La maladie de Parkinson au Canada (serveur d'exploration)

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Susceptibility to leprosy is associated with PARK2 and PACRG

Identifieur interne : 000327 ( PascalFrancis/Curation ); précédent : 000326; suivant : 000328

Susceptibility to leprosy is associated with PARK2 and PACRG

Auteurs : Marcelo T. Mira [Canada, Brésil, France, Viêt Nam, Pays-Bas] ; Alexandre Alcaïs ; NGUYEN VAN THUC ; Milton O. Moraes ; Celestino Di Flumeri ; VU HONG THAI ; MAL CHI PHUONG ; NGUYEN THU HUONG ; NGUYEN NGOC BA ; PHAM XUAN KHOA ; Euzenir N. Sarno ; Andrea Alter ; Alexandre Montpetit ; Marla E. Moraes ; José R. Moraes ; Carole Dore ; Caroline J. Dallant ; Pierre Lepage ; Andrel Verner ; Esther Van De Vosse ; Thomas J. Hudson ; Laurent Abel ; Erwin Schurr

Source :

RBID : Pascal:04-0337837

Descripteurs français

English descriptors

Abstract

Leprosy is caused by Mycobacterium leprae and affects about 700,000 individuals each year'. It has long been thought that leprosy has a strong genetic component2, and recently we mapped a leprosy susceptibility locus to chromosome 6 region q25-q26 (ref. 3). Here we investigate this region further by using a systematic association scan of the chromosomal interval most likely to harbour this leprosy susceptibility locus. In 197 Vietnamese families we found a significant association between leprosy I and 17 markers located in a block of approx. 80 kilobases overlapping the 5' regulatory region shared by the Parkinson's disease gene PARK2 and the co-regulated gene PACRG. Possession of as few as two of the 17 risk alleles was highly predictive of leprosy. This was confirmed in a sample of 975 unrelated leprosy cases and controls from Brazil in whom the same alleles were strongly associated with leprosy. Variants in the regulatory region shared by PARK2 and PACRG therefore act as common risk factors for leprosy.
pA  
A01 01  1    @0 0028-0836
A02 01      @0 NATUAS
A03   1    @0 Nature : (Lond.)
A05       @2 427
A06       @2 6975
A08 01  1  ENG  @1 Susceptibility to leprosy is associated with PARK2 and PACRG
A11 01  1    @1 MIRA (Marcelo T.)
A11 02  1    @1 ALCAÏS (Alexandre)
A11 03  1    @1 NGUYEN VAN THUC
A11 04  1    @1 MORAES (Milton O.)
A11 05  1    @1 DI FLUMERI (Celestino)
A11 06  1    @1 VU HONG THAI
A11 07  1    @1 MAL CHI PHUONG
A11 08  1    @1 NGUYEN THU HUONG
A11 09  1    @1 NGUYEN NGOC BA
A11 10  1    @1 PHAM XUAN KHOA
A11 11  1    @1 SARNO (Euzenir N.)
A11 12  1    @1 ALTER (Andrea)
A11 13  1    @1 MONTPETIT (Alexandre)
A11 14  1    @1 MORAES (Marla E.)
A11 15  1    @1 MORAES (José R.)
A11 16  1    @1 DORE (Carole)
A11 17  1    @1 DALLANT (Caroline J.)
A11 18  1    @1 LEPAGE (Pierre)
A11 19  1    @1 VERNER (Andrel)
A11 20  1    @1 VAN DE VOSSE (Esther)
A11 21  1    @1 HUDSON (Thomas J.)
A11 22  1    @1 ABEL (Laurent)
A11 23  1    @1 SCHURR (Erwin)
A14 01      @1 McGill Centre for the Study of Host Résistance and Departments of Human Genetics, Medicine and Biochemistry, McGill University, 1650 Cedar Avenue @2 Montreal, PQ H3G 1A4 @3 CAN
A14 02      @1 Centro de Ciências Biológicas e da Saúde, Pontificia Universidade Católica do Paraná. Rua Imaculada Conceição, 1155 @2 CEP 80215-901, Curitiba, Paraná @3 BRA
A14 03      @1 Laboratoire de Génétique Humaine des Maladies Infectieuses, INSERM U.550, Faculté de Médecine Necker, Université de Paris René Descartes, 156 rue de Vaugirard @2 75015 Paris @3 FRA
A14 04      @1 Hospital for Dermato-Venereology, Nguyen Thong Street, District 3, Ho Chi Minh City @3 VNM
A14 05      @1 Leprosy Laboratory, Tropical Medicine Department Oswaldo Cruz Institute, FIOCRUZ 20221-903 Rio de Janeiro @3 BRA
A14 06      @1 McGill University and Genome Québec Innovation Centre, 740 Docteur Penfield @2 Montreal, PQ H3A 1A4 @3 CAN
A14 07      @1 Laboratório de Imunogénetica, Instituto Nacional do Cancer, Ministério da @2 Saúde, 20230-130 Rio de Janeiro, RJ @3 BRA
A14 08      @1 Department of Infections Diseases & Department of Immunohematology and Blood Transfusion, Leiden University Médical Center, Building 1, Albinusdreef 2 @2 2333 ZA Leiden @3 NLD
A20       @1 636-640
A21       @1 2004
A23 01      @0 ENG
A43 01      @1 INIST @2 142 @5 354000110106500220
A44       @0 0000 @1 © 2004 INIST-CNRS. All rights reserved.
A45       @0 18
A47 01  1    @0 04-0337837
A60       @1 P @3 LT
A61       @0 A
A64 01  1    @0 Nature : (London)
A66 01      @0 GBR
C01 01    ENG  @0 Leprosy is caused by Mycobacterium leprae and affects about 700,000 individuals each year'. It has long been thought that leprosy has a strong genetic component2, and recently we mapped a leprosy susceptibility locus to chromosome 6 region q25-q26 (ref. 3). Here we investigate this region further by using a systematic association scan of the chromosomal interval most likely to harbour this leprosy susceptibility locus. In 197 Vietnamese families we found a significant association between leprosy I and 17 markers located in a block of approx. 80 kilobases overlapping the 5' regulatory region shared by the Parkinson's disease gene PARK2 and the co-regulated gene PACRG. Possession of as few as two of the 17 risk alleles was highly predictive of leprosy. This was confirmed in a sample of 975 unrelated leprosy cases and controls from Brazil in whom the same alleles were strongly associated with leprosy. Variants in the regulatory region shared by PARK2 and PACRG therefore act as common risk factors for leprosy.
C02 01  X    @0 002B05A03
C03 01  X  FRE  @0 Lèpre @2 NM @5 01
C03 01  X  ENG  @0 Leprosy @2 NM @5 01
C03 01  X  SPA  @0 Lepra @2 NM @5 01
C03 02  X  FRE  @0 Prédisposition @5 02
C03 02  X  ENG  @0 Predisposition @5 02
C03 02  X  SPA  @0 Predisposición @5 02
C03 03  X  FRE  @0 Homme @5 03
C03 03  X  ENG  @0 Human @5 03
C03 03  X  SPA  @0 Hombre @5 03
C03 04  X  FRE  @0 Gène @5 04
C03 04  X  ENG  @0 Gene @5 04
C03 04  X  SPA  @0 Gen @5 04
C07 01  X  FRE  @0 Mycobactériose @2 NM
C07 01  X  ENG  @0 Mycobacterial infection @2 NM
C07 01  X  SPA  @0 Micobacteriosis @2 NM
C07 02  X  FRE  @0 Bactériose @2 NM
C07 02  X  ENG  @0 Bacteriosis @2 NM
C07 02  X  SPA  @0 Bacteriosis @2 NM
C07 03  X  FRE  @0 Infection @2 NM
C07 03  X  ENG  @0 Infection @2 NM
C07 03  X  SPA  @0 Infección @2 NM
C07 04  X  FRE  @0 Peau pathologie @5 37
C07 04  X  ENG  @0 Skin disease @5 37
C07 04  X  SPA  @0 Piel patología @5 37
N21       @1 201
N44 01      @1 PSI
N82       @1 PSI

