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R Allikmets

Showing results (21-30 of 48) with videos related to

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Ophthalmology|November 20, 2001
Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathyJ M Seddon, M A Afshari, S Sharma, et al.
Investigative Ophthalmology & Visual Science|March 11, 2000
New ABCR mutations and clinical phenotype in Italian patients with Stargardt diseaseF Simonelli, F Testa, G de Crecchio, et al.
Gene|July 17, 1998
Organization of the ABCR gene: analysis of promoter and splice junction sequencesR Allikmets, W W Wasserman, A Hutchinson, et al.
American Journal of Human Genetics|February 11, 1999
Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt diseaseR A Lewis, N F Shroyer, N Singh, et al.
American Journal of Ophthalmology|December 28, 1999
A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt diseaseK Zhang, D C Garibaldi, M Kniazeva, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1995
Characterization and mapping of three new mammalian ATP-binding transporter genes from an EST databaseR Allikmets, B Gerrard, D Glavac, et al.
Human Genetics|November 10, 2001
Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patientsA Fumagalli, M Ferrari, N Soriani, et al.
Cancer Genetics and Cytogenetics|June 1, 1995
A group of NotI jumping and linking clones cover 2.5 Mb in the 3p21-p22 region suspected to contain a tumor suppressor geneV I Kashuba, A Szeles, R Allikmets, et al.
Ophthalmic Genetics|September 17, 2004
Evaluation of the ARMD1 locus on 1q25-31 in patients with age-related maculopathy: genetic variation in laminin genes and in exon 104 of HEMICENTIN-1M Hayashi, J E Merriam, C C W Klaver, et al.
Investigative Ophthalmology & Visual Science|December 1, 2001
Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 geneP S Bernstein, J Tammur, N Singh, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Ophthalmology|November 20, 2001
Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathyJ M Seddon, M A Afshari, S Sharma, et al.
Investigative Ophthalmology & Visual Science|March 11, 2000
New ABCR mutations and clinical phenotype in Italian patients with Stargardt diseaseF Simonelli, F Testa, G de Crecchio, et al.
Gene|July 17, 1998
Organization of the ABCR gene: analysis of promoter and splice junction sequencesR Allikmets, W W Wasserman, A Hutchinson, et al.
American Journal of Human Genetics|February 11, 1999
Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt diseaseR A Lewis, N F Shroyer, N Singh, et al.
American Journal of Ophthalmology|December 28, 1999
A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt diseaseK Zhang, D C Garibaldi, M Kniazeva, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1995
Characterization and mapping of three new mammalian ATP-binding transporter genes from an EST databaseR Allikmets, B Gerrard, D Glavac, et al.
Human Genetics|November 10, 2001
Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patientsA Fumagalli, M Ferrari, N Soriani, et al.
Cancer Genetics and Cytogenetics|June 1, 1995
A group of NotI jumping and linking clones cover 2.5 Mb in the 3p21-p22 region suspected to contain a tumor suppressor geneV I Kashuba, A Szeles, R Allikmets, et al.
Ophthalmic Genetics|September 17, 2004
Evaluation of the ARMD1 locus on 1q25-31 in patients with age-related maculopathy: genetic variation in laminin genes and in exon 104 of HEMICENTIN-1M Hayashi, J E Merriam, C C W Klaver, et al.
Investigative Ophthalmology & Visual Science|December 1, 2001
Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 geneP S Bernstein, J Tammur, N Singh, et al.
Pageof 5