retinoblastoma

retinoblastoma

1. Interaction among Survivin, p53 and bcl-2 might participate in carcinogenesis of retinoblastoma.

(2)Survivin、P53和bel一2可能通过相互作用共同参与Rb的发生发展。

2. One eyes with retinoblastoma was wrongly diagnosised as PHPV.The arterial flow signal was detected in the central part of hyperplastic vitreous body in 11 eyes.

1只眼为视网膜母细胞瘤误诊为PHPV,11只眼在玻璃体增生区的中心部显示动脉血流信号。

3. Of the 26 eyes with initial macular involvement, final visual acuity was 20/200 or better in six (23%).No patient developed retinoblastoma metastasis, pinealoblastoma, or second malignant neoplasms.

26个最初有黄斑部剥离的眼球中，最后的视力量表为20/200或更好的有6个眼球（23%），没有任何一位患者发生视网膜母细胞瘤转移、松果体母细胞瘤，或第二恶性肿瘤。

4. Other respondents provided such answers as Waardenburg's syndrome, retinoblastoma, chimerism, Fuchs' syndrome, and varicella.

2岁以后的获得性神经损伤，很少见到虹膜异色。

5. CT SCAN IN 52 CASES OF RETINOBLASTOMA

52例视网膜母细胞瘤的CT扫描

6. Effect of 8-bromum-cyclic adenosine monophosphate on the telomerase activity and dynamics in retinoblastoma cells

8-溴-环腺苷酸对视网膜母细胞瘤细胞系端粒酶活性及动力学影响的研究

7. The Expression of CD44v6 in Human Retinoblastoma and Proliferative Membranes of PVR

CD44v6在人视网膜母细胞瘤及增生性玻璃体视网膜病变增生膜中的表达

8. the CT findings of retinoblastoma showed calcified plaque inside tumor 100%(11/11) and protruded soft tissue density mass on the wall of eyeball.

CT检查病灶区100%有斑点状或团块状钙化,眼球壁上还可见密度增高的软组织肿块隆起。

9. Expression of Ets-1 and CD34 in retinoblastoma and their signifiance

Ets-1和CD34在视网膜母细胞瘤中的表达及意义

10. Over expression of MDR1 and MRP genes is significantly involved in the mechanism of MDR phenotype in retinoblastoma.

MDR1和MRP基因的过度表达是Rb多药耐药现象发生的重要机制。

11. p16 INK4a is one of the inhibitors of cyclin dependent kinase(cdk),which inhibits cdk4/cdk6 mediated phosphorylation of retinoblastoma gene product (Rb) that leads to cell cycle arrest in G 1 phase.

p16 INK4a是一种细胞周期蛋白依赖激酶 (cdk)的抑制因子 ,它通过抑制cdk4与cdk6的活性 ,使视网膜母细胞瘤抑制蛋白Rb处于低磷酸化状态 ,从而使细胞阻滞于G1期 .

12. retinoblastoma gene

Rb gene

13. retinoblastoma protein

Rb protein

14. Retinoblastoma 94 Gene

Rb94基因

15. Retinoblastoma (Rb) suppressor-associated protein 46(RbAp46) gene

RbAp46基因

16. Keywords RNA interference;retinoblastoma;vascular endothelial growth factor;

RNA干扰;视网膜母细胞瘤;血管内皮生长因子;

17. trilateral retinoblastoma

三侧性视网膜母细胞瘤

18. The principal first symptom remains "galeamaurosis" The clinical characteristics of retinoblastoma in children are diversified、concealed、puzzling and easy to make missed diagnosis.

临床仍以“猫眼”为本病主要首诊症状，但临床特点具有多样性，隐蔽性，迷惑性，易漏诊。

19. Orbital swelling mimicking orbital cellulitis is also an uncommon presentation of retinoblastoma, and it does not necessarily indicate extrascleral extension of tumor.

事实上这通常是肿瘤细胞大量坏死所引起的免疫反应，并不意味著肿瘤之眼球外扩散。

20. Keywords Human papilloma virus;Retinoblastoma protein;Head and neck neoplasms;Carcinoma;squamous cell;

人乳头状瘤病毒;视网膜母细胞瘤蛋白;头颈部肿瘤;癌;鳞状细胞;

21. Hhuman retinoblastoma Rb cell

人视网膜母细胞瘤Rb细胞

22. Any decision to remove their daughter's eye -- a common option for those with retinoblastoma -- will wait until she is old enough to tell them how much she can see with that eye.

