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591.
Hunter KF Moore KN Glazener CM 《BJU international》2007,100(5):1191; author reply 1191-1191; author reply 1192
592.
Quartuccio L De Re V Fabris M Marzotto A Franzolini N Gasparotto D Caggiari L Ferraccioli G Scott CA De Vita S 《Haematologica》2006,91(5):691-694
A patient with rheumatoid arthritis (RA) developed an atypical lymphoproliferative disorder (LPD) after methotrexate and cyclosporine A, which regressed after suspension of both drugs. After subsequent treatment with rituximab, the LPD was still undetectable. Anti-tumor necrosis factor a therapy was used when the arthritis relapsed, but an aggressive B-cell non Hodgkin's lymphoma developed. Molecular analyses showed an oligoclonal B-cell expansion at the LPD step. A minor clone with significant sequence homology to B-cell lymphomas arising in Sjogren's syndrome and mixed cryoglobulinemia syndrome, given rise to the non-Hodgkin's lymphoma. Treatment of rheumatoid arthritis associated with lymphoproliferation represents a clinical challenge, and common pathogenetic pathways to lymphoma may occur in different autoimmune diseases. 相似文献
593.
Matthias Christen DVM Rodrigo Gutierrez-Quintana MVZ MVM Matthew James BVM BVS Kiterie M.E. Faller DVM DPhil Mark Lowrie MA VetMB MVM Clare Rusbridge BVMS PhD Kenny Bossens MVM Cathryn Mellersh PhD Louise Pettitt BSc Tiina Heinonen MSc Hannes Lohi PhD Vidhya Jagannathan PhD Tosso Leeb PhD 《Movement disorders》2023,38(6):1094-1099
594.
Mark Fife Sophia Steer Sheila Fisher Julia Newton Kirsten McKay Jane Worthington Chandrabala Shah Andreas Polley Andre Rosenthal William Ollier Cathryn Lewis Paul Wordsworth Jerry Lanchbury 《Arthritis \u0026amp; Rheumatology》2002,46(1):75-82
Objective
Rheumatoid arthritis (RA) is a common disabling autoimmune disease with a complex genetic component. We have previously described linkage of a region of chromosome 8q12.3 with RA and association of the microsatellite marker CRHRA1 with RA in 295 affected sibling‐pair families. In the current study we aimed to physically link the RA‐associated marker with the corticotropin‐releasing hormone (CRH) candidate gene, and to examine the genomic region for additional short tandem repeat (STR) genetic markers in order to clarify the association with RA.Methods
We examined the association of 2 STR markers with disease in the original 295 multicase families and in a cohort of 131 simplex families to refine our understanding of this genetic region in disease susceptibility in sporadic and familial RA. Genomic library screening and sequencing were used to generate physical sequences in the CRH genomic region. Bioinformatic analysis of the sequence flanking the CRH structural gene was used to screen for additional STRs and other genetic features. Genotyping was carried out using a standard fluorescence approach. Estimations of haplotype frequencies were performed to assess linkage disequilibrium. The transmission disequilibrium test was performed using TRANSMIT.Results
Physical cloning and sequencing analyses identified the genomic region linking the CRHRA1 marker and the CRH structural locus. Moreover, we identified a further STR, CRHRA2, which was in strong linkage disequilibrium with CRHRA1 (P = 4.0 × 10−14). A haplotype, CRHRA1*10;CRHRA2*14, was preferentially carried by unaffected parents at a frequency of 8.6% compared with the expected frequency of 3.1%. This haplotype was overtransmitted in the multiply affected families (P = 0.0077) and, similarly, in the simplex families (P = 0.024). Combined analysis of both family cohorts confirmed significant evidence for linkage (P = 4.9 × 10−4) and association (P = 5.5 × 10−3) for this haplotype with RA.Conclusion
In demonstrating significant linkage disequilibrium between these 2 markers, we have refined the disease‐associated region to a single haplotype and confirmed the significance of this region in our understanding of the genetics of RA.595.