ro 5-4864 and cytochrome c-t

ro 5-4864 has been researched along with cytochrome c-t in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Braun, T; Carvalho, G; Codogno, P; Decaudin, D; Djavaheri-Mergny, M; Fabre, C; Feuillard, J; Gonzalez-Polo, RA; Kroemer, G; Larochette, N; Perfettini, JL; Raphael, M; Youlyouz-Marfak, I1
Azarashvili, T; Evtodienko, Y; Grachev, D; Krestinina, O; Papadopoulos, V; Reiser, G; Yurkov, I1
Campàs, C; Coll-Mulet, L; Cosialls, AM; de Frias, M; Domingo, A; Gil, J; González-Gironès, DM; Iglesias-Serret, D; Pons, G; Santidrián, AF1
Gavish, M; Kugler, W; Lakomek, M; Leschiner, S; Shandalov, Y; Spanier, I; Veenman, L1

Other Studies

4 other study(ies) available for ro 5-4864 and cytochrome c-t

ArticleYear
PK11195 potently sensitizes to apoptosis induction independently from the peripheral benzodiazepin receptor.
    Oncogene, 2005, Nov-17, Volume: 24, Issue:51

    Topics: Antineoplastic Agents; Apoptosis; ATP Binding Cassette Transporter, Subfamily B; Benzodiazepinones; Caspases; Chromatin; Cytochromes c; HeLa Cells; Humans; Hypolipidemic Agents; Isoquinolines; Ligands; Membrane Potentials; Mitochondria; NF-kappa B; Receptors, GABA-A; RNA, Small Interfering

2005
The peripheral-type benzodiazepine receptor is involved in control of Ca2+-induced permeability transition pore opening in rat brain mitochondria.
    Cell calcium, 2007, Volume: 42, Issue:1

    Topics: Adenosine Triphosphate; Animals; Antibodies; Apoptosis; Apoptosis Inducing Factor; Benzodiazepinones; Brain; Calcimycin; Calcium; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Carrier Proteins; Cyclosporine; Cytochromes c; Mitochondria; Mitochondrial ADP, ATP Translocases; Mitochondrial Membrane Transport Proteins; Mitochondrial Permeability Transition Pore; Phosphorylation; Protoporphyrins; Rats; Receptors, GABA-A

2007
The potential anticancer agent PK11195 induces apoptosis irrespective of p53 and ATM status in chronic lymphocytic leukemia cells.
    Haematologica, 2007, Volume: 92, Issue:12

    Topics: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Apoptosis; Ataxia Telangiectasia Mutated Proteins; B-Lymphocytes; Benzodiazepinones; Caspase Inhibitors; Caspases; Cell Cycle Proteins; Cytochromes c; DNA-Binding Proteins; Drug Screening Assays, Antitumor; Enzyme Activation; Female; Humans; Hypolipidemic Agents; Indoleacetic Acids; Isoquinolines; Leukemia, Lymphocytic, Chronic, B-Cell; Male; Membrane Potential, Mitochondrial; Middle Aged; Mitochondria; Protein Serine-Threonine Kinases; Receptors, GABA; T-Lymphocytes; Tumor Cells, Cultured; Tumor Suppressor Protein p53; Tumor Suppressor Proteins; Voltage-Dependent Anion Channels

2007
Ligands of the mitochondrial 18 kDa translocator protein attenuate apoptosis of human glioblastoma cells exposed to erucylphosphohomocholine.
    Cellular oncology : the official journal of the International Society for Cellular Oncology, 2008, Volume: 30, Issue:5

    Topics: Antineoplastic Agents; Apoptosis; Benzodiazepinones; Blotting, Western; Caspases; Cell Line, Tumor; Cell Proliferation; Cytochromes c; Erucic Acids; Glioblastoma; Humans; Isoquinolines; Ligands; Membrane Potential, Mitochondrial; Mitochondrial Membrane Transport Proteins; Mitochondrial Permeability Transition Pore; Phosphorylcholine; Receptors, GABA

2008