任何一个去除他女儿眼睛的决定--对于这种眼癌的一般选择--都会等到她长大到可以告诉他们她可以用的眼睛看到什么时.

23. His eleventh month old daughter, Tatum, had just been diagnosed with retinoblastoma, a rare type of eye cancer.

但是他11个月大的女儿Tatum被确证患上了眼癌，一种很罕见的眼癌。

24. Keywords Children;Eye neoplasma;Xeroderma Pigmentosum;Retinoblastoma;Lymphoma;

儿童;眼肿瘤;着色性干皮病;视网膜母细胞瘤;淋巴瘤;

25. Childreng retinoblastoma

儿童视网膜母细胞瘤

26. New suspicious gene loci correlated with the generation and development of children 's retinoblastoma

儿童视网膜母细胞瘤发生发展密切相关的可疑新基因位点研究

27. Keywords all-trans retinoic acid;mouse embryonic palatal mesenchymal cells;cell cycle;cyclins;retinoblastoma protein;

全反式视黄酸;胎鼠腭间质细胞;细胞周期;细胞周期蛋白;视网膜母细胞瘤蛋白;

28. Keywords all trans retinoid acid （ATRA） retinoblastoma cellular transduction Y79 growth inhibition;

关键词全反式维甲酸;视网膜母细胞瘤;信号转导;Y79;生长抑制;

29. endophytic retinoblastoma

内向性视网膜胶质瘤

30. retinoblastoma endophytum

内生性成视网膜细胞瘤, 内生性视网膜母细胞瘤

31. This is in contrast with developing countries, where retinoblastoma is generally diagnosed late, usually when extraocular dissemination has occurred and the prognosis is poor [3, 4] .

决然不同的是,发展中国家的视网膜母细胞瘤的诊断比较晚,通常是有了眼外转移,这时候预后是很差的.

32. Macular retinoblastoma managed with chemoreduction: Analysis of tumor control with or without adjuvant thermotherapy in 68 tumors

化学减容法治疗黄斑视网膜母细胞瘤:分析68例接受或未接受辅助温热疗法肿瘤患者的病情控制情况

33. Ou BX, Zhuo ZL, Yi YZ, et al: Dynamic investigation on chromosome aberration of a Human retinoblastoma cell line SO-Rb50.Eye Science 1993;

区宝祥,卓子兰,梁启万,等:视网膜母细胞瘤实体瘤的染色体研究.中华眼科杂志1988;

34. After threading a catheter through the body to the eye, doctors delivered a drug directly to retinoblastoma tumors through an artery in the eye.

医生将导管从身体一直伸到眼球，然后将药物通过眼球动脉直接注入视网膜母细胞瘤。

35. A missense mutation outside the large pocket of the retinoblastoma protein

发生在成视网膜细胞瘤蛋白大袋立体结构外的错义突变

36. Mutations analysis of RB1 gene in Chinese patients with retinoblastoma

国人视网膜母细胞瘤患者RB1基因突变的特性

37. There were 14 children pathologically proved retinoblastoma within the recent five years in our hospital.

在最近五年内，我们共有14例小孩由病理证实为视网膜瘤。

38. Here, we sought to explore whether RNA interference (RNAi) targeting VEGF could inhibit retinoblastoma angiogenesis and tumor growth.

在这里,我们试图探讨RNA干涉(RNA)针对血管内皮生长因子是否能抑制视网膜血管生成及肿瘤生长.

39. Keywords Genes;retinoblastoma;Gene thera py;Transfection;Plasmids;Osteosorcoma;

基因;视网膜母细胞瘤;基因疗法;转染;质粒;骨肉瘤;

40. Positive group includes cyclin, cyclin-dependent kinase (CDK), and downstream targets such as retinoblastoma protein (pRb) and so on.

