Prevalence of CARD15/NOD2 mutations in Caucasian healthy people. - sprookjes - yvandenbroek - TriplyDB

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

http://www.wikidata.org/entity/Q34576207

about

Revisiting Crohn's disease as a primary immunodeficiency of macrophages Identification and utilization of donor and recipient genetic variants to predict survival after HCT: are we ready for primetime?Assessment of heterogeneity between European Populations: a Baltic and Danish replication case-control study of SNPs from a recent European ulcerative colitis genome wide association study.The polymorphism rs3024505 proximal to IL-10 is associated with risk of ulcerative colitis and Crohns disease in a Danish case-control study.The functional -765G→C polymorphism of the COX-2 gene may reduce the risk of developing crohn's disease An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.Insufficient evidence for association of NOD2/CARD15 or other inflammatory bowel disease-associated markers on GVHD incidence or other adverse outcomes in T-replete, unrelated donor transplantation.Evidence of expression variation and allelic imbalance in Crohn's disease susceptibility genes NOD2 and ATG16L1 in human dendritic cells Induction and rescue of Nod2-dependent Th1-driven granulomatous inflammation of the ileum A case-only study of gene-environment interaction between genetic susceptibility variants in NOD2 and cigarette smoking in Crohn's disease aetiology.Association of NOD2 and IL23R with inflammatory bowel disease in Puerto Rico.Nucleotide oligomerization domain 2 polymorphisms in patients with intestinal failure.NOD1 and NOD2: signaling, host defense, and inflammatory disease.Microbially driven TLR5-dependent signaling governs distal malignant progression through tumor-promoting inflammation.Recipient's genetic R702W NOD2 variant is associated with an increased risk of bacterial infections after orthotopic liver transplantation.Granulocyte-macrophage colony stimulating factor blockade promotes ccr9(+) lymphocyte expansion in Nod2 deficient mice.Cutting edge: Crohn's disease-associated Nod2 mutation limits production of proinflammatory cytokines to protect the host from Enterococcus faecalis-induced lethality Size does not matter: commensal microorganisms forge tumor-promoting inflammation and anti-tumor immunity.Dissecting the genetics of complex inheritance: linkage disequilibrium mapping provides insight into Crohn disease NOD2/CARD15 gene mutations in North Algerian patients with inflammatory bowel disease.NOD2 mutations and anti-Saccharomyces cerevisiae antibodies are risk factors for Crohn's disease in African Americans The association between environmental exposures during childhood and the subsequent development of Crohn's disease: A score analysis approach.New global map of Crohn's disease: Genetic, environmental, and socioeconomic correlations.The TLR2-MyD88-NOD2-RIPK2 signalling axis regulates a balanced pro-inflammatory and IL-10-mediated anti-inflammatory cytokine response to Gram-positive cell walls Apical junction complex proteins and ulcerative colitis: a focus on the PTPRS gene.Contribution of higher risk genes and European admixture to Crohn's disease in African Americans.Disordered macrophage cytokine secretion underlies impaired acute inflammation and bacterial clearance in Crohn's disease Phenotypic and genotypic characteristics of inflammatory bowel disease in French Canadians: comparison with a large North American repository.Role of Nod2 in the development of Crohn's disease.The immunopathogenesis of Crohn's disease: a three-stage model.Molecular epidemiology of nontuberculous mycobacteria.Genome-wide association studies and Crohn's disease.NOD2 Polymorphisms and Their Impact on Haematopoietic Stem Cell Transplant Outcome.Crohn's as an immune deficiency: from apparent paradox to evolving paradigm.Hydroxylases as therapeutic targets in inflammatory bowel disease.NOD2 gene polymorphism rs2066844 associates with need for combined liver-intestine transplantation in children with short-gut syndrome.A novel crosstalk between TLR4- and NOD2-mediated signaling in the regulation of intestinal inflammation.Understanding the regulation of pattern recognition receptors in inflammatory diseases - a 'Nod' in the right direction.Cross-tolerization between Nod1 and Nod2 signaling results in reduced refractoriness to bacterial infection in Nod2-deficient macrophages.Emerging drugs to treat Crohn's disease.

