Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells. - Wikidata - awgldk - TriplyDB

Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells.

Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells.

http://www.wikidata.org/entity/Q43988423

about

Laser selection significantly affects cell viability following single-cell nanosurgery.FoxO3a governs early microglial proliferation and employs mitochondrial depolarization with caspase 3, 8, and 9 cleavage during oxidant induced apoptosis.Oxidative stress: Biomarkers and novel therapeutic pathways.New strategies for Alzheimer's disease and cognitive impairment.Diabetes mellitus: channeling care through cellular discovery FOXO3a governs early and late apoptotic endothelial programs during elevated glucose through mitochondrial and caspase signaling.Early apoptotic vascular signaling is determined by Sirt1 through nuclear shuttling, forkhead trafficking, bad, and mitochondrial caspase activation.Novel avenues of drug discovery and biomarkers for diabetes mellitus.Cytotoxic and apoptotic evaluations of marine bacteria isolated from brine-seawater interface of the Red Sea.miR-22 represses cancer progression by inducing cellular senescence EPO relies upon novel signaling of Wnt1 that requires Akt1, FoxO3a, GSK-3β, and β-catenin to foster vascular integrity during experimental diabetes.Erythropoietin fosters both intrinsic and extrinsic neuronal protection through modulation of microglia, Akt1, Bad, and caspase-mediated pathways Erythropoietin employs cell longevity pathways of SIRT1 to foster endothelial vascular integrity during oxidant stress.Mammalian target of rapamycin: hitting the bull's-eye for neurological disorders.Targeting WNT, protein kinase B, and mitochondrial membrane integrity to foster cellular survival in the nervous system.Activating Akt and the brain's resources to drive cellular survival and prevent inflammatory injury Attempted cell cycle induction in post-mitotic neurons occurs in early and late apoptotic programs through Rb, E2F1, and caspase 3 Erythropoietin requires NF-kappaB and its nuclear translocation to prevent early and late apoptotic neuronal injury during beta-amyloid toxicity The sirtuin inhibitor nicotinamide enhances neuronal cell survival during acute anoxic injury through AKT, BAD, PARP, and mitochondrial associated "anti-apoptotic" pathways.Vital elements of the Wnt-Frizzled signaling pathway in the nervous system.Winding through the WNT pathway during cellular development and demise Driving cellular plasticity and survival through the signal transduction pathways of metabotropic glutamate receptors.Cell Life versus cell longevity: the mysteries surrounding the NAD+ precursor nicotinamide.Erythropoietin: elucidating new cellular targets that broaden therapeutic strategies Mechanistic insights into diabetes mellitus and oxidative stress The Src homology 2 domain tyrosine phosphatases SHP-1 and SHP-2: diversified control of cell growth, inflammation, and injury.Erythropoietin and oxidative stress.The vitamin nicotinamide: translating nutrition into clinical care.ADAM17 is a survival factor for microglial cells in vitro and in vivo after spinal cord injury in mice.Regulation of spontaneous eosinophil apoptosis-a neglected area of importance.Cellular imaging assay for early evaluation of an apoptosis inducer.The effect of seal oil on paclitaxel induced cytotoxicity and apoptosis in breast carcinoma MCF-7 and MDA-MB-231 cell lines.The NAD+ precursor nicotinamide governs neuronal survival during oxidative stress through protein kinase B coupled to FOXO3a and mitochondrial membrane potential.DMSO modifies structural and functional properties of RPMI-8402 cells by promoting programmed cell death.Influence of zinc deficiency on cell-membrane fluidity in Jurkat, 3T3 and IMR-32 cells.Selective apoptosis of multiple myeloma cells in primary samples induced by arsenic trioxide.

P2860

Q33475086-F7D68AD6-1B87-4E88-BDCB-FF74CFA1097D Q33604706-D4AE77E7-949D-4A05-BC84-EDE0D8D71A52 Q33682262-7E534FBE-571C-4D92-B6AF-95DF5EFD7D6E Q33717008-336A9483-2BAA-475C-88B1-56BF74D55CE5 Q33749358-D4CAE243-8FED-44A2-8B73-CD56A361004C Q33802721-9E01F132-FDB9-4DD9-895E-4D4CB96308F6 Q33877687-7D5E4225-8BD5-42C1-9FD1-DDEFE19E95A3 Q34552287-028D7BAA-9A96-477F-B72E-C2E6928967B8 Q34578844-8491B11A-69E0-4B54-B291-D5B66D13A9B5 Q34825182-9116F57D-3BA2-4144-96F2-6F342C454773 Q34887803-6D0A4C79-F769-40B2-A91C-242640BBF6A1 Q35045115-66A79525-F2ED-45A3-BFBF-BB3CBF08379C Q35146283-54E48A16-D012-46AE-A1C4-8A0D6B4FD7FE Q35157985-E60BBBED-AB36-413B-BAA0-4EE7F5265B19 Q35692773-7494C4B5-EA2B-41F0-B201-FD3CACA9C31D Q35971676-A7C755E2-959D-41BA-B4FB-6111C123F50D Q36002822-294D8DF7-4287-4120-B661-9BCB3CB8E59E Q36002879-2274B608-33ED-4142-8D14-C7B8045C3B8B Q36002884-E92BA27C-41F1-458B-A41C-CDD5116C6ED5 Q36266255-05D167DA-D481-49C0-B832-C5EF837415CA Q36305544-854B31E9-FFC4-4C55-A753-677F39A1C792 Q36352348-FDEF1D22-117F-47CA-A9D5-AD0BFBC98BE8 Q36447198-8043111E-9F09-4BD2-A958-40D174FD3360 Q36740470-DC56A755-8245-4D6D-9AEA-1E96DAA0DFB0 Q36748171-C2BB42E4-EE71-428D-9205-2EFF1F076F73 Q36836455-268E4567-460B-40F7-96F5-58C03D7E14D1 Q36944477-4409920B-61B1-4BF1-A851-56A5032FB357 Q37374047-252F0335-B35A-4764-9F54-D0B9418FF271 Q37424039-6F798A0F-C41D-402A-B04D-F35F97C65320 Q38256352-3E545FD5-0073-4B5C-96B4-181ECE404F89 Q39492519-A2A9C607-D3B7-4567-9985-FF13755642ED Q40105127-29893679-41FD-4267-B43C-4E59E106CC9D Q40498088-ABD451A8-D9C6-451F-8F85-2E1FFB45C0DF Q40617710-ACF3954C-960E-49B9-A976-93C397E6AF35 Q41776462-C519B117-23A0-40E1-87EF-03CB33654CF6 Q44670178-45629FF6-2EB3-4735-92A1-11A4C89F2087

