490 related articles for article (PubMed ID: 8670109)
1. Benzyloxycarbonyl-Val-Ala-Asp (OMe) fluoromethylketone (Z-VAD.FMK) inhibits apoptosis by blocking the processing of CPP32.
Slee EA; Zhu H; Chow SC; MacFarlane M; Nicholson DW; Cohen GM
Biochem J; 1996 Apr; 315 ( Pt 1)(Pt 1):21-4. PubMed ID: 8670109
[TBL] [Abstract][Full Text] [Related]
2. Processing/activation of CPP32-like proteases is involved in transforming growth factor beta1-induced apoptosis in rat hepatocytes.
Inayat-Hussain SH; Couet C; Cohen GM; Cain K
Hepatology; 1997 Jun; 25(6):1516-26. PubMed ID: 9185777
[TBL] [Abstract][Full Text] [Related]
3. Processing/activation of at least four interleukin-1beta converting enzyme-like proteases occurs during the execution phase of apoptosis in human monocytic tumor cells.
MacFarlane M; Cain K; Sun XM; Alnemri ES; Cohen GM
J Cell Biol; 1997 Apr; 137(2):469-79. PubMed ID: 9128256
[TBL] [Abstract][Full Text] [Related]
4. Camptothecin-induced apoptosis in p53-null human leukemia HL60 cells and their isolated nuclei: effects of the protease inhibitors Z-VAD-fmk and dichloroisocoumarin suggest an involvement of both caspases and serine proteases.
Shimizu T; Pommier Y
Leukemia; 1997 Aug; 11(8):1238-44. PubMed ID: 9264376
[TBL] [Abstract][Full Text] [Related]
5. Ligation of CD40 rescues Ramos-Burkitt lymphoma B cells from calcium ionophore- and antigen receptor-triggered apoptosis by inhibiting activation of the cysteine protease CPP32/Yama and cleavage of its substrate PARP.
An S; Knox KA
FEBS Lett; 1996 May; 386(2-3):115-22. PubMed ID: 8647264
[TBL] [Abstract][Full Text] [Related]
6. Effector caspases are dispensable for the early nuclear morphological changes during chemical-induced apoptosis.
Johnson VL; Ko SC; Holmstrom TH; Eriksson JE; Chow SC
J Cell Sci; 2000 Sep; 113 ( Pt 17)():2941-53. PubMed ID: 10934034
[TBL] [Abstract][Full Text] [Related]
7. Inhibition of interleukin 1beta converting enzyme family proteases reduces ischemic and excitotoxic neuronal damage.
Hara H; Friedlander RM; Gagliardini V; Ayata C; Fink K; Huang Z; Shimizu-Sasamata M; Yuan J; Moskowitz MA
Proc Natl Acad Sci U S A; 1997 Mar; 94(5):2007-12. PubMed ID: 9050895
[TBL] [Abstract][Full Text] [Related]
8. Caspase-independent cell death induced by anti-CD2 or staurosporine in activated human peripheral T lymphocytes.
Déas O; Dumont C; MacFarlane M; Rouleau M; Hebib C; Harper F; Hirsch F; Charpentier B; Cohen GM; Senik A
J Immunol; 1998 Oct; 161(7):3375-83. PubMed ID: 9759854
[TBL] [Abstract][Full Text] [Related]
9. Systemic injection of a tripeptide inhibits the intracellular activation of CPP32-like proteases in vivo and fully protects mice against Fas-mediated fulminant liver destruction and death.
Rodriguez I; Matsuura K; Ody C; Nagata S; Vassalli P
J Exp Med; 1996 Nov; 184(5):2067-72. PubMed ID: 8920897
[TBL] [Abstract][Full Text] [Related]
10. A DEVD-inhibited caspase other than CPP32 is involved in the commitment of cerebellar granule neurons to apoptosis induced by K+ deprivation.
