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51. Evolutionary implications of inversions that have caused intra-strand parity in DNA

52. NUDT15variants confer high incidence of second malignancies in children with acute lymphoblastic leukemia

53. Recurrent RARB Translocations in Acute Promyelocytic Leukemia Lacking RARA Translocation

55. Collision-energy-resolved Penning ionization electron spectroscopy of p-benzoquinone: Study of electronic structure and anisotropic interaction with He*(2 3S) metastable atoms.

58. Molecular characteristics of the KCNJ5 mutated aldosterone-producing adenomas

61. A novel missense variant of the GNAI3gene and recognisable morphological characteristics of the mandibula in ARCND1

71. Fetal therapy model of myelomeningocele with three-dimensional skin using amniotic fluid cell-derived induced pluripotent stem cells

72. ZNF384 -related fusion genes define a subgroup of childhood B-cell precursor acute lymphoblastic leukemia with a characteristic immunotype

74. Complex Genomic Rearrangement Within theGNASRegion Associated With Familial Pseudohypoparathyroidism Type 1b

75. Distinctive features of single nucleotide alterations in induced pluripotent stem cells with different types of DNA repair deficiency disorders

78. Human genetic variation database, a reference database of genetic variations in the Japanese population

80. NR0B1 Frameshift Mutation in a Boy with Idiopathic Central Precocious Puberty

83. RARB Translocations in Acute Promyelocytic Leukemia without Rara translocation

84. Genomic, Epigenomic, and Transcriptomic Profiling towards Identifying Omics Features and Specific Biomarkers That Distinguish Uterine Leiomyosarcoma and Leiomyoma at Molecular Levels

86. DNA methylation analysis of human myoblasts during in vitro myogenic differentiation: de novo methylation of promoters of muscle-related genes and its involvement in transcriptional down-regulation

87. Ataxia telangiectasia derived iPS cells show preserved x-ray sensitivity and decreased chromosomal instability

88. Compilation of copy number variants identified in phenotypically normal and parous Japanese women

90. Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment

95. A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 11q: Comparison with chromosome 21q

97. Complex Genomic Rearrangement Within the GNASRegion Associated With Familial Pseudohypoparathyroidism Type 1b

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