المؤلفون: Liane Schuster, Nina Ardjomandi, Marita Munz, Felix Umrath, Christian Klein, Frank Rupp, Siegmar Reinert, Dorothea Alexander

المصدر: Materials, Vol 13, Iss 5, p 1203 (2020)

مصطلحات موضوعية: collagen/hydroxyapatite scaffolds, bmp-2 mimicry peptides, electrostatic binding on hydroxyapatite, quartz crystal microbalance, Technology, Electrical engineering. Electronics. Nuclear engineering, TK1-9971, Engineering (General). Civil engineering (General), TA1-2040, Microscopy, QH201-278.5, Descriptive and experimental mechanics, QC120-168.85

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/1996-1944/13/5/1203Test; https://doaj.org/toc/1996-1944Test

الوصول الحر: https://doaj.org/article/c563ce5c07ce47cabc2a8d146a46494fTest

المؤلفون: Marina Danalache, Sophie-Maria Kliesch, Marita Munz, Andreas Naros, Siegmar Reinert, Dorothea Alexander

المصدر: International Journal of Molecular Sciences, Vol 20, Iss 17, p 4193 (2019)

مصطلحات موضوعية: bone mineral formation, fetal calf serum, human platelet lysate, osteoprogenitor jaw periosteal cells, mechanical properties, atomic force microscopy, Raman spectroscopy, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/1422-0067/20/17/4193Test; https://doaj.org/toc/1422-0067Test

الوصول الحر: https://doaj.org/article/d2acb852932c4638851c53532e07db7bTest

المؤلفون: Stefanie Krüger, Florian Battke, Andrea Sprecher, Marita Munz, Matthis Synofzik, Ludger Schöls, Thomas Gasser, Torsten Grehl, Johannes Prudlo, Saskia Biskup

المصدر: Frontiers in Molecular Neuroscience, Vol 9 (2016)

مصطلحات موضوعية: Amyotrophic Lateral Sclerosis, Genetic Heterogeneity, neurodegeneration, next generation sequencing, polygenic inheritance, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

العلاقة: http://journal.frontiersin.org/Journal/10.3389/fnmol.2016.00092/fullTest; https://doaj.org/toc/1662-5099Test

الوصول الحر: https://doaj.org/article/3cf298d7a3fe4172b481bd74d787a147Test

المؤلفون: Wolfgang Wurst, Thomas Ott, Kathrin Brockmann, Daniela Vogt-Weisenhorn, Andrea Wenninger-Weinzierl, Marita Munz, Ralf Kühn, Saskia Biskup, Florian Giesert, Natalja Funk, Thomas Gasser

المصدر: Scientific Reports, Vol 9, Iss 1, Pp 1-16 (2019)
Scientific reports 9(1), 4515 (2019). doi:10.1038/s41598-019-40808-y
Scientific Reports

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, drug effects [Neuronal Outgrowth], metabolism [Leucine-Rich Repeat Serine-Threonine Protein Kinase-2], lcsh:Medicine, pharmacology [Fibroblast Growth Factors], Mice, 0302 clinical medicine, cytology [Fibroblasts], Insulin, Phosphorylation, lcsh:Science, pharmacology [Insulin], Glucose Transporter Type 4, Multidisciplinary, Kinase, Parkinson Disease, LRRK2, metabolism [rab GTP-Binding Proteins], Cell biology, ddc, Intracellular signal transduction, metabolism [Proto-Oncogene Proteins c-akt], Signal transduction, Technology Platforms, metabolism [Fibroblasts], Signal Transduction, drug effects [Signal Transduction], Cell Survival, drug effects [Cell Survival], Neuronal Outgrowth, metabolism [Parkinson Disease], Biology, Leucine-rich repeat, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Animals, Humans, Protein kinase B, lcsh:R, Fibroblasts, metabolism [Glucose Transporter Type 4], pathology [Parkinson Disease], Rats, nervous system diseases, Fibroblast Growth Factors, 030104 developmental biology, rab GTP-Binding Proteins, biology.protein, genetics [Leucine-Rich Repeat Serine-Threonine Protein Kinase-2], lcsh:Q, Proto-Oncogene Proteins c-akt, ddc:600, 030217 neurology & neurosurgery, GLUT4

