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Complement Deficiencies Result in Surrogate Pathways of Complement Activation in Novel Polygenic Lupus-like Models of Kidney Injury.
Skopelja-Gardner, Sladjana; Colonna, Lucrezia; Hermanson, Payton; Sun, Xizhang; Tanaka, Lena; Tai, Joyce; Nguyen, Yenly; Snyder, Jessica M; Alpers, Charles E; Hudkins, Kelly L; Salant, David J; Peng, YuFeng; Elkon, Keith B.
Afiliación
  • Skopelja-Gardner S; Division of Rheumatology, University of Washington, Seattle, WA 98109.
  • Colonna L; Division of Rheumatology, University of Washington, Seattle, WA 98109.
  • Hermanson P; Division of Rheumatology, University of Washington, Seattle, WA 98109.
  • Sun X; Division of Rheumatology, University of Washington, Seattle, WA 98109.
  • Tanaka L; Division of Rheumatology, University of Washington, Seattle, WA 98109.
  • Tai J; Division of Rheumatology, University of Washington, Seattle, WA 98109.
  • Nguyen Y; Division of Rheumatology, University of Washington, Seattle, WA 98109.
  • Snyder JM; Department of Comparative Medicine, University of Washington, Seattle, WA 98109.
  • Alpers CE; Department of Nephrology, University of Washington, Seattle, WA 98109.
  • Hudkins KL; Department of Nephrology, University of Washington, Seattle, WA 98109.
  • Salant DJ; Division of Nephrology, Boston University, Boston, MA 02215; and.
  • Peng Y; Division of Rheumatology, University of Washington, Seattle, WA 98109; yfpeng2014@gmail.com kelkon@medicine.washington.edu.
  • Elkon KB; Division of Rheumatology, University of Washington, Seattle, WA 98109; yfpeng2014@gmail.com kelkon@medicine.washington.edu.
J Immunol ; 204(10): 2627-2640, 2020 05 15.
Article en En | MEDLINE | ID: mdl-32238460
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Nefritis Lúpica / Enfermedades por Deficiencia de Complemento Hereditario / Riñón Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Immunol Año: 2020 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Nefritis Lúpica / Enfermedades por Deficiencia de Complemento Hereditario / Riñón Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Immunol Año: 2020 Tipo del documento: Article