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Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 2/2018, Volume 75, Issue 3, pp. 527 - 546
The survival of motor neuron (SMN) protein plays an essential role in the biogenesis of spliceosomal snRNPs and the molecular assembly of Cajal bodies (CBs).... 
Biomedicine, general | Biochemistry, general | Cajal bodies | Nuclear speckles | SMN interactome | SMA | SMN complex | Cell Biology | Life Sciences | CBP | Life Sciences, general | Protein acetylation | SMN | HDAC inhibitor | SnRNP | P53 ACETYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | MOUSE-MODEL | AMYOTROPHIC-LATERAL-SCLEROSIS | DISEASE MECHANISMS | MOTOR-NEURON PROTEIN | CELL BIOLOGY | MESSENGER-RNAS | NUCLEAR-BODIES | PREMATURE SENESCENCE | SPINAL MUSCULAR-ATROPHY | PROMYELOCYTIC LEUKEMIA | MCF-7 Cells | Humans | Cells, Cultured | HEK293 Cells | Coiled Bodies - metabolism | Cytoplasm - metabolism | Protein Processing, Post-Translational | Acetylation | Cyclic AMP Response Element-Binding Protein - physiology | Protein Transport | SMN Complex Proteins - metabolism | Nervous system diseases | Lysine | Oncology, Experimental | Leukemia | Biosynthesis | Research | Binding proteins | Cells | Cancer | Protein binding | Histone deacetylase | Chromatin | Diffusion rate | Ribonucleoproteins (small nuclear) | SMN protein | Gene deletion | Spinal muscular atrophy | Proteins | Atrophy | Promyeloid leukemia | CREB-binding protein | Clonal deletion | Deletion | Evolution | Degeneration | Acetyltransferase | Localization | Motor neurons | Cell survival | Splicing | Radioactive half-life | Cyclic AMP response element-binding protein | Mutation | Index Medicus
Journal Article
Translational Neuroscience, ISSN 2081-3856, 01/2017, Volume 8, Issue 1, pp. 1 - 6
Journal Article
Journal Article
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 | Muscular system | Cellular biology | Neurological disorders | SMN1 gene | spinal muscular atrophy | Smn protein | Heterogeneous-nuclear ribonucleoprotein R | Index Medicus | SMA; SMN; RNA transport; β-actin; hnRNP R
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 06/2012, Volume 32, Issue 25, pp. 8703 - 8715
Journal Article
SCIENTIFIC REPORTS, ISSN 2045-2322, 03/2019, Volume 9, Issue 1, pp. 3701 - 14
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterized by the degeneration of spinal motor neurons and muscle atrophy.... 
SURVIVAL | DEFECTS | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | DISEASE | PHENOTYPE | MICE | SMN GENE | ASTROGENESIS | SMN-DELTA-7 | ONSET | Atrophy | Motor neurons | Spinal cord | Cell survival | Astrocytes | SMN protein | Degeneration | Spinal muscular atrophy | Hereditary diseases
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2013, Volume 110, Issue 48, pp. 19348 - 19353
Journal Article