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e9ccd730fe7023ec1eb8e959bc4ec6fTest
http://link.springer.com/article/10.1038/s41598-019-40808-yTest

المؤلفون: Marita Munz, Christer Nilsson, Julia Fuchs, Matthew J. Farrer, Thomas Gasser, Mary M. Hulihan, Owen A. Ross, Elna-Marie Larsson, Frank A. Middleton, Birgitt Schüle, Jennifer M. Kachergus, J. W. Langston

المساهمون: Centre interdisciplinaire de recherche en biologie (CIRB), Labex MemoLife, École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Collège de France (CdF (institution))-Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris (ESPCI Paris), Université Paris sciences et lettres (PSL)-École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Neurology
Neurology, American Academy of Neurology, 2007, 68 (12), pp.916-922. ⟨10.1212/01.wnl.0000254458.17630.c5⟩
Fuchs, J, Nilsson, C, Kachergus, J, Munz, M, Larsson, E-M, Schüle, B, Langston, J W, Middleton, F A, Ross, O A, Hulihan, M, Gasser, T & Farrer, M J 2007, ' Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication. ', Neurology, vol. 68, no. 12, pp. 916-22 . https://doi.org/10.1212/01.wnl.0000254458.17630.c5Test

مصطلحات موضوعية: Male, Proband, [SDV]Life Sciences [q-bio], DNA Mutational Analysis, Gene Dosage, Disease, MESH: Gene Dosage, 0302 clinical medicine, Gene duplication, MESH: Blood Proteins, MESH: DNA Mutational Analysis, Oligonucleotide Array Sequence Analysis, MESH: Aged, Genetics, 0303 health sciences, MESH: Middle Aged, MESH: Genetic Testing, medicine.diagnostic_test, Genetic Screening, Parkinsonism, MESH: Genetic Predisposition to Disease, Blood Proteins, Middle Aged, MESH: Autonomic Nervous System Diseases, MESH: Dementia, Pedigree, Phenotype, MESH: Sweden, alpha-Synuclein, Female, Chromosomes, Human, Pair 4, Adult, MESH: Chromosomes, Human, Pair 4, MESH: Mutation, MESH: Pedigree, Biology, MESH: Phenotype, MESH: Tomography, Emission-Computed, Single-Photon, 03 medical and health sciences, Parkinsonian Disorders, Spect imaging, MESH: alpha-Synuclein, medicine, Humans, MESH: Americas, Dementia, Genetic Predisposition to Disease, Genetic Testing, Genotyping, Aged, 030304 developmental biology, Genetic testing, Sweden, Tomography, Emission-Computed, Single-Photon, MESH: Genealogy and Heraldry, MESH: Humans, MESH: Parkinsonian Disorders, MESH: Adult, medicine.disease, MESH: Male, Autonomic Nervous System Diseases, Mutation, MESH: Oligonucleotide Array Sequence Analysis, MESH: Microsatellite Repeats, Neurology (clinical), Americas, MESH: Female, 030217 neurology & neurosurgery, Genealogy and Heraldry, Microsatellite Repeats

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85d02631bf570a5de135ebc514256058Test
https://doi.org/10.1212/01.wnl.0000254458.17630.c5Test

المؤلفون: Kathrin Brockmann, Eva Schaeffer, T. Gasser, Claudia Schulte, Andrea Pilotto, Matthis Synofzik, Marita Munz, Ulrike Suenkel, Daniela Berg, Saskia Biskup, Walter Maetzler, Karin Srulijes, Ann-Kathrin Hauser

المصدر: European journal of neurology 23(3), 520-526 (2015). doi:10.1111/ene.12894

