Similar songs, but different mate localization strategies of the three species of Phaneroptera occurring in Western Europe (Orthoptera: Phaneropteridae)
HELLER, Klaus-Gerhard, HELLER, Martina, VOLLETH, Marianne, SAMIETZ, Jörg, HEMP, Claudia
Published in European journal of entomology (01.04.2021)
Published in European journal of entomology (01.04.2021)
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Journal Article
Generation of functional cardiomyocytes from rat embryonic and induced pluripotent stem cells using feeder-free expansion and differentiation in suspension culture
Dahlmann, Julia, Awad, George, Dolny, Carsten, Weinert, Sönke, Richter, Karin, Fischer, Klaus-Dieter, Munsch, Thomas, Leßmann, Volkmar, Volleth, Marianne, Zenker, Martin, Chen, Yaoyao, Merkl, Claudia, Schnieke, Angelika, Baraki, Hassina, Kutschka, Ingo, Kensah, George
Published in PloS one (07.03.2018)
Published in PloS one (07.03.2018)
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Early embryonic chromosome instability results in stable mosaic pattern in human tissues
Mkrtchyan, Hasmik, Gross, Madeleine, Hinreiner, Sophie, Polytiko, Anna, Manvelyan, Marina, Mrasek, Kristin, Kosyakova, Nadezda, Ewers, Elisabeth, Nelle, Heike, Liehr, Thomas, Volleth, Marianne, Weise, Anja
Published in PloS one (09.03.2010)
Published in PloS one (09.03.2010)
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Are molecular cytogenetics and bioinformatics suggesting diverging models of ancestral mammalian genomes?
Froenicke, Lutz, Caldés, Montserrat Garcia, Graphodatsky, Alexander, Müller, Stefan, Lyons, Leslie A, Robinson, Terence J, Volleth, Marianne, Yang, Fengtang, Wienberg, Johannes
Published in Genome Research (01.03.2006)
Published in Genome Research (01.03.2006)
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Journal Article
The Human Genome Puzzle - the Role of Copy Number Variation in Somatic Mosaicism
Mkrtchyan, Hasmik, Gross, Madeleine, Hinreiner, Sophie, Polytiko, Anna, Manvelyan, Marina, Mrasek, Kristin, Kosyakova, Nadezda, Ewers, Elisabeth, Nelle, Heike, Liehr, Thomas, Bhatt, Samarth, Thoma, Karen, Gebhart, Erich, Wilhelm, Sylvia, Fahsold, Raimund, Volleth, Marianne, Weise, Anja
Published in Current genomics (01.09.2010)
Published in Current genomics (01.09.2010)
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The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophy
Cortese, Rene, Eckhardt, Florian, Volleth, Marianne, Wehnert, Manfred, Koelsch, Uwe, Wieacker, Peter, Brune, Thomas
Published in Journal of molecular endocrinology (01.06.2007)
Published in Journal of molecular endocrinology (01.06.2007)
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Increased genome size is caused by heterochromatin addition in two non-related bat species, Hesperoptenus doriae and Philetor brachypterus (Vespertilionidae, Chiroptera, Mammalia)
Volleth, Marianne, Greilhuber, Johann, Heller, Klaus-Gerhard, Müller, Stefan, Yong, Hoi-Sen, Loidl, Josef
Published in Chromosoma (01.11.2023)
Published in Chromosoma (01.11.2023)
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Evidence for multi-copy Mega-NUMTs in the human genome
Lutz-Bonengel, Sabine, Niederstätter, Harald, Naue, Jana, Koziel, Rafal, Yang, Fengtang, Sänger, Timo, Huber, Gabriela, Berger, Cordula, Pflugradt, René, Strobl, Christina, Xavier, Catarina, Volleth, Marianne, Weiß, Sandra Carina, Irwin, Jodi A, Romsos, Erica L, Vallone, Peter M, Ratzinger, Gudrun, Schmuth, Matthias, Jansen-Dürr, Pidder, Liehr, Thomas, Lichter, Peter, Parsons, Thomas J, Pollak, Stefan, Parson, Walther
