摘要:
The present invention pertains to a novel treatment of renal cell carcinoma and other a solid tumors which harbor a VHL inactivation, based on the combination of a first agent inhibiting a protein kinase CK2 (CK2) and a second agent inhibiting an Ataxia Telangiectasia Mutated (ATM) kinase.
摘要:
The invention relates to small interfering RNA specific to sub-units α, α′ and &bgr; of the kinase protein CK2, and to the applications of the same, especially for treating cancer and viral illnesses.
摘要:
The invention relates to small interfering RNA specific to sub-units α, α' and ß of the kinase protein CK2, and to the applications of the same, especially for treating cancer and viral illnesses.
摘要:
The present invention pertains to a novel treatment of renal cell carcinoma and other a solid tumors which harbor a VHL inactivation, based on the combination of a first agent inhibiting a protein kinase CK2 (CK2) and a second agent inhibiting an Ataxia Telangiectasia Mutated (ATM) kinase.
摘要:
The invention relates to the use of specific compounds of formula (I) and their pharmaceutically-acceptable salts:(Formula 1) (I) as a new family of protein kinase CK2 inhibitors; the invention also relates to the use of compounds of formula (I) for the preparation of pharmaceutical compositions for the prevention and/or treatment of disorders and/or diseases chosen amongst cancers; autoimmune and inflammatory diseases; infectious diseases; diabetes angiogenesis related disorders; retinopathies and cardiac hypertrophy.