Pseudolinear C4d deposits in a hereditary glomerulopathy caused by a rare NC1 collagen-4-alpha-5 missense mutation: a “new disease entity”?-Reference-Cited by-同舟云学术

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Pseudolinear C4d deposits in a hereditary glomerulopathy caused by a rare NC1 collagen-4-alpha-5 missense mutation: a “new disease entity”?

Published:2019-09-03 Issue:4-5 Volume:43 Page:209-215
ISSN:0191-3123
Container-title:Ultrastructural Pathology
language:en
Short-container-title:Ultrastructural Pathology

Author:

Roy Sanjeet¹,Nalwa Aasma¹,Keith Jared²,Weck Karen³,Singh Harsharan¹,Nickeleit Volker¹

Affiliation:

1. Department of Pathology, Division of Nephropathology, University of North Carolina at Chapel Hill, Chapel Hill, United States

2. Blue Ridge Nephrology and Hypertension Center, Boone, NC, USA

3. Department of Pathology, Molecular Genetics Laboratory, University of North Carolina at Chapel Hill, Chapel Hill, USA

Publisher

Informa UK Limited

Subject

Structural Biology,Pathology and Forensic Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/01913123.2019.1683666

Reference24 articles.

1. Kidney transplants, antibodies and rejection: is C4d a magic marker?

2. Classical pathway of complement activation in normal and diseased human glomeruli

3. Capillary Deposition of Complement Split Product C4d in Renal Allografts is Associated with Basement Membrane Injury in Peritubular and Glomerular Capillaries: A Contribution of Humoral Immunity to Chronic Allograft Rejection

4. C4d as a Diagnostic Tool in Proliferative GN

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