143 results on '"Ohye, T."'
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2. Virological analysis of inherited chromosomally integrated human herpesvirus-6 in three hematopoietic stem cell transplant patients
3. Nine-year follow-up in a child with chromosomal integration of human herpesvirus 6 transmitted from an unrelated donor through the Japan Marrow Donor Program
4. The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements
5. Quantification of mRNA of tyrosine hydroxylase and aromatic L-amino acid decarboxylase in the substantia nigra in Parkinson's disease and schizophrenia
6. High accuracy calculation of magnetic field by improved 3-D boundary magnetic charge method
7. High accuracy calculation of electric field in composite dielectric system by improved 3-D boundary charge method
8. Identification of an enhancer region for immune activation in the human GTP cyclohydrolase i gene
9. Localization of sepiapterin reductase in the human brain
10. Characterization of wild-type and mutants of recombinant human GTP cyclohydrolase I: Relationship to etiology of dopa-responsive dystonia
11. A new splicing variant for human tyrosine hydroxylase in the adrenal medulla
12. DOPA-responsive dystonia. From causative gene to molecular mechanism
13. Catecholamines and serotonin are differently regulated by tetrahydrobiopterin. A study from 6-pyruvoyltetrahydropterin synthase knockout mice
14. The relation between metabolism of biopterin and dystonia-parkinsonism
15. Molecular aspects of the dopaminergic neurotoxins in relation to tyrosine hydroxylase isoforms
16. Alterations in Multiple Tyrosine Hydroxylase mRNAs in the Substantia Nigra, Locus Coeruleus and Adrenal Gland of MPTP-treated Parkinsonian Monkeys
17. Characterization of mouse and human GTP cyclohydrolase I genes: Mutations in patients with GTP cyclohydrolase I deficiency
18. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene
19. Tissue-specific alternative splicing of the first exon generates two types of mRNAs in human aromatic L-amino acid decarboxylase
20. Molecular mechanisms of hereditary progressive dystonia with marked diurnal fluctuation, Segawa's disease
21. Decrease in GTP cyclohydrolase I gene expression caused by inactivation of one allele in hereditary progressive dystonia with marked diurnal fluctuation
22. Molecular cloning of the human Nurr1 gene: characterization of the human gene and cDNAs
23. Genomic organization and chromosomal localization of the human sepiapterin reductase gene
24. GTP cyclohydrolase I gene in hereditary progressive dystonia with marked diurnal fluctuation
25. GTP cyclohydrolase I activity in mononuclear blood cells in juvenile parkinsonism
26. Characterization of mouse and human GTP cyclohydrolase I genes. Mutations in patients with GTP cyclohydrolase I deficiency
27. Characterization of curved cathode guns by the generalized trajectory method: upgrade of G-optk programme for applications to non-planar objects
28. Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm
29. Increased heterogeneity of tyrosine hydroxylase in humans
30. Two different forms of palindrome resolution in the human genome: deletion or translocation
31. Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats
32. Optimization of Operating Conditions for the FE Gun System of HVEM
33. Electrostatic force microscope imaging analyzed by the surface charge method.
34. Molecular genetics of dopa-responsive dystonia
35. Computer analysis of electron gun characteristics by surface charge method
36. Optimization of the operating condition of the accelerating tube for the high voltage electron microscope equipped with the field emission gun
37. Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes.
38. Andrographolide, isolated from Andrographis paniculata , induces apoptosis in monocytic leukemia and multiple myeloma cells via augmentation of reactive oxygen species production.
39. Inherited Chromosomally Integrated Human Herpesvirus 6 Is a Risk Factor for Spontaneous Abortion.
40. Coinfection With Human Herpesvirus (HHV)-6B in Immunocompetent, Healthy Individuals With Chromosomally Integrated HHV-6A.
41. Tyrosine hydroxylase conditional KO mice reveal peripheral tissue-dependent differences in dopamine biosynthetic pathways.
42. Inherited chromosomally integrated human herpesvirus-6 in a patient with XIAP deficiency.
43. Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal Inversion.
44. Chromosomally integrated human herpesvirus 6 in the Japanese population.
45. Analysis of the origin of inherited chromosomally integrated human herpesvirus 6 in the Japanese population.
46. Transmission of chromosomally integrated human herpesvirus 6 via cord blood transplantation.
47. Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements.
48. A simple cytogenetic method to detect chromosomally integrated human herpesvirus-6.
49. Intragenic duplication in the PKHD1 gene in autosomal recessive polycystic kidney disease.
50. Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome.
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