Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Astrid Bechtold"'
Autor:
Markus Loeffler, Monika Graeser, Carolin Nestle-Kraemling, Mohammad Zaino, Marion Kiechle, Sabine Preisler-Adams, Karin Kast, Dorothea Gadzicki, Norbert Arnold, Christoph Engel, Astrid Bechtold, Ursula G. Froster, Rita K. Schmutzler, Dominic Varga, Alfons Meindl, Ulrich Bick, B. Schlehe, Kerstin Rhiem
Publikováno v:
Journal of Clinical Oncology. 27:5887-5892
Purpose To estimate the risk for contralateral breast cancer in members of BRCA1- and BRCA2-positive families and to determine predictive risk factors. Patients and Methods A retrospective, multicenter, cohort study was performed from 1996 until 2008
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddecb0e2b397718be7cfb047433878e7
https://doi.org/10.1200/jco.2008.19.9430
https://doi.org/10.1200/jco.2008.19.9430
Autor:
Natalio Garbi, Ruth Ganss, Astrid Bechtold, Bernd Arnold, Günter J. Hämmerling, Simone H. Stahl, Torsten Sacher, Ulrike Protzer
Publikováno v:
Immunology letters. 123(1)
Tumors often induce tolerance in the immune system, which may contribute to the limited success of clinical vaccination against tumors. In order to develop strategies for overcoming tumor tolerance we have developed an inducible mouse model of autoch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff94b71b481de14a8b2252e38187d622
https://pubmed.ncbi.nlm.nih.gov/19428549
https://pubmed.ncbi.nlm.nih.gov/19428549
Autor:
Joerg Seidel, Raymonda Varon, Holger Hoehn, Bernd Gruhn, Holger Tönnies, Heidemarie Neitzel, Felix Zintl, Astrid Bechtold, Detlev Schindler
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 2, Iss 1, p 5 (2007)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
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 Seckel syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a25acbec5d6301967d3d085bde505757
http://www.OJRD.com/content/2/1/5
http://www.OJRD.com/content/2/1/5
Autor:
Holger Hoehn, Kornelia Neveling, Ioannis Gavvovidis, Astrid Bechtold, Richard Friedl, Reinhard Kalb, Sabine Herterich, Detlev Schindler, Benni Gottwald
Publikováno v:
Fetal diagnosis and therapy. 21(1)
Objective: To explore the potential of flow cytometry in the prenatal exclusion or confirmation of Fanconi anemia (FA). Methods: Indications for prenatal diagnosis were (1) FA-negative family history, but suspicious ultrasound findings such as radial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ce193704f331498d7c745c1e0cb7729
https://pubmed.ncbi.nlm.nih.gov/16354989
https://pubmed.ncbi.nlm.nih.gov/16354989