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J Bolz

Showing results (61-70 of 148) with videos related to

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The Journal of Comparative Neurology|December 1, 1994
GABAA receptor alpha 1 subunit, an early marker for area specification in developing rat cerebral cortexJ Paysan, J Bolz, H Mohler, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 24, 1997
Area-specific regulation of gamma-aminobutyric acid type A receptor subtypes by thalamic afferents in developing rat neocortexJ Paysan, A Kossel, J Bolz, et al.
Ophthalmology|April 14, 2015
Ophthalmic Features of Children Not Yet Diagnosed with Alstrom SyndromeArif O Khan, Inam N Bifari, Hanno J Bolz
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|December 6, 2014
[Genetics of congenital aniridia]C Neuhaus, C Betz, C Bergmann, et al.
Clinical Genetics|January 21, 2016
Hermansky-Pudlak syndrome genes are frequently mutated in patients with albinism from the Arabian PeninsulaA O Khan, M Tamimi, S Lenzner, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 5, 1998
Membrane-associated molecules guide limbic and nonlimbic thalamocortical projectionsF Mann, V Zhukareva, A Pimenta, et al.
The British Journal of Ophthalmology|October 25, 2014
A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod-cone dystrophy phenotype on the Arabian PeninsulaArif O Khan, Carsten Bergmann, Tobias Eisenberger, et al.
Neuroscience|September 13, 2005
Neurogenesis in the adult dentate gyrus after cortical infarcts: effects of infarct location, N-methyl-D-aspartate receptor blockade and anti-inflammatory treatmentM M Kluska, O W Witte, J Bolz, et al.
Journal of Pediatric Ophthalmology and Strabismus|July 18, 2014
Limited ocular motility in a child with 3q23 microdeletion ("blepharophimosis syndrome plus")Arif O Khan, Sandra Nagl, Carsten Bergmann, et al.
Ophthalmic Genetics|December 6, 2014
A distinct vitreo-retinal dystrophy with early-onset cataract from recessive KCNJ13 mutationsArif O Khan, Carsten Bergmann, Christine Neuhaus, et al.
Pageof 15

Showing results (61-70 of 148) with videos related to

Sort By:
Pageof 15
The Journal of Comparative Neurology|December 1, 1994
GABAA receptor alpha 1 subunit, an early marker for area specification in developing rat cerebral cortexJ Paysan, J Bolz, H Mohler, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 24, 1997
Area-specific regulation of gamma-aminobutyric acid type A receptor subtypes by thalamic afferents in developing rat neocortexJ Paysan, A Kossel, J Bolz, et al.
Ophthalmology|April 14, 2015
Ophthalmic Features of Children Not Yet Diagnosed with Alstrom SyndromeArif O Khan, Inam N Bifari, Hanno J Bolz
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|December 6, 2014
[Genetics of congenital aniridia]C Neuhaus, C Betz, C Bergmann, et al.
Clinical Genetics|January 21, 2016
Hermansky-Pudlak syndrome genes are frequently mutated in patients with albinism from the Arabian PeninsulaA O Khan, M Tamimi, S Lenzner, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 5, 1998
Membrane-associated molecules guide limbic and nonlimbic thalamocortical projectionsF Mann, V Zhukareva, A Pimenta, et al.
The British Journal of Ophthalmology|October 25, 2014
A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod-cone dystrophy phenotype on the Arabian PeninsulaArif O Khan, Carsten Bergmann, Tobias Eisenberger, et al.
Neuroscience|September 13, 2005
Neurogenesis in the adult dentate gyrus after cortical infarcts: effects of infarct location, N-methyl-D-aspartate receptor blockade and anti-inflammatory treatmentM M Kluska, O W Witte, J Bolz, et al.
Journal of Pediatric Ophthalmology and Strabismus|July 18, 2014
Limited ocular motility in a child with 3q23 microdeletion ("blepharophimosis syndrome plus")Arif O Khan, Sandra Nagl, Carsten Bergmann, et al.
Ophthalmic Genetics|December 6, 2014
A distinct vitreo-retinal dystrophy with early-onset cataract from recessive KCNJ13 mutationsArif O Khan, Carsten Bergmann, Christine Neuhaus, et al.
Pageof 15