Jan Klooster
Amsterdam, NH 1105BA, Netherlands
Last Updated: 09/26/2026
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Found 40 publications
Degenerated Cones in Cultured Human Retinas Can Successfully Be Optogenetically Reactivated.
Journal: International journal of molecular sciences
Published: December 05, 2019
Saltatory Conduction along Myelinated Axons Involves a Periaxonal Nanocircuit.
Journal: Cell
Published: March 11, 2019
Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.
Journal: Human molecular genetics
Published: August 08, 2018
CRB2 in immature photoreceptors determines the superior-inferior symmetry of the developing retina to maintain retinal structure and function.
Journal: Human molecular genetics
Published: March 20, 2018
Specific connectivity between photoreceptors and horizontal cells in the zebrafish retina.
Journal: Journal of neurophysiology
Published: June 06, 2016
An Ultrastructural and Immunohistochemical Analysis of the Outer Plexiform Layer of the Retina of the European Silver Eel (Anguilla anguilla L).
Journal: PloS one
Published: October 13, 2015
Astrocytes are central in the pathomechanisms of vanishing white matter.
Journal: The Journal of clinical investigation
Published: July 27, 2015
Gene therapy into photoreceptors and Müller glial cells restores retinal structure and function in CRB1 retinitis pigmentosa mouse models.
Journal: Human molecular genetics
Published: December 09, 2014
Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.
Journal: Anatomical record (Hoboken, N.J. : 2007)
Published: March 25, 2014
CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice.
Journal: Human molecular genetics
Published: February 26, 2014
Targeted ablation of Crb2 in photoreceptor cells induces retinitis pigmentosa.
Journal: Human molecular genetics
Published: February 05, 2014
Last Updated: 09/26/2026