Comparative Stages of Expression of Human Squamous Carcinoma Cells and Carcinogen Transformed Keratinocytes-Reference-Cited by-同舟云学术

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Comparative Stages of Expression of Human Squamous Carcinoma Cells and Carcinogen Transformed Keratinocytes

Published:1989-06 Issue:6 Volume:92 Page:848-853
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Milo George E.,Yohn Joseph,Schuller David,Noyes Inge,Lehman Teresa

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference30 articles.

1. Neoplastic transformation of normal human epithelial cells in vitro after exposure to chemical carcinogens;Milo;Cancer Res,1981

2. Human squamous cell carcinomas contain multiple subpopulations;Milo;Proc Amer Assoc Cancer Res,1986

3. Isolation and characterization of a monoclonal antibody specific for epithelial cells;Hamburger;Cancer Res,1985

4. Keratin filaments of cultured human epidermal cells;Sun;J Biol Chem,1978

5. Tumorigenic keratinocyte lines requiring anchorage and fibroblast support cultured from human squamous cell carcinomas;Rheinwald;Cancer Res,1981

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ineffectiveness of the presence of H-ras/p53 combination of mutations in squamous cell carcinoma cells to induce a conversion of a nontumorigenic to a tumorigenic phenotype;Cell Biology and Toxicology;1997

2. DOK, a cell line established from human dysplastic oral mucosa, shows a partially transformed non-malignant phenotype;International Journal of Cancer;1992-12-02

3. Conversion of premalignant human cells to tumorigenic cells by methylmethane sulfonate and methylnitronitrosoguanidine;Cell Biology and Toxicology;1992

4. Molecular Control of Expression of Plasticity of Tumorigenic/Metastatic Phenotypes;Neoplastic Transformation in Human Cell Culture;1991

5. Nontumorigenic squamous cell carcinoma line converted to tumorigenicity with methyl methanesulfonate without activation of HRAS or MYC.;Proceedings of the National Academy of Sciences;1990-02-01

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