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Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN.

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Individual Studies
  • OMIM - Kidney diseases

    Homo sapiens Homo sapiens | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

    Source: NextBio Library/Mutation and Phenotypic data

  • Mouse Phenotypes - Kidney diseases

    Mus musculus Mus musculus | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated mouse gene mutation data extracted from the Mouse Genome Database (MGD) at The Jackson Laboratory, Bar Harbor, Maine. Additional computational processing and curation of mouse phenotype data was performed to further organize and group data from related phenotypes into uni…

    Source: NextBio Library/Mutation and Phenotypic data

View All Individual Studies

Thought leaders and organizations working on research involving membranoproliferative glomerulonephritis.

  • Charles E Alpers
  • Christoph Licht
  • Peter F Zipfel
  • Pilar Sánchez-Corral
  • Kikuo Iitaka
  • Mayo Clinic
  • University of Iowa
  • National Institute of Arthritis and Musculoskeletal and Skin Diseases …
  • Kenta Biotech Ltd
  • ClinTrio Ltd.
  • University of Washington
  • Manchester Royal Eye Hospital
  • Hospital for Sick Children
  • University of Erlangen-Nürnberg
  • Imperial College

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