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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 circuits
V 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 projections
D 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 cones
D 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 axons
P 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 development
S 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 dystrophy
Inam 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 subtilis
Nicholas 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 dystrophies
Arif 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 consanguinity
Rami A Mahfouz, Hanno J Bolz, Zaher K Otrock, et al.
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of 15
Search research articles
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Showing results (71-80 of 148) with videos related to
Sort By:
Page
of 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 circuits
V 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 projections
D 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 cones
D 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 axons
P 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 development
S 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 dystrophy
Inam 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 subtilis
Nicholas 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 dystrophies
Arif 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 consanguinity
Rami A Mahfouz, Hanno J Bolz, Zaher K Otrock, et al.
Page
of 15