others. Until today, however, no specific genes (=hereditary disposition) could be identified that actually causes tics. The aim of this study is to discover the genes responsible for the inheritance of tics

, Faix, J., Di Donato, N., Taft, M. H. , Manstein, D. J. (2022) Frameshift mutation S368fs in the gene encoding cytoskeletal β-actin leads to ACTB-associated syndromic thrombocytopenia by impairing actin [...] Taft, M. H. , Manstein, D. J., and Henn, A. (2017) N-terminal splicing extensions of the human MYO1C gene fine-tune the kinetics of the three full-length myosin IC isoforms. J. Biol. Chem. pii: jbc.M117.794008

the Vascular Endothelium to Silence MHC Expression During Normothermic Ex Vivo Lung Perfusion. Hum Gene Ther. 2018 Nov 20. doi: 10.1089/hum.2018.117. 5. Sander J, Schmidt S, Cirovic B, McGovern N, Papa

um einen wesentlichen genetischen Faktor der PAH-Entwicklung, loss-of-function Mutationen im BMPR2 Gen, die bei über 70 % der Patienten mit familiärer PAH vorliegen, besser abbilden zu können. Das neue

Srivaratharajan S, Manns MP, Schambach A, Grimm D, Bohne J, Sharma AD , Buning H, Ott M. Ex Vivo/In vivo Gene Editing in Hepatocytes Using "All-in-One" CRISPR-Adeno-Associated Virus Vectors with a Self-Linearizing

Myosin essential light chain 1sa decelerates actin and thin filament gliding on β-myosin molecules. J Gen Physiol. Oct 3; 154(10):e202213149. Doi: 10.1085/jgp.202213149. Wang, T., Spahiu, E., Osten, J., Behrens

integrity in the murine ureter by activating the expression of Shh and superficial cell-specific genes. Development. 2025 Apr 15;152(8):dev204324. doi: 10.1242/dev.204324. Epub 2025 Apr 17. PMID: 40167323 [...] nt C6 Glioma Cells Restores Cardiolipin Composition but Not Proliferation Rate and Alterations in Gene Expression. Front Genet. 2022 Jul 25;13:931017. doi: 10.3389/fgene.2022.931017. eCollection 2022. [...] Seegers CII , Ramón Roth I , Zarnovican P, Buettner FFR, Routier FH (2022). Characterization of a gene cluster involved in Aspergillus fumigatus zwitterionic glycosphingolipid synthesis. Glycobiology.

WOLF S, PRELLER M, ARETZ S, WIESE B, HARTMANN C, WEBER RG: Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin. Acta [...] C, NAUMANN N, BIKAR S-E, GIESE A, BUZDIN A. Intratumoral heterogeneity and longitudinal changes in gene expression predict differential drug sensitivity in newly diagnosed and recurrent glioblastoma. Cancers [...] PRELLER M, ARETZ S, WIESE B, HARTMANN C, WEBER RG (2021) Rare germline variants in the E-cadherin gene CDH1 predispose to brain tumors of neuroepithelial and epithelial origin. Acta Neuropathol Apr 30

Martinez-Aviles LM, Paricio BB, Giraudier S, Skoda R, Lippert E, Hermouet S, Cario H: Clinical utility gene card for: Hereditary thrombocythemia. Eur J Hum Genet 2014; 22(2) doi: 10.1038/ejhg.2013.117 [Review] [...] the breast.] Pathologe 2014; 35(1): 36-44 [German] Lehmann U: Aberrant DNA methylation of microRNA genes in human breast cancer - a critical appraisal. Cell Tissue Res 2014; 356(3): 657-664 [Review] Liessem [...] Vollmer-Kary B, Metzgeroth G, Sotlar K, Horny HP, Kreipe HH , Fisch P, Reiter A: The FIP1L1-PDGFRA fusion gene and the KIT D816V mutation are coexisting in a small subset of myeloid/lymphoid neoplasms with eo

Subprojektpartner ordnen Ihre Daten möglicherweise aufgrund unterschiedlicher gesetzlicher Anforderun-gen in anderen Bundesländern anders ein als wir. Die Sicherheit Ihrer Daten ist jedoch gleichbleibend [...] Subprojektpartner ordnen Ihre Daten möglicherweise aufgrund unterschiedlicher gesetzlicher Anforderun-gen in anderen Bundesländern anders ein als wir. Die Sicherheit Ihrer Daten ist jedoch gleichbleibend