47 results on '"Nagai, Jun-ichi"'
Search Results
2. A short-term three dimensional culture-based drug sensitivity test is feasible for malignant bone tumors
3. Familial total anomalous pulmonary venous return with 15q11.2 (BP1-BP2) microdeletion
4. Diamond-Blackfan anemia caused by chromosome 1p22 deletion encompassing RPL5
5. Peak parking-moment analysis: A strategy for the measurement of molecular diffusivity in liquid phase
6. Using the in vitro drug sensitivity test to identify candidate treatments for transient abnormal myelopoiesis
7. Delineation of the KIAA2022 mutation phenotype: Two patients with X-linked intellectual disability and distinctive features
8. Microdeletion of 19p13.3 in a girl with Peutz–Jeghers syndrome, intellectual disability, hypotonia, and distinctive features
9. Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2
10. Refinement of the deletion in 8q22.2–q22.3: The minimum deletion size at 8q22.3 related to intellectual disability and epilepsy
11. De novo duplication of 17p13.1–p13.2 in a patient with intellectual disability and obesity
12. Negative priming and stimulus familiarity: What causes opposite results?
13. Pure duplication of 19p13.3
14. An efficient genetic test flow for multiple congenital anomalies and intellectual disability
15. Using the in vitro drug sensitivity test to identify candidate treatments for transient abnormal myelopoiesis.
16. Whole‐exome sequencing reveals the subclonal expression of NUP214 ‐ ABL1 fusion gene in T‐cell acute lymphoblastic leukemia
17. Hemoglobin beta Kanagawa [c.443A>C; p.(Ter148Serext*21)]: A novel β‐globin gene mutation causing dominantly inherited β‐thalassemia
18. 17q21.32‐q22 Deletion in a girl with osteogenesis imperfecta, tricho‐dento‐osseous syndrome, and intellectual disability
19. Evaluation of a patient with classical Ehlers‐Danlos syndrome due to a 9q34 duplication affecting COL5A1
20. A splicing mutation of proteolipid protein 1 in Pelizaeus-Merzbacher disease
21. Biases and regularities of grapheme–colour associations in Japanese nonsynaesthetic population
22. Delineation of theKIAA2022mutation phenotype: Two patients with X-linked intellectual disability and distinctive features
23. Microdeletion of 19p13.3 in a girl with Peutz–Jeghers syndrome, intellectual disability, hypotonia, and distinctive features
24. Deletion ofUBE3Ain brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2
25. Gene alterations involving the CRLF2-JAK pathway and recurrent gene deletions in Down syndrome-associated acute lymphoblastic leukemia in Japan
26. Grapheme-color synesthetic cognition among non-synesthetes
27. DNA Elements Reducing Transcriptional Gene Silencing Revealed by a Novel Screening Strategy
28. Networking System Employing near Infrared Spectroscopy for Sugarcane Payment in Japan
29. Grapheme-Color Synesthetic Tendency Test Without Color Presentation
30. Mild phenotype in Pelizaeus-Merzbacher disease caused by a PLP1-specific mutation
31. A Case of De Novo Acute Myeloid Leukemia With der(11)t(7;11)(q11;q23) and −7
32. Does Stimulus Familiarity Influence the Preview Effect in Visual Search?
33. Color diagnosticity or category: Which determines the role of color in visual object recognition?
34. Retinoic Acid Induces Neuroblastoma Cell Death by Inhibiting Proteasomal Degradation of Retinoic Acid Receptor α
35. Inactivation of O6-Methylguanine-DNA Methyltransferase in Human Lung Adenocarcinoma Relates to High-grade Histology and Worse Prognosis among Smokers
36. Ewing's sarcoma family of tumor arising in the adrenal gland—Possible diagnostic pitfall in pediatric pathology: Histologic, immunohistochemical, ultrastructural, and molecular study
37. Does negative priming occur by rotated characters?
38. A New Sensitive and Specific Combination of CD81/CD56/CD45 Monoclonal Antibodies for Detecting Circulating Neuroblastoma Cells in Peripheral Blood Using Flow Cytometry
39. Clinical Significance of Detecting p53 Protein in Burkitt Lymphoma and B-cell Acute Lymphoblastic Leukemia Using Immunocytochemistry
40. Whole-exome sequencing reveals the subclonal expression of NUP214-ABL1 fusion gene in T-cell acute lymphoblastic leukemia.
41. Inactivation of O6-Methylguanine-DNA Methyltransferase in Human Lung Adenocarcinoma Relates to High-grade Histology and Worse Prognosis among Smokers.
42. Expressed Sequence Tags from Immature Female Sexual Organ of a Liverwort, Marchantia polymorpha.
43. 17q21.32‐q22 Deletion in a girl with osteogenesis imperfecta, tricho‐dento‐osseous syndrome, and intellectual disability.
44. Inactivation of O6‐Methylguanine‐DNA Methyltransferase in Human Lung Adenocarcinoma Relates to High‐grade Histology and Worse Prognosis among Smokers
45. A Case of De Novo Acute Myeloid Leukemia With der(11)t(7;11)(q11;q23) and -7.
46. A case of de novo acute myeloid leukemia with der(11)t(7;11)(q11;q23)and -7.
47. Retinoic acid induces neuroblastoma cell death by inhibiting proteasomal degradation of retinoic acid receptor alpha.
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