BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

283 related articles for article (PubMed ID: 26493816)

  • 1. Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis.
    Lintner KE; Patwardhan A; Rider LG; Abdul-Aziz R; Wu YL; Lundström E; Padyukov L; Zhou B; Alhomosh A; Newsom D; White P; Jones KB; O'Hanlon TP; Miller FW; Spencer CH; Yu CY
    Ann Rheum Dis; 2016 Sep; 75(9):1599-606. PubMed ID: 26493816
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations.
    Chen JY; Wu YL; Mok MY; Wu YJ; Lintner KE; Wang CM; Chung EK; Yang Y; Zhou B; Wang H; Yu D; Alhomosh A; Jones K; Spencer CH; Nagaraja HN; Lau YL; Lau CS; Yu CY
    Arthritis Rheumatol; 2016 Jun; 68(6):1442-1453. PubMed ID: 26814708
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Low copy numbers of complement
    Zhou D; King EH; Rothwell S; Krystufkova O; Notarnicola A; Coss S; Abdul-Aziz R; Miller KE; Dang A; Yu GR; Drew J; Lundström E; Pachman LM; Mamyrova G; Curiel RV; De Paepe B; De Bleecker JL; Payton A; Ollier W; O'Hanlon TP; Targoff IN; Flegel WA; Sivaraman V; Oberle E; Akoghlanian S; Driest K; Spencer CH; Wu YL; Nagaraja HN; Ardoin SP; Chinoy H; Rider LG; Miller FW; Lundberg IE; Padyukov L; Vencovský J; Lamb JA; Yu CY;
    Ann Rheum Dis; 2023 Feb; 82(2):235-245. PubMed ID: 36171069
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetically determined partial complement C4 deficiency states are not independent risk factors for SLE in UK and Spanish populations.
    Boteva L; Morris DL; Cortés-Hernández J; Martin J; Vyse TJ; Fernando MM
    Am J Hum Genet; 2012 Mar; 90(3):445-56. PubMed ID: 22387014
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Low C4, C4A and C4B gene copy numbers are stronger risk factors for juvenile-onset than for adult-onset systemic lupus erythematosus.
    Pereira KM; Faria AG; Liphaus BL; Jesus AA; Silva CA; Carneiro-Sampaio M; Andrade LE
    Rheumatology (Oxford); 2016 May; 55(5):869-73. PubMed ID: 26800705
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gene CNVs and protein levels of complement C4A and C4B as novel biomarkers for partial disease remissions in new-onset type 1 diabetes patients.
    Kingery SE; Wu YL; Zhou B; Hoffman RP; Yu CY
    Pediatr Diabetes; 2012 Aug; 13(5):408-18. PubMed ID: 22151770
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Low copy numbers of complement C4 and homozygous deficiency of C4A may predispose to severe disease and earlier disease onset in patients with systemic lupus erythematosus.
    Jüptner M; Flachsbart F; Caliebe A; Lieb W; Schreiber S; Zeuner R; Franke A; Schröder JO
    Lupus; 2018 Apr; 27(4):600-609. PubMed ID: 29050534
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4.
    Blanchong CA; Chung EK; Rupert KL; Yang Y; Yang Z; Zhou B; Moulds JM; Yu CY
    Int Immunopharmacol; 2001 Mar; 1(3):365-92. PubMed ID: 11367523
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Impact of C4, C4A and C4B gene copy number variation in the susceptibility, phenotype and progression of systemic lupus erythematosus.
    Pereira KMC; Perazzio S; Faria AGA; Moreira ES; Santos VC; Grecco M; da Silva NP; Andrade LEC
    Adv Rheumatol; 2019 Aug; 59(1):36. PubMed ID: 31387635
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases.
    Zhou D; Rudnicki M; Chua GT; Lawrance SK; Zhou B; Drew JL; Barbar-Smiley F; Armstrong TK; Hilt ME; Birmingham DJ; Passler W; Auletta JJ; Bowden SA; Hoffman RP; Wu YL; Jarjour WN; Mok CC; Ardoin SP; Lau YL; Yu CY
    Front Immunol; 2021; 12():739430. PubMed ID: 34764957
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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.
    Wu YL; Savelli SL; Yang Y; Zhou B; Rovin BH; Birmingham DJ; Nagaraja HN; Hebert LA; Yu CY
    J Immunol; 2007 Sep; 179(5):3012-25. PubMed ID: 17709516
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4-deficient patients with systemic lupus erythematosus (SLE).
    Dragon-Durey MA; Rougier N; Clauvel JP; Caillat-Zucman S; Remy P; Guillevin L; Liote F; Blouin J; Ariey F; Lambert BU; Kazatchkine MD; Weiss L
    Clin Exp Immunol; 2001 Jan; 123(1):133-9. PubMed ID: 11168010
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complement C4A and C4B Gene Copy Number Study in Alzheimer's Disease Patients.
    Zorzetto M; Datturi F; Divizia L; Pistono C; Campo I; De Silvestri A; Cuccia M; Ricevuti G
    Curr Alzheimer Res; 2017; 14(3):303-308. PubMed ID: 27758680
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Insights on the relationship between complement component C4 serum concentrations and C4 gene copy numbers in a Western Australian systemic lupus erythematosus cohort.
    Margery-Muir AA; Bundell C; Wetherall JD; Whidborne R; Martinez P; Groth DM
    Lupus; 2018 Sep; 27(10):1687-1696. PubMed ID: 30041577
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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.
    Yang Y; Chung EK; Wu YL; Savelli SL; Nagaraja HN; Zhou B; Hebert M; Jones KN; Shu Y; Kitzmiller K; Blanchong CA; McBride KL; Higgins GC; Rennebohm RM; Rice RR; Hackshaw KV; Roubey RA; Grossman JM; Tsao BP; Birmingham DJ; Rovin BH; Hebert LA; Yu CY
    Am J Hum Genet; 2007 Jun; 80(6):1037-54. PubMed ID: 17503323
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genes.
    Lokki ML; Circolo A; Ahokas P; Rupert KL; Yu CY; Colten HR
    J Immunol; 1999 Mar; 162(6):3687-93. PubMed ID: 10092831
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Copy number variations of complement component C4 are associated with Behçet's disease but not with ankylosing spondylitis associated with acute anterior uveitis.
    Hou S; Qi J; Liao D; Zhang Q; Fang J; Zhou Y; Liu Y; Bai L; Zhang M; Kijlstra A; Yang P
    Arthritis Rheum; 2013 Nov; 65(11):2963-70. PubMed ID: 23918728
    [TBL] [Abstract][Full Text] [Related]  

  • 18. High-throughput analysis of the C4 polymorphism by a combination of MLPA and isotype-specific ELISA's.
    Wouters D; van Schouwenburg P; van der Horst A; de Boer M; Schooneman D; Kuijpers TW; Aarden LA; Hamann D
    Mol Immunol; 2009 Feb; 46(4):592-600. PubMed ID: 19062096
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Relationship between copy number of genes (C4A, C4B) encoding the fourth component of complement and the clinical course of hereditary angioedema (HAE).
    Blaskó B; Széplaki G; Varga L; Ronai Z; Prohászka Z; Sasvari-Szekely M; Visy B; Farkas H; Füst G
    Mol Immunol; 2007 Apr; 44(10):2667-74. PubMed ID: 17229465
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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.
    Saxena K; Kitzmiller KJ; Wu YL; Zhou B; Esack N; Hiremath L; Chung EK; Yang Y; Yu CY
    Mol Immunol; 2009 Apr; 46(7):1289-303. PubMed ID: 19135723
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.