La maladie de Parkinson en France (serveur d'exploration)

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Functions of poly(ADP-ribose) polymerase (PARP) in DNA repair, genomic integrity and cell death

Identifieur interne : 001130 ( PascalFrancis/Corpus ); précédent : 001129; suivant : 001131

Functions of poly(ADP-ribose) polymerase (PARP) in DNA repair, genomic integrity and cell death

Auteurs : Zdenko Herceg ; Zhao-Qi Wang

Source :

RBID : Pascal:02-0234959

Descripteurs français

English descriptors

Abstract

Poly(ADP-ribose) polymerase (PARP) is responsible for post-translational modification of proteins in the response to numerous endogenous and environmental genotoxic agents. PARP and poly(ADP-ribosyl)ation are proposed to be important for the regulation of many cellular processes such as DNA repair, cell death, chromatin functions and genomic stability. Activation of PARP is one of the early DNA damage responses, among other DNA sensing molecules, such as DNA-PK, ATM and p53. The generation and characterization of PARP deficient mouse models have been instrumental in defining the biological role of the molecule and its involvement in the pathogenesis of various diseases including diabetes, stroke, Parkinson disease, general inflammation as well as tumorigenesis, and have, therefore, provided information for the development of pharmaceutical strategies for the treatment of diseases.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0027-5107
A02 01      @0 MUREAV
A03   1    @0 Mutat. res.
A05       @2 477
A06       @2 1-2
A08 01  1  ENG  @1 Functions of poly(ADP-ribose) polymerase (PARP) in DNA repair, genomic integrity and cell death
A09 01  1  ENG  @1 Analysis and prevention of carcinogenesis in animal models
A11 01  1    @1 HERCEG (Zdenko)
A11 02  1    @1 WANG (Zhao-Qi)
A12 01  1    @1 NAKAGAMA (H.) @9 ed.
A12 02  1    @1 ISHIKAWA (T.) @9 ed.
A12 03  1    @1 MIWA (M.) @9 ed.
A12 04  1    @1 SETLOW (R. B.) @9 ed.
A14 01      @1 International Agency for Research on Cancer (IARC), 150 cours Albert-Thomas @2 69008 Lyon @3 FRA @Z 1 aut. @Z 2 aut.
A15 01      @1 Biochemistry Division, National Cancer Center Research Institute @2 Tokyo 104-0045 @3 JPN @Z 1 aut.
A15 02      @1 Faculty of Medicine, University of Tokyo @2 Tokyo @3 JPN @Z 2 aut.
A15 03      @1 Department of Biochemistry and Molecular Oncology, Institute of Basic Medical Sciences, University of Tsukuba @2 Tsukuba, Ibaraki @3 JPN @Z 3 aut.
A15 04      @1 Biology Department, Brookhaven National Laboratory @2 Upton, NY @3 USA @Z 4 aut.
A20       @1 97-110
A21       @1 2001
A23 01      @0 ENG
A43 01      @1 INIST @2 12206A @5 354000095503940110
A44       @0 0000 @1 © 2002 INIST-CNRS. All rights reserved.
A45       @0 105 ref.
A47 01  1    @0 02-0234959
A60       @1 P
A61       @0 A
A64 01  1    @0 Mutation research
A66 01      @0 NLD
C01 01    ENG  @0 Poly(ADP-ribose) polymerase (PARP) is responsible for post-translational modification of proteins in the response to numerous endogenous and environmental genotoxic agents. PARP and poly(ADP-ribosyl)ation are proposed to be important for the regulation of many cellular processes such as DNA repair, cell death, chromatin functions and genomic stability. Activation of PARP is one of the early DNA damage responses, among other DNA sensing molecules, such as DNA-PK, ATM and p53. The generation and characterization of PARP deficient mouse models have been instrumental in defining the biological role of the molecule and its involvement in the pathogenesis of various diseases including diabetes, stroke, Parkinson disease, general inflammation as well as tumorigenesis, and have, therefore, provided information for the development of pharmaceutical strategies for the treatment of diseases.
