Pages that link to "Q58062339"

The following pages link to Integrated Map of the Chromosome 8p12–p21 Region, a Region Involved in Human Cancers and Werner Syndrome (Q58062339):

Displaying 19 items.

• Cancer incidence in relatives of a population-based set of cases of early-onset breast cancer with a known BRCA1 and BRCA2 mutation status (Q24802534) (← links)
• PRK, a cell cycle gene localized to 8p21, is downregulated in head and neck cancer (Q28145001) (← links)
• Genetic alteration of chromosome 8 is a common feature of human mammary epithelial cell lines transformed in vitro with benzo[a]pyrene (Q31881445) (← links)
• NEFL mRNA expression level is a prognostic factor for early-stage breast cancer patients (Q34154749) (← links)
• TrnR2, a novel receptor that mediates neurturin and GDNF signaling through Ret. (Q34428727) (← links)
• Deletion mapping and linkage analysis provide strong indication for the involvement of the human chromosome region 8p12-p22 in breast carcinogenesis (Q36431232) (← links)
• From old organisms to new molecules: integrative biology and therapeutic targets in accelerated human ageing. (Q36895328) (← links)
• A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene (Q40640693) (← links)
• gamma-heregulin is the product of a chromosomal translocation fusing the DOC4 and HGL/NRG1 genes in the MDA-MB-175 breast cancer cell line (Q40922469) (← links)
• A 2.8 megabase YAC contig spanning D8S339, which is tightly linked to the Werner syndrome locus (Q41130003) (← links)
• Instability of the CAG repeat in immortalized fibroblast cell cultures from Huntington's disease transgenic mice (Q45298851) (← links)
• Mathematical modeling of noise and discovery of genetic expression classes in gliomas (Q48473479) (← links)
• Refined deletion mapping in sporadic breast cancer at chromosomal region 8p12-p21 and association with clinicopathological parameters. (Q52970508) (← links)
• Frequent multiplication of chromosomal region 8q24.1 associated with aggressive histologic types of breast cancers. (Q53421391) (← links)
• Genetic alterations detected by comparative genomic hybridization in BRCAX breast and ovarian cancers of Brazilian population. (Q55191144) (← links)
• Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22 (Q57903143) (← links)
• Association of NEFL Gene Polymorphisms with Wilms’ Tumor Susceptibility in Chinese Children (Q64095210) (← links)
• Differential expression assay of chromosome arm 8p genes identifies Frizzled-related (FRP1/FRZB) and Fibroblast Growth Factor Receptor 1 (FGFR1) as candidate breast cancer genes (Q74623191) (← links)
• Two novel regions of interstitial deletion on chromosome 8p in colorectal cancer (Q78171325) (← links)