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B H Weber

Showing results (41-50 of 91) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 2, 1999
Isolation and characterization of the murine X-linked juvenile retinoschisis (Rs1h) geneA E Gehrig, R Warneke-Wittstock, C G Sauer, et al.
Biochimica Et Biophysica Acta|January 10, 2002
Identification of a novel retina-specific gene located in a subtelomeric region with polymorphic distribution among multiple human chromosomesN Mah, H Stoehr, H L Schulz, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
L- and M-cone-driven electroretinograms in Stargardt's macular dystrophy-fundus flavimaculatusH P Scholl, J Kremers, R Vonthein, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 25, 2001
Clinical electrophysiology of two rod pathways: normative values and clinical applicationH P Scholl, H Langrová, B H Weber, et al.
Archives of Biochemistry and Biophysics|May 1, 1988
Glycyl-tRNA synthetase of Escherichia coli: immunological homology with phenylalanyl-tRNA synthetaseG M Nagel, M S Johnson, J Rynd, et al.
Nucleic Acids Research|May 25, 1984
The beta subunit of E. coli glycyl-tRNA synthetase plays a major role in tRNA recognitionG M Nagel, S Cumberledge, M S Johnson, et al.
American Journal of Human Genetics|December 1, 1994
High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11B H Weber, G Vogt, H Stöhr, et al.
Clinical Genetics|August 18, 1999
Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisisA Gehrig, K White, B Lorenz, et al.
Nature Genetics|June 1, 1994
Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qterB H Weber, G Vogt, W Wolz, et al.
Cytogenetics and Cell Genetics|February 15, 2001
EST mining of the UniGene dataset to identify retina-specific genesH Stöhr, N Mah, H L Schulz, et al.
Pageof 10

Showing results (41-50 of 91) with videos related to

Sort By:
Pageof 10
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 2, 1999
Isolation and characterization of the murine X-linked juvenile retinoschisis (Rs1h) geneA E Gehrig, R Warneke-Wittstock, C G Sauer, et al.
Biochimica Et Biophysica Acta|January 10, 2002
Identification of a novel retina-specific gene located in a subtelomeric region with polymorphic distribution among multiple human chromosomesN Mah, H Stoehr, H L Schulz, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
L- and M-cone-driven electroretinograms in Stargardt's macular dystrophy-fundus flavimaculatusH P Scholl, J Kremers, R Vonthein, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 25, 2001
Clinical electrophysiology of two rod pathways: normative values and clinical applicationH P Scholl, H Langrová, B H Weber, et al.
Archives of Biochemistry and Biophysics|May 1, 1988
Glycyl-tRNA synthetase of Escherichia coli: immunological homology with phenylalanyl-tRNA synthetaseG M Nagel, M S Johnson, J Rynd, et al.
Nucleic Acids Research|May 25, 1984
The beta subunit of E. coli glycyl-tRNA synthetase plays a major role in tRNA recognitionG M Nagel, S Cumberledge, M S Johnson, et al.
American Journal of Human Genetics|December 1, 1994
High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11B H Weber, G Vogt, H Stöhr, et al.
Clinical Genetics|August 18, 1999
Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisisA Gehrig, K White, B Lorenz, et al.
Nature Genetics|June 1, 1994
Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qterB H Weber, G Vogt, W Wolz, et al.
Cytogenetics and Cell Genetics|February 15, 2001
EST mining of the UniGene dataset to identify retina-specific genesH Stöhr, N Mah, H L Schulz, et al.
Pageof 10