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The EMBO Journal|February 15, 1994
Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen)K Steinmeyer, C Lorenz, M Pusch, et al.
International Journal of Molecular Medicine|November 8, 2005
Mutational risk in highly repetitive exon ORF15 of the RPGR multidisease gene is not associated with haplotype backgroundFelix K Jacobi, Daniela Karra, Martina Broghammer, et al.
Journal of Applied Genetics|October 18, 2003
Adaptor-mediated amplification of minute amounts of severely fragmented ancient nucleic acidsC M Pusch, N Blin, M Broghammer, et al.
American Journal of Physical Anthropology|May 16, 2002
Detection of bone glue treatment as a major source of contamination in ancient DNA analysesGraeme J Nicholson, Jürgen Tomiuk, Alfred Czarnetzki, et al.
Human Mutation|October 29, 2002
Ten novel ORF15 mutations confirm mutational hot spot in the RPGR gene in European patients with X-linked retinitis pigmentosaCarsten M Pusch, Martina Broghammer, Bernhard Jurklies, et al.
Ocular Immunology and Inflammation|July 16, 2005
Autoimmune retinopathy with RPE hypersensitivity and 'negative ERG' in X-linked hyper-IgM syndromeAndreas Schuster, Eckart Apfelstedt-Sylla, Carsten M Pusch, et al.
British Journal of Pharmacology|December 12, 2001
A kinetic study on the stereospecific inhibition of KCNQ1 and I(Ks) by the chromanol 293BG Seebohm, C Lerche, M Pusch, et al.
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