Peter Westenskow

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.

Compound mutations: a common cause of severe long-QT syndrome.

Mutation of colocalized residues of the pore helix and transmembrane segments S5 and S6 disrupt deactivation and modify inactivation of KCNQ1 K+ channels.

Beta-catenin controls differentiation of the retinal pigment epithelium in the mouse optic cup by regulating Mitf and Otx2 expression.

Ectopic Mitf in the embryonic chick retina by co-transfection of β-catenin and Otx2.

Astrocyte pVHL and HIF-α isoforms are required for embryonic-to-adult vascular transition in the eye.

Generation of retinal pigment epithelial cells from small molecules and OCT4 reprogrammed human induced pluripotent stem cells.

Using flow cytometry to compare the dynamics of photoreceptor outer segment phagocytosis in iPS-derived RPE cells.

Targeted deletion of Vegfa in adult mice induces vision loss.

Ras pathway inhibition prevents neovascularization by repressing endothelial cell sprouting.

Hypoxia-inducible factor (HIF)/vascular endothelial growth factor (VEGF) signaling in the retina.

Utilizing stem cell-derived RPE cells as a therapeutic intervention for age-related macular degeneration.

Local acting Sticky-trap inhibits vascular endothelial growth factor dependent pathological angiogenesis in the eye.

Interactive XCMS Online: simplifying advanced metabolomic data processing and subsequent statistical analyses.