Search Results

Cre recombinase promotes leukemogenesis in the presence of both homozygous and heterozygous FLT3-ITD by Yang, Min (Author) , Ma, Zhiyuan (Author) , Wang, Chonggang (Author) , Agca, Muammer Cihan (Author) , Liu, Hongyun (Author) , Huang, Kezhi (Author) , Glage, Silke (Author) , Rumpel, Regina (Author) , Gerbaulet, Alexander (Author) , Roers, Axel (Author) , Liu, Xuemei (Author) , Noyan, Fatih (Author) , von Neuhoff, Nils (Author) , Ganser, Arnold (Author) , Liu, Ligen (Author) , Yun, Haiyang (Author) , Li, Zhixiong (Author) ,

• Verlag, kostenfrei, Volltext
• Resolving-System, kostenfrei, Volltext

Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis by Yang, Yongjie (Author) , März, Winfried (Author) ,

Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 f... by Fischer, Christine (Author) , Kuchenbäcker, Karoline (Author) , Engel, Christoph (Author) , Zachariae, Silke (Author) , Rhiem, Kerstin (Author) , Meindl, Alfons (Author) , Rahner, Nils (Author) , Dikow, Nicola (Author) , Plendl, Hansjörg (Author) , Debatin, Irmgard (Author) , Grimm, Tiemo (Author) , Gadzicki, Dorothea (Author) , Flöttmann, Ricarda (Author) , Horvath, Judit (Author) , Schröck, Evelin (Author) , Stock, Friedrich (Author) , Schäfer, Dieter (Author) , Schwaab, Ira (Author) , Kartsonaki, Christiana (Author) , Mavaddat, Nasim (Author) , Schlegelberger, Brigitte (Author) , Antoniou, Antonis C. (Author) , Schmutzler, Rita (Author) ,

• Verlag, lizenzpflichtig, Volltext

Impaired ion channel function related to a common KCNQ1 mutation: implications for risk stratification in long QT syndrome 1 by Aidery, Parwez (Author) , Kisselbach, Jana (Author) , Schweizer, Patrick Alexander (Author) , Becker, Rüdiger (Author) , Katus, Hugo (Author) , Thomas, Dierk (Author) ,

• Verlag, Volltext

Motivational reserve: motivation-related occupational abilities and risk of mild cognitive impairment and Alzheimer disease by Forstmeier, Simon (Author) , Weyerer, Siegfried (Author) ,

• Verlag, Volltext
• Verlag, Volltext

Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone by Bleyer, Anthony J. (Author) , Zivná, M. (Author) , Hulková, H. (Author) , Hodanová, K. (Author) , Vyletal, P. (Author) , Sikora, J. (Author) , Zivný, J. (Author) , Sovová, J. (Author) , Hart, T. C. (Author) , Adams, J. N. (Author) , Elleder, M. (Author) , Kapp, Katharina (Author) , Haws, R. (Author) , Cornell, L. D. (Author) , Kmoch, S. (Author) , Hart, P. S. (Author) ,

The haploinsufficient Col3a1 mouse as a model for vascular Ehlers-Danlos syndrome by Cooper, Timothy K. (Author) , Zhong, Q. (Author) , Krawczyk, M. (Author) , Tae, H.-J. (Author) , Müller, G. A. (Author) , Schubert, Rudolf (Author) , Myers, L. A. (Author) , Dietz, H. C. (Author) , Talan, M. I. (Author) , Briest, W. (Author) ,

• Verlag, lizenzpflichtig, Volltext

TIMP-2 gene polymorphism is associated with intracerebral hemorrhage by Reuter, Björn (Author) , Bugert, Peter (Author) , Stroick, Mark Gregor (Author) , Bukow, Simone (Author) , Griebe, Martin (Author) , Hennerici, Michael G. (Author) , Fatar, Marc (Author) ,

• Verlag, lizenzpflichtig, Volltext

Disease manifestations and X inactivation in heterozygous females with Fabry disease by Maier, Esther M. (Author) , Schatz, Stephanie Barbara (Author) , Whybra-Trümpler, Catharina (Author) , Ries, Markus (Author) , Gal, Andreas (Author) , Beck, Michael (Author) , Roscher, Adelbert A. (Author) , Muntau, Ania (Author) ,

Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2 by Samman, Irene (Author) , Schulz-Schaeffer, Walter J. (Author) , Wöhrle, Johannes C. (Author) , Sommer, André (Author) , Kretzschmar, Hans A. (Author) , Hennerici, Michael G. (Author) ,

• Verlag, lizenzpflichtig, Volltext