增多的细胞不是血液中炎性细胞的浸润，而是受损组织固有细胞的增生。

41. exophytic retinoblastoma

外向性视网膜胶质瘤

42. retinoblastoma exophytum

外生性成视网膜细胞瘤, 外生性视网膜母细胞瘤

43. Treatment of intraocular retinoblastoma with local treatment and chemotherapy

局部治疗加化疗治疗眼内视网膜母细胞瘤

44. 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。

45. retinoblastoma planum

平坦部成视网膜细胞瘤, 平坦部视网膜母细胞瘤

46. Keywords acute leukemia;child acute leukeima;retinoblastoma protein;MRD monitor;

急性白血病;儿童急性白血病;视网膜母细胞瘤蛋白;MRD监测;

47. retinoblastoma protein(Rb protein)

成视网膜母细胞瘤蛋白, Rb蛋白[一种抑癌蛋白, 参与细胞周期调控]

48. retinoblastoma susceptibility gene

成视网膜细胞瘤易感基因[即Rb蛋白]

49. CT manifestations of retinoblastoma and their clinical diagnostic value

成视网膜细胞瘤的CT表现及其临床诊断价值

50. Retinoblastoma is rare, but life-endangering tumor of childhood.We reported a even more rare, but much benign retinal anlage tumor of eyelid.

摘要一位十天大的婴儿，因右下眼睑肿瘤且日益影响眼球运动而住院。

51. Trilateral retinoblastoma is a rare malignancy of childhood with high mortality.We reported such a case with delayed treatment.

摘要双眼视网膜母细胞瘤合并松果体母细胞瘤是一种罕见而具高致死率的小儿恶性肿瘤。

52. Objective: To investigate the relationship between CT findings and pathologic diagnosis of retinoblastoma and their value in diagnosis and differentiation.

摘要目的：探讨视网膜母细胞瘤的CT表现与病理诊断的关系及其诊断、鉴别诊断价值。

53. The LDH activity in aqueous humor of retinoblastoma of our people are characterict: colly higher than that of control group in our research.

摘要网膜芽细胞瘤病人房水内乳酸脱氢酶活性值，以我国人所做的研究显示，亦有明显的增高现象。

54. Methods:Hemoporphyrin derivative (HPD) was used as photosensitizer in this study. Fifteen nude mice, associated with intraocular transplanted heterogeneous retinoblastoma in right eye, were divided into five groups (group A,B,C,D and E).

方法 :将 15只裸小鼠视网膜母细胞瘤眼内动物模型眼分成A、B、C、D及E五组 ,其中A和B组为观察组 ,即既给光敏剂HPD又照光 ,但光照剂量不同 ,A组为 15 0mw/cm2 ,B组为 30 0mw/cm2 ;

55. Methods Observation of choroidal invasion in 297 primary enucleated retinoblastoma eyes by drawing materials with five planes (151 eyes) and with one plane (146 eyes) was compared.

方法:复查297只原发摘除的视网膜母细胞瘤眼球的病理切片,比较五平面取材法(151只眼)和单平面取材法(146只眼)对脉络膜浸润的检出率。

56. Method 27 patients with retinoblastoma proved by pathology and clinical symptom,were analysed retrospectively.

方法回顾分析27例经病理或临床证实的视网膜母细胞瘤的CT表现。

57. Methods 12 cases as a result of retinoblastoma line enucleation surgery for children with modified hydroxyapatite orbital implant surgery, the lunwen114surgery under general anesthesia.

方法对12例因视网膜母细胞瘤行眼球摘除术患儿进行改良式羟基磷灰石义眼台植入术，手术在全身麻醉下进行。

58. Methods Hep3B cells which lack the expression of both p53 and retinoblastoma tumor suppressor genes because of deletions, were transfected with a wild-type (wt) p53 cDNA and control vector by a liposome method.

方法通过采用脂质体介导转染技术，将野生型p53 cDNA导入一种p53和Rb基因缺失的肝癌细胞株Hep3B。

59. Methods: To analyze the age, sexuality, symptom, the accompaniment of symptom and the diagnostic feature of 53 retinoblastoma cases.

方法：就我院53例视网膜母细胞瘤门诊患儿年龄、性别、发病年龄、眼别、临床症状进行回顾性分析。

60. No patients developed retinoblastoma metastasis, pinealoblastoma, secondary tumor (leukemia), dysfunction of hepatic, renal or auditory.

