N. Torben Bech‐Hansen
University of Calgary(CA)Alberta Children's Hospital(CA)
Publications by Year
Research Areas
Retinal Development and Disorders, Photoreceptor and optogenetics research, Connexins and lens biology, Neuroscience and Neuropharmacology Research, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness(2000)349 cited
- → Pleiotropic phenotype of colchicine‐resistant CHO cells: Cross‐resistance and collateral sensitivity(1976)313 cited
- → Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina(2005)267 cited
- → Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism(2008)115 cited
- → A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants(2001)102 cited
- → The CaV1.4 Calcium Channel Is a Critical Regulator of T Cell Receptor Signaling and Naive T Cell Homeostasis(2011)100 cited