406 results on '"Tsujino, S"'
Search Results
52. Highly collimated electron beams from double-gate field emitter arrays with large collimation gate apertures
53. Coherent science at the SwissFEL x-ray laser
54. The molecular genetic basis of muscle phosphoglycerate mutase (PGAM) deficiency
55. Field-emission characteristics of single- and double-gate all-metallic field emitter arrays fabricated by molding and self-aligned gate process
56. Fabrication of all-metal field emitter arrays with controlled apex sizes by molding
57. Four-terminal field-emission characteristics of double-gate metallic field-emitter array cathodes with controlled apex sizes fabricated by molding and self-aligned gate process
58. Static and optical field enhancement in metallic nanotips studied by two-photon photoemission microscopy and spectroscopy excited by picosecond laser pulses
59. Case report Myophosphorylase deficiency and limb-girdle muscular dystrophy in the same pedigree
60. Ultrafast electron emission from metallic nanotip arrays induced by near infrared femtosecond laser pulses
61. SiGe double barrier resonant tunneling diodes on bulk SiGe substrates with high peak-to-valley current ratio
62. In situinvestigations of Si and Ge interdiffusion in Ge-rich Si/SiGe multilayers using x-ray scattering
63. Characterization of metallic field emitter array devices fabricated by molding for x-ray free electron laser applications
64. Myophosphorylase gene transfer in McArdle's disease myoblasts in vitro
65. Investigations of gene therapy for McArdle's disease using the sheep model
66. Photocurrent and transmission spectroscopy of direct-gap interband transitions in Ge∕SiGe quantum wells
67. Total angular momentum conservation during tunnelling through semiconductor barriers
68. SiGe Quantum Cascade Structures: Physics, Growth and Technology
69. Intra-valence-band mixing in strain-compensatedSiGequantum wells
70. Intersubband absorption of strain-compensated Si1−xGex valence-band quantum wells with 0.7⩽x⩽0.85
71. High temperature investigations of Si/SiGe based cascade structures using x-ray scattering methods
72. Interface-roughness-induced broadening of intersubband electroluminescence in p-SiGe and n-GaInAs∕AlInAs quantum-cascade structures
73. Hall mobility of narrow Si0.2Ge0.8–Si quantum wells on Si0.5Ge0.5 relaxed buffer substrates
74. Adenovirus-mediated myophosphorylase gene transfer in myophosphorylase-deficient cells in vitro
75. Reverse Seroconversion of Hepatitis B Virus after Hematopoietic Stem Cell Transplantation
76. Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis
77. Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis: a common mutation, R179X
78. Quantum Control of Electron Transfer
79. Coherent Transfer and Electron Teleportation in Semiconductor Double Quantum Well
80. Crystallographic Features and Subband Transitions of Al/InAs Metal-Semiconductor Junctions
81. Peak position of the intersubband absorption spectrum of quantum wells with controlled electron concentrations
82. Midinfrared studies of the contact region at superconductor–semiconductor interfaces
83. Myophosphorylase gene transfer in McArdle's disease myoblasts in vitro
84. Negative vertical photovoltaic response of two-dimensional electrons in the quantum Hall regime
85. Transient negative photoconductance in a charge transfer double quantum well under optical intersubband excitation
86. Pyk2 is a downstream mediator of the IL-2 receptor-coupled Jak signaling pathway
87. Glycogen Storage Disease Type II: Identification of Four Novel Missense Mutations (D645N, G648S, R672W, R672Q) and Two Insertions/Deletions in the Acid α-Glucosidase Locus of Patients of Differing Phenotype
88. Enhancement of intersubband transition energies in GaAs quantum wells by Si delta doping of high concentration
89. Saturation of Intersubband Absorption by Real-Space Transfer in Modulation Doped Single GaAs–AlAs Quantum Well
90. Delayed luminescence induced by intersubband optical excitation in a charge transfer double quantum well structure
91. Sudden infant death syndrome (SIDS) in a family with myosphosphorylase deficiency
92. Acute pandysautonomia: mass spectrometric and histopathological studies of the sympathetic nervous system during long term L-threo-3,4-dihydroxyphenylserine treatment.
93. Molecular characterization of myophosphorylase deficiency in a group of patients from Northern Italy
94. Myophosphorylase deficiency associated with rhabdomyolysis and exercise intolerance in 6 related charolais cattle
95. Control of electron population by intersubband optical excitation in potential‐inserted double quantum well structures
96. Phosphoglycerate kinase deficiency
97. Aberrant splicing in adult onset glycogen storage disease type II (GSDII): molecular identification of an IVS1 (– 13T→G) mutation in a majority of patients and a novel IVS10 (+ 1GT → CT) mutation
98. Phosphoglycerate kinase deficiency: Biochemical and molecular genetic studies in a new myopathic variant (PGK Alberta)
99. A single MEF-2 site is a major positive regulatory element required for transcription of the muscle-specific subunit of the human phosphoglycerate mutase gene in skeletal and cardiac muscle cells
100. Effect of long-term L-threo-3,4-dihydroxyphenylserine administration on α-2-adrenergic receptors in platelet membranes in neurologic disorders
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