about
A review on the dietary flavonoid kaempferolEvaluating the cancer therapeutic potential of cardiac glycosidesTargeting SAMHD1 with the Vpx protein to improve cytarabine therapy for hematological malignancies.Discovery of the First Potent and Selective Inhibitors of Human dCTP Pyrophosphatase 1Pro-oxidant natural products as anticancer agents.Effect of DNA repair deficiencies on the cytotoxicity of drugs used in cancer therapy - a review.Design, synthesis and biological studies of a library of NK1-Receptor Ligands Based on a 5-arylthiosubstituted 2-amino-4,6-diaryl-3-cyano-4H-pyran core: Switch from antagonist to agonist effect by chemical modification.Zebularine induces replication-dependent double-strand breaks which are preferentially repaired by homologous recombination.Piperazin-1-ylpyridazine Derivatives Are a Novel Class of Human dCTP Pyrophosphatase 1 Inhibitors.Cancer-Specific Synthetic Lethality between ATR and CHK1 Kinase Activities.In vitro and in vivo evaluation of Δ⁹-tetrahidrocannabinol/PLGA nanoparticles for cancer chemotherapy.Sulforaphane homologues: Enantiodivergent synthesis of both enantiomers, activation of the Nrf2 transcription factor and selective cytotoxic activity.The PARP inhibitor Olaparib disrupts base excision repair of 5-aza-2'-deoxycytidine lesions.A hydroalcoholic extract from the leaves of Nerium oleander inhibits glycolysis and induces selective killing of lung cancer cells.Selective cytotoxic activity of new lipophilic hydroxytyrosol alkyl ether derivatives.Cells Deficient in the Fanconi Anemia Protein FANCD2 are Hypersensitive to the Cytotoxicity and DNA Damage Induced by Coffee and Caffeic Acid.Comment on 'Quiescence and γH2AX in neuroblastoma are regulated by ouabain/Na,K-ATPase': ouabain and cancer.The dark side of curcumin.Aziridines from alkenyl-β-D-galactopyranoside derivatives: Stereoselective synthesis and in vitro selective anticancer activity.Identification of Triazolothiadiazoles as Potent Inhibitors of the dCTP Pyrophosphatase 1.Avoiding the ingestion of cytotoxic concentrations of ethanol may reduce the risk of cancer associated with alcohol consumption.Guanidine-reactive agent phenylglyoxal induces DNA damage and cancer cell death.Does the Nerium oleander extract PBI-05204 have potential for pancreatic cancer therapy?A 30-s exposure to ethanol 20% is cytotoxic to human keratinocytes: possible mechanistic link between alcohol-containing mouthwashes and oral cancerAre most cancer cases a consequence of an immune deficiency caused by thymic involution?Screening for selective anticancer activity of plants from Grazalema Natural Park, SpainSelective cytotoxic activity and DNA damage by an epoxyalkyl galactopyranosideMore research is needed to establish the benefit-risk profile of curcuminBufalin is a steroid receptor coactivator inhibitor-letterThe in vivo antitumor activity of cardiac glycosides in mice xenografted with human cancer cells is probably an experimental artifactAnticancer Activities of Meroterpenoids Isolated from the Brown Alga Cystoseira usneoides against the Human Colon Cancer Cells HT-29
P50
Q28307823-3F4198B1-B3B0-4D3A-8061-D16C70948C25Q28386608-AB8ACECC-B089-4378-A80B-2608C45C165EQ34548815-B9375C3C-FA00-4602-91BB-D5FC892148CCQ36580244-FB22AAD1-EB21-4C30-8D2D-51F88580A0A5Q38010738-74D294E9-D3FA-40F3-BBB2-76765771A564Q38220654-4C301231-4C19-4CDC-A6D7-9E7539DBA5F0Q38657218-65E91C35-7EC9-4838-94D0-6986B6AA4DBEQ38667772-6E6BABEC-4C64-4933-9389-44A58158DF35Q38703379-85216835-0A13-4483-90E1-05DA171825FCQ38805276-89D54BBD-9B41-4E5F-AD67-6B49B230A9C5Q38883898-1B3BE163-55A5-465E-B047-772844E485AEQ38949448-B60ED5E4-BDC7-44C7-A17B-0A1BD52DB57BQ38970507-22DDBFDE-ED1C-43CA-A2E3-177E40FFD9FAQ39130887-4AB04ED0-9BE5-49F9-8E3F-40885FE9B381Q39157189-F0AC7BF0-2988-41E5-B1BC-169FF1BC6AE9Q39614379-F9FECA0B-4ED9-4869-B268-1B853C907B2BQ43143252-A358FF28-034D-4731-8390-740C76878DA5Q43261037-BB980341-A086-4B8B-A9D0-2096B1743900Q46071875-F9DBD4AF-81D0-4664-9BCA-C2DA826A12E0Q48289734-37DB87BB-D1B9-4718-944C-C6CCA80C56A4Q48554077-ADB15C7B-0815-45DE-B46B-45A3AEF6F7D1Q51754682-C95D782D-C537-45B5-92D7-96849390587EQ55067193-7398186F-C5C7-4F7A-A659-7CE3BB29389EQ57669564-28F386A2-F705-41E6-8AE2-A03BF1C59FCFQ57669580-2BAD9EBE-0587-42B7-ABE9-8A48AA56F1D4Q57669592-FA6C79CD-E5C1-41E7-AA9A-748DBEA9196FQ58094606-9B743A8F-18AE-4918-A225-0D9DC87647FFQ83112532-0596E421-3DE0-4A38-9D56-041B50C72936Q86862860-01E83FD3-5E42-496B-95C5-7DDB1329CF57Q86927793-9399EFF7-7F96-4E28-91EA-DD7969D522B5Q90189705-5421C9A1-9984-4C39-8505-7BF3434EA5D1
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0001-6845-797X
@en
name
José Manuel Calderón-Montaño
@ast
José Manuel Calderón-Montaño
@en
José Manuel Calderón-Montaño
@es
José Manuel Calderón-Montaño
@nl
type
label
José Manuel Calderón-Montaño
@ast
José Manuel Calderón-Montaño
@en
José Manuel Calderón-Montaño
@es
José Manuel Calderón-Montaño
@nl
prefLabel
José Manuel Calderón-Montaño
@ast
José Manuel Calderón-Montaño
@en
José Manuel Calderón-Montaño
@es
José Manuel Calderón-Montaño
@nl
P108
P106
P108
P1153
35602834400
P21
P31
P496
0000-0001-6845-797X