Cargando…
Allelotype of 28 human breast cancer cell lines and xenografts
Heterozygous loss of relatively large chromosomal regions is a hallmark of the inactivation of tumour suppressor genes. Searching for deletions in cancer genomes therefore provides an attractive option to identify new tumour suppressor genes. Here, we have performed a genome-wide survey for regions...
Autores principales: | Harkes, I C, Elstrodt, F, Dinjens, W N M, Molier, M, Klijn, J G M, Berns, E M J J, Schutte, M |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2003
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395277/ https://www.ncbi.nlm.nih.gov/pubmed/14676808 http://dx.doi.org/10.1038/sj.bjc.6601448 |
Ejemplares similares
-
Genetic alterations in primary osteosarcoma from 54 children and adolescents by targeted allelotyping
por: Entz-Werle, N, et al.
Publicado: (2003) -
High resolution chromosome 3p, 8p, 9q and 22q allelotyping analysis in the pathogenesis of gallbladder carcinoma
por: Wistuba, I I, et al.
Publicado: (2002) -
High-resolution genome-wide allelotype analysis identifies loss of chromosome 14q as a recurrent genetic alteration in astrocytic tumours
por: Hu, J, et al.
Publicado: (2002) -
The CHEK2(*)1100delC mutation has no major contribution in oesophageal carcinogenesis
por: Koppert, L B, et al.
Publicado: (2004) -
Low-risk susceptibility alleles in 40 human breast cancer cell lines
por: Riaz, Muhammad, et al.
Publicado: (2009)