P2860

Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells.

http://www.wikidata.org/entity/Q43988423

description

2002 nî lūn-bûn

@nan

2002年の論文

@ja

2002年学术文章

@wuu

2002年学术文章

@zh-cn

2002年学术文章

@zh-hans

2002年学术文章

@zh-my

2002年学术文章

@zh-sg

2002年學術文章

@yue

2002年學術文章

@zh

2002年學術文章

@zh-hant

name

Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells.

@en

Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells.

@nl

type

label

Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells.

@en

Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells.

@nl

prefLabel

Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells.

@en

Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells.

@nl

P1433

Q43988423-D1729841-2ADA-4375-AF1C-B75E77A8DB83

P1476

Q43988423-818250A4-442F-4B7F-BCD0-78CDD4A8DD2B

P2093

Q43988423-3599571D-95D9-46B5-84DF-BE458CDEA566

Q43988423-9D77C7DD-6828-4A95-A40F-D15298C74C91

Q43988423-AB4AB267-3B07-41B2-AC36-DDC2405CBD31

Q43988423-B1D723BF-9E7B-40D1-BDF4-61F6A8BC240C

Q43988423-BE103D23-F2F0-462D-935D-139B90BBCF2B

P2860

Q43988423-0C7532E4-98ED-4053-B75D-5661AEEDD9E2

Q43988423-41C9B0C9-0F33-4C86-B06E-A5BE047CECA1

Q43988423-4A22D722-A956-4D51-8363-793758FAB3DB

Q43988423-4CE97F15-4317-4262-8C4D-75CB1A2C4A63

Q43988423-5DF947A8-BA52-440A-8A00-04D59EBB3ADF

Q43988423-60E45034-E9A8-45C1-BD9E-DD8E8D314984

Q43988423-71736EA8-07EF-476E-A730-8BB9FEAF86E7

Q43988423-99D34D40-AD8E-4A35-8071-D60BFC999205

Q43988423-A1298642-D0E5-4B51-9D53-EFD5A3F8916D

Q43988423-AE080AF9-5B65-4BDF-A2AE-0A7F68839B8D

P304

Q43988423-626CD289-19B0-4D74-A029-284D4EE9CCF5

P31

Q43988423-468EF5AA-0167-4839-AA30-9BAC99999D79

P356

Q43988423-D95A0720-7D70-4F4A-BDE4-37DAF268FA32

P433

Q43988423-F403894A-0AD7-4097-AAFD-8046A9391554

P478

Q43988423-4A43E80D-51EE-4B08-B34E-35D5CD3ECBA4

P577

Q43988423-B299E714-8076-441A-B022-CE142AED3761

P5875

Q43988423-AA4AF6F5-16A5-4C8B-874E-62A56995F804

P698

Q43988423-4F2FE76B-3C3C-41C0-8666-8D83D00AC04A

P921

Q43988423-EC55934B-D323-4FA5-80AA-77BDEADE7A19

P932

Q43988423-C0ACA0EC-8403-4BA2-ABB8-B0A78B9C6EAB

P356

J.1582-4934.2002.TB00313.X

P1433

Journal of Cellular and Molecular Medicine

P1476

Kinetics of apoptotic markers in exogeneously induced apoptosis of EL4 cells

@en

P2093

Carmen Socaciu

http://www.w3.org/2001/XMLSchema#string

Horst A Diehl

http://www.w3.org/2001/XMLSchema#string

Robert Jessel

http://www.w3.org/2001/XMLSchema#string

Steffen Haertel

http://www.w3.org/2001/XMLSchema#string

Svetlana Tykhonova

http://www.w3.org/2001/XMLSchema#string

P2860

Oxidative signaling pathway for externalization of plasma membrane phosphatidylserine during apoptosis

Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics

Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

Apoptosis: definition, mechanisms, and relevance to disease.

Role of reactive oxygen species in apoptosis: implications for cancer therapy.

Role of Ced-3/ICE-family proteases in staurosporine-induced programmed cell death.

Plasma membrane alterations and cytoskeletal changes in apoptosis.

Fluidity parameters of lipid regions determined by fluorescence polarization.

Lipid asymmetry in membranes.

Apoptosis: the biochemistry and molecular biology of programmed cell death.

P304

82-92

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/J.1582-4934.2002.TB00313.X

http://www.w3.org/2001/XMLSchema#string

P433

1

http://www.w3.org/2001/XMLSchema#string

P478

6

http://www.w3.org/2001/XMLSchema#string

P577

2002-01-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

11366715

http://www.w3.org/2001/XMLSchema#string

P698

12003671

http://www.w3.org/2001/XMLSchema#string

P921

apoptotic process

P932

6740285

http://www.w3.org/2001/XMLSchema#string