| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1030964719 |
| P356 | DOI | 10.1007/S00251-008-0274-6 |
| P698 | PubMed publication ID | 18253730 |
| P50 | author | Robert Schwarzenbacher | Q2158777 |
| Christoph Gasche | Q56704803 | ||
| P2093 | author name string | Peter Ferenci | |
| Claudia Willheim-Polli | |||
| Paul Grundtner | |||
| Manuela Nemeth | |||
| P2860 | cites work | CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease | Q37216685 |
| Bacterial flagellin is a dominant antigen in Crohn disease. | Q37698878 | ||
| Muramyl dipeptide-induced differential gene expression in NOD2 mutant and wild-type Crohn's disease patient-derived dendritic cells | Q38297299 | ||
| Both donor and recipient NOD2/CARD15 mutations associate with transplant-related mortality and GvHD following allogeneic stem cell transplantation | Q40516766 | ||
| Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan | Q40679561 | ||
| Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15. | Q42695065 | ||
| Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations. | Q44210447 | ||
| Nod2 mutation in Crohn's disease potentiates NF-kappaB activity and IL-1beta processing | Q45251378 | ||
| CARD15 gene mutations in sarcoidosis. | Q54138585 | ||
| Genetic variants in the NOD2/CARD15 gene are associated with early mortality in sepsis patients | Q57569138 | ||
| CARD15 gene mutations are not associated with ankylosing spondylitis | Q73024233 | ||
| Prognostic significance of NOD2/CARD15 variants in HLA-identical sibling hematopoietic stem cell transplantation: effect on long-term outcome is confirmed in 2 independent cohorts and may be modulated by the type of gastrointestinal decontamination | Q82312167 | ||
| Nod1, an Apaf-1-like activator of caspase-9 and nuclear factor-kappaB | Q22010046 | ||
| Gene-culture coevolution between cattle milk protein genes and human lactase genes | Q22122052 | ||
| A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease | Q22251291 | ||
| GRIM-19 interacts with nucleotide oligomerization domain 2 and serves as downstream effector of anti-bacterial function in intestinal epithelial cells | Q24297555 | ||
| Cytochrome c and dATP-dependent formation of Apaf-1/caspase-9 complex initiates an apoptotic protease cascade | Q24311006 | ||
| The Crohn's disease protein, NOD2, requires RIP2 in order to induce ubiquitinylation of a novel site on NEMO | Q24336822 | ||
| Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease | Q27860821 | ||
| Host recognition of bacterial muramyl dipeptide mediated through NOD2. Implications for Crohn's disease | Q28201834 | ||
| The application of molecular genetic approaches to the study of human evolution | Q28212794 | ||
| A human genome diversity cell line panel | Q28214742 | ||
| Genetic structure of human populations | Q28218564 | ||
| Nod2-dependent regulation of innate and adaptive immunity in the intestinal tract | Q28587612 | ||
| Role of Nod2 in the Response of Macrophages to Toll-Like Receptor Agonists | Q28592332 | ||
| Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance | Q29614684 | ||
| Autoimmunity and apoptosis: the Crohn's connection | Q34326177 | ||
| The NOD: a signaling module that regulates apoptosis and host defense against pathogens | Q34405567 | ||
| Phylogenetic analysis of the evolution of lactose digestion in adults. | Q34439496 | ||
| Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases. | Q34870666 | ||
| Toll-like receptor 4 and NOD2/CARD15 mutations in Hungarian patients with Crohn's disease: phenotype-genotype correlations | Q35010434 | ||
| Analytic review: some current problems of human population genetics | Q35569212 | ||
| Expression of NOD2 in Paneth cells: a possible link to Crohn's ileitis | Q35596103 | ||
| Intracellular pattern recognition receptors in the host response | Q36528528 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 115-120 | |
| P577 | publication date | 2008-02-06 | |
| P1433 | published in | Immunogenetics | Q15709984 |
| P1476 | title | Evolution of Crohn's disease-associated Nod2 mutations | |
| P478 | volume | 60 |
| Q34232094 | A novel single nucleotide polymorphism within the NOD2 gene is associated with pulmonary tuberculosis in the Chinese Han, Uygur and Kazak populations |
| Q28085271 | Adult lactose digestion status and effects on disease |
| Q37724700 | Association between NOD2/CARD15 gene polymorphisms and Crohn's disease in Chinese Zhuang patients |
| Q36084227 | Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixture |
| Q45863398 | Confirmation of three inflammatory bowel disease susceptibility loci in a Chinese cohort |
| Q35204635 | Cutting edge: Crohn's disease-associated Nod2 mutation limits production of proinflammatory cytokines to protect the host from Enterococcus faecalis-induced lethality |
| Q37333657 | First description of NOD2 variant associated with defective neutrophil responses in a woman with granulomatous mastitis related to corynebacteria |
| Q33806340 | Latitude, sunshine, and human lactase phenotype distributions may contribute to geographic patterns of modern disease: the inflammatory bowel disease model |
| Q35919095 | NOD2 mutations and anti-Saccharomyces cerevisiae antibodies are risk factors for Crohn's disease in African Americans |
| Q35819548 | NOD2/CARD15 gene mutations in North Algerian patients with inflammatory bowel disease |
| Q55231820 | Periodontal Infectogenomics. |
| Q92885468 | Relationship(s) between obesity and inflammatory bowel diseases: possible intertwined pathogenic mechanisms |
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