hMSH6 deficiency and inactivation of the αE-catenin invasion-suppressor gene in HCT-8 colon cancer cells
暂无分享,去创建一个
F. Speleman | M. Mareel | F. van Roy | J. Jiricny | P. Boukamp | P. Debruyne | G. Marra | S. Vermeulen | A. Cuthbert | R. Newbold | F. Nollet
[1] Frank Speleman,et al. The αE-catenin gene (CTNNA1) acts as an invasion-suppressor gene in human colon cancer cells , 1999, Oncogene.
[2] F. Speleman,et al. Did the four human cancer cell lines DLD-1, HCT-15, HCT-8, and HRT-18 originate from one and the same patient? , 1998, Cancer genetics and cytogenetics.
[3] J. Jiricny,et al. Mismatch repair deficiency associated with overexpression of the MSH3 gene. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[4] J. Jiricny,et al. hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSα , 1998, The EMBO journal.
[5] R. Kucherlapati,et al. Mutation in the Mismatch Repair Gene Msh6 Causes Cancer Susceptibility , 1997, Cell.
[6] M. Koike,et al. Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer , 1997, Nature Genetics.
[7] T. Kunkel,et al. Correction of hypermutability, N-methyl-N'-nitro-N-nitrosoguanidine resistance, and defective DNA mismatch repair by introducing chromosome 2 into human tumor cells with mutations in MSH2 and MSH6. , 1997, Cancer research.
[8] Y. Yuasa,et al. Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred. , 1997, Cancer research.
[9] D. Notterman,et al. Expression of wild-type alpha-catenin protein in cells with a mutant alpha-catenin gene restores both growth regulation and tumor suppressor activities , 1997, Molecular and cellular biology.
[10] K. Kinzler,et al. Lessons from Hereditary Colorectal Cancer , 1996, Cell.
[11] E. Stanbridge,et al. The microsatellite mutator phenotype of colon cancer cells is often recessive. , 1995, Oncogene.
[12] W. Isaacs,et al. Chromosome 5 suppresses tumorigenicity of PC3 prostate cancer cells: correlation with re-expression of alpha-catenin and restoration of E-cadherin function. , 1995, Cancer research.
[13] G. Berx,et al. Transition from the noninvasive to the invasive phenotype and loss of alpha-catenin in human colon cancer cells. , 1995, Cancer research.
[14] N. Fusenig,et al. Step-wise progression in human skin carcinogenesis in vitro involves mutational inactivation of p53, rasH oncogene activation and additional chromosome loss. , 1995, Oncogene.
[15] K. Kinzler,et al. Mutations of GTBP in genetically unstable cells. , 1995, Science.
[16] M. Themis,et al. Novel use of a selectable fusion gene as an “In‐Out” marker for studying genetic loss in mammalian cells , 1995, Molecular carcinogenesis.
[17] R. Ekong,et al. Construction and characterization of a highly stable human: rodent monochromosomal hybrid panel for genetic complementation and genome mapping studies. , 1995, Cytogenetics and cell genetics.
[18] A. Chapelle,et al. Polymerase δ variants in RER colorectal tumours , 1995, Nature Genetics.
[19] E. van Marck,et al. Malignant melanoma of soft parts. Further cytogenetic characterization. , 1992, Cancer genetics and cytogenetics.
[20] T. Kunkel,et al. Heteroduplex repair in extracts of human HeLa cells. , 1991, The Journal of biological chemistry.