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Applicants have described methods in which library members comprise a fusion protein having a first polypeptide portion with DNA binding activity and a second polypeptide portion having the library member unique peptide sequence

No additional loci reached genome-wide significance under the random-effects framework, reinforcing the stability of the findings

carboplatin e.g., PARAPLATIN Cisplatin e.g., PLATINOL, PLATINOL-AQ Cyclophosphamide e.g., CYTOXAN, NEOSAR Docetaxel e.g., TAXOTERE GEMZAR gemcitabine imatinib mesylate e.g., GLEEVEC Irinotecan e.g., CAMPTOSAR Methotrexate e.g., FOLEX, MEXATE, AMETHOPTERIN Paclitaxel e.g., TAXOL, ABRAXANE Sorafmib e.g., NEXAVAR Sunitinib e.g., SUTENT Topotecan e.g., HYCAMTIN Vinblastine e.g., VELBAN Vincristine e.g

Protein Expres Purif 2006, 48 (1):104-111