reverse genetics of mouse models for mitochondrial disease
22. Deletion-mutant mtDNA increases in somatic tissues but decreases in female germ cells with age
23. Mito-mice∆ and mitochondrial Mito-mice∆ and mitochondrial DNA mutator mice as models of human osteoporosis caused not by aging but by hyperparathyroidism
24. Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment
25. Neuronal degeneration and cognitive impairment can be prevented via the normalization of mitochondrial dynamics
26. Ditercalinium chloride, a pro-anticancer drug, intimately associates with mammalian mitochondrial DNA and inhibits its replication
27. In vivo interaction between mitochondria carrying mtDNAs from different mouse species
28. Immunohistochemical studies on regulation of alternative splicing of fast skeletal muscle troponin T: non-uniform distribution of the exon x3 epitope in a single muscle fiber
29. The structure of the avian fast skeletal muscle troponin T gene: seven novel tandem-arranged exons in the exon x region
30. Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA
31. Distal control of mitochondrial biogenesis and respiratory activity by extracellular lactate caused by large-scale deletion of mitochondrial DNA
32. The accessory subunit of human DNA polymerase γ is required for mitochondrial DNA maintenance and is able to stabilize the catalytic subunit
33. Lactic acidemia in the pathogenesis of mice carrying mitochondrial DNA with a deletion
34. p62/SQSTM1 cooperates with Parkin for perinuclear clustering of depolarized mitochondria
35. Skeletal muscle regeneration induced by chorio-allantoic grafting
36. Mitochondrial complementation preventing respiratory dysfunction caused by mutant mtDNA
37. Suppression of disease phenotypes of adult mito-mice carrying pathogenic mtDNA by bone marrow transplantation
38. Generation of trans-mitochondrial mice carrying homoplasmic mtDNAs with a missense mutation in a structural gene using ES cells
39. Determination of Normal Ranges of Mitochondrial Respiratory Activities by mtDNA Transfer from 54 Human Subjects to mtDNA-less HeLa Cells for Identification of the Pathogenicities of Mutated mtDNAs
40. Expression of multiple troponin T isoforms in chicken breast muscle regeneration induced by sub-serous implantation
41. Disruption of the mouse Shmt2 gene confers embryonic anaemia via foetal liver-specific metabolomic disorders
42. Diabetic conditions induce intolerance to accumulation of pathogenic mitochondrial DNAs
43. Concentration of mitochondrial DNA mutations by cytoplasmic transfer from platelets to cultured mouse cells
44. Acquired expression of mutant Mitofusin 2 causes progressive neurodegeneration and abnormal behavior
45. G7731A mutation in mouse mitochondrial tRNALys regulates late-onset disorders in transmitochondrial mice
46. Normal mitochondrial respiratory function is essential for spatial remote memory in mice
47. Administration of an Antioxidant Prevents Lymphoma Development in Transmitochondrial Mice Overproducing Reactive Oxygen Species
48. Mice deficient in the Shmt2 gene have mitochondrial respiration defects and are embryonic lethal
49. Mito-mice∆ and mitochondrial DNA mutator mice as models of human osteoporosis caused not by aging but by hyperparathyroidism
50. RLR-mediated antiviral innate immunity requires oxidative phosphorylation activity
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