J. T. Ten Brink

发表

Gene expression-based comparison of the human secretory neuroepithelia of the brain choroid plexus and the ocular ciliary body: potential implications for glaucoma

T. Gorgels, A. Bergen, N. Jansonius, 2014, Fluids and Barriers of the CNS.

Sorsby fundus dystrophy without a mutation in the TIMP-3 gene

P. D. de Jong, F. Meire, Jacqueline J M Assink, 2000, The British journal of ophthalmology.

Genotypic and Phenotypic Characteristics of CRB1-Associated Retinal Dystrophies: A Long-Term Follow-up Study.

C. Klaver, N. Schalij-Delfos, G. Dagnelie, 2017, Ophthalmology.

The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR Gene.

C. Klaver, N. Schalij-Delfos, G. Dagnelie, 2018, Investigative ophthalmology & visual science.

CRB1-associated retinal dystrophies: a prospective natural history study in anticipation of future clinical trials.

C. Klaver, N. Schalij-Delfos, J. Wijnholds, 2021, American journal of ophthalmology.

Dietary magnesium, not calcium, prevents vascular calcification in a mouse model for pseudoxanthoma elasticum

J. Waarsing, T. Gorgels, A. Bergen, 2010, Journal of molecular medicine.

Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region.

F. Riemslag, A. Bergen, J. T. ten Brink, 1995, Human molecular genetics.

Gene Expression and Functional Annotation of the Human Ciliary Body Epithelia

P. J. van der Spek, T. Gorgels, A. Bergen, 2012, PloS one.

Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa

P. D. de Jong, F. Meire, M. V. van Schooneveld, 2005, Journal of Medical Genetics.

Frequent Mutation in the ABCC6 Gene (R1141X) Is Associated With a Strong Increase in the Prevalence of Coronary Artery Disease

A. Zwinderman, J. Boer, E. Feskens, 2002, Circulation.