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Journal Article
Molecular and Cellular Neuroscience, ISSN 1044-7431, 07/2019, Volume 98, pp. 97 - 108
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 03/2018, Volume 115, Issue 12, pp. E2859 - E2868
Disturbed RNA processing and subcellular transport contribute to the pathomechanisms of motoneuron diseases such as amyotrophic lateral sclerosis and spinal... 
Axon | Motoneuron | HnRNP R | ICLIP | 7SK | MOTOR-NEURONS | CORD | hnRNP R | POLYMERASE-II ELONGATION | MULTIDISCIPLINARY SCIENCES | HUMAN APOLIPOPROTEIN E4 | P-TEFB | GROWTH CONES | DETERMINING GENE-PRODUCT | SPINAL MUSCULAR-ATROPHY | motoneuron | axon | ACTIN MESSENGER-RNA | iCLIP | TRANSGENIC MICE | Biological Sciences | PNAS Plus
Journal Article
Journal Article
Acta neuropathologica communications, ISSN 2051-5960, 02/2019, Volume 7, Issue 1, pp. 18 - 13
Frontotemporal lobar degeneration (FTLD) is pathologically subdivided based on the presence of particular pathological proteins that are identified in... 
Frontotemporal lobar degeneration | hnRNP Q | FUS | Heterogeneous nuclear ribonucleoprotein | hnRNP R | FTLD | METHYLATION | RNA | BINDING PROTEIN | NEUROSCIENCES | PHASE-SEPARATION | FET PROTEINS | IMPORT | SARCOMA FUS | EXPRESSION | Ethylenediaminetetraacetic acid | Proteins | Brain | Sarcoma | Pathology | Hypotheses | Disease | Pathogenesis | DNA methylation | Metabolism | Cytoplasm | Deoxyribonucleic acid--DNA
Journal Article
Journal Article
Journal Article
Frontiers in molecular biosciences, ISSN 2296-889X, 2018, Volume 5, p. 79
Heteregeneous ribonucleoproteins (hnRNPs) are a family of RNA-binding proteins that take part in all processes that involve mRNA maturation. As a consequence,... 
Journal Article
Frontiers in Molecular Biosciences, ISSN 2296-889X, 08/2018, Volume 5
Heteregeneous ribonucleoproteins (hnRNPs) are a family of RNA-binding proteins that take part in all processes that involve mRNA maturation. As a consequence,... 
Brain | HnRNP Q | Syncrip | RNA-seq | HnRNP R | Immune system | Physiological aspects | Molecular evolution | Genetic aspects | Research | Binding proteins | RNA processing | immune system | hnRNP Q | brain | hnRNP R
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 11/2003, Volume 163, Issue 4, pp. 801 - 812
Spinal muscular atrophy (SMA), a common autosomal recessive form of motoneuron disease in infants and young adults, is caused by mutations in the survival... 
Growth cones | Axons | Neurites | Messenger RNA | Neurons | Heterogeneous nuclear ribonucleoproteins | Cell lines | Actins | Antibodies | PC12 cells | β-actin | RNA transport | SMN | HnRNP R | SMA | SURVIVAL | GRY-RBP | hnRNP R | PROGRESSIVE-MOTOR-NEURONOPATHY | CYTOPLASMIC LOCALIZATION | beta-actin | BINDING PROTEIN | SNRNP BIOGENESIS | SINGLE NUCLEOTIDE | CELL-DEATH | CELL BIOLOGY | MOUSE MODEL | MISSENSE MUTATION | Spinal Cord - metabolism | Spinal Cord - growth & development | Nerve Tissue Proteins - deficiency | 3' Untranslated Regions - genetics | Cell Survival - genetics | Axons - physiology | RNA-Binding Proteins | RNA, Messenger - metabolism | PC12 Cells | Actins - genetics | Cell Differentiation - genetics | Motor Neurons - cytology | Spinal Cord - cytology | Cyclic AMP Response Element-Binding Protein | Disease Models, Animal | Nerve Tissue Proteins - physiology | Survival of Motor Neuron 1 Protein | Heterogeneous-Nuclear Ribonucleoproteins - metabolism | Rats | Mice, Transgenic | SMN Complex Proteins | Nerve Tissue Proteins - genetics | Heterogeneous-Nuclear Ribonucleoproteins - genetics | Motor Neurons - metabolism | Animals | Growth Cones - metabolism | Growth Cones - ultrastructure | Mice | SMN1 gene | spinal muscular atrophy | Smn protein | Heterogeneous-nuclear ribonucleoprotein R | SMA; SMN; RNA transport; β-actin; hnRNP R
Journal Article