Yee-Ling Wu

发表

DNA deaminases induce break-associated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis

M. Stratton, P. Campbell, L. Stebbings, 2013, eLife.

Elevated serum complement levels and higher gene copy number of complement C4B are associated with hypertension and effective response to statin therapy in childhood-onset systemic lupus erythematosus (SLE)

H. Nagaraja, Yee-Ling Wu, L. Schanberg, 2019, Lupus Science & Medicine.

Three distinct profiles of serum complement C4 proteins in pediatric systemic lupus erythematosus (SLE) patients: tight associations of complement C4 and C3 protein levels in SLE but not in healthy subjects.

H. Nagaraja, B. Rovin, D. Birmingham, 2006, Advances in experimental medicine and biology.

Complement Components C4A and C4B in Human Lupus

B. Rovin, D. Birmingham, C. Y. Yu, 2005 .

Sensitive and Specific Real-Time Polymerase Chain Reaction Assays to Accurately Determine Copy Number Variations (CNVs) of Human Complement C4A, C4B, C4-Long, C4-Short, and RCCX Modules: Elucidation of C4 CNVs in 50 Consanguineous Subjects with Defined HLA Genotypes

H. Nagaraja, B. Rovin, D. Birmingham, 2007 .

Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies

J. Lamb, H. Nagaraja, A. Payton, 2022, Annals of the Rheumatic Diseases.

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans.

Bi Zhou, H. Nagaraja, B. Rovin, 2007, American journal of human genetics.

Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome

K. Lindblad-Toh, R. Jonsson, L. Rönnblom, 2022, Arthritis & Rheumatology (Hoboken, N.j.).

Chapter 19 – Complement Deficiencies in Human Systemic Lupus Erythematosus (SLE) and SLE Nephritis: Epidemiology and Pathogenesis

B. Rovin, D. Birmingham, C. Y. Yu, 2007 .

Human Complement Components C4A and C4B Genetic Diversities: Complex Genotypes and Phenotypes

C. Y. Yu, Yee-Ling Wu, Erwin K. Chung, 2005, Current protocols in immunology.

Sensitive and specific real-time PCR assays to accurately determine gene copy-number variations (CNVs) of human complement C4A, C4B, C4-Long, C4-Short and RCCX modules: Elucidation of C4 GCNVs in 50 consanguineous subjects with defined HLA genotypes

H. Nagaraja, B. Rovin, C. Y. Yu, 2007 .

The complement system and human autoimmune diseases.

Yee-Ling Wu, J. Atkinson, Chack-Yung Yu, 2022, Journal of autoimmunity.

Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune Diseases

C. Y. Yu, L. Hebert, Yee-Ling Wu, 2016, Front. Immunol..

Active RNAP pre-initiation sites are highly mutated by cytidine deaminases in yeast, with AID targeting small RNA genes

C. Rada, Benjamin J M Taylor, Yee-Ling Wu, 2014, eLife.

Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases

M. Rudnicki, Y. Lau, D. Birmingham, 2021, Frontiers in Immunology.

Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations.

Kapil Saxena, Bi Zhou, C. Y. Yu, 2009, Molecular immunology.

Complement Component C4 in Human Systemic Lupus Erythematosus: from Genetic Deficiencies to Copy-Number Variations

Yee-Ling Wu, 2009 .

H. Nagaraja, B. Rovin, D. Birmingham, 2007, The Journal of Immunology.

A Dinucleotide Deletion in CD24 Confers Protection against Autoimmune Diseases

Yang Liu, Xincheng Zheng, Pan Zheng, 2007, PLoS genetics.

Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis

L. Padyukov, Yee-Ling Wu, F. Miller, 2015, Annals of the rheumatic diseases.

Gene CNVs and protein levels of complement C4A and C4B as novel biomarkers for partial disease remissions in new‐onset type 1 diabetes patients

C. Y. Yu, Yee-Ling Wu, R. Hoffman, 2012, Pediatric diabetes.

Frequency of Carriers of 8.1 Ancestral Haplotype and its Fragments in Two Caucasian Populations

C. Y. Yu, Yee-Ling Wu, Z. Prohászka, 2007, Immunological investigations.

The HLA 8.1 ancestral haplotype is strongly linked to the C allele of -429T>C promoter polymorphism of receptor of the advanced glycation endproduct (RAGE) gene. Haplotype-independent association of the -429C allele with high hemoglobinA1C levels in diabetic patients.

Yee-Ling Wu, G. Füst, L. Madácsy, 2007, Molecular immunology.

Assessment of complement C4 gene copy number using the paralog ratio test

J. Rioux, D. Morris, T. Vyse, 2010, Human mutation.

Intrinsic transcriptional heterogeneity in B cells controls early class switching to IgE

Sarah A Teichmann, Michael J. T. Stubbington, S. Teichmann, 2017, The Journal of experimental medicine.

Sex-specific association of X-linked Toll-like receptor 7 (TLR7) with male systemic lupus erythematosus

R. Cantor, Y. Lau, C. Y. Yu, 2010, Proceedings of the National Academy of Sciences.

Determination of the Loss of Function Complement C4 Exon 29 CT Insertion Using a Novel Paralog-Specific Assay in Healthy UK and Spanish Populations

Javier Martín, T. Vyse, Yee-Ling Wu, 2011, PloS one.

Opposite Profiles of Complement in Antiphospholipid Syndrome (APS) and Systemic Lupus Erythematosus (SLE) Among Patients With Antiphospholipid Antibodies (aPL)

H. Nagaraja, Yee-Ling Wu, Chack-Yung Yu, 2019, Front. Immunol..

Increased frequency of complement C4B deficiency in rheumatoid arthritis.

C. Y. Yu, Yee-Ling Wu, W. Rigby, 2012, Arthritis and rheumatism.

Loop extrusion promotes an alternate pathway for isotype switching

A. Kenter, Yee-Ling Wu, S. Priyadarshi, 2021, Cell reports.

Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome

K. Lindblad-Toh, R. Jonsson, L. Rönnblom, 2022, Arthritis & rheumatology.

Molecular basis of complete complement C4 deficiency in two North-African families with systemic lupus erythematosus

C. Y. Yu, Yee-Ling Wu, M. Viguier, 2009, Genes and Immunity.

Molecular fine-tuning of affinity maturation in germinal centers.

C. Rada, Yee-Ling Wu, 2016, The Journal of clinical investigation.

Sex-specific association of X-linked Toll-like receptor 7 (TLR7) with male systemic lupus erythematosus

R. Cantor, Y. Lau, S. Bang, 2010, Proceedings of the National Academy of Sciences.

Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations.

Yee-Ling Wu, K. Saxena, L. Hiremath, 2009, Molecular immunology.