Artlett C M

Top coauthors of Artlett C M

Jimenez S A (11 papers)

Welsh K I (6 papers)

Briggs D C (5 papers)

Varga J (4 papers)

Black C M (3 papers)

List of Artlett C M publications


Otieno F G, Lopez A M, Jimenez S A, Gentiletti J, Artlett C M 2007. "Allograft inflammatory factor-1 and tumor necrosis factor single nucleotide polymorphisms in systemic sclerosis." Tissue antigens 69 (6) doi:10.1111/j.1399-0039.2007.00830.x


Sawaya H H B, Jimenez S A, Artlett C M 2004. "Quantification of fetal microchimeric cells in clinically affected and unaffected skin of patients with systemic sclerosis." Rheumatology (Oxford, England) 43 (8) doi:10.1093/rheumatology/keh211


Artlett C M, Rasheed M, Russo-Stieglitz K E, Sawaya H H B, Jimenez S A 2002. "Influence of prior pregnancies on disease course and cause of death in systemic sclerosis." Annals of the rheumatic diseases 61 (4) doi:


Artlett C M, Miller F W, Rider L G 2001. "Persistent maternally derived peripheral microchimerism is associated with the juvenile idiopathic inflammatory myopathies." Rheumatology (Oxford, England) 40 (11) doi:


Christner P J, Artlett C M, Conway R F, Jiménez S A 2000. "Increased numbers of microchimeric cells of fetal origin are associated with dermal fibrosis in mice following injection of vinyl chloride." Arthritis and rheumatism 43 (11) doi:10.1002/1529-0131(200011)43:11<2598::AID-ANR30>3.0.CO;2-8
Rider L G, Artlett C M, Foster C B, Ahmed A, Neeman T, et al. 2000. "Polymorphisms in the IL-1 receptor antagonist gene VNTR are possible risk factors for juvenile idiopathic inflammatory myopathies." Clinical and experimental immunology 121 (1) doi:
Artlett C M, Cox L A, Jimenez S A 2000. "Detection of cellular microchimerism of male or female origin in systemic sclerosis patients by polymerase chain reaction analysis of HLA-Cw antigens." Arthritis and rheumatism 43 (5) doi:10.1002/1529-0131(200005)43:5<1062::AID-ANR16>3.0.CO;2-P
Artlett C M, Ramos R, Jiminez S A, Patterson K, Miller F W, Rider L G 2000. "Chimeric cells of maternal origin in juvenile idiopathic inflammatory myopathies. Childhood Myositis Heterogeneity Collaborative Group." Lancet 356 (9248) doi:


Artlett C M, Smith J B, Jimenez S A 1999. "New perspectives on the etiology of systemic sclerosis." Molecular medicine today 5 (2) doi:


Hitraya E G, Varga J, Artlett C M, Jiménez S A 1998. "Identification of elements in the promoter region of the alpha1(I) procollagen gene involved in its up-regulated expression in systemic sclerosis." Arthritis and rheumatism 41 (11) doi:10.1002/1529-0131(199811)41:11<2048::AID-ART21>3.0.CO;2-X
Artlett C M, Chen S J, Varga J, Jimenez S A 1998. "Modulation of basal expression of the human alpha1(I) procollagen gene (COL1A1) by tandem NF-1/Sp1 promoter elements in normal human dermal fibroblasts." Matrix biology : journal of the International Society for Matrix Biology 17 (6) doi:
Chen S J, Artlett C M, Jimenez S A, Varga J 1998. "Modulation of human alpha1(I) procollagen gene activity by interaction with Sp1 and Sp3 transcription factors in vitro." Gene 215 (1) doi:
Artlett C M, Smith J B, Jimenez S A 1998. "Identification of fetal DNA and cells in skin lesions from women with systemic sclerosis." The New England journal of medicine 338 (17) doi:10.1056/NEJM199804233381704


Artlett C M, Welsh K I, Black C M, Jimenez S A 1997. "Fetal-maternal HLA compatibility confers susceptibility to systemic sclerosis." Immunogenetics 47 (1) doi:


Artlett C M, Black C M, Briggs D C, Stephens C, Welsh K I 1996. "DNA allelic alterations within VNTR loci of scleroderma families." British journal of rheumatology 35 (12) doi:
Artlett C M, Black C M, Briggs D C, Stevens C O, Welsh K I 1996. "Telomere reduction in scleroderma patients: a possible cause for chromosomal instability." British journal of rheumatology 35 (8) doi:


Li L, Artlett C M, Jimenez S A, Hall D J, Varga J 1995. "Positive regulation of human alpha 1 (I) collagen promoter activity by transcription factor Sp1." Gene 164 (2) doi:
Shornick J K, Jenkins R E, Artlett C M, Briggs D C, Welsh K I, et al. 1995. "Class II MHC typing in pemphigoid gestationis." Clinical and experimental dermatology 20 (2) doi:


Stephens C O, Briggs D C, Whyte J, Artlett C M, Scherbakov A B, et al. 1994. "Familial scleroderma--evidence for environmental versus genetic trigger." British journal of rheumatology 33 (12) doi:
Cox A, Gonzalez A M, Wilson A G, Wilson R M, Ward J D, et al. 1994. "Comparative analysis of the genetic associations of HLA-DR3 and tumour necrosis factor alpha with human IDDM." Diabetologia 37 (5) doi:


Shornick J K, Artlett C M, Jenkins R E, Briggs D C, Welsh K I, et al. 1993. "Complement polymorphism in herpes gestationis: association with C4 null allele." Journal of the American Academy of Dermatology 29 (4) doi: