the group of Dr. Bernhard Herrmann. ("Isolation and characterisation of an S6 kinase II homologous gene from the T/t-complex region of the mouse") Doctoral training 1990-1993 Ph.D. thesis in the laboratory

Methionine Adenosyltransferase I/III Deficiency Detected by Newborn Screening. Genes (Basel). 2022 Jun 27;13(7). doi: 10.3390/genes13071163. PubMed PMID: 35885946; PubMed Central PMCID: PMC9323693. Mütze U

h S, Davis MJ, Pearson RB, Sanij E, Alexander WS, Ng AP. (2024) ERG and c-MYC regulate a critical gene network in BCR::ABL1-driven B-cell acute lymphoblastic leukaemia. Science Advances 10(10): 1126. Deng [...] H, Koch J, Serve H, Bonig H, Stocking C, Rieger MA, Lausen J. (2015) RUNX1 represses the erythroid gene expression program during megakaryocytic differentiation. Blood 125(23): 3570-9. Skokowa J, Steinemann

Science Publishers Link Kirsten Haastert-Talini Editorial for special issue: Gene Therapy approaches for Neuroregeneration Curr Gene Ther 2011 in press (Vol 11 No 2, April 2011) Ratzka A, Baron O, Grothe C [...] hypothesis. Placenta 2007;28(4):353-60. Kirsten Haastert, Claudia Grothe Gene Therapy in Peripheral Nerve Reconstruction Approaches Curr Gene Ther, 2007 Jun, 7:221-228 Grothe C and Timmer M The physiological [...] Vol. 108(3) 1–27. https://doi.org/10.1177/00368504251360728 The lincRNA Pantr1 is a FOXG1 target gene conferring site-specific chromatin binding of FOXG1. Gather F, Rauleac T, Akol I, Arumugam G, Fullio

r-Rezeptor-2. Bei Gallenwegstumoren ist FGFR2 aufgrund einer genetischen Fehlbildung mit anderen Genen sozusagen verschmolzen. Diese Fusionsumlagerungen führen zu einer dauerhaften Aktivierung von Signalwegen

questions remain unanswered. For example, in the majority of cases, it is unknown how and if the marker genes or regions are functionally involved in the cancerogenesis or progression. Likewise, it is unclear

herausragende Rolle. Aufgrund des erheblichen Polymorphismus der dem HLA-Komplex zugrunde liegenden Gene können derzeit an den transplantationsrelevanten HLA-Genorten A, B, C, DRB1, DQB1 und DPB1 mehr als

Becker JU , Cremer R, Hoefele J, Benz MR, Weber LT, Buettner R, Zerres K: Mutations in multiple PKD genes may explain early and severe polycystic kidney disease. J Am Soc Nephrol 2011; 22(11): 2047-56 Beutel [...] Wicke DC, Brugman MH, Meyer J, Schambach A, Büsche G , Ballmaier M, Baum C, Modlich U: Lentiviral gene transfer regenerates hematopoietic stem cells in a mouse model for Mpl-deficient aplastic anemia. [...] 32(2): 152-8 [German] Janciauskiene S, Ferrarotti I, Laenger F, Jonigk D, Luisetti M: Clinical utility gene card for: α-1-antitrypsin deficiency. Eur J Hum Genet 2011; 19(5): doi:10.1038/ejhg.2010.246 Jonigk

cardiomyopathy (HCM) is one of the most commonly inherited cardiovascular diseases caused by mutations in genes encoding key cardiac sarcomeric proteins and is associated with a high risk of sudden cardiac death

Down-Regulation of MHC Class I Expression in Human Keratinocytes Using Viral Vectors Containing US11 Gene of Human Cytomegalovirus and Cultivation on Bovine Collagen-Elastin Matrix (Matriderm®): Potential