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Dirk Korthaus

12

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911

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N-ethyl-N-nitrosourea-based generation of mouse models for mutant G protein-coupled receptors

2006 Physiological Genomics
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Efficient and fast targeted production of murine models based on ENU mutagenesis.

2005 Mammalian Genome
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The dominant alopecia phenotypes Bareskin, Rex-denuded, and Reduced Coat 2 are caused by mutations in gasdermin 3.

2004 Genomics
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Mutations in dynein link motor neuron degeneration to defects in retrograde transport

2003 Science
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Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency

2003 Journal of Investigative Dermatology
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A non-human animal model for growth deficiency and defects of information processing or cognitive function and its use

2000
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Homology between human chromosome 2p13.3 and the wobbler critical region on mouse chromosome 11: comparative high-resolution mapping of STS and EST loci on YAC/BAC contigs

1998 Mammalian Genome
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Integrated radiation hybrid map of human chromosome 2p13: possible involvement of dynactin in neuromuscular diseases

1997 Genomics
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The gene for cytoplasmatic malate dehydrogenase, Mor2, is closely linked to the wobbler spinal muscular atrophy gene (wr).

1996 Mammalian Genome
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YAC Contigs of the Rab1 and wobbler (wr) Spinal Muscular Atrophy Gene Region on Proximal Mouse Chromosome 11 and of the Homologous Region on Human Chromosome 2p

1996 Genomics
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Citations (16)