Search Results - "Kwitek, A. E."

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    Effects of chromosome 17 on features of the metabolic syndrome in the Lyon hypertensive rat by Gilibert, S, Kwitek, A. E, Hubner, N, Tschannen, M, Jacob, H. J, Sassard, J, Bataillard, A

    Published in Physiological genomics (22-04-2008)
    “…1 Département de Physiologie et Pharmacologie Clinique, Institut des Sciences Pharmaceutiques et Biologiques, Université Lyon 1, Lyon, France 2 Human and…”
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    Journal Article
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    Genetic dissection reveals diabetes loci proximal to the gimap5 lymphopenia gene by Fuller, J. M, Bogdani, M, Tupling, T. D, Jensen, R. A, Pefley, R, Manavi, S, Cort, L, Blankenhorn, E. P, Mordes, J. P, Lernmark, A, Kwitek, A. E

    Published in Physiological genomics (10-06-2009)
    “…1 Department of Clinical Sciences, Lund University, and Clinical Research Center, Malmö, Sweden 2 Department of Medicine, University of Washington 3 Pacific…”
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    The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutions by Sheffield, V C, Beck, J S, Kwitek, A E, Sandstrom, D W, Stone, E M

    Published in Genomics (San Diego, Calif.) (01-05-1993)
    “…Single-strand conformation polymorphism (SSCP) analysis has proven to be a simple and effective technique for the detection of single base substitutions. We…”
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    Screening of Living Kidney Donors for Genetic Diseases Using a Comprehensive Genetic Testing Strategy by Thomas, C. P., Mansilla, M. A., Sompallae, R., Mason, S. O., Nishimura, C. J., Kimble, M. J., Campbell, C. A., Kwitek, A. E., Darbro, B. W., Stewart, Z. A., Smith, R. J. H.

    Published in American journal of transplantation (01-02-2017)
    “…Related living kidney donors (LKDs) are at higher risk of end‐stage renal disease (ESRD) compared with unrelated LKDs. A genetic panel was developed to screen…”
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    Rat Genome Database, update 2007--Easing the path from disease to data and back again by Twigger, Simon N, Shimoyama, Mary, Bromberg, Susan, Kwitek, Anne E, Jacob, Howard J

    Published in Nucleic acids research (01-01-2007)
    “…The Rat Genome Database (RGD, http://rgd.mcw.edu) is one of the core resources for rat genomics and recent developments have focused on providing support for…”
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    Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma by Johnson, A T, Drack, A V, Kwitek, A E, Cannon, R L, Stone, E M, Alward, W L

    Published in Ophthalmology (Rochester, Minn.) (01-04-1993)
    “…Juvenile glaucoma is an uncommon form of open-angle glaucoma that is usually recognized during childhood or early adulthood and which often has a strong family…”
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    Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15 by Carmi, R, Rokhlina, T, Kwitek-Black, A E, Elbedour, K, Nishimura, D, Stone, E M, Sheffield, V C

    Published in Human molecular genetics (01-01-1995)
    “…Bardet-Biedl syndrome is a heterogeneous autosomal recessive disorder characterized by obesity, mental retardation, polydactyly, retinitis pigmentosa and…”
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    Usher syndrome in the Samaritans: Strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders by Bonné-Tamir, B., Nystuen, A., Seroussi, E., Kalinsky, H., Kwitek-Black, A. E., Korostishevsky, M., Adato, A., Sheffield, V. C.

    Published in American journal of physical anthropology (01-10-1997)
    “…We have previously reported significant linkage between markers on 11q13.5 and Usher syndrome type 1 (USH1B) in a large Samaritan kindred. USH1B is an…”
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    Mapping of human chromosome 5 microsatellite DNA polymorphisms by Weber, J L, Polymeropoulos, M H, May, P E, Kwitek, A E, Xiao, H, McPherson, J D, Wasmuth, J J

    Published in Genomics (San Diego, Calif.) (01-11-1991)
    “…Thirteen moderately to highly informative microsatellite DNA polymorphisms based on (dC-dA)n.(dG-dT)n repeats were mapped to segments of human chromosome 5…”
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