BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 31357913)

  • 1. Complex medical history of a patient with a compound heterozygous mutation in
    Lubbers R; Beaart-van de Voorde LJJ; van Leeuwen K; de Boer M; Gelderman KA; van den Berg MJ; Ketel AG; Simon A; de Ree J; Huizinga TWJ; Steup-Beekman GM; Trouw LA
    Lupus; 2019 Sep; 28(10):1255-1260. PubMed ID: 31357913
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of a novel non-coding mutation in C1qB in a Dutch child with C1q deficiency associated with recurrent infections.
    van Schaarenburg RA; Daha NA; Schonkeren JJ; Nivine Levarht EW; van Gijlswijk-Janssen DJ; Kurreeman FA; Roos A; van Kooten C; Koelman CA; Ernst-Kruis MR; Toes RE; Huizinga TW; Lankester AC; Trouw LA
    Immunobiology; 2015 Mar; 220(3):422-7. PubMed ID: 25454803
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Survey of Turkish systemic lupus erythematosus patients for a particular mutation of C1Q deficiency.
    Topaloglu R; Bakkaloglu A; Slingsby JH; Aydintug O; Besbas N; Saatci U; Walport MJ
    Clin Exp Rheumatol; 2000; 18(1):75-7. PubMed ID: 10728448
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PCR-RFLP genotyping of C1q mutations and single nucleotide polymorphisms in Malaysian patients with systemic lupus erythematosus.
    Chew CH; Chua KH; Lian LH; Puah SM; Tan SY
    Hum Biol; 2008 Feb; 80(1):83-93. PubMed ID: 18505047
    [TBL] [Abstract][Full Text] [Related]  

  • 5. New C1q mutation in a Tunisian family.
    Jlajla H; Sellami MK; Sfar I; Laadhar L; Zerzeri Y; Abdelmoula MS; Gorgi Y; Dridi MF; Makni S
    Immunobiology; 2014 Mar; 219(3):241-6. PubMed ID: 24331529
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole Exome Sequencing in Early-onset Systemic Lupus Erythematosus.
    Batu ED; Koşukcu C; Taşkıran E; Sahin S; Akman S; Sözeri B; Ünsal E; Bilginer Y; Kasapcopur O; Alikaşifoğlu M; Ozen S
    J Rheumatol; 2018 Dec; 45(12):1671-1679. PubMed ID: 30008451
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family.
    Topaloglu R; Bakkaloglu A; Slingsby JH; Mihatsch MJ; Pascual M; Norsworthy P; Morley BJ; Saatci U; Schifferli JA; Walport MJ
    Kidney Int; 1996 Aug; 50(2):635-42. PubMed ID: 8840296
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of novel coding mutation in C1qA gene in an African-American pedigree with lupus and C1q deficiency.
    Namjou B; Keddache M; Fletcher D; Dillon S; Kottyan L; Wiley G; Gaffney PM; Wakeland BE; Liang C; Wakeland EK; Scofield RH; Kaufman K; Harley JB
    Lupus; 2012 Sep; 21(10):1113-8. PubMed ID: 22472776
    [TBL] [Abstract][Full Text] [Related]  

  • 9. C1q deficiency in an Inuit family: identification of a new class of C1q disease-causing mutations.
    Marquart HV; Schejbel L; Sjoholm A; Martensson U; Nielsen S; Koch A; Svejgaard A; Garred P
    Clin Immunol; 2007 Jul; 124(1):33-40. PubMed ID: 17513176
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exome sequencing revealed C1Q homozygous mutation in Pediatric Systemic Lupus Erythematosus.
    Zoghi S; Ziaee V; Hirschmugl T; Jimenez-Heredia R; Krolo A; Boztug K; Rezaei N
    Allergol Immunopathol (Madr); 2018; 46(6):594-598. PubMed ID: 29739689
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus.
    Liphaus BL; Umetsu N; Jesus AA; Bando SY; Silva CA; Carneiro-Sampaio M
    Clinics (Sao Paulo); 2015 Mar; 70(3):220-7. PubMed ID: 26017655
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Homozygous hereditary C1q deficiency and systemic lupus erythematosus. A new family and the molecular basis of C1q deficiency in three families.
    Slingsby JH; Norsworthy P; Pearce G; Vaishnaw AK; Issler H; Morley BJ; Walport MJ
    Arthritis Rheum; 1996 Apr; 39(4):663-70. PubMed ID: 8630118
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of C1q polymorphisms suggests association with systemic lupus erythematosus, serum C1q and CH50 levels and disease severity.
    Martens HA; Zuurman MW; de Lange AH; Nolte IM; van der Steege G; Navis GJ; Kallenberg CG; Seelen MA; Bijl M
    Ann Rheum Dis; 2009 May; 68(5):715-20. PubMed ID: 18504288
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Monogenic interferonopathies: Phenotypic and genotypic findings of CANDLE syndrome and its overlap with C1q deficient SLE.
    Al-Mayouf SM; AlSaleem A; AlMutairi N; AlSonbul A; Alzaid T; Alazami AM; Al-Mousa H
    Int J Rheum Dis; 2018 Jan; 21(1):208-213. PubMed ID: 29115062
    [TBL] [Abstract][Full Text] [Related]  

  • 15. C1q Deficiency and Neuropsychiatric Systemic Lupus Erythematosus.
    van Schaarenburg RA; Magro-Checa C; Bakker JA; Teng YK; Bajema IM; Huizinga TW; Steup-Beekman GM; Trouw LA
    Front Immunol; 2016; 7():647. PubMed ID: 28082982
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Common silent mutations in all types of hereditary complement C1q deficiencies.
    Petry F; Loos M
    Immunogenetics; 2005 Sep; 57(8):566-71. PubMed ID: 16086173
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Classical pathway deficiencies - A short analytical review.
    Truedsson L
    Mol Immunol; 2015 Nov; 68(1):14-9. PubMed ID: 26038300
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey.
    Berkel AI; Birben E; Oner C; Oner R; Loos M; Petry F
    Immunobiology; 2000 Jan; 201(3-4):347-55. PubMed ID: 10776791
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Structure and function of complement protein C1q and its role in the development of autoimmune diseases].
    Smykał-Jankowiak K; Niemir ZI
    Postepy Hig Med Dosw (Online); 2009 Apr; 63():134-41. PubMed ID: 19373194
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Systemic lupus erythematosus with C1q deficiency: treatment with fresh frozen plasma.
    Ekinci Z; Ozturk K
    Lupus; 2018 Jan; 27(1):134-138. PubMed ID: 29113537
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.