视网膜母细胞瘤基因在人类癌症发生和发展中的作用。 - Suppr

Suppr

超能文献

Role of the retinoblastoma gene in the initiation and progression of human cancer.

作者信息

Benedict W F, Xu H J, Hu S X, Takahashi R

机构信息

Center for Biotechnology, Baylor College of Medicine, Woodlands, Texas 77381.

出版信息

J Clin Invest. 1990 Apr;85(4):988-93. doi: 10.1172/JCI114575.

DOI:10.1172/JCI114575

PMID:2180983

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC296526/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907a/296526/51da52efda06/jcinvest00070-0016-a.jpg

相似文献

Role of the retinoblastoma gene in the initiation and progression of human cancer.视网膜母细胞瘤基因在人类癌症发生和发展中的作用。

J Clin Invest. 1990 Apr;85(4):988-93. doi: 10.1172/JCI114575.

Genetic suppression of tumor formation: a new frontier in cancer research.肿瘤形成的基因抑制：癌症研究的新前沿。

Cancer Res. 1986 Apr;46(4 Pt 1):1573-80.

[A gene inhibiting the development of human retinoblastoma: the prototype of tumor suppressor genes].一种抑制人类视网膜母细胞瘤发生发展的基因：肿瘤抑制基因的原型

Orv Hetil. 1990 Jun 17;131(24):1287-90.

[Hereditary tumors and chromosome aberrations with special reference to retinoblastoma].[遗传性肿瘤与染色体畸变，特别涉及视网膜母细胞瘤]

Gan To Kagaku Ryoho. 1986 Mar;13(3 Pt 2):645-51.

The retinoblastoma gene: its role in human malignancies.

Cancer Invest. 1990;8(5):535-40. doi: 10.3109/07357909009012078.

[A case of bilateral retinoblastoma in light of genetic counseling].[一例双侧视网膜母细胞瘤的遗传咨询情况]

Klin Oczna. 1985 Apr;87(4):167-8.

Chromosomal deletion and retinoblastoma.染色体缺失与视网膜母细胞瘤

N Engl J Med. 1976 Nov 11;295(20):1120-3. doi: 10.1056/NEJM197611112952007.

Retinoblastoma and partial deletion of the long arm of chromosome 13.视网膜母细胞瘤与13号染色体长臂部分缺失

Trans Am Ophthalmol Soc. 1978;76:172-83.

Increased number of chromosome aberrations in the peripheral blood culture of a retinoblastoma patient.一名视网膜母细胞瘤患者外周血培养中染色体畸变数量增加。

Acta Paediatr Hung. 1990;30(2):303-8.

Chromosome errors in retinoblastoma.视网膜母细胞瘤中的染色体错误。

Birth Defects Orig Artic Ser. 1982;18(6):703-27.

引用本文的文献

Using a Novel Diagnostic Nomogram to Differentiate Malignant from Benign Parathyroid Neoplasms.应用新型诊断列线图鉴别甲状旁腺良恶性肿瘤。

Endocr Pathol. 2019 Dec;30(4):285-296. doi: 10.1007/s12022-019-09592-3.

Reduced expression of the retinoblastoma protein shows that the related signaling pathway is essential for mediating the antineoplastic activity of erufosine.视网膜母细胞瘤蛋白表达降低表明相关信号通路对于介导依鲁替尼的抗肿瘤活性至关重要。

PLoS One. 2014 Jul 2;9(7):e100950. doi: 10.1371/journal.pone.0100950. eCollection 2014.

Altered p16(INK4) and RB1 Expressions Are Associated with Poor Prognosis in Patients with Nonsmall Cell Lung Cancer.p16(INK4) 和 RB1 表达改变与非小细胞肺癌患者预后不良相关。

J Oncol. 2012;2012:957437. doi: 10.1155/2012/957437. Epub 2012 Apr 30.

Promoter hypermethylation profile of cell cycle regulator genes in pituitary adenomas.垂体腺瘤中细胞周期调节基因的启动子高甲基化谱

J Neurooncol. 2007 Jun;83(2):153-62. doi: 10.1007/s11060-006-9316-9. Epub 2007 Jan 11.

