about
Iscador Qu inhibits doxorubicin-induced senescence of MCF7 cellsA combined ligand- and structure-based approach for the identification of rilmenidine-derived compounds which synergize the antitumor effects of doxorubicin.Synthesis of the vitamin E amino acid esters with an enhanced anticancer activity and in silico screening for new antineoplastic drugs.Synthesis and in vitro antitumour activity of crassalactone D, its stereoisomers and novel cinnamic ester derivatives.Design, synthesis and in vitro antitumour activity of new goniofufurone and 7-epi-goniofufurone mimics with halogen or azido groups at the C-7 position.Novel selenosemicarbazone metal complexes exert anti-tumor effect via alternative, caspase-independent necroptotic cell death.Imidazoline-1 receptor ligands as apoptotic agents: pharmacophore modeling and virtual docking study.Anti-metastatic and anti-angiogenic properties of potential new anti-cancer drugs based on metal complexes of selenosemicarbazones.Targeted therapy and personalized medicine in hepatocellular carcinoma: drug resistance, mechanisms, and treatment strategies.Synthesis, characterization, cytotoxic activity and DNA binding properties of the novel dinuclear cobalt(III) complex with the condensation product of 2-acetylpyridine and malonic acid dihydrazide.TNF-α induced apoptosis is accompanied with rapid CD30 and slower CD45 shedding from K-562 cells.Synthesis, structure and characterization of novel Cd(II) and Zn(II) complexes with the condensation product of 2-formylpyridine and selenosemicarbazide Antiproliferative activity of the synthesized complexes and related selenosemicarbazone complexeSynthesis and antiproliferative activity of goniobutenolides A and B, 5-halogenated crassalactone D derivatives and the corresponding 7-epimers.Sensitization of K562 Leukemia Cells to Doxorubicin by the Viscum album Extract.Rilmenidine suppresses proliferation and promotes apoptosis via the mitochondrial pathway in human leukemic K562 cells.Biological evaluation of transdichloridoplatinum(II) complexes with 3- and 4-acetylpyridine in comparison to cisplatin.Effects of bioactive-rich extracts of pomegranate, persimmon, nettle, dill, kale and Sideritis and isolated bioactives on arachidonic acid induced markers of platelet activation and aggregation.Chemical characterization, antioxidant, genotoxic and in vitro cytotoxic activity assessment of Juniperus communis var. saxatilis.Acute effects of black currant consumption on salivary flow rate and secretion rate of salivary immunoglobulin a in healthy smokers.Decreased expression of pSTAT, IRF-1 and DAP10 signalling molecules in peripheral blood lymphocytes of patients with metastatic melanoma.Author Correction: Iscador Qu inhibits doxorubicin-induced senescence of MCF7 cellsAntibody Epitope Specificity for dsDNA Phosphate Backbone Is an Intrinsic Property of the Heavy Chain Variable Germline Gene Segment UsedThe absence of immunoreactivity to donkey’s milk in patients with recurrent aphthous ulcers and immunoreactivity to cow’s milkSpecific Binding of Paraprotein to Platelet Receptors as a Cause of Platelet Dysfunction in Monoclonal GammopathiesNaturally occurring V region connected antibodies inhibit anti-dsDNA antibody reactivity with dsDNASerum DPPIV activity and CD26 expression on lymphocytes in patients with benign or malignant breast tumorsExpression of ERCC1 protein in biopsy specimen predicts survival in advanced ovarian cancer patients treated with platinum-based chemotherapyCooperation of intrathymic T15 idiotype-bearing B and complementary T cells in ontogeny of natural Treg cells involved in establishment of T15 clonal dominanceTelmisartan induces melanoma cell apoptosis and synergizes with vemurafenib in vitro by altering cell bioenergeticsBenzothiazole carbamates and amides as antiproliferative speciesNovel O-methyl goniofufurone and 7-epi-goniofufurone derivatives: synthesis, in vitro cytotoxicity and SAR analysisA Model for Potential B-cell Precursors of Broadly Neutralizing HIV-1 Antibodies Selection and Antibody Affinity Maturation
P50
Q33812688-717E314F-F8F4-410B-B42C-931D433A9147Q36041718-E078AD0E-A408-45C8-A01D-5F0699EB6684Q38779456-CAE10A06-1B0A-4D9B-BAAD-0C5F8377D48BQ38828392-64D4F6BC-53C4-4FF4-AD14-F3F61BE6E17EQ38991819-C0D48327-ADE5-4929-955F-9F65FA762307Q39010619-3F1FE058-AA85-445C-A4A1-E22C89AB25EAQ39202618-43DBA4FA-9EC3-4C39-97B6-B9BDDC79ACB9Q39348667-2748193E-26BE-4E32-8BF1-9117F37B4BC6Q39458547-253367B3-6258-4EDE-90F3-2CC06ED104E1Q39514489-A581D223-FC0B-4059-BB27-4860698D40A7Q39609504-C40A3A4B-CD04-46F3-80BD-A1AE013E3953Q39720460-560E0DCE-927C-479B-BEA8-9C696693A35FQ40155508-2B0FCE72-7617-4272-A8DE-4AF12301644EQ40182949-150899CD-6805-479E-8726-D12DE72B660FQ40284464-427838AD-4ABA-440A-8614-1F617142A811Q42925820-E209A6E2-CDE8-4D14-AE38-C7E7242A8D7BQ45168153-85BC2AAA-647F-41C3-B4A9-5C93357E5242Q49488199-AEED59BD-BACA-47B0-8D30-0007DD61C518Q51002658-8C589E4D-3921-45D3-8824-74D17B30E23BQ52911759-7A40837B-8595-4968-B5AB-D287378BEAE6Q58116374-F843CE15-4E36-4CE0-910D-220D3C6F0F0CQ58596162-027310C4-AE44-47B1-B1F8-F0C8718BBEC4Q61847299-23487163-7F61-4C1C-B1C3-1D2FF358CB35Q61847303-55759746-D102-457E-B3D0-8CDE64532039Q64386685-9DCABCB9-A533-4E8C-973C-4CA8EDF2A3A5Q83332373-83C45DE7-5364-4767-93DE-2875F8C0B3B9Q83439811-BAE584FC-92DD-439D-97EF-DA83DADA0DE7Q89499242-C123DAB6-472B-4376-B320-436085A46729Q90088009-C8CDE488-9D6E-4ED6-A88A-FBAD87C6B8AFQ91282916-7E2C2810-F236-4AFA-A40F-2F4FF8219A12Q91470249-3B1D52CF-DCBA-4965-918C-C7AA7BBC7090Q95794311-5F914ED0-14B8-4668-9105-2A25A472F378
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Tatjana Srdic-Rajic
@ast
Tatjana Srdic-Rajic
@en
Tatjana Srdic-Rajic
@es
Tatjana Srdic-Rajic
@nl
type
label
Tatjana Srdic-Rajic
@ast
Tatjana Srdic-Rajic
@en
Tatjana Srdic-Rajic
@es
Tatjana Srdic-Rajic
@nl
prefLabel
Tatjana Srdic-Rajic
@ast
Tatjana Srdic-Rajic
@en
Tatjana Srdic-Rajic
@es
Tatjana Srdic-Rajic
@nl
P106
P1153
16432965100
P31
P496
0000-0001-9840-6970