Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Annelore Junge"'
Autor:
Pavlina Havlikova, Pavel Zak, Michal Karas, Annelore Junge, Alzbeta Zavrelova, Radek Cmejla, Lenka Zejskova, Nadezda Kosyakova, Lucie Zemankova, Christian Ramel, Radek Plachy, David Hardekopf, Thomas Liehr, Tereza Jancuskova, Jiri Stika, Tomas Kozak, Sona Pekova
Publikováno v:
Leukemia Research. 37:1363-1373
Acute leukemias (AL) comprise a heterogeneous group of hematologic malignancies, and individual patient responses to treatment can be difficult to predict. Monitoring of minimal residual disease (MRD) is thus very important and holds great potential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9b140a8c3bca2d730bc58e042dd9b99
https://doi.org/10.1016/j.leukres.2013.06.009
https://doi.org/10.1016/j.leukres.2013.06.009
Autor:
Thomas Eggermann, Herdit M. Schüler, Britta Belitz, Andreas Roos, Klaus Zerres, Annelore Junge, Kristin Mrasek, Almuth Caliebe, Anja Weise, Gesa Schwanitz, Christine Löffler, Constantin von Kaisenberg, Simone Heidemann, Monika Kautza
Publikováno v:
Archives of Gynecology and Obstetrics. 288:1153-1158
To test the hypothesis that mutations of SYCP3 encoding synaptonemal complex protein 3, result in increased frequency of aneuploidies in humans. Mutation analysis of the PCR-amplified 8 coding exons and exon–intron boundaries of the SYCP3 gene was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cdda444b867875eb2df670c078bb90e
https://doi.org/10.1007/s00404-013-2861-5
https://doi.org/10.1007/s00404-013-2861-5
Autor:
Monika Ziegler, Hanne Tittelbach, Elisabeth Klein, Nadezda Kosyakova, Florian Kubek, Annelore Junge, Thomas Liehr, Laura Rodríguez, Fedora Stipoljev, Marcelo de Bello Cioffi, Marianne Volleth, Peter Kozlowski, Faezeh Vasheghani, Hannes Spittel, Gopakumar Radhakrishnan, Karl Mehnert, Xiaobo Fan, Ahmed B. Hamid, Dagmar Huhle, Thomas Martin, Mehmet Ali Ergun, Catherine Sarri, Berndt Schulze, Mariela Militaru, Katharina Kreskowski, Shaymaa S. Hussein
Small supernumerary marker chromosomes (sSMC) are known for being present in mosaic form as 47,+mar/46 in >50% of the cases with this kind of extra chromosomes. However, no detailed studies have been done for the mitotic stability of sSMC so far, mai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67e3995ba37117c0f9523cc560d16241
https://avesis.gazi.edu.tr/publication/details/6a2aafb0-4506-4b4e-ac6e-fcb424562647/oai
https://avesis.gazi.edu.tr/publication/details/6a2aafb0-4506-4b4e-ac6e-fcb424562647/oai
Autor:
Rita Exeler, Annelore Junge, Juergen Horst, Ingo Kennerknecht, Thomas Schmitt-John, Oliver Bartsch, Bettina Prager, Daniela Ehling, Beate Behre, J. Wirth
Publikováno v:
Ehling, D, Kennerknecht, I, Junge, A, Prager, B, Exeler, R, Lemcke, B, Horst, J, Bartsch, O, Schmitt-John, T & Wirth, J 2004, ' Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies ', American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, vol. 131A, pp. 265-372 .
We describe two unrelated patients with cytogenetically visible deletions of 21q22.2-q22.3 and mild phenotypes. Both patients presented minor dysmorphic features including thin marfanoid build, facial asymmetry, downward-slanting palpebral fissures,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6977f7d559556b4cd066b271ffdb104
https://pure.au.dk/portal/da/publications/mild-phenotype-in-two-unrelated-patients-with-a-partial-deletion-of-21q222q223-defined-by-fish-and-molecular-studies(5cd91e00-6396-11dd-9251-000ea68e967b).html
https://pure.au.dk/portal/da/publications/mild-phenotype-in-two-unrelated-patients-with-a-partial-deletion-of-21q222q223-defined-by-fish-and-molecular-studies(5cd91e00-6396-11dd-9251-000ea68e967b).html
Autor:
Hanne Tittelbach, M. Miyachi, P.A. Lima-Filho, V. Genualdo, W. Rens, Gopakumar Radhakrishnan, C. Nishida, M.B. Cioffi, W.F. Molina, Alfredo Pauciullo, Alessandra Iannuzzi, Berndt Schulze, H. Hosoi, Karl Mehnert, Ahmed B. Hamid, Clara Iannuzzi, Darren K. Griffin, V. Zukin, Nadezda Kosyakova, M. Röser, Fedora Stipoljev, Shaymaa S. Hussein, H. Yamane, Marcelo de Bello Cioffi, Dagmar Huhle, Monika Ziegler, L. Kratochvíl, D. Mykytenko, Hannes Spittel, K. Shiwaku, Peter Kozlowski, Y. Matsuda, Katharina Kreskowski, Satz Mengensatzproduktion, J. Schneider, Annelore Junge, Faezeh Vasheghani, L. Spinenko, Thomas Martin, Xiaobo Fan, Petra Musilova, M. Rovatsos, Domenico Incarnato, L.A.C. Bertollo, Angela Perucatti, S. Ishishita, L. Pylyp, G. Winterfeld, Jiri Rubes, N. Kakazu, K. Yamada, Laura Rodríguez, Catherine Sarri, Mehmet Ali Ergun, K. Perner, Thomas Liehr, Mariela Militaru, G.W.W.F. Costa, M. Pokorná, Florian Kubek, Druckerei Stückle, Marianne Volleth, Elisabeth Klein
Publikováno v:
Cytogenetic and Genome Research. 142:226-226
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a68efb555d083fb69bd606edece3646
https://doi.org/10.1159/000360710
https://doi.org/10.1159/000360710