Chack Yung Yu
Affiliations: | Ohio State University, Columbus, Columbus, OH |
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"Chack Yu"Mean distance: 15.83 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentor| César Milstein | grad student | (Chemistry Tree) | |
| Rodney Robert Porter | grad student | (Chemistry Tree) |
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Publications
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| Mulvihill E, Ardoin S, Thompson SD, et al. (2019) Elevated serum complement levels and higher gene copy number of complement are associated with hypertension and effective response to statin therapy in childhood-onset systemic lupus erythematosus (SLE). Lupus Science & Medicine. 6: e000333 |
| Savelli SL, Roubey RAS, Kitzmiller KJ, et al. (2019) Opposite Profiles of Complement in Antiphospholipid Syndrome (APS) and Systemic Lupus Erythematosus (SLE) Among Patients With Antiphospholipid Antibodies (aPL). Frontiers in Immunology. 10: 885 |
| Yu C, Savelli S, Roubey R, et al. (2019) 190 Opposite profiles of complement in antiphospholipid syndrome (APS) and systemic lupus erythematosus (SLE) among patients with antiphospholipid antibodies Lupus Science & Medicine. 6 |
| Copenhaver M, Yu C, Hoffman RP. (2018) Complement Components, C3 and C4, and the Metabolic Syndrome. Current Diabetes Reviews. 15: 44-48 |
| Mok CC, King E, Zhou B, et al. (2018) SAT0424 Complement c4 gene copy number variations bestow large ranges of serum c4 protein levels in chinese patients with systemic lupus erythematosus (SLE) and contribute to organ and cardiovascular damages over time Annals of the Rheumatic Diseases |
| Yu C, Mulvihill E, Ardoin S, et al. (2018) Higher copy number of C4B genes and serum C4 are associated with hypertension and effective response to statins in pediatric lupus Molecular Immunology. 102: 230-231 |
| Lintner KE, Patwardhan A, Rider LG, et al. (2015) Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis. Annals of the Rheumatic Diseases |
| Mueller M, Barros P, Witherden AS, et al. (2013) Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus. American Journal of Human Genetics. 92: 28-40 |
| Kaiser R, Taylor KE, Deng Y, et al. (2013) Brief Report: Single-nucleotide polymorphisms in VKORC1 are risk factors for systemic lupus erythematosus in Asians. Arthritis and Rheumatism. 65: 211-5 |
| Kaufman KM, Zhao J, Kelly JA, et al. (2013) Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups. Annals of the Rheumatic Diseases. 72: 437-44 |