These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 7900940)

  • 21. 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]  

  • 22. C1q: structure, function, and receptors.
    Kishore U; Reid KB
    Immunopharmacology; 2000 Aug; 49(1-2):159-70. PubMed ID: 10904115
    [TBL] [Abstract][Full Text] [Related]  

  • 23. C1q--how many functions? How many receptors?
    Eggleton P; Reid KB; Tenner AJ
    Trends Cell Biol; 1998 Nov; 8(11):428-31. PubMed ID: 9854308
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Family study of natural killer cell activity in C1q-deficient patients with systemic lupus erythematosus-like syndrome: association between impaired natural killer cell function and C1q deficiency.
    Tóth J; Starsia Z; Buc M; Stefanovic J
    Immunobiology; 1989 Nov; 180(1):47-54. PubMed ID: 2625354
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. SLE like syndrome and functional deficiency of C1q in members of a large family.
    Hannema AJ; Kluin-Nelemans JC; Hack CE; Eerenberg-Belmer AJ; Mallée C; van Helden HP
    Clin Exp Immunol; 1984 Jan; 55(1):106-14. PubMed ID: 6319055
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. The complement system in systemic lupus erythematosus: an update.
    Leffler J; Bengtsson AA; Blom AM
    Ann Rheum Dis; 2014 Sep; 73(9):1601-6. PubMed ID: 24845390
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Marked variability in clinical presentation and outcome of patients with C1q immunodeficiency.
    van Schaarenburg RA; Schejbel L; Truedsson L; Topaloglu R; Al-Mayouf SM; Riordan A; Simon A; Kallel-Sellami M; Arkwright PD; Åhlin A; Hagelberg S; Nielsen S; Shayesteh A; Morales A; Tam S; Genel F; Berg S; Ketel AG; Merlijn van den Berg J; Kuijpers TW; Olsson RF; Huizinga TW; Lankester AC; Trouw LA
    J Autoimmun; 2015 Aug; 62():39-44. PubMed ID: 26119135
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Investigation of C1-complex regions reveals new C1Q variants associated with protection from systemic lupus erythematosus, and affect its transcript abundance.
    Guo J; Gao Y; Wang Y; Zou Y; Du Y; Luo C; Shi Y; Yang Y; Wu X; Su Y; Wu L; Chen S; Li Z
    Sci Rep; 2018 May; 8(1):8048. PubMed ID: 29795138
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Hereditary C1q deficiency: a new family with C1qA deficiency.
    Sun-Tan C; Ozgür TT; Kilinç G; Topaloğlu R; Gököz O; Ersoy-Evans S; Sanal O
    Turk J Pediatr; 2010; 52(2):184-6. PubMed ID: 20560256
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of the Raji cell membrane-derived C1q inhibitor as a receptor for human C1q. Purification and immunochemical characterization.
    Ghebrehiwet B; Silvestri L; McDevitt C
    J Exp Med; 1984 Nov; 160(5):1375-89. PubMed ID: 6436431
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The binding protein for globular heads of complement C1q, gC1qR. Functional expression and characterization as a novel vitronectin binding factor.
    Lim BL; Reid KB; Ghebrehiwet B; Peerschke EI; Leigh LA; Preissner KT
    J Biol Chem; 1996 Oct; 271(43):26739-44. PubMed ID: 8900153
    [TBL] [Abstract][Full Text] [Related]  

  • 37. SLE: Novel Postulates for Therapeutic Options.
    Hosszu KK; Valentino A; Peerschke EI; Ghebrehiwet B
    Front Immunol; 2020; 11():583853. PubMed ID: 33117397
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Anti-C1q autoantibodies from systemic lupus erythematosus patients activate the complement system via both the classical and lectin pathways.
    Thanei S; Vanhecke D; Trendelenburg M
    Clin Immunol; 2015 Oct; 160(2):180-7. PubMed ID: 26148903
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A patient with hereditary C1q deficiency.
    Ozsoylu S
    Turk J Pediatr; 2010; 52(6):674; author reply 674. PubMed ID: 21428208
    [No Abstract]   [Full Text] [Related]  

  • 40. C1q-binding proteins and C1q receptors.
    Nicholson-Weller A; Klickstein LB
    Curr Opin Immunol; 1999 Feb; 11(1):42-6. PubMed ID: 10047536
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.