D'Mello SR; Aglieco F; Roberts MR; Borodezt K; Haycock JW
J Neurochem; 1998 May; 70(5):1809-18. PubMed ID: 9572264
[TBL] [Abstract][Full Text] [Related]
11. Activation of the CED3/ICE-related protease CPP32 in cerebellar granule neurons undergoing apoptosis but not necrosis.
Armstrong RC; Aja TJ; Hoang KD; Gaur S; Bai X; Alnemri ES; Litwack G; Karanewsky DS; Fritz LC; Tomaselli KJ
J Neurosci; 1997 Jan; 17(2):553-62. PubMed ID: 8987778
[TBL] [Abstract][Full Text] [Related]
12. Caspases (interleukin-1beta-converting enzyme family proteases) are involved in the regulation of the survival of osteoclasts.
Okahashi N; Koide M; Jimi E; Suda T; Nishihara T
Bone; 1998 Jul; 23(1):33-41. PubMed ID: 9662128
[TBL] [Abstract][Full Text] [Related]
13. Involvement of ICE (Caspase) family in gamma-radiation-induced apoptosis of normal B lymphocytes.
Hallan E; Blomhoff HK; Smeland EB; Lømo J
Scand J Immunol; 1997 Dec; 46(6):601-8. PubMed ID: 9420624
[TBL] [Abstract][Full Text] [Related]
14. The apoptosis-necrosis paradox. Apoptogenic proteases activated after mitochondrial permeability transition determine the mode of cell death.
Hirsch T; Marchetti P; Susin SA; Dallaporta B; Zamzami N; Marzo I; Geuskens M; Kroemer G
Oncogene; 1997 Sep; 15(13):1573-81. PubMed ID: 9380409
[TBL] [Abstract][Full Text] [Related]
15. Caspases-3 and -7 are activated in goniothalamin-induced apoptosis in human Jurkat T-cells.
Inayat-Hussain SH; Osman AB; Din LB; Ali AM; Snowden RT; MacFarlane M; Cain K
FEBS Lett; 1999 Aug; 456(3):379-83. PubMed ID: 10462048
[TBL] [Abstract][Full Text] [Related]
16. Processing/activation of caspases, -3 and -7 and -8 but not caspase-2, in the induction of apoptosis in B-chronic lymphocytic leukemia cells.
King D; Pringle JH; Hutchinson M; Cohen GM
Leukemia; 1998 Oct; 12(10):1553-60. PubMed ID: 9766499
[TBL] [Abstract][Full Text] [Related]
17. Distinct steps in DNA fragmentation pathway during camptothecin-induced apoptosis involved caspase-, benzyloxycarbonyl- and N-tosyl-L-phenylalanylchloromethyl ketone-sensitive activities.
Sané AT; Bertrand R
Cancer Res; 1998 Jul; 58(14):3066-72. PubMed ID: 9679972
[TBL] [Abstract][Full Text] [Related]
18. Activation of CPP32-like proteases is not sufficient to trigger apoptosis: inhibition of apoptosis by agents that suppress activation of AP24, but not CPP32-like activity.
Wright SC; Schellenberger U; Wang H; Kinder DH; Talhouk JW; Larrick JW
J Exp Med; 1997 Oct; 186(7):1107-17. PubMed ID: 9314559
[TBL] [Abstract][Full Text] [Related]
19. Inhibition of Ced-3/ICE-related proteases does not prevent cell death induced by oncogenes, DNA damage, or the Bcl-2 homologue Bak.
McCarthy NJ; Whyte MK; Gilbert CS; Evan GI
J Cell Biol; 1997 Jan; 136(1):215-27. PubMed ID: 9008715
[TBL] [Abstract][Full Text] [Related]
20. Need for caspases in apoptosis of trophic factor-deprived PC12 cells.
Haviv R; Lindenboim L; Li H; Yuan J; Stein R
J Neurosci Res; 1997 Oct; 50(1):69-80. PubMed ID: 9379495
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]