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J Bolz

Showing results (71-80 of 148) with videos related to

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Klinische Monatsblatter Fur Augenheilkunde|March 30, 2017
[Genotype-Phenotype Correlations in Patients with CRB1 Mutations]C Papadopoulou Laiou, M N Preising, H J Bolz, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 10, 1998
Dual action of a ligand for Eph receptor tyrosine kinases on specific populations of axons during the development of cortical circuitsV Castellani, Y Yue, P P Gao, et al.
Development (Cambridge, England)|November 13, 1998
Semaphorins act as attractive and repulsive guidance signals during the development of cortical projectionsD Bagnard, M Lohrum, D Uziel, et al.
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 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.
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.
Pageof 15

Showing results (71-80 of 148) with videos related to

Sort By:
Pageof 15
Klinische Monatsblatter Fur Augenheilkunde|March 30, 2017
[Genotype-Phenotype Correlations in Patients with CRB1 Mutations]C Papadopoulou Laiou, M N Preising, H J Bolz, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 10, 1998
Dual action of a ligand for Eph receptor tyrosine kinases on specific populations of axons during the development of cortical circuitsV Castellani, Y Yue, P P Gao, et al.
Development (Cambridge, England)|November 13, 1998
Semaphorins act as attractive and repulsive guidance signals during the development of cortical projectionsD Bagnard, M Lohrum, D Uziel, et al.
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 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.
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.
Pageof 15