P2860

Q22242983-C7D6A6AB-60BF-4390-A7C8-EA0C17579929 Q28080914-7E8597ED-D4CB-40ED-AEFA-0B72F19697F2 Q31034250-85C45C28-2C50-4DD3-888A-1FBB02C67CD8 Q33590163-F36BC07F-A8E9-4CD1-A885-CC6EDFC34C7E Q33760727-98EB703A-B22B-4E31-8001-5B3394D96709 Q33815678-1DB2AE66-32BC-4041-8D24-E494E1FD6FAE Q33839876-0B75A1F0-09C6-4573-8C47-E0C0FDD7665B Q34056080-3C22C3CE-F354-4871-AFF5-CE3103AB40EF Q34093119-180C4885-04ED-465B-93A5-56556D47AEB6 Q34195178-99000A86-E71C-47BD-8A29-8E3CB132F41C Q34258465-DD373B67-5FB5-4251-BFE5-4AA4A2D371A5 Q34313205-A34B1B5B-1DBE-4F30-BF22-F52EBC14233E Q34745603-39949ABB-8AF8-4A38-83A8-2C4044063F59 Q34944118-0EB7D4BA-4202-45ED-8F4E-6583B3DE2A59 Q34973978-BB965B6B-7120-4373-88DC-02511B21F821 Q35036733-C0E34C6B-8922-478C-BEA6-26A01A639D27 Q35204635-487F1121-7FC2-40DF-ADF6-9854B7B29B95 Q35376137-52F35632-8E42-4065-BEEC-F9CAB1BE6628 Q35603251-035D0365-A164-4C13-BA5E-01A1001EB4F7 Q35819548-D1962170-8D23-4B38-92F1-5CA4A29E41A6 Q35919095-0E25FD43-AE21-4B19-AA24-E916D0C9BBE4 Q36272975-C42AD688-61A9-4937-93B4-6FF86B1F6A55 Q37038665-9E645491-DD27-4FCE-BCE9-883DEA224585 Q37139051-A84D7D9C-3EF0-47A9-832D-7663DAA4FCE1 Q37206258-90355879-C25F-4C34-87D2-0F017C1BD70F Q37261147-AB16FC1D-522A-4DC8-BD94-97C56D89F164 Q37331540-56BBB2B7-7A1B-44B3-B4A7-615E4AB98B95 Q37343481-77C470F4-930D-4431-894D-2B81B7D3423D Q37539114-EB3562AF-FFF5-4EFE-88E9-054B98673D2B Q37576645-09042866-46E3-4D75-9D94-87F63BFF3B56 Q37613672-B6198F2C-2DF9-4B34-91C2-D59AD58A9919 Q37857566-20F85948-7B25-461F-9EED-63298844C105 Q38057238-B3EFA79C-8A62-421B-BC58-C3FC82A6B7FC Q38068957-AD76C071-92A2-41EA-99EB-35263A4CE738 Q38082620-0F0AA088-2F98-4C87-80FE-C5F1AA8291BB Q38414222-88A0853B-5AEF-49E6-8FEA-DD6A22B0975D Q38855496-0D1FE172-235E-47AE-881B-AD09661CE8C7 Q38972852-A96E1B7E-B440-41FB-BB05-5D000618FDE2 Q39353816-DBE19A53-D613-4B93-A135-A619F493A0DE Q39881787-21DBDAAE-4475-40C4-B1B9-DC34632AB89E

