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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 29, 2000
Spatial distributions of guidance molecules regulate chemorepulsion and chemoattraction of growth conesD Bagnard, N Thomasset, M Lohrum, et al.Developmental Biology|January 3, 2001
The polysialic acid moiety of the neural cell adhesion molecule is involved in intraretinal guidance of retinal ganglion cell axonsP P Monnier, S G Beck, J Bolz, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 1, 1996
Dual action of a carbohydrate epitope on afferent and efferent axons in cortical developmentS Henke-Fahle, F Mann, M Götz, et al.The European Journal of Neuroscience|December 14, 1999
Orientation topography of layer 4 lateral networks revealed by optical imaging in cat visual cortex (area 18)T Yousef, T Bonhoeffer, D S Kim, et al.The British Journal of Ophthalmology|September 12, 2015
The ophthalmic phenotype of IFT140-related ciliopathy ranges from isolated to syndromic congenital retinal dystrophyInam N Bifari, Sahar M Elkhamary, Hanno J Bolz, et al.Journal of Bacteriology|July 31, 2012
Residues in the N-terminal domain of MutL required for mismatch repair in Bacillus subtilisNicholas J Bolz, Justin S Lenhart, Steven C Weindorf, et al.Ophthalmic Genetics|February 9, 2016
C8orf37 is mutated in Bardet-Biedl syndrome and constitutes a locus allelic to non-syndromic retinal dystrophiesArif O Khan, Eva Decker, Nadine Bachmann, et al.The European Journal of Neuroscience|October 10, 1998
The layout of orientation and ocular dominance domains in area 17 of strabismic catsS Löwel, K E Schmidt, D S Kim, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 21, 2012
Novel mutation in the glycoprotein Ibβ in a patient with Bernard-Soulier syndrome: possibility of distant parental consanguinityRami A Mahfouz, Hanno J Bolz, Zaher K Otrock, et al.The British Journal of Ophthalmology|June 11, 2015
Peripherin mutations cause a distinct form of recessive Leber congenital amaurosis and dominant phenotypes in asymptomatic parents heterozygous for the mutationArif O Khan, Saba Al Rashaed, Christine Neuhaus, et al.Pageof 19