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1.
Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies.
Ann Rheum Dis
; 82(2): 235-245, 2023 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-36171069
2.
The complement system and human autoimmune diseases.
J Autoimmun
; 137: 102979, 2023 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-36535812
3.
Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis.
Ann Rheum Dis
; 75(9): 1599-606, 2016 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-26493816
4.
Increased frequency of complement C4B deficiency in rheumatoid arthritis.
Arthritis Rheum
; 64(5): 1338-44, 2012 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-22076784
5.
Sex-specific association of X-linked Toll-like receptor 7 (TLR7) with male systemic lupus erythematosus.
Proc Natl Acad Sci U S A
; 107(36): 15838-43, 2010 Sep 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-20733074
6.
Gene CNVs and protein levels of complement C4A and C4B as novel biomarkers for partial disease remissions in new-onset type 1 diabetes patients.
Pediatr Diabetes
; 13(5): 408-18, 2012 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-22151770
7.
Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome.
Arthritis Rheumatol
; 74(11): 1842-1850, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-35729719
8.
Loop extrusion promotes an alternate pathway for isotype switching.
Cell Rep
; 37(8): 110059, 2021 11 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-34818547
9.
Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases.
Front Immunol
; 12: 739430, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34764957
10.
Assessment of complement C4 gene copy number using the paralog ratio test.
Hum Mutat
; 31(7): 866-74, 2010 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-20506482
11.
Opposite Profiles of Complement in Antiphospholipid Syndrome (APS) and Systemic Lupus Erythematosus (SLE) Among Patients With Antiphospholipid Antibodies (aPL).
Front Immunol
; 10: 885, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31134052
12.
Elevated serum complement levels and higher gene copy number of complement C4B are associated with hypertension and effective response to statin therapy in childhood-onset systemic lupus erythematosus (SLE).
Lupus Sci Med
; 6(1): e000333, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31448126
13.
The HLA 8.1 ancestral haplotype is strongly linked to the C allele of -429T>C promoter polymorphism of receptor of the advanced glycation endproduct (RAGE) gene. Haplotype-independent association of the -429C allele with high hemoglobinA1C levels in diabetic patients.
Mol Immunol
; 44(4): 648-55, 2007 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-16504296
14.
Intrinsic transcriptional heterogeneity in B cells controls early class switching to IgE.
J Exp Med
; 214(1): 183-196, 2017 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27994069
15.
Three distinct profiles of serum complement C4 proteins in pediatric systemic lupus erythematosus (SLE) patients: tight associations of complement C4 and C3 protein levels in SLE but not in healthy subjects.
Adv Exp Med Biol
; 586: 227-47, 2006.
Artículo
en Inglés
| MEDLINE | ID: mdl-16893076
16.
Molecular fine-tuning of affinity maturation in germinal centers.
J Clin Invest
; 126(1): 32-4, 2016 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-26657856
17.
Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune Diseases.
Front Immunol
; 7: 36, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-26913032
18.
Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations.
Arthritis Rheumatol
; 68(6): 1442-1453, 2016 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-26814708
19.
Active RNAP pre-initiation sites are highly mutated by cytidine deaminases in yeast, with AID targeting small RNA genes.
Elife
; 3: e03553, 2014 Sep 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-25237741
20.
DNA deaminases induce break-associated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis.
Elife
; 2: e00534, 2013 Apr 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-23599896