C02 01  X    @0 002A04C07
C03 01  X  FRE  @0 Mort cellulaire @5 07
C03 01  X  ENG  @0 Cell death @5 07
C03 01  X  SPA  @0 Muerte celular @5 07
C03 02  X  FRE  @0 Réparation @5 08
C03 02  X  ENG  @0 Repair @5 08
C03 02  X  SPA  @0 Reparación @5 08
C03 03  X  FRE  @0 DNA @5 09
C03 03  X  ENG  @0 DNA @5 09
C03 03  X  SPA  @0 DNA @5 09
C03 04  X  FRE  @0 DNA-directed DNA polymerase @2 FE @5 10
C03 04  X  ENG  @0 DNA-directed DNA polymerase @2 FE @5 10
C03 04  X  SPA  @0 DNA-directed DNA polymerase @2 FE @5 10
C03 05  X  FRE  @0 Génomique @5 11
C03 05  X  ENG  @0 Genomics @5 11
C03 05  X  SPA  @0 Genómica @5 11
C03 06  X  FRE  @0 Intégrité @5 12
C03 06  X  ENG  @0 Integrity @5 12
C03 06  X  SPA  @0 Integridad @5 12
C03 07  X  FRE  @0 Apoptose @5 13
C03 07  X  ENG  @0 Apoptosis @5 13
C03 07  X  SPA  @0 Apoptosis @5 13
C07 01  X  FRE  @0 Nucleotidyltransferases @2 FE
C07 01  X  ENG  @0 Nucleotidyltransferases @2 FE
C07 01  X  SPA  @0 Nucleotidyltransferases @2 FE
C07 02  X  FRE  @0 Transferases @2 FE
C07 02  X  ENG  @0 Transferases @2 FE
C07 02  X  SPA  @0 Transferases @2 FE
C07 03  X  FRE  @0 Enzyme
C07 03  X  ENG  @0 Enzyme
C07 03  X  SPA  @0 Enzima
N21       @1 140
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 02-0234959 INIST
ET : Functions of poly(ADP-ribose) polymerase (PARP) in DNA repair, genomic integrity and cell death
AU : HERCEG (Zdenko); WANG (Zhao-Qi); NAKAGAMA (H.); ISHIKAWA (T.); MIWA (M.); SETLOW (R. B.)
AF : International Agency for Research on Cancer (IARC), 150 cours Albert-Thomas/69008 Lyon/France (1 aut., 2 aut.); Biochemistry Division, National Cancer Center Research Institute/Tokyo 104-0045/Japon (1 aut.); Faculty of Medicine, University of Tokyo/Tokyo/Japon (2 aut.); Department of Biochemistry and Molecular Oncology, Institute of Basic Medical Sciences, University of Tsukuba/Tsukuba, Ibaraki/Japon (3 aut.); Biology Department, Brookhaven National Laboratory/Upton, NY/Etats-Unis (4 aut.)
DT : Publication en série; Niveau analytique
SO : Mutation research; ISSN 0027-5107; Coden MUREAV; Pays-Bas; Da. 2001; Vol. 477; No. 1-2; Pp. 97-110; Bibl. 105 ref.
LA : Anglais
EA : Poly(ADP-ribose) polymerase (PARP) is responsible for post-translational modification of proteins in the response to numerous endogenous and environmental genotoxic agents. PARP and poly(ADP-ribosyl)ation are proposed to be important for the regulation of many cellular processes such as DNA repair, cell death, chromatin functions and genomic stability. Activation of PARP is one of the early DNA damage responses, among other DNA sensing molecules, such as DNA-PK, ATM and p53. The generation and characterization of PARP deficient mouse models have been instrumental in defining the biological role of the molecule and its involvement in the pathogenesis of various diseases including diabetes, stroke, Parkinson disease, general inflammation as well as tumorigenesis, and have, therefore, provided information for the development of pharmaceutical strategies for the treatment of diseases.
CC : 002A04C07
FD : Mort cellulaire; Réparation; DNA; DNA-directed DNA polymerase; Génomique; Intégrité; Apoptose
FG : Nucleotidyltransferases; Transferases; Enzyme
ED : Cell death; Repair; DNA; DNA-directed DNA polymerase; Genomics; Integrity; Apoptosis
EG : Nucleotidyltransferases; Transferases; Enzyme
SD : Muerte celular; Reparación; DNA; DNA-directed DNA polymerase; Genómica; Integridad; Apoptosis
LO : INIST-12206A.354000095503940110
ID : 02-0234959

Links to Exploration step

Pascal:02-0234959

Le document en format XML

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