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Systemic sclerosis: the susceptible host (genetics and environment)

Rheumatic diseases clinics of North America, 2003-05, Vol.29 (2), p.211-237

Tan, Filemon K

2003

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Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis

Annals of the rheumatic diseases, 2011-03, Vol.70 (3), p.454-462

2011

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Signatures of differentially regulated interferon gene expression and vasculotrophism in the peripheral blood cells of systemic sclerosis patients

Rheumatology (Oxford, England), 2006-06, Vol.45 (6), p.694-702

2006

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Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study

Annals of the rheumatic diseases, 2013-04, Vol.72 (4), p.602-607

2013

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

Rheumatology (Oxford, England), 2005-10, Vol.44 (10), p.1303-1307

2005

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Genetics of scleroderma: update on single nucleotide polymorphism analysis and microarrays

Current opinion in rheumatology, 2005-11, Vol.17 (6), p.761-767

2005

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

Lupus, 2006-01, Vol.15 (1), p.26-31

2006

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Identification of novel targets in scleroderma: update on population studies, cDNA arrays, SNP analysis, and mutations

Current opinion in rheumatology, 2003-11, Vol.15 (6), p.766-771

2003

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Genetic factors in the etiology of systemic sclerosis and Raynaud phenomenon

Current opinion in rheumatology, 2000-11, Vol.12 (6), p.511-519

2000

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Glutathione S-transferase genotypes in systemic sclerosis and their association with clinical manifestations in early disease

Genes and immunity, 2001-06, Vol.2 (4), p.236-238

2001

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Lack of association of a functionally relevant single nucleotide polymorphism of matrix metalloproteinase-1 promoter with systemic sclerosis (scleroderma)

Genes and immunity, 2001-08, Vol.2 (5), p.273-275

2001

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Monozygotic twins clinically discordant for scleroderma show concordance for fibroblast gene expression profiles

Arthritis and rheumatism, 2005-10, Vol.52 (10), p.3305-3314

2005

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Genome‐wide association study for regions of systemic sclerosis susceptibility in a Choctaw Indian population with high disease prevalence

Arthritis and rheumatism, 2003-09, Vol.48 (9), p.2585-2592

2003

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Association of novel polymorphisms with the expression of SPARC in normal fibroblasts and with susceptibility to scleroderma

Arthritis and rheumatism, 2002-11, Vol.46 (11), p.2990-2999

2002

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Mutations of bone morphogenetic protein receptor type II are not found in patients with pulmonary hypertension and underlying connective tissue diseases

Arthritis and rheumatism, 2002-10, Vol.46 (10), p.2829-2830

2002

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Small interfering RNA inhibition of SPARC attenuates the profibrotic effect of transforming growth factor beta 1 in cultured normal human fibroblasts

Arthritis and rheumatism, 2005-01, Vol.52 (1), p.257-261

2005

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Association of microsatellite markers near the fibrillin 1 gene on human chromosome 15q with scleroderma in a Native American population

Arthritis and rheumatism, 1998-10, Vol.41 (10), p.1729-1737

1998

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

Arthritis and rheumatism, 2000-05, Vol.43 (5), p.1068-1073

2000

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A molecular analysis of the low serum deoxyribonuclease activity in lupus patients

Arthritis and rheumatism, 2001-10, Vol.44 (10), p.2446-2447

2001

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

Arthritis and rheumatism, 2001-08, Vol.44 (8), p.1855-1864

2001

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Examination of the possible role of biologically relevant genes around FBN1 in systemic sclerosis in the Choctaw population

Arthritis and rheumatism, 2003-11, Vol.48 (11), p.3295-3296

2003

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Systemic lupus erythematosus in a multiethnic US cohort: XXXVI. Influence of mannose‐binding lectin exon 1 polymorphisms in disease manifestations, course, and outcome

Arthritis and rheumatism, 2006-05, Vol.54 (5), p.1703-1704

2006

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Autoantibodies to the extracellular matrix microfibrillar protein, fibrillin 1, in patients with localized scleroderma

Arthritis and rheumatism, 1999-12, Vol.42 (12), p.2656-2659

1999

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Fibrillin 1 abnormalities in dermal fibroblast cultures from first‐degree relatives of patients with systemic sclerosis (scleroderma)

Arthritis and rheumatism, 2004-01, Vol.50 (1), p.329-332

2004

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Systemic lupus erythematosus in three ethnic groups. VIII. Lack of association of glutathione S‐transferase null alleles with disease manifestations

Arthritis and rheumatism, 2001-04, Vol.44 (4), p.981-983

2001

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Systemic sclerosis: the susceptible host (genetics and environment)

Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis

Signatures of differentially regulated interferon gene expression and vasculotrophism in the peripheral blood cells of systemic sclerosis patients

Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study

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

Genetics of scleroderma: update on single nucleotide polymorphism analysis and microarrays

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

Identification of novel targets in scleroderma: update on population studies, cDNA arrays, SNP analysis, and mutations

Genetic factors in the etiology of systemic sclerosis and Raynaud phenomenon

Glutathione S-transferase genotypes in systemic sclerosis and their association with clinical manifestations in early disease

Lack of association of a functionally relevant single nucleotide polymorphism of matrix metalloproteinase-1 promoter with systemic sclerosis (scleroderma)

Monozygotic twins clinically discordant for scleroderma show concordance for fibroblast gene expression profiles

Genome‐wide association study for regions of systemic sclerosis susceptibility in a Choctaw Indian population with high disease prevalence

Association of novel polymorphisms with the expression of SPARC in normal fibroblasts and with susceptibility to scleroderma

Mutations of bone morphogenetic protein receptor type II are not found in patients with pulmonary hypertension and underlying connective tissue diseases

Small interfering RNA inhibition of SPARC attenuates the profibrotic effect of transforming growth factor beta 1 in cultured normal human fibroblasts

Association of microsatellite markers near the fibrillin 1 gene on human chromosome 15q with scleroderma in a Native American population

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

A molecular analysis of the low serum deoxyribonuclease activity in lupus patients

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

Examination of the possible role of biologically relevant genes around FBN1 in systemic sclerosis in the Choctaw population

Systemic lupus erythematosus in a multiethnic US cohort: XXXVI. Influence of mannose‐binding lectin exon 1 polymorphisms in disease manifestations, course, and outcome

Autoantibodies to the extracellular matrix microfibrillar protein, fibrillin 1, in patients with localized scleroderma

Fibrillin 1 abnormalities in dermal fibroblast cultures from first‐degree relatives of patients with systemic sclerosis (scleroderma)

Systemic lupus erythematosus in three ethnic groups. VIII. Lack of association of glutathione S‐transferase null alleles with disease manifestations

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