32 results on '"Inoue, Kimiko"'
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2. Loss of H3K27me3 Imprinting in Somatic Cell Nuclear Transfer Embryos Disrupts Post-Implantation Development
3. Histone H3 Methylated at Arginine 17 Is Essential for Reprogramming the Paternal Genome in Zygotes
4. The Rodent-Specific MicroRNA Cluster within the Sfmbt2 Gene Is Imprinted and Essential for Placental Development
5. Mouse D1Pas1, a DEAD-box RNA helicase, is required for the completion of first meiotic prophase in male germ cells
6. Impact of glucocerebrosidase mutations on motor and nonmotor complications in Parkinson's disease
7. Functional Differences between GDNF-Dependent and FGF2-Dependent Mouse Spermatogonial Stem Cell Self-Renewal
8. Histone Variants Enriched in Oocytes Enhance Reprogramming to Induced Pluripotent Stem Cells
9. Naive-like Conversion Overcomes the Limited Differentiation Capacity of Induced Pluripotent Stem Cells
10. ROS Are Required for Mouse Spermatogonial Stem Cell Self-Renewal
11. Reconstitution of Mouse Spermatogonial Stem Cell Niches in Culture
12. Intracytoplasmic sperm injection induces transcriptome perturbation without any transgenerational effect
13. P39. Enhancer of Polycomb 1 is essential for spermiogenesis by regulating histone hyperacetylation status
14. Generation of Induced Pluripotent Stem Cells in Rabbits
15. Stable embryonic stem cell lines in rabbits: potential small animal models for human research
16. Production of knockout mice by gene targeting in multipotent germline stem cells
17. Centromeric DNA hypomethylation as an epigenetic signature discriminates between germ and somatic cell lineages
18. Chorioallantoic placenta defects in cloned mice
19. Generation of Cloned Mice by Direct Nuclear Transfer from Natural Killer T Cells
20. Generation of Pluripotent Stem Cells from Neonatal Mouse Testis
21. Epigenetic regulation in mammalian development and dysfunction: the effects of somatic cloning and genomic imprinting
22. Mito-mice: animal models for mitochondrial DNA-based diseases
23. Interaction Theory of Mammalian Mitochondria
24. Correlation of Functional and Ultrastructural Abnormalities of Mitochondria in Mouse Heart Carrying a Pathogenic Mutant mtDNA with a 4696-bp Deletion
25. Homozygosity Mapping to Chromosome 5p15 of a Gene Responsible for Hartnup Disorder
26. Long-Term Postmortem Survival of Mitochondrial Genomes in Mouse Synaptosomes and Their Rescue in a Mitochondrial DNA-less Mouse Cell Line
27. Isolation and Characterization of Mitochondrial DNA-less Lines from Various Mammalian Cell Lines by Application of an Anticancer Drug, Ditercalinium
28. Isolation of Mitochondrial DNA-less Mouse Cell Lines and Their Application for Trapping Mouse Synaptosomal Mitochondrial DNA with Deletion Mutations
29. Identification of Inheritance Modes of Mitochondrial Diseases by Introduction of Pure Nuclei from mtDNA-less HeLa Cells to Patient-derived Fibroblasts
30. The Interorganellar Interaction between Distinct Human Mitochondria with Deletion Mutant mtDNA from a Patient with Mitochondrial Disease and with HeLa mtDNA
31. Mitochondrial DNA Is Required for Regulation of Glucose-stimulated Insulin Secretion in a Mouse Pancreatic Beta Cell Line, MIN6
32. Mutant mtDNA at 1555 A to G in 12S rRNA Gene and Hypersusceptibility of Mitochondrial Translation to Streptomycin Can Be Co-Transferred to ρ0HeLa Cells
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