Searching for microsatellite mutations in coding regions in lung, breast, ovarian and colorectal cancers
暂无分享,去创建一个
J. Minna | A. Gazdar | Xie L Xu | S. Markowitz | J. Wren | H. Garner | C. Muller | M. Kondo | G. Tomlinson | Xie L. Xu | É. Forgács | C. Kamibayashi
[1] H R Garner,et al. Repeat polymorphisms within gene regions: phenotypic and evolutionary implications. , 2000, American journal of human genetics.
[2] A. Lindblom,et al. Missense mutations in hMLH1 associated with colorectal cancer. , 1999 .
[3] R. Wells,et al. Genetic Instabilities in (CTG·CAG) Repeats Occur by Recombination* , 1999, The Journal of Biological Chemistry.
[4] J. Boyd,et al. Causes and consequences of microsatellite instability in endometrial carcinoma. , 1999, Cancer research.
[5] H R Garner,et al. Computerized polymorphic marker identification: experimental validation and a predicted human polymorphism catalog. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[6] J. Herman,et al. Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[7] P. Patel,et al. The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure. , 1998, American journal of human genetics.
[8] T. Takenawa,et al. A novel ligand for an SH3 domain of the adaptor protein Nck bears an SH2 domain and nuclear signaling motifs. , 1997, Biochemical and biophysical research communications.
[9] A. Otte,et al. Interference with the expression of a novel human polycomb protein, hPc2, results in cellular transformation and apoptosis , 1997, Molecular and cellular biology.
[10] Y. Pekarsky,et al. Activation of a novel gene in 3q21 and identification of intergenic fusion transcripts with ecotropic viral insertion site I in leukemia. , 1997, Cancer research.
[11] J C Reed,et al. Somatic Frameshift Mutations in the BAX Gene in Colon Cancers of the Microsatellite Mutator Phenotype , 1997, Science.
[12] Hiroyuki Yamamoto,et al. Frameshift mutator mutations , 1996, Nature.
[13] L. Girard,et al. Frequent provirus insertional mutagenesis of Notch1 in thymomas of MMTVD/myc transgenic mice suggests a collaboration of c-myc and Notch1 for oncogenesis. , 1996, Genes & development.
[14] K. Kinzler,et al. Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients , 1996, Nature Medicine.
[15] R. Wells. Molecular Basis of Genetic Instability of Triplet Repeats (*) , 1996, The Journal of Biological Chemistry.
[16] K. Kinzler,et al. Microsatellite instability and mutations of the transforming growth factor beta type II receptor gene in colorectal cancer. , 1995, Cancer research.
[17] K. Kinzler,et al. Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability. , 1995, Science.
[18] A. Chapelle,et al. Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability , 1995, Nature Genetics.
[19] A. Bowcock,et al. Genetic instability in human ovarian cancer cell lines. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[20] R. Fleischmann,et al. Mutations of two P/WS homologues in hereditary nonpolyposis colon cancer , 1994, Nature.
[21] D. Ward,et al. Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer , 1994, Nature.
[22] M. Brown,et al. SREBP-2, a second basic-helix-loop-helix-leucine zipper protein that stimulates transcription by binding to a sterol regulatory element. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[23] M. Hayden,et al. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease , 1993, Nature Genetics.
[24] J. Sklar,et al. TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms , 1991, Cell.