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index medicus (97) 97
humans (92) 92
6q23 (69) 69
female (54) 54
male (54) 54
polymorphism, single nucleotide (47) 47
adult (44) 44
chromosome 6q23 (39) 39
genetic predisposition to disease (39) 39
genome-wide association (36) 36
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nuclear proteins - genetics (33) 33
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middle aged (32) 32
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genetic aspects (28) 28
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risk (27) 27
tumor necrosis factor alpha-induced protein 3 (27) 27
genetics & heredity (26) 26
association (25) 25
intracellular signaling peptides and proteins - genetics (25) 25
susceptibility (25) 25
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alleles (22) 22
nf-kappa-b (22) 22
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tnfaip3 (18) 18
dna-binding proteins (17) 17
hematology (17) 17
variants (17) 17
immunology (16) 16
polymorphism (16) 16
polymorphism, single nucleotide - genetics (16) 16
disease (15) 15
expression (15) 15
biochemistry & molecular biology (14) 14
fetal hemoglobin - genetics (14) 14
haplotypes (14) 14
schizophrenia (14) 14
schizophrenia - genetics (14) 14
a20 (13) 13
genetic research (13) 13
linkage disequilibrium (13) 13
responses (13) 13
single nucleotide polymorphism (13) 13
animals (12) 12
article (12) 12
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beta-thalassemia (10) 10
beta-thalassemia - genetics (10) 10
dna-binding proteins - genetics (10) 10
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gene expression (10) 10
genetic association studies (10) 10
genetic predisposition to disease - genetics (10) 10
locus (10) 10
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single nucleotide polymorphisms (10) 10
adaptor proteins, signal transducing - genetics (9) 9
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lupus erythematosus, systemic - genetics (9) 9
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anemia, sickle cell - genetics (8) 8
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arthritis, rheumatoid - immunology (7) 7
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Gut, ISSN 0017-5749, 08/2009, Volume 58, Issue 8, pp. 1078 - 1083
Objective:Our previous coeliac disease genome-wide association study (GWAS) implicated risk variants in the human leucocyte antigen (HLA) region and eight... 
RHEUMATOID-ARTHRITIS | IMMUNE-RESPONSE | SYSTEMIC-LUPUS-ERYTHEMATOSUS | 6Q23 | INFLAMMATION | GENE-EXPRESSION | GASTROENTEROLOGY & HEPATOLOGY | GENOME-WIDE ASSOCIATION | A20 | REGION
Journal Article
by Xu, EB and Cao, HL and Lin, LM and Liu, HL
PLOS ONE, ISSN 1932-6203, 04/2017, Volume 12, Issue 4, p. e0195181
Previous studies have found that the polymorphisms of tumor necrosis factor-a induced protein 3 (TNFAIP3) were associated with several autoimmune diseases.... 
RHEUMATOID-ARTHRITIS | CELLS | SYSTEMIC-LUPUS-ERYTHEMATOSUS | METAANALYSIS | VARIANTS | 6Q23 | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | REGION
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 08/2010, Volume 69, Issue 8, pp. 1548 - 53
Journal Article
Nature, ISSN 0028-0836, 2014, Volume 512, Issue 1, pp. 69 - 73
Rheumatoid arthritis is a chronic autoinflammatory disease that affects 1-2% of the world's population and is characterized by widespread joint inflammation.... 
RHEUMATOID-ARTHRITIS | COLLAGEN-INDUCED ARTHRITIS | ACTIVATION | 6Q23 | CASPASE-1 | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | MICE | INHIBITOR | NF-KAPPA-B | ASSOCIATION | Inflammasomes - metabolism | NLR Family, Pyrin Domain-Containing 3 Protein | Caspase 1 - metabolism | Male | Intracellular Signaling Peptides and Proteins - metabolism | Intracellular Signaling Peptides and Proteins - deficiency | Arthritis, Rheumatoid - metabolism | Arthritis, Rheumatoid - prevention & control | Cysteine Endopeptidases - metabolism | Receptors, Interleukin-1 - deficiency | Cysteine Endopeptidases - deficiency | Female | Tumor Necrosis Factor alpha-Induced Protein 3 | DNA-Binding Proteins | Disease Models, Animal | Calcium-Binding Proteins - metabolism | Interleukin-1 - metabolism | Signal Transduction | Nuclear Proteins - metabolism | Apoptosis Regulatory Proteins - metabolism | Arthritis, Rheumatoid - pathology | Mice, Knockout | Receptors, Interleukin-1 - metabolism | Macrophages - metabolism | Phenotype | Animals | Carrier Proteins - metabolism | Caspase 1 - deficiency | Mice | Arthritis, Rheumatoid - immunology | Prevention | Rheumatoid arthritis | Physiological aspects | NLRP3 | Properties | Macrophages | Risk factors | Proteins | Pathology | Dehydrogenases | Histopathology | Pathogenesis | Rodents | Protein expression | Index Medicus | Nlrp3 | IL1R1 | caspase-1 | inflammasome | A20
Journal Article
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2011, Volume 43, Issue 3, pp. 253 - 258
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2008, Volume 105, Issue 33, pp. 11869 - 11874
Journal Article
FRONTIERS IN GENETICS, ISSN 1664-8021, 07/2019, Volume 10
We report on a 34-year-old woman and her mother who both have clinical features suggestive for otofaciocervical syndrome (OTFCS), a disorder characterized by a... 
otofaciocervical syndrome | 6q23 deletion | EYA1 | array CGH | EYA4 | MUTATION | GENETICS & HEREDITY | PATIENT | DEAFNESS | PROTEINS | Genetic research | Branchio-Oto-Renal syndrome | Research | Diagnosis | Gene expression
Journal Article
by Li, GM and Liu, HM and Guan, WZ and Xu, H and Wu, BB and Sun, L
BMC MEDICAL GENETICS, ISSN 1471-2350, 07/2019, Volume 20, Issue 1, pp. 124 - 124
BackgroundThe association between mutations in the TNFAIP3 gene and a new autoinflammatory disease (called A20 haploinsufficiency, HA20) has recently been... 
APOPTOSIS | 6Q23 | TNFAIP3 | MECHANISMS | Liver fibrosis | Hypothyroidism | Interstitial lung disease | TNFAIP3 gene | POLYMORPHISMS | DISEASES | GENETICS & HEREDITY | A20 haploinsufficiency | ASSOCIATION | Macrophage activation syndrome | Skin diseases | Crohn's disease | Research | Gene mutations
Journal Article
Journal Article