Britt Johnson

Multiple sclerosis patients have a distinct gut microbiota compared to healthy controls

A pupal transcriptomic screen identifies Ral as a target of store-operated calcium entry in Drosophila neurons

Carbonic Anhydrase Related Protein VIII and its Role in Neurodegeneration and Cancer

The molecular basis of human retinal and vitreoretinal diseases

Update on hypoxia-inducible factors and hydroxylases in oxygen regulatory pathways: from physiology to therapeutics

Decoding multiple sclerosis: an update on genomics and future directions

Diabetic Retinopathy

Metazoan MicroRNAs

Leber congenital amaurosis: Genes, proteins and disease mechanisms

Mutant Isocitrate Dehydrogenase Inhibitors as Targeted Cancer Therapeutics

Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling

MiR-211 is essential for adult cone photoreceptor maintenance and visual function

Oxidative Stress in Cancer

Retinal Ganglion Cells Survive and Maintain Normal Dendritic Morphology in a Mouse Model of Inherited Photoreceptor Degeneration

Diabetes downregulates presynaptic proteins and reduces basal synapsin I phosphorylation in rat retina

Molecular oncogenesis of chondrosarcoma: impact for targeted treatment

Interaction between the Photoreceptor-Specific Tubby-like Protein 1 and the Neuronal-Specific GTPase Dynamin-1

Reversible Photocontrol of Biological Systems by the Incorporation of Molecular Photoswitches

Molecular genetics and protein function involved in nocturnal vision

Piccolo and bassoon maintain synaptic vesicle clustering without directly participating in vesicle exocytosis

Early Synaptic Defects intulp1^−/−Mice

Accurate proteome-wide missense variant effect prediction with AlphaMissense

Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms?

Treatment with a Small Molecule Mutant IDH1 Inhibitor Suppresses Tumorigenic Activity and Decreases Production of the Oncometabolite 2-Hydroxyglutarate in Human Chondrosarcoma Cells

Thenob2mouse, a null mutation inCacna1f: Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses

Reduced synaptic vesicle density and aberrant synaptic localization caused by a splice site mutation in the Rs1h gene

Aggregation of multiple sclerosis genetic risk variants in multiple and single case families

Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum

Prioritizing genes for systematic variant effect mapping