Pages that link to "Q36431232"
Jump to navigation
Jump to search
The following pages link to Deletion mapping and linkage analysis provide strong indication for the involvement of the human chromosome region 8p12-p22 in breast carcinogenesis (Q36431232):
Displaying 15 items.
- HLS5, a novel RBCC (ring finger, B box, coiled-coil) family member isolated from a hemopoietic lineage switch, is a candidate tumor suppressor (Q24301505) (← links)
- Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility (Q24679438) (← links)
- ST18 is a breast cancer tumor suppressor gene at human chromosome 8q11.2. (Q30032679) (← links)
- Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer (Q33901652) (← links)
- Genetic imbalances in pleomorphic xanthoastrocytoma detected by comparative genomic hybridization and literature review (Q34500804) (← links)
- Models of genetic susceptibility to breast cancer (Q36602581) (← links)
- Transfer of chromosome 8 into two breast cancer cell lines: total exclusion of three regions indicates location of putative in vitro growth suppressor genes (Q38483754) (← links)
- Genetic background of different cancer cell lines influences the gene set involved in chromosome 8 mediated breast tumor suppression (Q40301219) (← links)
- A network of clinically and functionally relevant genes is involved in the reversion of the tumorigenic phenotype of MDA-MB-231 breast cancer cells after transfer of human chromosome 8. (Q40484664) (← links)
- Analysis of DLC-1 expression in human breast cancer. (Q52951470) (← links)
- Refined deletion mapping in sporadic breast cancer at chromosomal region 8p12-p21 and association with clinicopathological parameters. (Q52970508) (← links)
- Mutation analysis and mRNA expression of trail-receptors in human breast cancer. (Q53386106) (← links)
- Comparative genomic hybridization of microdissected familial ovarian carcinoma: two deleted regions on chromosome 15q not previously identified in sporadic ovarian carcinoma. (Q53395169) (← links)
- Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22 (Q57903143) (← links)
- Three discrete areas within the chromosomal 8p21.3-23 region are associated with the development of breast carcinoma of Indian patients (Q80049754) (← links)