768 results on '"Inazawa J"'
Search Results
2. P964: IMMUNOPHENOTYPED-SUSPENSION-MULTIPLEX FISH BY IMAGING FLOW CYTOMETRY FOR THE SIMULTANEOUS DIAGNOSIS OF THREE PIVOTAL IGH TRANSLOCATIONS IN MULTIPLE MYELOMA
3. Integrated genomic and functional analyses reveal glyoxalase I as a novel metabolic oncogene in human gastric cancer
4. SIX1 promotes epithelial–mesenchymal transition in colorectal cancer through ZEB1 activation
5. A transcriptional variant of the LC3A gene is involved in autophagy and frequently inactivated in human cancers
6. Stabilization of phenotypic plasticity through mesenchymal-specific DNA hypermethylation in cancer cells
7. Expression of cIAP-1 correlates with nodal metastasis in squamous cell carcinoma of the tongue
8. DEK oncoprotein regulates transcriptional modifiers and sustains tumor initiation activity in high-grade neuroendocrine carcinoma of the lung
9. Etiology of orofacial dysmorphologies explained by genomic analysis: S1-2
10. POU2AF1, an amplification target at 11q23, promotes growth of multiple myeloma cells by directly regulating expression of a B-cell maturation factor, TNFRSF17
11. PRTFDC1, a possible tumor-suppressor gene, is frequently silenced in oral squamous-cell carcinomas by aberrant promoter hypermethylation
12. Epigenetic silencing of prostaglandin E receptor 2 (PTGER2) is associated with progression of neuroblastomas
13. Frequent methylation-associated silencing of a candidate tumor-suppressor, CRABP1, in esophageal squamous-cell carcinoma
14. RGC32, a novel p53-inducible gene, is located on centrosomes during mitosis and results in G2/M arrest
15. A novel amplification target, DUSP26, promotes anaplastic thyroid cancer cell growth by inhibiting p38 MAPK activity
16. Genomic loss and epigenetic silencing of very-low-density lipoprotein receptor involved in gastric carcinogenesis
17. Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient with left-right axis malformation
18. Recessive mutations in KIAA1632 cause Vici syndrome, a multisystem disorder with defective autophagy
19. Cytogenetic investigation of miscarriages by array comparative genomic hybridization: MS-3
20. Genetic diagnosis of cancer
21. Aurora kinase B is a predictive factor for the aggressive recurrence of hepatocellular carcinoma after curative hepatectomy
22. Chromosomal location and structure of amplicons in two human cell lines with coamplification of c-myc and Ki-ras oncogenes
23. Precise localization of the human gene encoding cell adhesion kinase β (CAKβ/PYK2) to chromosome 8 at p21.1 by fluorescence in situ hybridization
24. Mutational analysis of abcd1 in 86 adrenoleukodystrophy patients, including identification of complex mutations
25. Autophagy is required for cell survival under L-asparaginase-induced metabolic stress in acute lymphoblastic leukemia cells
26. Juvenile myoclonic epilepsy in chromosome 6p11: Recombinations and haplotype sharing reduce the candidate region to 500 kb
27. Overexpression of SMYD2 contributes to malignant outcome in gastric cancer
28. Overexpression of SMYD2 contributes to malignant outcome in gastric cancer
29. Integrated genomic and functional analyses reveal glyoxalase I as a novel metabolic oncogene in human gastric cancer
30. Potential of tumor-suppressive miR-596 targeting LGALS3BP as a therapeutic agent in oral cancer
31. Esophageal Squamous Cell Carcinoma Developed 11 Years After Allogeneic Bone Marrow Transplantation for Acute Lymphatic Leukemia
32. 434 Four loci at 11q12, 10q26, 3p11.2, and 2p11 are associated with prostate cancer susceptibility in the Japanese population
33. 904 Copy number alterations in urothelial carcinomas: Their clinicopathological significance and correlation with DNA methylation alterations
34. Mutations in EFHC1 cause juvenile myoclonic epilepsy
35. Mutations in EFHC1 cause juvenile myoclonic epilepsy
36. Stabilization of phenotypic plasticity through mesenchymal-specific DNA hypermethylation in cancer cells
37. Neuroradiologic Features ofCASKMutations
38. [i(17q) appearing in acute phase in Ph1-negative, BCR-negative CML]
39. POU2AF1, an amplification target at 11q23, promotes growth of multiple myeloma cells by directly regulating expression of a B-cell maturation factor, TNFRSF17
40. Genetic analysis of multifocal superficial urothelial cancers by array-based comparative genomic hybridisation
41. Overexpression of SMYD2 contributes to malignant outcome in gastric cancer.
42. RGC32, a novel p53-inducible gene, is located on centrosomes during mitosis and results in G2/M arrest
43. A novel amplification target, DUSP26, promotes anaplastic thyroid cancer cell growth by inhibiting p38 MAPK activity
44. Diagnostic clinical application of two-color fluorescence in situ hybridization that detects chromosome 1 and 17 alterations to direct touch smear and liquid-based thin-layer cytologic preparations of endometrial cancers
45. Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
46. MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas
47. Molecular Cloning and Genomic Analysis of Mouse Glucuronyltransferase Involved in Biosynthesis of the HNK-1 Epitope
48. Human arylhydrocarbon receptor repressor (AHRR) gene: genomic structure and analysis of polymorphism in endometriosis
49. The c-Jun NH2-terminal kinase3 (JNK3) gene: genomic structure, chromosomal assignment, and loss of expression in brain tumors
50. Molecular cloning, tissue expression, and chromosomal assignment of a novel gene encoding a subunit of the human signal-recognition particle
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