Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Melanie Ronsiek"'
Autor:
Dirk Korthaus, Cora S. Thiel, Harald Jockusch, Karin Resch, Thomas Schmitt-John, Melanie Ronsiek, Niels Wedemeyer, Kristin Baer, Andreas Lengeling
Publikováno v:
Mammalian Genome. 9:893-898
Human Chr 2p13-14 and homologous regions on mouse Chrs 6 and 11 have been subjects of previous studies because they comprise the loci for several neuromuscular diseases. Here we report on high-resolution mapping of 55 STS and EST loci on human Chr 2p
Autor:
Melanie Ronsiek, Yoshitaka Ono, Nobuaki Takahashi, Sonja Fuchs, Harald Jockusch, Jörg W. Bartsch, Hideyuki Mukai
Publikováno v:
Genomics. 49:129-132
Protein kinase N (PKN) is a fatty acid- and Rho-activated serine/threonine protein kinase involved in the regulation of cell motility by association with cytoskeletal components such as neurofilament and cu-actinin. We determined the chromosomal loca
Autor:
Melanie Ronsiek, Anke Mussmann, Harald Jockusch, Volker C. Schmidt, Michael Ulbrich, Martin Augustin, Jörg W. Bartsch, Thomas Schmitt-John
Publikováno v:
Ulbrich, M, Schmidt, V, Ronsiek, M, Mussmann, A, Bartsch, J, Augustin, M, Jockusch, H & Schmitt-John, T 2002, ' Genetic modifiers that aggravate the neurological phenotype of the wobbler mouse ', NeuroReport, vol. 13, pp. 535-539 .
The autosomal recessive mutation wobbler of the mouse (phenotype WR; genotype wr/wr) causes muscular atrophy due to motoneuron degeneration with 100% penetrance on the standard Mus musculus laboratorius C57BL/6J background. In inter- and backcrosses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0641175d1f130131b6d06e2f57a55037
https://doi.org/10.1097/00001756-200203250-00035
https://doi.org/10.1097/00001756-200203250-00035
Autor:
Herwig Ponstingl, Melanie Ronsiek, Katherine Rojas, Claudia Disqué-Kochem, Ingeborg Sobek-Klocke, Ursula Eichenlaub-Ritter, Joan Overhauser, Astrid Breuning, Harald Jockusch, Rainer Klocke
Publikováno v:
Genomics. 43(2)
A clone from a lambda gt11 cDNA expression library of HeLa cells was isolated, sequenced, and shown to encode a new human zinc finger protein. The cDNA of the gene termed ZFP161 has an open reading frame of 1347 bp. The predicted protein comprises 44
Autor:
Melanie Ronsiek, Rainer Klocke, André Augustin, Herman van der Putten, Aribert Stief, Harald Jockusch
Publikováno v:
Genomics. 41(2)
Dynamins, microtubule-binding GTPases, are encoded by at least three genes in mammals. Two distinct gene-specific cDNAs were used to analyze the segregation of dynamin genes Dnm1 and Dnm2 in a mouse interspecies backcross. The nervous system expresse
Autor:
Melanie Ronsiek, Niels Wedemeyer, Andreas Lengeling, Harald Jockusch, Dirk Korthaus, Thomas Schmitt-John
Publikováno v:
Korthaus, D, Wedemeyer, N, Lengeling, A, Ronsiek, M, Jockusch, H & Schmitt-John, T 1997, ' Integrated Radiation Hybrid Map of Human Chromosome 2p13: Possible Involvement of Dynactin in Neuromuscular Diseases ', Genomics, vol. 43, pp. 242-244 .
The genes for the human neuromuscular diseases limb-girdle muscular dystrophy type 2B (LGMD2B) and Miyoshi myopathy are located on chromosome 2p13p14, and two neuromuscular mutations of the mouse have been mapped to regions homologous to human chromo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5233daed6757c976153b2523769716e
https://doi.org/10.1006/geno.1997.4789
https://doi.org/10.1006/geno.1997.4789
Autor:
Melanie Ronsiek, Harald Jockusch, Andreas Lengeling, Niels Wedemeyer, Dirk Korthaus, Martina Wuttke, Kristin Baer
Publikováno v:
Wedemeyer, N, Lengeling, A, Ronsiek, M, Korthaus, D, Baer, K, Wuttke, M & Jockusch, H 1996, ' 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 ', Genomics, vol. 32, no. 3, pp. 447-54 . https://doi.org/10.1006/geno.1996.0140
Despite rapid progress in the physical characterization of murine and human genomes, little molecular information is available on certain regions, e.g., proximal mouse chromosome 11 (Chr 11) and human chromosome 2p (Chr 2p). We have localized the wob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d35d7e10f98fc1e94270a2ff09b64c4c
https://hdl.handle.net/20.500.11820/6e903f39-f1ac-4e99-a012-fd2195f13e44
https://hdl.handle.net/20.500.11820/6e903f39-f1ac-4e99-a012-fd2195f13e44
Autor:
Monika Gronemeier, Thomas J. Jentsch, Melanie Ronsiek, Andreas Lengeling, Astrid Thiemann, Harald Jockusch
Publikováno v:
Europe PubMed Central
SummaryTheClc2gene of the mouse codes for the ubiquitously expressed chloride channel ClC-2, a member of a family of at least seven voltage gated chloride channels, some of which are implicated in hereditary diseases. Using a mouse interspecies back-
Autor:
Martin Rothkegel, Hans-Georg Mannherz, Melanie Ronsiek, Brigitte M. Jockusch, Rudolf Valenta, Klaudia Giehl
Publikováno v:
European journal of biochemistry. 226(2)
The mode of interaction of birch and bovine profilins with actin was compared using a number of techniques. Birch profilin was purified from pollen or as a recombinant protein from Escherichia coli, using poly(l-proline) affinity chromatography and a