2002
DOI: 10.1080/030097402320817095
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The significance of mannan-binding lectin gene alleles in patients with primary Sjo¨gren's syndrome

Abstract: Our findings suggest that MBL structural gene polymorphisms do not influence on susceptibility to pSS. However, MBL may be associated with salivary gland destruction in pSS, and its concentration may be comparable with the intensity of inflammatory reaction. Further studies are warranted to clarify the possible mechanisms involved.

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Cited by 15 publications
(10 citation statements)
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References 22 publications
(22 reference statements)
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“…This association, however, is not observed in patients who did not produce anti-Ro52 autoantibodies [38]. Wang et al [40] 104 (143) Mullighan et al [42] 97 (106) Aittoniemi et al [43] 65 (138) Homozygous mutant allele Lupus and SS and rheumatoid factor…”
Section: Other Polymorphisms and Candidate Genes Ro52mentioning
confidence: 85%
See 3 more Smart Citations
“…This association, however, is not observed in patients who did not produce anti-Ro52 autoantibodies [38]. Wang et al [40] 104 (143) Mullighan et al [42] 97 (106) Aittoniemi et al [43] 65 (138) Homozygous mutant allele Lupus and SS and rheumatoid factor…”
Section: Other Polymorphisms and Candidate Genes Ro52mentioning
confidence: 85%
“…This study group consisted of 97 patients with primary SS and 106 ethnically matched healthy control individuals from Australia. Similarly, Aittoniemi et al [43] did not find any difference in the frequency of MBL polymorphisms in a group of 65 patients with primary SS compared with 138 control individuals. However, they associated lower concentrations of MBL with the 52/W genotype in patients who also had less salivary gland destruction [43].…”
Section: Mannose-binding Lectinmentioning
confidence: 94%
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“…Exon 1 of the MBL gene was amplified by polymerase chain reaction (PCR). Genotyping of codon 52 (CGT TGT; 52), 54 (GGC GAC; 54) and 57 (GGA GAA; 57) mutations was performed by restriction fragment length polymorphism (RFLP) as described elsewhere [9,10]. Alleles lacking these point mutations were classified as wild-type (w).…”
mentioning
confidence: 99%