Expression of altered retinoblastoma protein inversely correlates with tumor invasion in gastric carcinoma.视网膜母细胞瘤蛋白表达改变与胃癌肿瘤侵袭呈负相关。

World J Gastroenterol. 2006 Nov 28;12(44):7188-91. doi: 10.3748/wjg.v12.i44.7188.

Changes in retinoblastoma gene expression during cervical cancer progression.宫颈癌进展过程中视网膜母细胞瘤基因表达的变化。

Int J Exp Pathol. 2002 Dec;83(6):275-86. doi: 10.1046/j.1365-2613.2002.00198.x.

Immunohistochemical Analysis of the Cell Cycle-Associated Antigens Ki-67 and Retinoblastoma Protein in Parathyroid Carcinomas and Adenomas.甲状旁腺癌和腺瘤中细胞周期相关抗原Ki-67和视网膜母细胞瘤蛋白的免疫组织化学分析

Endocr Pathol. 1995 Winter;6(4):279-287. doi: 10.1007/BF02738728.

Molecular pathogenesis of acromegaly.肢端肥大症的分子发病机制。

Pituitary. 1999 Jun;2(1):43-50. doi: 10.1023/a:1009917920589.

Retinoblastoma (RB1) gene product expression in breast carcinoma. Correlation with Ki-67 growth fraction and biopathological profile.视网膜母细胞瘤（RB1）基因产物在乳腺癌中的表达。与Ki-67增殖分数及生物病理学特征的相关性。

J Clin Pathol. 1998 Nov;51(11):818-24. doi: 10.1136/jcp.51.11.818.

Differential retinoblastoma protein expression in neuroendocrine tumors of the lung. Potential diagnostic implications.视网膜母细胞瘤蛋白在肺神经内分泌肿瘤中的差异表达。潜在的诊断意义。

Am J Pathol. 1997 Feb;150(2):393-400.

本文引用的文献

Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes.具有正常染色体核型个体的视网膜母细胞瘤中13号染色体异常。

Cancer Genet Cytogenet. 1982 Jul;6(3):213-21. doi: 10.1016/0165-4608(82)90058-9.

Homozygosity of chromosome 13 in retinoblastoma.视网膜母细胞瘤中13号染色体的纯合性。

N Engl J Med. 1984 Mar 1;310(9):550-3. doi: 10.1056/NEJM198403013100902.

Nonrandom chromosomal changes in untreated retinoblastomas.未经治疗的视网膜母细胞瘤中的非随机染色体变化。

Cancer Genet Cytogenet. 1983 Dec;10(4):311-33. doi: 10.1016/0165-4608(83)90090-0.

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma.视网膜母细胞瘤中隐性等位基因通过染色体机制的表达。

Nature. 1983;305(5937):779-84. doi: 10.1038/305779a0.

Second nonocular tumors in retinoblastoma survivors. Are they radiation-induced?视网膜母细胞瘤幸存者中的第二种非眼部肿瘤。它们是辐射诱发的吗？

Ophthalmology. 1984 Nov;91(11):1351-5. doi: 10.1016/s0161-6420(84)34127-6.

Retinoblastoma: clues to human oncogenesis.视网膜母细胞瘤：人类肿瘤发生的线索

Science. 1984 Mar 9;223(4640):1028-33. doi: 10.1126/science.6320372.

A nonrandom chromosomal abnormality, del 3p(14-23), in human small cell lung cancer (SCLC).人类小细胞肺癌（SCLC）中一种非随机的染色体异常，即3p(14 - 23)缺失。

Cancer Genet Cytogenet. 1982 Jun;6(2):119-34. doi: 10.1016/0165-4608(82)90077-2.

Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus.从流式细胞分选的染色体中克隆出的、可能与视网膜母细胞瘤基因座相关的人13号染色体特异性DNA序列的分离。

Cancer Genet Cytogenet. 1984 Dec;13(4):283-95. doi: 10.1016/0165-4608(84)90073-6.

Mutation and cancer: statistical study of retinoblastoma.突变与癌症：视网膜母细胞瘤的统计学研究

Proc Natl Acad Sci U S A. 1971 Apr;68(4):820-3. doi: 10.1073/pnas.68.4.820.

Human retinoblastoma susceptibility gene: cloning, identification, and sequence.人类视网膜母细胞瘤易感基因：克隆、鉴定及序列分析

Science. 1987 Mar 13;235(4794):1394-9. doi: 10.1126/science.3823889.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验