-Detlev Schindler Researcher Activity Profile

Research Author Detailed Information 

Detlev Schindler Publication Rate By Year

Detlev Schindler has published 6 paper(s) in 2007, 2 paper(s) in 2008, for a total of 8 research publications in total.

Detlev D Schindler Author Information

LAST NAME: schindler

FIRST NAME: detlev

INITIALS: D

AFFILIATION:

Papers

Detlev Schindler's Publication Record

1. FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway. Year Published: 2007
Laboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
2. Genetic heterogeneity among Fanconi anemia heterozygotes and risk of cancer. Year Published: 2007
Cancer Research and Treatment Center/Internal Medicine, University of New Mexico, Albuquerque, New Mexico, USA.
3. Inhibition of primordial germ cell proliferation by the medaka male determining gene Dmrt I bY. Year Published: 2007
University of Wurzburg, Physiological Chemistry I, Biozentrum, Am Hubland, D-97074 Wurzburg, Germany. amaury.herpin@biozentrum.uni-wuerzburg.de
4. Inhibition of primordial germ cell proliferation by the medaka male determining gene Dmrt I bY. Year Published: 2007
University of Wurzburg, Physiological Chemistry I, Biozentrum, Am Hubland, D-97074 Wurzburg, Germany. amaury.herpin@biozentrum.uni-wuerzburg.de
5. Decreased platelet reactivity identified by whole blood flow cytometry in Fanconi anaemia patients. Year Published: 2007
Haemophilia Centre, Department of Internal Medicine III, Institute of Transfusion Medicine, Johann Wolfgang Goethe-University, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany. E-mail: ralf.grossmann@kgu.de.
6. Decreased platelet reactivity identified by whole blood flow cytometry in Fanconi anaemia patients. Year Published: 2007
University Children's Hospital, University of Wuerzburg, Germany.
7. Mutations in the pericentrin (PCNT) gene cause primordial dwarfism. Year Published: 2008
Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany. Anita.Rauch@humgenet.uni-erlangen.de
8. Mutations in the pericentrin (PCNT) gene cause primordial dwarfism. Year Published: 2008
Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany. Anita.Rauch@humgenet.uni-erlangen.de