Bereich umfassen elektrophysiologische Störungen (z. B. Brugada-Syndrom aufgrund von Mutationen im SCN5A-Gen), die Störung kardialer Transkriptionsfaktoren (z. B. NKX2.5 Knock Out in HFOs) und die Untersuchung [...] Ansatz gehören elektrophysiologische Störungen (z. B. Brugada-Syndrom aufgrund von Mutationen im SCN5A-Gen), die Inaktivierung kardialer Transkriptionsfaktoren (z. B. NKX2.5-Knock-out in HFOs) und jüngste [...] and MHHi021-B) from a patient with hypertrophic cardiomyopathy with p.Arg723Gly mutation in the MYH7 gene. Stem Cell Res. 2021 Apr;52:102208. doi: 10.1016/j.scr.2021.102208. Epub 2021 Feb 3. PMID: 33578365
chronic lung disease initiation. By using patient-derived iPS cells, we also study the effect of gene deficiencies on alveolar cell functionality. Single-cell transcriptomics, data integration approaches
Viable pigs after simultaneous inactivation of porcine MHC class I and three xenoreactive antigen genes GGTA1, CMAH and B4GALNT2. Fischer K, Rieblinger B, Hein R, Sfriso R, Zuber J, Fischer A, Klinger B
Hämatologie Molekularbiologie der Zelle Alberts Alternativ: Molecular Biology of the cell Alberts Gene therapy immunology Herzog Textbook of Hematology / McKenzie Principles of regenerative medicine Atala
rv ( Nervus trigeminus ) weitervermittelt. Wie auch bei der Migräne scheint das CGRP ( calcitonin-gene related peptide ) Transmittersystem – genauer gesagt Neurotransmitter, also die Botenstoffe mit denen
Sewald K; U-BIOPRED Study Group. Rhinovirus-induced Human Lung Tissue Responses Mimic COPD and Asthma Gene Signatures. Am J Respir Cell Mol Biol. 2021 Jun 28. doi: 10.1165/rcmb.2020-0337OC. Epub ahead of print
Supervisor: Prof. Dr. Michael Heuser, Department of Haematology / Oncology, Project: Targeting fusion genes in acute myeloid leukemia. Final exam June 2023 Johannes Greve GERMANY Greve.Johanne@mh-hannover.de
supervisor: Prof. Dr. Baum, Experimental Hematology, OE 6960, project: Correction of MPL deficiency by gene transfer Final exam June 2011 Yarua Jaimes VENEZUELA supervisor: Prof. Dr. Blasczyk, Transfusion Medicine
Schwäbe FV, Pokrant T, Faix J, Di Donato N, Taft MH, Manstein DJ. Frameshift mutation S368fs in the gene encoding cytoskeletal β-actin leads to ACTB -associated syndromic thrombocytopenia by impairing actin
6(4): 847-51 Leonhardt J, Stanulla M, von Wasielewski R, Skokowa J, Kubler J, Ure BM, Petersen C: Gene expression profile of the infective murine model for biliary atresia. Pediatr Surg Int 2006; 22(1): [...] TJ, Brehm C, Hanack J, von Wasielewski R, Musholt PB: Identification of Differentially Expressed Genes in Papillary Thyroid Carcinomas with and without Rearrangements of the Tyrosine Kinase Receptors RET