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progressive motor neuronopathy (64) 64
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by Smith, Bradley N and Ticozzi, Nicola and Fallini, Claudia and Gkazi, Athina Soragia and Topp, Simon and Kenna, Kevin P and Scotter, Emma L and Kost, Jason and Keagle, Pamela and Miller, Jack W and Calini, Daniela and Vance, Caroline and Danielson, Eric W and Troakes, Claire and Tiloca, Cinzia and Al-Sarraj, Safa and Lewis, Elizabeth A and King, Andrew and Colombrita, Claudia and Pensato, Viviana and Castellotti, Barbara and de Belleroche, Jacqueline and Baas, Frank and ten Asbroek, Anneloor LMA and Sapp, Peter C and McKenna-Yasek, Diane and McLaughlin, Russell L and Polak, Meraida and Asress, Seneshaw and Esteban-Pérez, Jesús and Muñoz-Blanco, José Luis and Simpson, Michael and D’Alfonso, Sandra and Mazzini, Letizia and Comi, Giacomo P and Del Bo, Roberto and Ceroni, Mauro and Gagliardi, Stella and Querin, Giorgia and Bertolin, Cinzia and van Rheenen, Wouter and Diekstra, Frank P and Lauria, Giuseppe and Duga, Stefano and Corti, Stefania and Cereda, Cristina and Corrado, Lucia and Sorarù, Gianni and Morrison, Karen E and Williams, Kelly L and Nicholson, Garth A and Blair, Ian P and Dion, Patrick A and Leblond, Claire S and Rouleau, Guy A and Hardiman, Orla and Veldink, Jan H and van den Berg, Leonard H and Al-Chalabi, Ammar and Pall, Hardev and Shaw, Christopher E and Shaw, Pamela J and Turner, Martin R and Talbot, Kevin and Taroni, Franco and García-Redondo, Alberto and Wu, Zheyang and Glass, Jonathan D and Gellera, Cinzia and Ratti, Antonia and Brown, Robert H and Silani, Vincenzo and Landers, John E and SLAGEN Consortium
Neuron, ISSN 0896-6273, 10/2014, Volume 84, Issue 2, pp. 324 - 331
Journal Article
Trends in Genetics, ISSN 0168-9525, 2009, Volume 25, Issue 12, pp. 555 - 566
Journal Article
Journal Article
Progress in Retinal and Eye Research, ISSN 1350-9462, 2005, Volume 24, Issue 6, pp. 639 - 662
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 | SMN1 gene | spinal muscular atrophy | Smn protein | Heterogeneous-nuclear ribonucleoprotein R | SMA; SMN; RNA transport; β-actin; hnRNP R
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 12/2018, Volume 75, Issue 23, pp. 4301 - 4319
Journal Article
Journal Article