Pages that link to "Q48105355"
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The following pages link to A common region of homozygous deletion in malignant human gliomas lies between the IFN alpha/omega gene cluster and the D9S171 locus (Q48105355):
Displaying 8 items.
- Clinical significance of EGFR amplification and the aberrant EGFRvIII transcript in conventionally treated astrocytic gliomas. (Q33628302) (← links)
- MTS1/p16/CDKN2 lesions in primary glioblastoma multiforme. (Q35794912) (← links)
- Low-frequency loss of heterozygosity in Moloney murine leukemia virus-induced tumors in BRAKF1/J mice. (Q35883808) (← links)
- Loss of tumor suppressive microRNA-31 enhances TRADD/NF-κB signaling in glioblastoma (Q36232178) (← links)
- Loss of heterozygosity at chromosome 9p in ductal carcinoma in situ and invasive carcinoma of the breast (Q36292461) (← links)
- Genetic alterations in gliomas (Q40923819) (← links)
- Multiple deleted regions on the long arm of chromosome 6 in astrocytic tumours (Q41903586) (← links)
- Infrequent methylation of CDKN2A(MTS1/p16) and rare mutation of both CDKN2A and CDKN2B(MTS2/p15) in primary astrocytic tumours (Q41909854) (← links)