无一例发生白血病，肝肾功能及听力损害等严重化疗毒性反应者。

61. There is evidence suggesting a role for VEGF in the neovascularization of retinoblastoma.

有证据表明在视网膜母细胞瘤中VEGF起了比较重要的作用。

62. This article reports our experiences in the clinical treatment of these complicated retinoblastoma.

本文主要介绍这类肿瘤病例的治疗结果和一些临床体会。

63. Materials and Methods: The CT findings of 11 cases with retinoblastoma confirmed by operation and pathology were analyzed retrospectively.

材料和方法:回顾性分析11例经临床和手术病理证实的视网膜母细胞瘤的CT表现。

64. Pathologic examination confirmed a case of retinoblastoma.

核磁共振检查更察觉松果腺有一肿瘤。

65. nuclear retinoblastoma protein

核视网膜神经胶质瘤蛋白, 核成视网膜细胞瘤蛋白

66. The giving up treatment of retinoblastoma is relatively common in our country at present time and its early diagnosis and early treatment is very important.T...

治疗性放弃对临床医生是一个全新的概念,医生在特殊情况下对某些可治性疾病可采用放弃治疗的方法。

67. Keywords Carcinoma;squamous cell;Genes;retinoblastoma;Two-hybrid system techniques;

癌;鳞状细胞;基因;视网膜母细胞瘤;双杂交系统技术;

68. Purpose:To investigate palitaxel (Tax) induct io n of apoptosis in human retinoblastoma Y79 cells and the role of Bcl-2 phosphor ylation in the mechanism.

目的 :研究紫杉醇 (Tax)抑制视网膜母细胞瘤 (Rb)细胞生长并诱导其凋亡及磷酸化Bcl 2在其中的作用。

69. Objective：To observe the therapeutic ef fect of chemoreduction treatm ent combined with local focal therapy for advanced intraocular retinoblastoma (R B).

目的:察化学减容术联合眼肿瘤局部加强治疗方法治疗晚期眼内 视网膜母细胞瘤 的疗效。

70. AIM: To study RB1 heterozugous mutations in patients with retinoblastoma and compare the characteristics of the RB1 gene mutation in Chinese and foreigners with retinoblastoma.

目的:检测国人RB患者体细胞中RB1基因突变,分析我国RB1基因突变的特性,探讨RB1基因突变的分子生物学机制。

71. Objective: To acquire the variable region gene of light chain of monoclonal antibodyagainst 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。

72. Objective:To observe the effect of intraorbital implantation of hydroxyapatite(HA)sphere in enucleation of retinoblastoma.

目的:观察视网膜母细胞瘤眼球摘除术后眶内植入羟基磷灰石(HA)眼台的疗效。

73. Objective To study the CT findings and clinical features of retinoblastoma(RB).

目的分析视网膜母细胞瘤的CT和临床特征。

74. Objective To search for a classification of the visual and living prognosis of patients with retinoblastoma.

目的探讨视网膜母细胞瘤患者视力和生命预后的分类方法。

75. Objective Observe and analyze the pathology and clinic of retinoblastoma(Rb).Methods Observe the pathological pattern and clinic.

目的观察分析视网膜母细胞瘤的病理形态和临床表现。

76. Purpose:To observe the morphologic changes of retinoblastoma on CT images in order to improve the recognition of this disease.

目的：研究视网膜母细胞瘤的CT形态学改变，旨在提高对本病的认识。

77. The extraocular extension account for about 20% of retinoblastoma of the same period.

眼外蔓延的发生率约占同期视网膜母细胞瘤的20%。

78. Keywords Cyclin E;Retinoblastoma gene;Cervical intraepithelial neoplasm;Cervical squamous cell carcinoma;

细胞周期素E;视网膜母细胞瘤基因;子宫颈上皮内瘤变;子宫颈鳞状上皮癌;

79. At 27 months after therapy, one patient was free of measurable retinoblastoma.

经过 27个月的治疗后，其中一个患者已经没有可测量的视网膜胚细胞瘤。

80. Results All the 12 cases of retinoblastoma showed increased and inhomogeneous density of vitreous body.

结果12例成视网膜细胞瘤均表现为玻璃体密度增高,密度不均匀,常见钙化灶,呈密集点状或斑块状。