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K B Sims

Showing results (11-20 of 27) with videos related to

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Nature Genetics|June 1, 1992
Isolation and characterization of a candidate gene for Norrie diseaseZ Y Chen, R W Hendriks, M A Jobling, et al.
Human Molecular Genetics|June 1, 1992
Characterization of a YAC containing part or all of the Norrie disease locusZ Y Chen, K B Sims, M Coleman, et al.
Journal of Neurochemistry|October 1, 1988
Structural features of human monoamine oxidase A elucidated from cDNA and peptide sequencesY P Hsu, W Weyler, S Chen, et al.
Journal of Neural Transmission. General Section|January 1, 1991
Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidaseD L Murphy, K B Sims, F Karoum, et al.
Applied and Theoretical Electrophoresis : the Official Journal of the International Electrophoresis Society|January 1, 1991
Abnormal protein in the cerebrospinal fluid of patients with a submicroscopic X-chromosomal deletion associated with Norrie disease: preliminary reportJ E Joy, R Poglod, D L Murphy, et al.
The New England Journal of Medicine|October 3, 1996
Clinical and biochemical manifestations of hyaluronidase deficiencyM R Natowicz, M P Short, Y Wang, et al.
Genomics|May 1, 1993
Norrie disease gene: characterization of deletions and possible functionZ Y Chen, E M Battinelli, R W Hendriks, et al.
Ophthalmology|December 1, 1996
Peripheral retinopathy in offspring of carriers of Norrie disease gene mutations. Possible transplacental effect of abnormal NorrinH A Mintz-Hittner, R E Ferrell, K B Sims, et al.
Human Mutation|January 1, 1997
Norrie disease gene mutation in a large Costa Rican kindred with a novel phenotype including venous insufficiencyH L Rehm, G A Gutiérrez-Espeleta, R Garcia, et al.
American Journal of Human Genetics|September 1, 1989
Norrie disease gene is distinct from the monoamine oxidase genesK B Sims, L Ozelius, T Corey, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Nature Genetics|June 1, 1992
Isolation and characterization of a candidate gene for Norrie diseaseZ Y Chen, R W Hendriks, M A Jobling, et al.
Human Molecular Genetics|June 1, 1992
Characterization of a YAC containing part or all of the Norrie disease locusZ Y Chen, K B Sims, M Coleman, et al.
Journal of Neurochemistry|October 1, 1988
Structural features of human monoamine oxidase A elucidated from cDNA and peptide sequencesY P Hsu, W Weyler, S Chen, et al.
Journal of Neural Transmission. General Section|January 1, 1991
Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidaseD L Murphy, K B Sims, F Karoum, et al.
Applied and Theoretical Electrophoresis : the Official Journal of the International Electrophoresis Society|January 1, 1991
Abnormal protein in the cerebrospinal fluid of patients with a submicroscopic X-chromosomal deletion associated with Norrie disease: preliminary reportJ E Joy, R Poglod, D L Murphy, et al.
The New England Journal of Medicine|October 3, 1996
Clinical and biochemical manifestations of hyaluronidase deficiencyM R Natowicz, M P Short, Y Wang, et al.
Genomics|May 1, 1993
Norrie disease gene: characterization of deletions and possible functionZ Y Chen, E M Battinelli, R W Hendriks, et al.
Ophthalmology|December 1, 1996
Peripheral retinopathy in offspring of carriers of Norrie disease gene mutations. Possible transplacental effect of abnormal NorrinH A Mintz-Hittner, R E Ferrell, K B Sims, et al.
Human Mutation|January 1, 1997
Norrie disease gene mutation in a large Costa Rican kindred with a novel phenotype including venous insufficiencyH L Rehm, G A Gutiérrez-Espeleta, R Garcia, et al.
American Journal of Human Genetics|September 1, 1989
Norrie disease gene is distinct from the monoamine oxidase genesK B Sims, L Ozelius, T Corey, et al.
Pageof 3