Published in Nucleic acids research (22.02.2021)
Published in Nucleic acids research (22.02.2021)
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Journal Article
Evidence for multi-copy Mega-NUMT s in the human genome
Lutz-Bonengel, Sabine, Niederstätter, Harald, Naue, Jana, Koziel, Rafal, Yang, Fengtang, Sänger, Timo, Huber, Gabriela, Berger, Cordula, Pflugradt, René, Strobl, Christina, Xavier, Catarina, Volleth, Marianne, Weiß, Sandra Carina, Irwin, Jodi A, Romsos, Erica L, Vallone, Peter M, Ratzinger, Gudrun, Schmuth, Matthias, Jansen-Dürr, Pidder, Liehr, Thomas, Lichter, Peter, Parsons, Thomas J, Pollak, Stefan, Parson, Walther
Published in Nucleic acids research (22.02.2021)
Published in Nucleic acids research (22.02.2021)
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Integration of molecular cytogenetics, dated molecular phylogeny, and model-based predictions to understand the extreme chromosome reorganization in the Neotropical genus Tonatia (Chiroptera: Phyllostomidae)
Sotero-Caio, Cibele G, Volleth, Marianne, Hoffmann, Federico G, Scott, LuAnn, Wichman, Holly A, Yang, Fengtang, Baker, Robert J
Published in BMC evolutionary biology (06.10.2015)
Published in BMC evolutionary biology (06.10.2015)
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Wing Membrane Biopsies for Bat Cytogenetics: Finding of 2n = 54 in Irish Rhinolophushipposideros (Rhinolophidae, Chiroptera, Mammalia) Supports Two Geographically Separated Chromosomal Variants in Europe
Kacprzyk, Joanna, Teeling, Emma C, Kelleher, Conor, Volleth, Marianne
Published in Cytogenetic and genome research (2016)
Published in Cytogenetic and genome research (2016)
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A cryptic unbalanced translocation der(4)t(4;17)(p16.1;q25.3) identifies Wittwer syndrome as a variant of Wolf-Hirschhorn syndrome
Wieland, Ilse, Schanze, Denny, Schanze, Ina, Volleth, Marianne, Muschke, Petra, Zenker, Martin
Published in American journal of medical genetics. Part A (01.12.2014)
Published in American journal of medical genetics. Part A (01.12.2014)
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Journal Article
Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres — A long term in vitro study
Hussein, Shaymaa Subhi, Kreskowski, Katharina, Ziegler, Monika, Klein, Elisabeth, Hamid, Ahmed B., Kosyakova, Nadezda, Volleth, Marianne, Liehr, Thomas, Fan, Xiaobo, Piaszinski, Katja
Published in Gene (01.12.2014)
Published in Gene (01.12.2014)
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Deletions in the 3′ Part of the NFIX Gene Including a Recurrent Alu-Mediated Deletion of Exon 6 and 7 Account for Previously Unexplained Cases of Marshall-Smith Syndrome
Schanze, Denny, Neubauer, Dorothée, Cormier-Daire, Valerie, Delrue, Marie-Ange, Dieux-Coeslier, Anne, Hasegawa, Tomonobu, Holmberg, Eva E., Koenig, Rainer, Krueger, Gabriele, Schanze, Ina, Seemanova, Eva, Shaw, Adam C., Vogt, Julie, Volleth, Marianne, Reis, André, Meinecke, Peter, Hennekam, Raoul C.M., Zenker, Martin
Published in Human mutation (01.09.2014)
Published in Human mutation (01.09.2014)
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Greig Cephalopolysyndactyly (GCPS) Contiguous Gene Syndrome in a Boy with a 14 Mb Deletion in Region 7p13-14 Caused by a Paternal Balanced Insertion (5; 7) [Expression of Concern]
Schulz, Solveig, Volleth, Marianne, Muschke, Petra, Wieland, Isle, Wieacker, Peter
Published in Application of clinical genetics (01.01.2021)
Published in Application of clinical genetics (01.01.2021)
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