184 results on '"Horai, S."'
Search Results
2. Severe lactic acidosis and neonatal death in Pearson syndrome
3. HLA-A, HLA-B, and HLA-DRB1 alleles and haplotypes in Naxi and Han populations in southwestern China (Yunnan province)
4. The geographic distribution of human Y chromosome variation
5. A new type of mitochondrial DNA deletion in patients with encephalomyopathy
6. In situ hybridization of muscle mitochondrial mRNA in mitochondrial myopathies
7. Shoots formation by rhizome culture of Anemone keiskeana©
8. Differently deleted mitochondrial genomes in maternally inherited chronic progressive external ophthalmoplegia
9. Evolutionary Implications of Mitochondrial DNA Polymorphism in Human Populations
10. Differential enzyme activities in human esterase D phenotypes
11. PD-1/PD-L1 expression in human T-cell leukemia virus type 1 carriers and adult T-cell leukemia/lymphoma patients
12. Dynamical Calling Behavior Experimentally Observed in Japanese Tree Frogs (Hyla japonica)
13. Mitochondrial DNA polymorphisms in Yunnan nationalities in China
14. Mitochondrial DNA polymorphisms in Thailand
15. Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications
16. Molecular phylogeny of macaques: implications of nucleotide sequences from an 896-base pair region of mitochondrial DNA
17. Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs.
18. Enzymatic and genetic adaptation of soleus muscle mitochondria to physical training in rats
19. A Caucasian Family with the 3271 Mutation in Mitochondrial DNA
20. A New Point Mutation at Nucleotide Pair-3291 of the Mitochondrial Transfer-RNALeu(Uur) Gene in a Patient with Mitochondrial Myopathy, Encephalopathy, Lactic-Acidosis, and Stroke-Like Episodes (MELAS)
21. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS)
22. A new congenital muscular dystrophy with mitochondrial structural abnormalities.
23. Seroepidemiological survey of human T-lymphotropic retrovirus among indigenous populations in Taiwan.
24. Differential recognition of the serologically defined HLA-A2 antigen by allogeneic cytotoxic T Cells
25. Polymorphism of the HLA-DRB1 Locus in Colombian, Ecuadorian, and Chilean Amerinds
26. Peopling of the Americas, founded by four major lineages of mitochondrial DNA.
27. A New Point Mutation at Nucleotide Pair-3291 of the Mitochondrial Transfer-RNALeu(Uur)Gene in a Patient with Mitochondrial Myopathy, Encephalopathy, Lactic-Acidosis, and Stroke-Like Episodes (MELAS)
28. Mitochondrial myopathy encephalopathy lactic acidosis and strokelike episodes MELAS
29. Heteroplasmy and polymorphism in the major noncoding region of mitochondrial DNA in Japanese monkeys: association with tandemly repeated sequences.
30. Phylogenetic relationships among Japanese, rhesus, Formosan, and crab-eating monkeys, inferred from restriction-enzyme analysis of mitochondrial DNAs.
31. Molecular phylogeny and evolution of primate mitochondrial DNA.
32. Differential recognition of the serologically defined HLA-A2 antigen by allogeneic cytotoxic T cells
33. Detection of platelet antibodies by enzyme-linked immunosorbent assay (ELISA). Comparative studies with the indirect immunofluorescence assay
34. Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndrome
35. The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).
36. Mitochondrial DNA mutation and Leigh's syndrome.
37. Mitochondrial DNA mutations at nucleotide positions 3243 and 3271 in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: a comparative study
38. Environmental monitoring of trace elements and evaluation of environmental impacts to organisms near a former uranium mining site in Nigyo-toge, Japan.
39. Concentrations of nucleophilic sulfur species in small Indian mongoose (Herpestes auropunctatus) in Okinawa, Japan.
40. Forecasting wind power ramps with prediction coordinates.
41. The fate of methylmercury through the formation of bismethylmercury sulfide as an intermediate in mice.
42. Concentration ratios of 238U and 226Ra for insects and amphibians living in the vicinity of the closed uranium mine at Ningyo-toge, Japan.
43. Simultaneous total analysis of core and polar membrane lipids in archaea by high-performance liquid chromatography/high-resolution mass spectrometry coupled with heated electrospray ionization.
44. Deepest and hottest hydrothermal activity in the Okinawa Trough: the Yokosuka site at Yaeyama Knoll.
45. Facile analysis of contents and compositions of the chondroitin sulfate/dermatan sulfate hybrid chain in shark and ray tissues.
46. Clinical significance of CD70 expression on T cells in human T-lymphotropic virus type-1 carriers and adult T cell leukemia/ lymphoma patients.
47. Parsimonious description for predicting high-dimensional dynamics.
48. Establishment of a primary hepatocyte culture from the small Indian mongoose (Herpestes auropunctatus) and distribution of mercury in liver tissue.
49. Concentrations of trace elements in American alligators (Alligator mississippiensis) from Florida, USA.
50. Hepatocyte growth factor enhances the barrier function in primary cultures of rat brain microvascular endothelial cells.
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