P2860

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

http://www.wikidata.org/entity/Q34576207

description

2007 nî lūn-bûn

@nan

2007 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

name

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

@ast

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

@en

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

@nl

type

label

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

@ast

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

@en

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

@nl

prefLabel

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

@ast

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

@en

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

@nl

P1433

Q34576207-DD938EE3-27C6-454B-B0E1-2E3D942DF3DE

P1476

Q34576207-3F18BA72-2192-4F5F-A5BD-3ECA955EBA14

P2093

Q34576207-019CD8BB-E38E-45CA-ABCC-ED23B0A66106

Q34576207-1C60FC01-32F5-4D50-9A55-2CDC2D391462

Q34576207-1E0FC858-9249-418B-8944-69F8116E2C10

Q34576207-21B055C6-1146-46AA-AA8D-88377282602D

Q34576207-2E4B904D-3D89-4A7B-B4A3-58F79EA7530A

Q34576207-37B8B4B2-49FD-4AAC-AF28-1EA1F2672DF1

Q34576207-58E94C84-D20F-4B81-9934-18EC2224E0DA

Q34576207-84BFF6DF-82B0-41FD-8BF6-450F40CEF6C1

Q34576207-904034DF-0541-4BDC-8A29-4620AE3DB4EF

Q34576207-C0BA243C-0BC7-4B42-8176-0ECB2FD0BE9C

P2860

Q34576207-00BE0933-5266-411E-892A-C816E5A33164

Q34576207-013A5724-3A9F-49B9-A9B1-1F35A46CCD2E

Q34576207-03CA2480-A332-4BB6-87DC-7A865B44A004

Q34576207-0560662F-3C79-4B76-9D6F-EFA9C802793E

Q34576207-0BC62663-6993-4398-B04B-776783094C3F

Q34576207-0CA61A1B-288A-4093-942F-1EC163233624

Q34576207-118D008B-711E-4779-BF75-7B6C4B8FB9BA

Q34576207-1F6199EA-CBC3-4619-8AC5-24A7BB919528

Q34576207-1FB0FDBA-AB62-423F-9490-955C3C895E6C

Q34576207-22BC89E6-7311-4E46-BA17-903F4B778920

P304

Q34576207-43900617-3334-4A91-BA04-3CDEF6AD04E7

P31

Q34576207-E6E45FD5-B409-4BEB-B610-701984CE991B

P356

Q34576207-FFC58CEB-C00E-4141-90FC-57C55FD3CBB8

P407

Q34576207-AD762EAA-0B84-4CD4-B06A-F6622D08A030

P433

Q34576207-6C91785C-627D-49C3-A246-285EFBBB4242

P478

Q34576207-F9FF7626-EA24-4B8A-8FCE-9B5609A4E46D

P50

Q34576207-07D390F8-79F8-4738-B452-74CA09EA804E

Q34576207-5C937B13-C85E-43B8-B290-E934593A1D28

Q34576207-B3BFC470-02C7-4AF8-8DAC-686C22D267E4

P577

Q34576207-D21B1039-35F9-4C3C-9C84-B64359B4999F

P698

Q34576207-B91492E5-837D-4ED2-9688-B6F6514D0281

P356

J.1572-0241.2007.01149.X

P1433

The American Journal of Gastroenterology

P1476

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.

@en

P2093

Derek P Jewell

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

Elizabeth V Fowler

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

Huiying Yang

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

IBD International Genetics Consortium

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

Isabelle Zaccaria

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

Jack Satsangi

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

Judy Cho

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

Juleen Cavanaugh

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

Maarit Lappalainen

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

Mark S Silverberg

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

P2860

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

Nod2 is a general sensor of peptidoglycan through muramyl dipeptide (MDP) detection

Genetics and the population history of Europe

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

Host recognition of bacterial muramyl dipeptide mediated through NOD2. Implications for Crohn's disease

Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15.

International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16.

A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews

CARD15: a pleiotropic autoimmune gene that confers susceptibility to psoriatic arthritis.

P304

1259-1267

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

P31

scholarly article

P356

10.1111/J.1572-0241.2007.01149.X

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

P407

P433

6

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

P478

102

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

P50

Séverine Vermeire

Jean-Pierre Hugot

P577

2007-02-23T00:00:00Z

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

P698

17319929

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