Understanding Type IV Collagens in Kidney Disease

Development of novel genetic tools for the study of type IV collagens

NIH-funded research University of California, San Francisco · NIH-11171687

This project aims to create new tools to better understand how certain collagen proteins work in the body and how their changes lead to inherited kidney diseases like Alport syndrome.

Quick facts

Grant typeR21 grant
Study typeNIH-funded research
Funding institutionUniversity of California, San Francisco NIH-funded
Lab location1 site (San Francisco, United States)
Project IDNIH-11171687 on NIH RePORTER

What this research studies

Our bodies rely on special proteins called type IV collagens, especially in the kidney's filtering units. When these collagens have mutations, they can cause inherited kidney diseases such as Alport syndrome. Currently, it's very difficult to study these collagens because they are stable and hard to isolate. This project will develop new mouse models where these collagens are marked with fluorescent proteins, allowing scientists to see exactly where and when they are deposited and how they change. These advanced tools will help us learn more about how these collagens function in both healthy and diseased kidneys.

Who could benefit from this research

Good fit: This foundational research is relevant to patients with Alport syndrome and other inherited kidney diseases caused by type IV collagen mutations.

Not a fit: Patients without inherited kidney diseases related to type IV collagen mutations would not directly benefit from this specific research.

Why it matters

Potential benefit: If successful, this work could provide fundamental insights into the causes of Alport syndrome and other inherited kidney diseases, paving the way for new diagnostic methods or treatments.

How similar studies have performed: While the role of type IV collagens in Alport syndrome is well-established, the specific genetic tools being developed in this project are novel and designed to overcome existing research barriers.

Where this research is happening

San Francisco, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Conditions Alport syndromeAlport syndrome (AS, ATS)Alport syndrome-like hereditary nephritisAlport syndrome-like hereditary nephritis (ASLHN, ASLN)Alport's Syndrome
Last reviewed 2026-06-10 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.