eine familiäre genetische Belastung oder vorausgegangene Schwangerschaft mit einem Feten mit einer Gen-Mutation / einem genetischen Syndrom. Eine Chorionzottenbiopsie bedeutet, dass immer eine Direkpräparation
Gottlieb J, Welte T, Braubach P, Laenger F, Hoeper MM, Kuehnel MP, Jonigk DD. Comparative Analysis of Gene Expression in Fibroblastic Foci in Patients with Idiopathic Pulmonary Fibrosis and Pulmonary Sarcoidosis
P. & Hunt, D.M. (1995) Cloning vectors for the production of proteins in Dictyostelium discoideum Gene 162 , 129-134. (Abstract) (pdf, 436 kB) Schröder, R.R., Manstein, D.J., Jahn, W., Holden, H.M., Rayment [...] Biol. 137 , 359-367. (Abstract) Manstein, D.J., Titus, M.A., De Lozanne, A. & Spudich, J.A. (1989) Gene replacement in Dictyostelium: generation of myosin null mutants EMBO J. 8 , 923-932. (Abstract) Manstein
Daniel C, Kispert A, Haffner D, Weber RG: Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations. Hum Mol Genet 2017; 26(9): 1716-1731 Kröger [...] Schuster-Gossler K, Kühnel MP , Hegermann J, Ueffing M, Gossler A: 1700012B09Rik, a FOXJ1 effector gene active in ciliated tissues of the mouse but not essential for motile ciliogenesis. Dev Biol 2017;
and/or indirect microglia/neuron-interactions and subsequently controls neuronal excitability and gene expression. We aim at revealing the therapeutic potential of microglia depletion on inflammation-related
and/or indirect microglia/neuron-interactions and subsequently controls neuronal excitability and gene expression. We aim at revealing the therapeutic potential of microglia depletion on inflammation-related
to answer whether early traumatic childhood experiences and the methylation of exon IV of the BDNF gene have an influence on the differential effectiveness of the two treatments. Mediator analyzes are used
Holger Prokisch, Tim Ripperger, and David Malkin. 2022. “ Heterozygous BRCA1/2 and Mismatch Repair Gene Pathogenic Variants in Children and Adolescents with Cancer .” JNCI: Journal of the National Cancer [...] Nilesh J. Samani. 2009. “Genome-Wide Haplotype Association Study Identifies the SLC22A3-LPAL2-LPA Gene Cluster as a Risk Locus for Coronary Artery Disease.” Nature Genetics 41(3):283–85. doi: 10.1038/ng [...] Novel Genetic Variant Predisposing to Coronary Artery Disease in the Region of the PSRC1 and CELSR2 Genes on Chromosome 1 Associates with Serum Cholesterol.” Journal of Molecular Medicine 86(11):1233–41.
Storage of Porcine Liver Grafts. Transpl Int. 2022 Oct 20;35:10712. Chruscinski A et al. Evaluation of a gene expression biomarker to identify operationally tolerant liver transplant recipients: the LITMUS trial [...] 2022;272:1-26. Valdivia E et al. Genetic Modification of Limbs Using Ex Vivo Machine Perfusion. Hum Gene Ther. 2022 Apr;33(7-8):460-471. Mund E et al. Clinically latent and autopsy-verified inflammatory [...] alpha-1 antitrypsin (AAT)-transgenic macrophages provides a source of functional human AAT in vivo. Gene Ther. 2021 Sep;28(9):477-493. Neubert L et al. Couples After Renal Transplantation: Impact of Sex
Lehmann U : Routine clinical mutation profiling using next generation sequencing and a customized gene panel improves diagnostic precision in myeloid neoplasms. Oncotarget 2016; 7(21):30084-30093 Baumann [...] Harbeck N: West German Study Group Phase III PlanB Trial: First Prospective Outcome Data for the 21-Gene Recurrence Score Assay and Concordance of Prognostic Markers by Central and Local Pathology Assessment