Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Hoehn Holger"'
Autor:
Bechtold Astrid, Neitzel Heidemarie, Tönnies Holger, Varon Raymonda, Zintl Felix, Seidel Joerg, Gruhn Bernd, Hoehn Holger, Schindler Detlev
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 2, Iss 1, p 5 (2007)
Abstract Background DNA Ligase IV deficiency syndrome is a rare autosomal recessive disorder caused by hypomorphic mutations in the DNA ligase IV gene (LIG4). The clinical phenotype shows overlap with a number of other rare syndromes, including Secke
Externí odkaz:
https://doaj.org/article/fe6c636648f549969287685d35f37099
Autor:
Kalb, Reinhard, Duerr, Michael, Wagner, Matthias, Herterich, Sabine, Gross, Michaela, Digweed, Martin, Joenje, Hans, Hoehn, Holger, Schindler, Detlev
Publikováno v:
Radiation Research, 2004 Mar 01. 161(3), 318-325.
Externí odkaz:
https://www.jstor.org/stable/3581034
Autor:
Djuzenova, Cholpon S, Rothfuss, Andreas, Oppitz, Ulrich, Speit, Günter, Schindler, Detlev, Hoehn, Holger, Flentje, Michael
Publikováno v:
In Laboratory Investigation 1 February 2001 81(2):185-192
Akademický článek
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Autor:
Oppitz, Ulrich *, Bernthaler, Ulrike, Schindler, Detlev, Sobeck, Alexandra, Hoehn, Holger, Platzer, Matthias, Rosenthal, André, Flentje, Michael
Publikováno v:
In International Journal of Radiation Oncology, Biology, Physics 1999 44(5):981-988
Autor:
Hoehn, Holger
Publikováno v:
Current Science, 1992 Oct . 63(8), 407-410.
Externí odkaz:
https://www.jstor.org/stable/24094683
Autor:
Kurnit, David M.1, Hoehn, Holger1
Publikováno v:
Annual Review of Genetics. 1979, Vol. 13, p235-258. 24p.
Autor:
Colle, Isabelle, Laureys, Geneviève, Raevens, Sarah, Libbrecht, Louis, Leroy, Juliaan G, Reyntjens, Koen, Geerts, Anja, Rogiers, Xavier, Troisi, Roberto I, Hoehn, Holger, Schindler, Detlev, Hanenberg, Helmut, De Wilde, Vincent, Van Vlierberghe, Hans
Publikováno v:
Hepatology research : the official journal of the Japan Society of Hepatology, 43(9), 991-998. Wiley
Fanconi anemia (FA) is an inherited bone marrow failure syndrome due to defective DNA inter-strand cross-link repair. Hematopoietic stem cell transplantation (HSCT) is curative for pancytopenia, but may not prevent the development of non-hematologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::388892b5438830a2c8d921b7338ad20d
https://research.rug.nl/en/publications/8aec773f-74c6-42c7-b1b5-afa52ee68369
https://research.rug.nl/en/publications/8aec773f-74c6-42c7-b1b5-afa52ee68369
Autor:
Kalba, Reinhard, Neveling, Kornelia, Hoehn, Holger, Schneider, Hildegard, Linka, Yvonne, Batishb, Sat Dev, Hunt, Curtis, Berwick, Marianne, Callén Moréu, Elsa, Surrallés i Calonge, Jordi, Casado, José A., Bueren, Juan, Dasí, Ángeles, Soulier, Jean, Gluckman, Eliane, Zwaan, C. Michel, Van Spaendonk, Rosalina, Pals, Gerard, Winter, Johan P. de, Joenje, Hans, Grompe, Markus, Auerbach, Arleen D., Hanenberg, Helmut, Schindler, Detlev
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Universitat Autònoma de Barcelona
Premi a l'excel·lència investigadora. Àmbit de les Ciències de la Salut. 2008 FANCD2 is an evolutionarily conserved Fanconi anemia (FA) gene that plays a central role in DNA double-strand type damage responses. Using complementation assays and im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e6ec6f8e4dbac51f589a2b693ffff2db
https://ddd.uab.cat/record/67767
https://ddd.uab.cat/record/67767