مصطلحات موضوعية: 0301 basic medicine, Oncology, Male, Pathology, physiopathology [Supranuclear Palsy, Progressive], genetics [Basal Ganglia Diseases], Disease, physiopathology [Frontotemporal Dementia], genetics [Glucosylceramidase], Primary progressive aphasia, C9orf72 expansion, 0302 clinical medicine, physiopathology [Aphasia, Primary Progressive], C9orf72, Supranuclear Palsy, genetics [Frontotemporal Dementia], genetics [Aphasia, Primary Progressive], Parkinsonism, genetics [Supranuclear Palsy, Progressive], Middle Aged, Corticobasal syndrome, Phenotype, Neurology, Frontotemporal Dementia, Glucosylceramidase, GBA, Female, Supranuclear Palsy, Progressive, Frontotemporal dementia, physiopathology [Basal Ganglia Diseases], medicine.medical_specialty, Primary Progressive, Progressive supranuclear palsy, 03 medical and health sciences, Progressive, Basal Ganglia Diseases, Internal medicine, medicine, Aphasia, Dementia, Humans, ddc:610, Aged, Synucleinopathies, business.industry, medicine.disease, 030104 developmental biology, Aphasia, Primary Progressive, Mutation, Neurology (clinical), business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7659a9e241aa0495db97bc08cdb4684cTest
https://pubmed.ncbi.nlm.nih.gov/26549049Test

المؤلفون: Marita Munz, Joerg Hennenlotter, Igor Tsaur, Ursula Kuehs, Elsie Oppermann, David Schilling, Arnulf Stenzl

المصدر: Cancer biomarkers : section A of Disease markers. 15(3)

مصطلحات موضوعية: PCA3, Male, Cancer Research, medicine.medical_specialty, Pathology, Adenocarcinoma, Real-Time Polymerase Chain Reaction, Metastasis, Prostate cancer, Single-cell analysis, Prostate, Antigens, Neoplasm, Genetics, medicine, Biomarkers, Tumor, Humans, RNA, Messenger, Lymph node, Prostatectomy, business.industry, Micrometastasis, Prostatic Neoplasms, General Medicine, Prostate-Specific Antigen, medicine.disease, Tumor Burden, medicine.anatomical_structure, Oncology, Lymphatic Metastasis, Lymph Node Excision, Histopathology, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b5bc837f4d843edc8f7303dfb97b65bTest
https://pubmed.ncbi.nlm.nih.gov/25769446Test

المؤلفون: Lena E. Hjermind, Andreas Kupsch, Andrea A. Kühn, Thomas Gasser, Erik Dupont, Marita Munz, Farid Salih, Friedrich Asmus, Karen Østergaard

المصدر: Annals of Neurology. 58:792-797

مصطلحات موضوعية: Adult, Male, Myoclonus, Adolescent, DNA Mutational Analysis, Nonsense mutation, Gene Dosage, Biology, medicine.disease_cause, Gene dosage, Exon, SGCE, Sarcoglycans, medicine, Humans, RNA, Messenger, Family Health, Genetics, Mutation, Reverse Transcriptase Polymerase Chain Reaction, Genetic heterogeneity, Exons, Stop codon, Pedigree, genomic DNA, Neurology, Dystonic Disorders, Female, Neurology (clinical), Gene Deletion

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a60c4eab35aed7db22f9b1d3c2cbfd5eTest
https://doi.org/10.1002/ana.20661Test

المؤلفون: Igor, Tsaur, Markus, Renninger, Joerg, Hennenlotter, Elsie, Oppermann, Marita, Munz, Ursula, Kuehs, Arnulf, Stenzl, David, Schilling

المصدر: Anticancer research. 33(12)

مصطلحات موضوعية: Adult, Male, Genes, Essential, Lymphatic Metastasis, Humans, Prostatic Neoplasms, Middle Aged, Real-Time Polymerase Chain Reaction, Aged

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::62fe0b8d19d57c88e3b76def24eae74fTest
https://pubmed.ncbi.nlm.nih.gov/24324056Test

المؤلفون: Marita Munz, Saskia Biskup, Dennis Döcker, Deborah Bartholdi, Christiane Spaich, M. Menzel, Max Schubach

مصطلحات موضوعية: medicine.medical_specialty, Genotype, Nonsense mutation, Rett syndrome, Biology, Bioinformatics, Article, Angelman syndrome, Gene Order, Genetics, medicine, Humans, Exome, Genetics (clinical), Exome sequencing, Genetic Association Studies, Facies, Matrix Attachment Region Binding Proteins, Sequence Analysis, DNA, medicine.disease, Fragile X syndrome, Phenotype, Genetic Loci, Child, Preschool, Chromosomes, Human, Pair 2, Mutation, Medical genetics, Female, Chromosome Deletion, Haploinsufficiency, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f5dc8be87e9ff343c5eceae2ad47ec2Test
https://europepmc.org/articles/PMC4350596Test/