Differential effects of Best disease causing missense mutations on bestrophin-1 trafficking

TREK-1 and Best1 Channels Mediate Fast and Slow Glutamate Release in Astrocytes upon GPCR Activation

(2012) Dong Ho Woo et al.   CELL

iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degeneration

(2012) Ruchira Singh et al.   HUMAN MOLECULAR GENETICS

Role of bestrophin-1 in store-operated calcium entry in retinal pigment epithelium

(2012) Néstor Más Gómez et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

Autosomal Recessive Best Vitelliform Macular Dystrophy

(2011) Alessandro Iannaccone   ARCHIVES OF OPHTHALMOLOGY

Disease-associated missense mutations in bestrophin-1 affect cellular trafficking and anion conductance

(2011) Vladimir M. Milenkovic et al.   JOURNAL OF CELL SCIENCE

Interaction of Bestrophin-1 and Ca2+ Channel β-Subunits: Identification of New Binding Domains on the Bestrophin-1 C-Terminus

(2011) Vladimir M. Milenkovic et al.   PLoS One

Effect of bestrophin-1 on L-type Ca2+ channel activity depends on the Ca2+ channel beta-subunit

(2010) Nadine Reichhart et al.   EXPERIMENTAL EYE RESEARCH

Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutations

(2010) A C Cohn et al.   EYE

Suppression of Ca2+ signaling in a mouse model of Best disease

(2010) Y. Zhang et al.   HUMAN MOLECULAR GENETICS

Bestrophin-2 mediates bicarbonate transport by goblet cells in mouse colon

(2010) Kuai Yu et al.   JOURNAL OF CLINICAL INVESTIGATION

Bestrophins and retinopathies

(2010) Qinghuan Xiao et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

The presence of bestrophin-1 modulates the Ca2+ recruitment from Ca2+ stores in the ER

(2010) Rudgar Neussert et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

Channel-Mediated Tonic GABA Release from Glia

(2010) S. Lee et al.   SCIENCE

Missense Mutations in a Retinal Pigment Epithelium Protein, Bestrophin-1, Cause Retinitis Pigmentosa

(2009) Alice E. Davidson et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Human Disease-causing Mutations Disrupt an N-C-terminal Interaction and Channel Function of Bestrophin 1

(2009) Zhiqiang Qu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Functional roles of bestrophins in ocular epithelia

(2009) Alan D. Marmorstein et al.   PROGRESS IN RETINAL AND EYE RESEARCH

The spectrum of ocular phenotypes caused by mutations in the BEST1 gene

(2009) Camiel J.F. Boon et al.   PROGRESS IN RETINAL AND EYE RESEARCH

Biallelic Mutation of BEST1 Causes a Distinct Retinopathy in Humans

(2008) Rosemary Burgess et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The Best Disease-Linked Cl- Channel hBest1 Regulates CaV1 (L-type) Ca2+ Channels via src-Homology-Binding Domains

(2008) K. Yu et al.   JOURNAL OF NEUROSCIENCE

Molecular Physiology of Bestrophins: Multifunctional Membrane Proteins Linked to Best Disease and Other Retinopathies

(2008) H. Criss Hartzell et al.   PHYSIOLOGICAL REVIEWS