Search Results - "Sauer, C G"

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    Expression of X-Linked Retinoschisis Protein RS1 in Photoreceptor and Bipolar Cells by Molday, Laurie L, Hicks, David, Sauer, Christian G, Weber, Bernhard H. F, Molday, Robert S

    “…To examine the biochemical properties, cell expression, and localization of RS1, the product of the gene responsible for X-linked juvenile retinoschisis. Rs1h…”
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    Positional cloning of the gene associated with X-linked juvenile retinoschisis by Sauer, Christian G, Gehrig, Andrea, Warneke-Wittstock, Regina, Marquardt, Andreas, Ewing, Cecil C, Gibson, Alice, Lorenz, Birgit, Jurklies, Bernhard, Weber, Bernhard H.F

    Published in Nature genetics (01-10-1997)
    “…X-linked juvenile retinoschisis(RS) is a recessively inherited vitreo-retinal degeneration characterized by macular pathology and intraretinal splitting of the…”
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    Impaired perception of self-motion (heading) in abstinent ecstasy and marijuana users by RIZZO, M, LAMERS, C. T. J, SAUER, C. G, RAMAEKERS, J. G, BECHARA, A, ANDERSEN, G. J

    Published in Psychopharmacologia (01-05-2005)
    “…Illicit drug use can increase driver crash risk due to loss of control over vehicle trajectory. This study asks, does recreational use of…”
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    Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration by Sauer, Christian G, White, Karen, Stöhr, Heidi, Grimm, Tiemo, Hutchinson, Amy, Bernstein, Paul S, Lewis, Richard Allan, Simonelli, Francesca, Pauleikhoff, Daniel, Allikmets, Rando, Weber, Bernhard H F

    Published in British journal of ophthalmology (01-08-2001)
    “…BACKGROUND A long term project was initiated to identify and to characterise genes that are expressed exclusively or preferentially in the retina as candidates…”
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    Clinical and Genetic Evidence for Autosomal Dominant North Carolina Macular Dystrophy in a German Family by Pauleikhoff, Daniel, Sauer, Christian G., Müller, Clemens R., Radermacher, Martin, Merz, Antje, Weber, Bernhard H.F.

    Published in American journal of ophthalmology (01-09-1997)
    “…To describe a German family with clinical and genetic evidence of autosomal dominant North Carolina macular dystrophy. Twenty-six individuals from a…”
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    An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1) by Sauer, C G, Schworm, H D, Ulbig, M, Blankenagel, A, Rohrschneider, K, Pauleikhoff, D, Grimm, T, Weber, B H

    Published in Journal of medical genetics (01-12-1997)
    “…Autosomal dominant North Carolina macular dystrophy (NCMD) or central areolar pigment epithelial dystrophy (CAPED) is an allelic disorder that maps to an…”
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    FT-IR kinetic and product study of the Br-radical initiated oxidation of α, β-unsaturated organic carbonyl compounds by Sauer, C.G., Barnes, I., Becker, K.H.

    Published in Atmospheric environment (1994) (01-08-1999)
    “…Using the relative kinetic technique the kinetics of the gas-phase reactions of Br radicals with acrolein, methacrolein and methylvinyl ketone have been…”
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    Atmospheric Chemistry of 1,3-Dioxolane:  Kinetic, Mechanistic, and Modeling Study of OH Radical Initiated Oxidation by Sauer, C. G, Barnes, I, Becker, K. H, Geiger, H, Wallington, T. J, Christensen, L. K, Platz, J, Nielsen, O. J

    “…An absolute rate pulse radiolysis technique was used to measure k(OH + 1,3-dioxolane) = (8.8 ± 0.9) × 10-12 cm3 molecule-1 s-1 at 295 K in 1000 mbar of Ar…”
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    Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies by Felbor, U, Gehrig, A, Sauer, C G, Marquardt, A, Köhler, M, Schmid, M, Weber, B H

    Published in Cytogenetics and cell genetics (1998)
    “…The interphotoreceptor matrix is a unique extracellular matrix occupying the space between the photoreceptors and the retinal pigment epithelium. Due to its…”
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    Standardization strategy for quantitative PCR in human seminoma and normal testis by Neuvians, Tanja Pascale, Gashaw, Isabella, Sauer, Christian Georg, Ostau, Christian von, Kliesch, Sabine, Bergmann, Martin, Häcker, Axel, Grobholz, Rainer

    Published in Journal of biotechnology (04-05-2005)
    “…Housekeeping genes are commonly used as endogenous references in quantitative RT-PCR. Ideally these genes are constitutionally expressed by all cell types and…”
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    Transcript Map of a 900-kb Genomic Region in Xp22.1–p22.2: Identification of 12 Novel Genes by Warneke-Wittstock, Regina, Marquardt, Andreas, Gehrig, Andrea, Sauer, Christian G., Gessler, Manfred, Weber, Bernhard H.F.

    Published in Genomics (San Diego, Calif.) (01-07-1998)
    “…The Xp22.1–p22.2 interval is a focus of interest as a number of hereditary disease loci have been mapped to this region, including X-linked nonsyndromic…”
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    Localization of the human membrane-type 2 matrix metalloproteinase gene (MMP15) to 16q12.1 near DNA elements that are part of centromeric and non-centromeric heterochromatin of 11 human chromosomes by Koehler, M R, Sauer, C G, Reismann, N, Steinlein, C, Weber, B H, Will, H, Schmid, M

    Published in Chromosome research (01-04-1998)
    “…We have localized a second gene for membrane-type matrix metalloproteinases, MT2-MMP, to chromosome 16q12 by in situ hybridization. FISH experiments using a…”
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    Tunable diode laser absorption spectrometer measurements of ambient nitrogen dioxide, nitric acid, formaldehyde, and hydrogen peroxide in Parlier, California by Sauer, Claudia G., Pisano, John T., Fitz, Dennis R.

    Published in Atmospheric environment (1994) (01-04-2003)
    “…Field measurements were conducted to determine atmospheric concentrations of nitrogen dioxide, nitric acid, formaldehyde, and hydrogen peroxide gases using two…”
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    Developing a comprehensive system for handling mental illness commitments by SAUER, G. C. JR, KIRK, S, GEORGE, C. E

    Published in Psychiatric quarterly (01-12-1982)
    “…A comprehensive system for processing individuals being evaluated for mental illness commitment is presented. The system comprises six levels making maximum…”
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    EFEMP1 is not associated with sporadic early onset drusen by Sauer, C.G., White, K., Kellner, U., Rudolph, G., Jurklies, B., Pauleikhoff, D., Weber, B.H.F.

    Published in Ophthalmic genetics (2001)
    “…The early onset of multiple drusen in the posterior pole of the retina is characteristic of a group of macular dystrophies often referred to as dominant or…”
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    Isolation and characterization of the murine X-linked juvenile retinoschisis (Rs1h) gene by Gehrig, A E, Warneke-Wittstock, R, Sauer, C G, Weber, B H

    Published in Mammalian genome (01-03-1999)
    “…X-linked juvenile retinoschisis (RS) is a vitreoretinal degeneration affecting only males. Recently, the RS1 gene underlying this common cause of early vision…”
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