retinoblastoma
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n.
眼癌（有遗传性）；
英英释义
retinoblastoma[ ,retinəublæs'təumə ]
n.malignant ocular tumor of retinal cells; usually occurs before the third year of life; composed of primitive small round retinal cells
权威例句
The retinoblastoma protein and cell cycle controlThe retinoblastoma protein and the cell cycle control
Weinberg, R. A. The retinoblastoma protein and cell control. Cell 81, 323-330
Mutation and cancer: statistical study of retinoblastoma.
Weinberg, R. A. The retinoblastoma gene and cell cycle control. Cell 81, 323-330
Functional interactions of the retinoblastoma protein with mammalian D-type cyclins
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
The human papilloma virus-16 E7 oncoprotein is able to bind to the retinoblastoma gene product
Knudson AG, Jr. Mutation and cancer: Statistical study of retinoblastoma. Proc Natl Acad Sci USA68: 820-823
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
1. Objective: to discuss ct characteristics of retinoblastoma.
目的：探讨视网膜母细胞瘤的CT表现特征。
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2. Objective to discuss the ct and MRI features of retinoblastoma.
目的探讨视网膜母细胞瘤的CT与MRI表现。
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3. Retinoblastoma is the most common intraocular malignant in children.
视网膜母细胞瘤是儿童最常见的眼内恶性肿瘤。
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4. Retinoblastoma is the commonest intraocular malignant tumor in children.
视网膜母细胞瘤是最常见的儿童眼内恶性肿瘤。
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5. The child with retinoblastoma had complete remission in a 6-months follow-up.
②视网膜母细胞瘤患儿随访6个月获完全缓解。
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6. Objective to explore the manifestation and diagnostic value of ct in retinoblastoma.
目的探讨视网膜母细胞瘤的CT表现及诊断价值。
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7. Retinoblastoma with massive tumor necrosis was proved by pathology after enucleation.
左眼眼球摘除后之病理报告显示为广泛坏死的视网膜胚胎母细胞瘤。
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8. The tumor is associated with mutations of a protein called Rb, or retinoblastoma protein.
这种肿瘤与一种称作rb的蛋白，或视网膜母细胞瘤蛋白(retinoblastomaprotein, prb)的突变有关。
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9. Results: 1, 15 of 16 cases of Retinoblastoma showed lumps with calcifications in eyeball.
结果：1、视网膜母细胞瘤16例中15例表现为球内肿块伴钙化。
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10. Objective to investigate ct diagnosis and differentiating diagnosis of the retinoblastoma.
目的研究视网膜母细胞瘤的CT诊断及鉴别诊断。
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11. These results suggested that ATRA might have clinical application for treatment of retinoblastoma.
提示，ATRA可能是一种潜在的抗视网膜母细胞瘤治疗药物。
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12. Objective to discuss the reliability of tissue microarray technique in research of retinoblastoma.
目的探讨组织芯片技术用于视网膜母细胞瘤研究中的可靠性。
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13. AIM: to investigate the expression of PTEN protein in retinoblastoma and its clinical significance.
目的：探讨pten蛋白在视网膜母细胞瘤组织中的表达及临床意义。
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14. ObjectiveTo observe whether apoptosis is the primary type of cell death in retinoblastoma (RB) or not.
目的观察凋亡是否为视网膜母细胞瘤(RB)细胞死亡的主要方式。
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15. Materials and Methods: 15 cases of Retinoblastoma examined with CT and confirmed by operation and pathology.
材料与方法：经ct检查及手术病理证实的15例视网膜母细胞瘤。
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16. Objective to explore ct manifestations of retinoblastoma and to understand the characteristics of its image.
目的探讨成视网膜细胞瘤的CT表现，了解其影像学特点。
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17. Intraocular tumors of retinoblastoma and melanoma demonstrate a high level of VEGF and VEGF receptor expression.
眼外的视网膜母细胞和黑色素瘤也表现出了VEGF和VEGF受体的高水平的表达。
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18. Methods The CT manifestations of 12 patients with retinoblastoma proved by operation and pathology were analyzed.
方法分析12例经手术及病理证实的成视网膜细胞瘤的CT表现。
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19. Objective: to acquire the variable region gene of light chain of monoclonal antibody against human retinoblastoma.
目的：获得抗人视网膜母细胞瘤单克隆抗体轻链可变区基因。
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20. The result suggests X-knife stereotactic radiotherapy is a safe and effective method for treatment of retinoblastoma.
认为颅脑x -刀立体定向治疗是一种安全有效的治疗视网膜母细胞瘤的新方法。
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21. Methods Immunohistochemical staining was used to determine the expression of P16 and P53 in 36 cases of retinoblastoma.
方法对36例视网膜母细胞瘤标本采用免疫组织化学方法观察P 16和P 53表达水平。
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22. Background: Subsequent malignant neoplasms are a major cause of premature death in survivors of hereditary retinoblastoma.
背景：继发恶性肿瘤是遗传性视网膜母细胞瘤生存者早死主要原因。
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23. Objective To study hyperthermia induced apoptosis and the effect of aspirin on hyperthermia induced apoptosis in retinoblastoma cells.
目的研究视网膜母细胞瘤的热凋亡现象及阿斯匹林对视网膜母细胞瘤热凋亡的影响。
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24. The results suggested that retinoblastoma originated from the retinoblast with potential of differentiation into photoreceptors and neurons.
结果提示：视网膜母细胞瘤来源于神经外胚层上皮，向神经元和光感受器方向分化。
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25. Dark adaptation ERGs of 11 cases with retinoblastoma demonstrated pathologically were analysed. 8 eyes were extinguish, 3 eyes were subnormal.
对11例已得到病理证实的视网膜母细胞瘤的暗适应erg作了分析。其中8只眼为无波型，3只眼为降低型。
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26. Dark adaptation ERGs of 11 cases with retinoblastoma demonstrated pathologically were analysed. 8 eyes were extinguish, 3 eyes were subnormal.
对11例已得到病理证实的视网膜母细胞瘤的暗适应erg作了分析。其中8只眼为无波型，3只眼为降低型。
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retinoblastoma
