Search Results - "Hoffman, Katrin"

Enriching Flaws of Scent عطر עטרה A Guava Scent Collection by Hoffman, Thalia Katrin

“…This essay is written around the art-action from an artist’s point of view. It connects the decision-making process and manifestations of the scent collection…”
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Nanoparticle-encapsulated vis- and NIR-emissive fluorophores with different fluorescence decay kinetics for lifetime multiplexing by Hoffmann, Katrin, Behnke, Thomas, Grabolle, Markus, Resch-Genger, Ute

“…Bioanalytical, clinical, and security applications increasingly require simple, efficient, and versatile strategies to measure an ever increasing number of…”
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Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly by SHULTZ, Leonard D, LYONS, Bonnie L, OLINS, Donald E, SPERLING, Karl, HOFFMANN, Katrin, BURZENSKI, Lisa M, GOTT, Bruce, SAMUELS, Rebecca, SCHWEITZER, Peter A, DREGER, Christine, HERRMANN, Harald, KALSCHEUER, Vera, OLINS, Ada L

“…The nature of the wild-type gene product at the mouse ichthyosis (ic) locus has been of great interest because mutations at this locus cause marked…”
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FragIdent--automatic identification and characterisation of cDNA-fragments by Seelow, Dominik, Goehler, Heike, Hoffmann, Katrin

“…Many genetic studies and functional assays are based on cDNA fragments. After the generation of cDNA fragments from an mRNA sample, their content is at first…”
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A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family by Sanggaard, Kirsten M., Kjaer, Klaus W., Eiberg, Hans, Nürnberg, Gudrun, Nürnberg, Peter, Hoffman, Katrin, Jensen, Hanne, Sørum, Charlotte, Rendtorff, Nanna D., Tranebjærg, Lisbeth

“…Autosomal dominant inheritance is described in about 20% of all nonsyndromic hearing loss with currently 54 distinct loci (DFNA1‐54), and >20 different genes…”
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A Novel Nonsense Mutation in MY06 Is Associated With Progressive Nonsyndromic Hearing Loss in a Danish DFNA22 Family by SANGGAARD, Kirsten M, KJAER, Klaus W, EIBERG, Hans, NUMBERS, Gudrun, NÜMBERG, Peter, HOFFMAN, Katrin, JENSEN, Hanne, SØRUM, Charlotte, RENDTORFF, Nanna D, TRANEBJAERG, Lisbeth

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Efficient two-trait-locus linkage analysis through program optimization and parallelization: application to hypercholesterolemia by DIETTER, Johannes, SPIEGEL, Alexander, AN MEY, Dieter, PFLUG, Hans-Joachim, AL-KATEB, Hussam, HOFFMANN, Katrin, WIENKER, Thomas F, STRAUCH, Konstantin

“…We have optimized and parallelized the GENEHUNTER-TWOLOCUS program that allows to perform linkage analysis with two trait loci in the multimarker context. The…”
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Similarity by state/descent and genetic vector spaces: analysis of a longitudinal family study by Stassen, Hans H, Hoffman, Katrin, Scharfetter, Christian

“…Using the genome-wide screening data of the Framingham Heart Study (394 nuclear families, 1328 genotyped subjects, 397 marker loci) we have quantified the…”
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