COMMD1 Exemplifies the Power of Inbred Dogs to Dissect Genetic Causes of Rare Copper-Related Disorders
Wilson’s Disease is a rare autosomal recessive disorder in humans, often presenting with hepatic copper overload. Finding the genetic cause of a rare disease, especially if it is related to food constituents like the trace element copper, is a Herculean task. This review describes examples of how th...
Main Authors: | Ronald Jan Corbee, Louis C. Penning |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-02-01
|
Series: | Animals |
Subjects: | |
Online Access: | https://www.mdpi.com/2076-2615/11/3/601 |
Similar Items
-
Regulation of murine copper homeostasis by members of the COMMD protein family
by: Amika Singla, et al.
Published: (2021-01-01) -
Reduced FXR Target Gene Expression in Copper-Laden Livers of COMMD1-Deficient Dogs
by: Xiaoyan Wu, et al.
Published: (2019-09-01) -
Does Subtelomeric Position of COMMD5 Influence Cancer Progression?
by: Carole G. Campion, et al.
Published: (2021-03-01) -
Contribution à l’étude du rôle de COMMD1 dans la physiopathologie de la mucoviscidose
by: Drévillon, Loïc
Published: (2009) -
Transcriptional analysis of the expression, prognostic value and immune infiltration activities of the COMMD protein family in hepatocellular carcinoma
by: Xiaobo Wang, et al.
Published: (2021-09-01)