المؤلفون: Katja Beck, Ulrich Schüller, Matthias A. Karajannis, Daniel Schrimpf, Andrey Korshunov, Svenja Boekhoff, Christina Bluecher, Arie Perry, Hermann L. Müller, Priscilla K. Brastianos, Christian Mawrin, Jens Schittenhelm, Felix Sahm, Damian Stichel, Nagarajan Paramasivam, Natalie Waldt, Stefan M. Pfister, Matthias Schlesner, Torsten Pietsch, Philipp Sievers, David Capper, Markus J. Riemenschneider, Siegfried Kropf, Elmar Kirches

المصدر: Acta neuropathologica, vol 142, iss 5
Acta Neuropathologica

مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, Pediatric Research Initiative, Adolescent, Clinical Sciences, Biology, DNA sequencing, Pathology and Forensic Medicine, Meningioma, Cellular and Molecular Neuroscience, Rare Diseases, Papillary Meningioma, Chromosome instability, medicine, otorhinolaryngologic diseases, Meningeal Neoplasms, Genetics, Humans, ddc:610, Child, Preschool, neoplasms, Cancer, Pediatric, Original Paper, Methylation profile, Neurology & Neurosurgery, Gene Expression Profiling, Human Genome, Neurosciences, medicine.disease, Dna methylation profiling, nervous system diseases, Brain Disorders, Brain Cancer, Child, Preschool, NF2, DNA methylation, Targeted sequencing, Female, Neurology (clinical), Unsupervised clustering, Transcriptome, Clear cell

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a72798dded58bd3ab3dedeb1fa1ab15
https://escholarship.org/uc/item/9xd344rz

المؤلفون: Andrej Teren, Holger Kirsten, Ralph Burkhardt, Katrin Horn, Valentin Schlegel, Juergen Kratzsch, Markus Scholz, Markus Loeffler, Joachim Thiery, Christina Bluecher, Janne Pott

المصدر: Circulation. Genomic and precision medicine. 11(5)

مصطلحات موضوعية: 0301 basic medicine, Male, Genome-wide association study, 030204 cardiovascular system & hematology, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Humans, ATHEROSCLEROTIC VASCULAR DISEASE, PCSK9, Subtilisin, General Medicine, Plasma levels, Mendelian Randomization Analysis, Middle Aged, Proprotein convertase, Atherosclerosis, Phenotype, 030104 developmental biology, Treatment Outcome, Genetic Loci, Cancer research, Kexin, Female, Proprotein Convertase 9, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1627a8366be14ef454f6332cce44ecc7
https://pubmed.ncbi.nlm.nih.gov/29748320