Completed Genetics & Molecular Biology NIHR-supported project Heart, Stroke & Blood

Molecular and phenotypic investigation of a CA12 loss-of-function variant associated with chronic kidney disease-defining traits

Funder NIHR (part of DHSC)
Recipient organisation NIHR Manchester Biomedical Research Centre
NIHR support Recorded as supported by this research centre
Period Feb 2025 — Mar 2026

About this grant

This summary is based on the grant title only — the full abstract was not available.

No substantive source abstract was published for this research project funded by NIHR.

Researchers

Amber Emmett (Principal Investigator)

Related Research

Grants with similar aims, by meaning.

Genetic Investigation of Kidney Disease.
Functional characterisation of genetic variants of relevance to hypertension and antihypertensive treatment
Deciphering the Role of DDX1 SNPs in Kidney Disease Using CRISPR Technology
A Study of the Natural History of Renal Disease in TSC2/PKD1 Contiguous Gene Deletion Syndrome.
A functional genomics pipeline for genetic discovery in diabetic kidney disease

Original classification

Next Generation Phenotyping and Diagnostics

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