Molecular evolution and functional divergence of the bestrophin protein family
<p>Abstract</p> <p>Background</p> <p>Mutations in human bestrophin 1 are associated with at least three autosomal-dominant macular dystrophies including Best disease, adult onset vitelliform macular dystrophy and autosomal dominant vitreo-retinochoroidopathy. The protei...
Main Authors: | Schreiber Rainer, Langmann Thomas, Milenkovic Vladimir M, Kunzelmann Karl, Weber Bernhard HF |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2008-02-01
|
Series: | BMC Evolutionary Biology |
Online Access: | http://www.biomedcentral.com/1471-2148/8/72 |
Similar Items
-
Lineage-specific expression of bestrophin-2 and bestrophin-4 in human intestinal epithelial cells.
by: Go Ito, et al.
Published: (2013-01-01) -
The Y227N mutation affects bestrophin-1 protein stability and impairs sperm function in a mouse model of Best vitelliform macular dystrophy
by: Andrea Milenkovic, et al.
Published: (2019-07-01) -
Molecular mechanisms of gating in the calcium-activated chloride channel bestrophin
by: Alexandria N Miller, et al.
Published: (2019-01-01) -
Structures and gating mechanisms of human bestrophin anion channels
by: Aaron P. Owji, et al.
Published: (2022-07-01) -
Targeting of Intracellular TMEM16 Proteins to the Plasma Membrane and Activation by Purinergic Signaling
by: Rainer Schreiber, et al.
Published: (2020-06-01)