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Experimental Eye Research
|
May 16, 2016
First insights into the expression of VAX2 in humans and its localization in the adult primate retina
Giovanna Alfano, Amna Z Shah, Glen Jeffery, et al.
American Journal of Human Genetics
|
June 24, 2003
Single-nucleotide polymorphisms and glaucoma severity
Catey Bunce, Roger A Hitchings, Shomi S Bhattacharya, et al.
Ophthalmic Genetics
|
June 28, 2018
Identification and characterization of the VAX2 p.Leu139Arg variant: possible involvement of VAX2 in cone dystrophy
Giovanna Alfano, Naushin H Waseem, Andrew R Webster, et al.
Journal of Clinical Pathology
|
July 1, 2017
Gene of the month: <i>PRPF31</i>
Anna M Rose, Rong Luo, Utsav K Radia, et al.
Investigative Ophthalmology & Visual Science
|
May 27, 2004
Developmental expression profile of the optic atrophy gene product: OPA1 is not localized exclusively in the mammalian retinal ganglion cell layer
Saima Aijaz, Lynda Erskine, Glen Jeffery, et al.
Journal of Glaucoma
|
January 17, 2007
A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG)
Mohamed F El-Ashry, Mai M Abd El-Aziz, Shomi S Bhattacharya
Current Protocols in Stem Cell Biology
|
March 15, 2012
Derivation of cerebellar neurons from human pluripotent stem cells
Slaven Erceg, Dunja Lukovic, Victoria Moreno-Manzano, et al.
European Journal of Human Genetics : EJHG
|
July 7, 2011
A novel locus for autosomal dominant congenital cerulean cataract maps to chromosome 12q
Vanita Berry, Alexander C W Ionides, Anthony T Moore, et al.
Trends in Genetics : TIG
|
June 13, 2003
Fox's in development and disease
Ordan J Lehmann, Jane C Sowden, Peter Carlsson, et al.
Stem Cells (Dayton, Ohio)
|
February 15, 2011
Concise review: stem cells for the treatment of cerebellar-related disorders
Slaven Erceg, Victoria Moreno-Manzano, Marcela Garita-Hernandez, et al.
Page
of 14
Search research articles
Search
Showing results (1-10 of 135) with videos related to
Sort By:
Page
of 14
Experimental Eye Research
|
May 16, 2016
First insights into the expression of VAX2 in humans and its localization in the adult primate retina
Giovanna Alfano, Amna Z Shah, Glen Jeffery, et al.
American Journal of Human Genetics
|
June 24, 2003
Single-nucleotide polymorphisms and glaucoma severity
Catey Bunce, Roger A Hitchings, Shomi S Bhattacharya, et al.
Ophthalmic Genetics
|
June 28, 2018
Identification and characterization of the VAX2 p.Leu139Arg variant: possible involvement of VAX2 in cone dystrophy
Giovanna Alfano, Naushin H Waseem, Andrew R Webster, et al.
Journal of Clinical Pathology
|
July 1, 2017
Gene of the month: <i>PRPF31</i>
Anna M Rose, Rong Luo, Utsav K Radia, et al.
Investigative Ophthalmology & Visual Science
|
May 27, 2004
Developmental expression profile of the optic atrophy gene product: OPA1 is not localized exclusively in the mammalian retinal ganglion cell layer
Saima Aijaz, Lynda Erskine, Glen Jeffery, et al.
Journal of Glaucoma
|
January 17, 2007
A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG)
Mohamed F El-Ashry, Mai M Abd El-Aziz, Shomi S Bhattacharya
Current Protocols in Stem Cell Biology
|
March 15, 2012
Derivation of cerebellar neurons from human pluripotent stem cells
Slaven Erceg, Dunja Lukovic, Victoria Moreno-Manzano, et al.
European Journal of Human Genetics : EJHG
|
July 7, 2011
A novel locus for autosomal dominant congenital cerulean cataract maps to chromosome 12q
Vanita Berry, Alexander C W Ionides, Anthony T Moore, et al.
Trends in Genetics : TIG
|
June 13, 2003
Fox's in development and disease
Ordan J Lehmann, Jane C Sowden, Peter Carlsson, et al.
Stem Cells (Dayton, Ohio)
|
February 15, 2011
Concise review: stem cells for the treatment of cerebellar-related disorders
Slaven Erceg, Victoria Moreno-Manzano, Marcela Garita-Hernandez, et al.
Page
of 14