The CTLA4 variants may interact with the IL23R- and NOD2-conferred risk in development of Crohn's disease
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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The CTLA4 variants may interact with the IL23R- and NOD2-conferred risk in development of Crohn's disease ; volume:11 ; number:1 ; day:10 ; month:6 ; year:2010 ; pages:1-9 ; date:12.2010
BMC medical genetics ; 11, Heft 1 (10.6.2010), 1-9, 12.2010
- Creator
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Hradsky, Ondrej
- Contributor
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Dusatkova, Petra
Lenicek, Martin
Bronsky, Jiri
Nevoral, Jiri
Vítek, Libor
Lukáš, Milan
Zeniskova, Ivana
Cinek, Ondrej
SpringerLink (Online service)
- DOI
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10.1186/1471-2350-11-91
- URN
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urn:nbn:de:1111-2016071511945
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:46 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Hradsky, Ondrej
- Dusatkova, Petra
- Lenicek, Martin
- Bronsky, Jiri
- Nevoral, Jiri
- Vítek, Libor
- Lukáš, Milan
- Zeniskova, Ivana
- Cinek, Ondrej
- SpringerLink (Online service)
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NOD2 function in Crohn's disease
Influence of NOD2 variants on Trichuris suis ova treatment outcome in Crohn’s disease
The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants
Age-of-onset-dependent influence of NOD2 gene variants on disease behaviour and treatment in Crohn’s disease
Funktionelle Bedeutung der NOD2-CARD15-Mutationen beim Morbus Crohn
The vesicle-associated function of NOD2 as a link between Crohn’s disease and mycobacterial infection
Emperipolesis and cell death in NOD2-related Blau Syndrome and Crohn’s disease
NOD2 deficiency increases retrograde transport of secretory IgA complexes in Crohn’s disease
Einfluss des NOD2-Mutationsstatus auf das therapeutische Drug-Monitoring bei M. Crohn
A case-only study of gene-environment interaction between genetic susceptibility variants in NOD2 and cigarette smoking in Crohn's disease aetiology
The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations
Untersuchungen zum monozytären Zytokinexpressionsmuster beim Morbus Crohn in Abhängigkeit vom CARD15-, NOD2-Genotyp
NOD2 function in Crohn's disease
Influence of NOD2 variants on Trichuris suis ova treatment outcome in Crohn’s disease
The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants
Age-of-onset-dependent influence of NOD2 gene variants on disease behaviour and treatment in Crohn’s disease
Funktionelle Bedeutung der NOD2-CARD15-Mutationen beim Morbus Crohn
The vesicle-associated function of NOD2 as a link between Crohn’s disease and mycobacterial infection
Emperipolesis and cell death in NOD2-related Blau Syndrome and Crohn’s disease
NOD2 deficiency increases retrograde transport of secretory IgA complexes in Crohn’s disease
Einfluss des NOD2-Mutationsstatus auf das therapeutische Drug-Monitoring bei M. Crohn
A case-only study of gene-environment interaction between genetic susceptibility variants in NOD2 and cigarette smoking in Crohn's disease aetiology
The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations