Výsledky vyhledávání

Systemic lupus erythematosus in a multi-ethnic cohort (LUMINA) XXXII: [corrected] contributions of admixture and socioeconomic status to renal involvement

Autor: G S, Alarcón, H M, Bastian, T M, Beasley, J M, Roseman, F K, Tan, B J, Fessler, L M, Vilá, G, McGwin

Publikováno v: Lupus. 15(1)

Renal involvement in systemic lupus erythematosus (SLE) is more frequent in minorities. We examined whether genetic or socioeconomic status (SES) explain these disparities in a large multiethnic (Hispanics from Texas and Puerto Rico, African American

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9cb9df10ba8854096fdff42d6a1b40c3
https://pubmed.ncbi.nlm.nih.gov/16482742

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Systemic lupus erythematosus in a multiethnic cohort (LUMINA): XXVIII. Factors predictive of thrombotic events

Autor: K. T. Ho, Chul Ahn, F. K. Tan, J. Calvo-Alén, Gerald McGwin, John D. Reveille, Holly M. Bastian, Luis M. Vilá, Graciela S. Alarcón, B. J. Fessler, Jeffrey M. Roseman, Bruce A. Baethge

Publikováno v: Rheumatology (Oxford, England). 44(10)

Objective. To determine the relationship between the presence of antiphospholipid (aPL) antibodies, hydroxychloroquine use and the occurrence of thrombotic events in patients with systemic lupus erythematosus (SLE). Methods: Four hundred and forty-tw

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce9570e82dad24e26e511196b3211564
https://pubmed.ncbi.nlm.nih.gov/16030085

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Abnormalities in fibrillin 1-containing microfibrils in dermal fibroblast cultures from patients with systemic sclerosis (scleroderma)

Autor: D D, Wallis, F K, Tan, C M, Kielty, M D, Kimball, F C, Arnett, D M, Milewicz

Publikováno v: Arthritis and rheumatism. 44(8)

To determine if there are abnormalities in fibrillin 1-containing microfibrils in the extracellular matrix (ECM) of primary dermal fibroblasts explanted from patients with systemic sclerosis (SSc).Explanted fibroblasts from unaffected skin of 12 SSc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4658de47adacd3c843cab9c7a00eae98
https://pubmed.ncbi.nlm.nih.gov/11508439

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FBN1 exon 2 splicing error in a patient with Marfan syndrome

Autor: D, Guo, F K, Tan, A, Cantu, S E, Plon, D M, Milewicz

Publikováno v: American journal of medical genetics. 101(2)

Mutations in FBN1 cause the autosomal dominant condition, Marfan syndrome. A single-base mutation that results in a skipping of exon 2 of FBN1 was found in a Marfan patient. By sequencing this proband's entire FBN1 gene and comparing the mutated DNA

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::645438a2777d59c32cc8b7184b7925f9
https://pubmed.ncbi.nlm.nih.gov/11391655

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Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations

Autor: F K, Tan, N, Wang, M, Kuwana, R, Chakraborty, C A, Bona, D M, Milewicz, F C, Arnett

Publikováno v: Arthritis and rheumatism. 44(4)

Previously, we demonstrated with the use of microsatellite markers that a 2-cM haplotype on chromosome 15q containing the fibrillin 1 gene (FBN1) was strongly associated with systemic sclerosis (SSc) in the Choctaw, a population with high SSc prevale

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c259a8910c6b32edbc7fff31da832678
https://pubmed.ncbi.nlm.nih.gov/11315929

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Autoantibodies to fibrillin 1 in systemic sclerosis: ethnic differences in antigen recognition and lack of correlation with specific clinical features or HLA alleles

Autor: F K, Tan, F C, Arnett, J D, Reveille, C, Ahn, S, Antohi, T, Sasaki, K, Nishioka, C A, Bona

Publikováno v: Arthritis and rheumatism. 43(11)

We previously reported the presence of autoantibodies to the extracellular matrix protein, fibrillin 1, in sera from patients with systemic sclerosis (SSc). These autoantibodies appeared to be highly disease-specific but had significantly different f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::96f1bbc395ebaa6e79d4c55a3b5afb6d
https://pubmed.ncbi.nlm.nih.gov/11083269

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Microsatellites and intragenic polymorphisms of transforming growth factor beta and platelet-derived growth factor and their receptor genes in Native Americans with systemic sclerosis (scleroderma): a preliminary analysis showing no genetic association

Autor: X, Zhou, F K, Tan, D N, Stivers, F C, Arnett

Publikováno v: Arthritis and rheumatism. 43(5)

Abnormalities of transforming growth factor beta (TGFbeta) and platelet-derived growth factor (PDGF) alpha and beta and/or their receptors have been demonstrated in systemic sclerosis (SSc). This study aimed to determine whether genetic polymorphisms

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::89c01c04b61b0d588724a2ca5506f56f
https://pubmed.ncbi.nlm.nih.gov/10817561

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