Search Results - "Klaften, M"

Mutation in the Ercc2 gene of the mouse causes cataracts by Graw, J., Kunze, S., Dalke, C., Fuchs, H., Klaften, M., Sabrautzki, S., Hrabe de Angelis, M.

“…Summary Cataracts have been associated with many mutations. In a large‐scale high‐throughput ENU mutagenesis screen we analyzed the offspring of paternally…”
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Splice‐site mutation in the Bmpr1b gene of the mouse causes optic nerve head dysgenesis and retinal gliosis by Graw, J., Yan, X., Amarie, O.V., Puk, O., Sabrautzki, S., Klaften, M., Thiele, F., Fuchs, H., Hrabe de Angelis, M.

“…Purpose A novel splice‐site mutation of the Bmpr1b gene was characterized in offspring of N‐ethyl‐N‐nitrosourea (ENU) ‐treated mice; besides irregular limb…”
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A Mutation in the Enamelin Gene in a Mouse Model by Seedorf, H., Klaften, M., Eke, F., Fuchs, H., Seedorf, U., Hrabe de Angelis, M.

“…Amelogenesis imperfecta is an inherited disorder affecting tooth enamel formation. We previously isolated a mouse strain with an amelogenesis imperfecta…”
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Phenotypic and pathomorphological characteristics of a novel mutant mouse model for maturity-onset diabetes of the young type 2 (MODY 2) by van Bürck, L, Blutke, A, Kautz, S, Rathkolb, B, Klaften, M, Wagner, S, Kemter, E, Hrabé de Angelis, M, Wolf, E, Aigner, B, Wanke, R, Herbach, N

“…Several mutant mouse models for human diseases such as diabetes mellitus have been generated in the large-scale Munich ENU (N-ethyl-N-nitrosourea) mouse…”
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ARTS: a web-based tool for the set-up of high-throughput genome-wide mapping panels for the SNP genotyping of mouse mutants by Klaften, Matthias, de Angelis, Martin Hrabé

“…Genome-wide mapping in the identification of novel candidate genes has always been the standard method in genetics and genomics to correlate a clinically…”
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Targeted inactivation of the murine Abca3 gene leads to respiratory failure in newborns with defective lamellar bodies by Hammel, Markus, Michel, Geert, Hoefer, Christina, Klaften, Matthias, Müller-Höcker, Josef, de Angelis, Martin Hrabé, Holzinger, Andreas

“…Mutations in the human ABCA3 gene, encoding an ABC-transporter, are associated with respiratory failure in newborns and pediatric interstitial lung disease. In…”
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Mutation in the Bmpr1b gene affects optic nerve development by GRAW, J, WEBER, S, PUK, O, WAGNER, S, KLAFTEN, M, THIELE, F, FUCHS, H, HRABé DE ANGELIS, M

“…Purpose Systematic analysis of the ocular defects in a new mouse mutant carrying a Bmpr1b mutation. Methods The Bmpr1b mutants were analyzed by slit lamp,…”
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To Professor I.A. Amreich, on his 70th birthday by KLAFTEN, E M

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