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Pascal:04-0337837

Le document en format XML

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<term>Lèpre</term>
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<div type="abstract" xml:lang="en">Leprosy is caused by Mycobacterium leprae and affects about 700,000 individuals each year'. It has long been thought that leprosy has a strong genetic component
<sup>2</sup>
, and recently we mapped a leprosy susceptibility locus to chromosome 6 region q25-q26 (ref. 3). Here we investigate this region further by using a systematic association scan of the chromosomal interval most likely to harbour this leprosy susceptibility locus. In 197 Vietnamese families we found a significant association between leprosy I and 17 markers located in a block of approx. 80 kilobases overlapping the 5' regulatory region shared by the Parkinson's disease gene PARK2 and the co-regulated gene PACRG. Possession of as few as two of the 17 risk alleles was highly predictive of leprosy. This was confirmed in a sample of 975 unrelated leprosy cases and controls from Brazil in whom the same alleles were strongly associated with leprosy. Variants in the regulatory region shared by PARK2 and PACRG therefore act as common risk factors for leprosy.</div>
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<sup>2</sup>
, and recently we mapped a leprosy susceptibility locus to chromosome 6 region q25-q26 (ref. 3). Here we investigate this region further by using a systematic association scan of the chromosomal interval most likely to harbour this leprosy susceptibility locus. In 197 Vietnamese families we found a significant association between leprosy I and 17 markers located in a block of approx. 80 kilobases overlapping the 5' regulatory region shared by the Parkinson's disease gene PARK2 and the co-regulated gene PACRG. Possession of as few as two of the 17 risk alleles was highly predictive of leprosy. This was confirmed in a sample of 975 unrelated leprosy cases and controls from Brazil in whom the same alleles were strongly associated with leprosy. Variants in the regulatory region shared by PARK2 and PACRG therefore act as common risk factors for leprosy.</s0>
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