易引发人类癌症的隐性突变基因。 - Suppr

Suppr

超能文献

Recessive mutant genes predisposing to human cancer.

作者信息

Cavenee W K, Koufos A, Hansen M F

出版信息

Mutat Res. 1986 Jul;168(1):3-14. doi: 10.1016/0165-1110(86)90019-9.

DOI:10.1016/0165-1110(86)90019-9

PMID:3012326

Abstract

摘要

相似文献

Recessive mutant genes predisposing to human cancer.

Mutat Res. 1986 Jul;168(1):3-14. doi: 10.1016/0165-1110(86)90019-9.

Recessive cancer genes and chromosomal mechanisms in tumorigenesis.

Ann Clin Res. 1986;18(5-6):307-13.

Carcinogenesis. Is imprinting to blame?

Nature. 1989 Jul 27;340(6231):264. doi: 10.1038/340264a0.

Mutagenesis and embryonal carcinogenesis.

Natl Cancer Inst Monogr. 1979 May(51):19-24.

Chromosome 13 homozygosity in osteosarcoma without retinoblastoma.

Am J Hum Genet. 1986 Jan;38(1):59-66.

Recessive mutations in cancer predisposition and progression.

Basic Life Sci. 1991;57:171-80; discussion 180-1. doi: 10.1007/978-1-4684-5994-4_15.

Identification of recessive mutations at human cancer loci.

Birth Defects Orig Artic Ser. 1987;23(3):93-107.

Hereditary cancer, oncogenes, and antioncogenes.

Cancer Res. 1985 Apr;45(4):1437-43.

Retinoblastoma: clues to human oncogenesis.

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

Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition.

Proc Natl Acad Sci U S A. 1985 Sep;82(18):6216-20. doi: 10.1073/pnas.82.18.6216.

引用本文的文献

Genetics and genomics of endometriosis.

Clin Obstet Gynecol. 2010 Jun;53(2):403-12. doi: 10.1097/GRF.0b013e3181db7ca1.

Phenotypic reversions at the W/Kit locus mediated by mitotic recombination in mice.

Mol Cell Biol. 1995 Nov;15(11):5898-905. doi: 10.1128/MCB.15.11.5898.

The specificity of UV-induced mutations at an endogenous locus in mammalian cells.

Proc Natl Acad Sci U S A. 1987 Dec;84(24):9103-7. doi: 10.1073/pnas.84.24.9103.

Functional hemizygosity in the human genome: direct estimate from twelve erythrocyte enzyme loci.

Hum Genet. 1987 Nov;77(3):241-5. doi: 10.1007/BF00284477.

Recurrent genomic rearrangements are not at the fragile sites on chromosomes 3 and 5 in human renal cell carcinomas.

Hum Genet. 1988 Sep;80(1):99-101. doi: 10.1007/BF00451467.

Mutations in human lymphocytes commonly involve gene duplication and resemble those seen in cancer cels.

Proc Natl Acad Sci U S A. 1988 May;85(9):3189-92. doi: 10.1073/pnas.85.9.3189.

Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma.

Proc Natl Acad Sci U S A. 1987 Dec;84(24):9275-9. doi: 10.1073/pnas.84.24.9275.

Analysis of 13q RFLP in multiple endocrine neoplasia type II kindreds.

Cancer Genet Cytogenet. 1987 Nov;29(1):183-5. doi: 10.1016/0165-4608(87)90049-5.

Role of a tumor-suppressor gene in the negative control of anchorage-independent growth of Syrian hamster cells.

Proc Natl Acad Sci U S A. 1989 Nov;86(22):8773-7. doi: 10.1073/pnas.86.22.8773.

Utility of short-term tests for genetic toxicity.

Cell Biol Toxicol. 1989 Jun;5(2):189-200. doi: 10.1007/BF00122652.

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