Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jasen Anderson"'
Autor:
O A Haas, Jasen Anderson, A Polityko, Laura Rodríguez, Heike Starke, N. Martínez Guardia, Joris Vermeesch, Uwe Claussen, Christian Ramel, A Sanchís, F. von Eggeling, Thomas Liehr, Kristin Mrasek, Anja Weise, Andreas Dufke
Publikováno v:
Cytogenetic and Genome Research. 112:23-34
Small supernumerary marker chromosomes (sSMC) are still a major problem in clinical cytogenetics as they are too small to be characterized for their chromosomal origin by traditional banding techniques, but require molecular cytogenetic techniques fo
Autor:
Jasen Anderson, John A. Allan, Rohini Edirisinghe, Michael Gattas, A.V. Nandini, Rodney Jemmott
Publikováno v:
The Australian and New Zealand Journal of Obstetrics and Gynaecology. 44:117-123
Background: An increased embryo aneuploidy rate is associated with advancing maternal age. Preimplantation genetic diagnosis (PGD) using fluorescence in situ hybridisation (FISH) coupled with in vitro fertilisation (IVF)/embryo biopsy provides a powe
Autor:
Nikolai Rubtsov, Martina Merkas, Ahmed B. Hamid, Thomas Liehr, Alma Küchler, Isolde Schreyer, Ferdinand von Eggeling, Raimund Fahsold, Jasen Anderson, Nadezda Kosyakova, Kristin Mrasek, Julia Hentschel, Elisabeth Ewers, Heike Nelle, Anikó Ujfalusi, Anja Weise
Mental retardation is correlated in approximately 0.4% of cases with the presence of a small supernumerary marker chromosome (sSMC). However, here we report a case of a carrier of a heterochromatic harmless sSMC with fragile X syndrome (Fra X). In ap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1c92d1ba50c42acbfef3d532589cb18
Autor:
A Polityko, Anja Weise, Marina Manvelyan, Dilek Aktas, Hans-Christoph Duba, Thomas Liehr, Franck Pellestor, Daniela Reich, Peter Küpferling, Bernt Schulze, Hanne Tittelbach, Ute Hehr, Marie-Luise Mazaurik, Elisabeth Gödde, Mònica Santos, Thomas Martin, Isolde Schreyer, Sigrid Köhler, Marianne Volleth, Gisela Reising-Ackermann, Carme Fuster, Britta Belitz, Elisabeth Ewers, Jasen Anderson, Andreas Dufke, Mariluce Riegel, Kristin Mrasek, Christina Kelbova
Publikováno v:
ResearcherID
Thirty-two patients with fertility problems were identified as carriers of small supernumerary marker chromosomes (sSMC). Molecular cytogenetic techniques were used to characterize their chromosomal origin. Together with the other cases available in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87b5f6d2769c959ecfadc2a02ae28a0f
https://doi.org/10.5167/uzh-57505
https://doi.org/10.5167/uzh-57505
Autor:
Nadezda Kosyakova, Thomas Liehr, Daniela Reich, Jasen Anderson, Elisabeth Ewers, Adayapalam Nandini, Simon Fluri, Hasmik Mkrtchyan, Vladimir A. Trifonov, Franz Binkert, Anja Weise, Laura Rodríguez, Madeleine Gross
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 1, Iss 1, p 6 (2008)
Repisalud
Instituto de Salud Carlos III (ISCIII)
Molecular Cytogenetics, Vol 1, Iss 1, p 6 (2008)
Repisalud
Instituto de Salud Carlos III (ISCIII)
Background Small supernumerary marker chromosomes (sSMC) are present ~2.6 × 106 human worldwide. sSMC are a heterogeneous group of derivative chromosomes concerning their clinical consequences as well as their chromosomal origin and shape. Besides t
Publikováno v:
ResearcherID
Rafts are small membrane domains containing discrete subsets of lipids and proteins. Although microscopic raft structures termed ‘caveolae’ were described nearly 50 years ago, the importance of rafts, particularly signalling within rafts, is only