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Article title matches

  1. Category:Chemotherapy (43 bytes)
    1: List of pages with the keyword Chemotherapy
  2. Category:Chemotherapy target (50 bytes)
    1: List of pages with the keyword Chemotherapy target
  3. Category:Cancer chemotherapy target (57 bytes)
    1: List of pages with the keyword Cancer chemotherapy target
  4. Category:Resistance to chemotherapy (57 bytes)
    1: List of pages with the keyword Resistance to chemotherapy

Page text matches

  1. 2iw9 (7,175 bytes)
    24: ...egulation and are an attractive target for cancer chemotherapy. The roles of four residues of the cyclin-depende...
  2. 2iw8 (7,143 bytes)
    24: ...egulation and are an attractive target for cancer chemotherapy. The roles of four residues of the cyclin-depende...
  3. 2iw6 (7,250 bytes)
    24: ...egulation and are an attractive target for cancer chemotherapy. The roles of four residues of the cyclin-depende...
  4. 1bj4 (4,347 bytes)
    23: ...ynthesis makes it an attractive target for cancer chemotherapy. RESULTS: We have solved the crystal structure of...
    25: ...ine hydroxymethyltransferase: a target for cancer chemotherapy.,Renwick SB, Snell K, Baumann U Structure. 1998 S...
  5. 2cbz (4,545 bytes)
    24: ...family of transport proteins. MRP1 contributes to chemotherapy failure by exporting a wide range of anti-cancer ...
  6. 2cg9 (5,524 bytes)
    24: ...ng systems and is an emerging target for rational chemotherapy of many cancers. Although the structures of isola...
  7. 2j87 (4,959 bytes)
    24: ...e of the most successful strategies for antiviral chemotherapy as demonstrated for anti-herpes drugs. Vaccinia v...
  8. 3zcw (4,576 bytes)
    16: ...in Eg5 is a target for drug development in cancer chemotherapy with compounds in phase II clinical trials. These...
  9. 1qnt (4,356 bytes)
    23: ...nt of drugs as chemoenhancers of alkylating agent chemotherapy.
  10. Deoxycytidine kinase 3D structures (1,844 bytes)
    6: *dCK complex with chemotherapy agent
    8: **[[1p5z]], [[1p62]], [[2a7q]] – hDCK + ADP + chemotherapy agent – human<br />
    9: ...0]], [[2no6]], [[2zi9]] – hDCK (mutant) + ADP + chemotherapy agent <br />
    10: **[[2zia]], [[4kcg]] – hDCK (mutant) + UDP + chemotherapy agent <br />
    11: ...5mqt]], [[5mql]] – hDCK (mutant) + UDP + dCMP + chemotherapy agent<br />
  11. 11gs (4,085 bytes)
    24: ... been tested in clinical trials as an adjuvant in chemotherapy. We recently solved the crystal structure of this...
  12. 1cb5 (4,677 bytes)
    23: ...major cause of tumor cell resistance to bleomycin chemotherapy. In addition, it has been reported that an alleli...
  13. 4hrc (3,961 bytes)
    14: ...to the design of proteasome inhibitors for cancer chemotherapy.
  14. 4hrd (4,011 bytes)
    14: ...to the design of proteasome inhibitors for cancer chemotherapy.
  15. 8f4b (3,590 bytes)
    14: ...ancers leads to acquired multidrug resistance and chemotherapy failure. Small-molecule inhibitors have the poten...
  16. 1g91 (4,448 bytes)
    23: ...es that could lead to therapeutics for preventing chemotherapy-associated myelotoxicity.
  17. 1hw3 (5,048 bytes)
    2: ...HUMAN THYMIDYLATE SYNTHASE SUGGESTS ADVANTAGES OF CHEMOTHERAPY WITH NONCOMPETITIVE INHIBITORS==
    24: ...hymidylate synthase (TS) is a major target in the chemotherapy of colorectal cancer and some other neoplasms. Th...
    26: ...human thymidylate synthase suggests advantages of chemotherapy with noncompetitive inhibitors.,Phan J, Steadman ...
  18. 1hw4 (5,045 bytes)
    2: ...RE OF THYMIDYLATE SYNTHASE SUGGESTS ADVANTAGES OF CHEMOTHERAPY WITH NONCOMPETITIVE INHIBITORS==
    24: ...hymidylate synthase (TS) is a major target in the chemotherapy of colorectal cancer and some other neoplasms. Th...
    26: ...human thymidylate synthase suggests advantages of chemotherapy with noncompetitive inhibitors.,Phan J, Steadman ...
  19. 1ke6 (7,409 bytes)
    24: ...have shown potential utility in the prevention of chemotherapy-induced alopecia.
  20. 1ke7 (7,413 bytes)
    24: ...have shown potential utility in the prevention of chemotherapy-induced alopecia.

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