Neuronal Nuclear Membrane Budding Occurs during a Developmental Window Modulated by Torsin Paralogs.
暂无分享,去创建一个
[1] Caterina Strambio-De-Castilla. Jumping over the fence: RNA nuclear export revisited , 2017 .
[2] P. Verstreken,et al. Torsins Are Essential Regulators of Cellular Lipid Metabolism. , 2016, Developmental cell.
[3] W. Dauer,et al. A novel conditional knock-in approach defines molecular and circuit effects of the DYT1 dystonia mutation. , 2015, Human molecular genetics.
[4] C. Cepeda,et al. Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons , 2015, eLife.
[5] E. Laudermilch,et al. The Torsin Activator LULL1 Is Required for Efficient Growth of Herpes Simplex Virus 1 , 2015, Journal of Virology.
[6] Lesilee S. Rose,et al. A novel function for the Caenorhabditis elegans torsin OOC-5 in nucleoporin localization and nuclear import , 2015, Molecular biology of the cell.
[7] L. Servais,et al. Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1 , 2014, Orphanet Journal of Rare Diseases.
[8] Jimin Wang,et al. The mechanism of Torsin ATPase activation , 2014, Proceedings of the National Academy of Sciences.
[9] H. Ploegh,et al. How lamina-associated polypeptide 1 (LAP1) activates Torsin , 2014, eLife.
[10] W. Dauer,et al. TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration. , 2014, The Journal of clinical investigation.
[11] W. Dauer,et al. Nuclear envelope breakdown induced by herpes simplex virus type 1 involves the activity of viral fusion proteins. , 2014, Virology.
[12] M. Moore,et al. Torsin mediates primary envelopment of large ribonucleoprotein granules at the nuclear envelope. , 2013, Cell reports.
[13] M. Eisele,et al. Regulation of Torsin ATPases by LAP1 and LULL1 , 2013, Proceedings of the National Academy of Sciences.
[14] M. Moore,et al. Nuclear Envelope Budding Enables Large Ribonucleoprotein Particle Export during Synaptic Wnt Signaling , 2012, Cell.
[15] W. Dauer,et al. Genetic Background Modulates the Phenotype of a Mouse Model of DYT1 Dystonia , 2012, PloS one.
[16] R. Goodchild,et al. The nuclear envelope localization of DYT1 dystonia torsinA-ΔE requires the SUN1 LINC complex component , 2011, BMC Cell Biology.
[17] David A Lewis,et al. Postnatal developmental trajectories of neural circuits in the primate prefrontal cortex: identifying sensitive periods for vulnerability to schizophrenia. , 2011, Schizophrenia bulletin.
[18] M. Hetzer,et al. Nuclear pore biogenesis into an intact nuclear envelope , 2010, Chromosoma.
[19] Philip Shaw,et al. Childhood psychiatric disorders as anomalies in neurodevelopmental trajectories , 2010, Human brain mapping.
[20] Mark Ellisman,et al. A molecular mechanism underlying the neural-specific defect in torsinA mutant mice , 2010, Proceedings of the National Academy of Sciences.
[21] Rose E Goodchild,et al. Relative tissue expression of homologous torsinB correlates with the neuronal specific importance of DYT1 dystonia-associated torsinA. , 2010, Human molecular genetics.
[22] Y. Sasai,et al. Purkinje cells originate from cerebellar ventricular zone progenitors positive for Neph3 and E-cadherin. , 2010, Developmental biology.
[23] Gabriel Wittum,et al. Synaptic Activity Induces Dramatic Changes in the Geometry of the Cell Nucleus: Interplay between Nuclear Structure, Histone H3 Phosphorylation, and Nuclear Calcium Signaling , 2009, The Journal of Neuroscience.
[24] S. Siniossoglou. Lipins, Lipids and Nuclear Envelope Structure , 2009, Traffic.
[25] S. Dalal,et al. Interaction of TorsinA with Its Major Binding Partners Is Impaired by the Dystonia-associated ΔGAG Deletion* , 2009, The Journal of Biological Chemistry.
[26] A. Sonnenberg,et al. TorsinA binds the KASH domain of nesprins and participates in linkage between nuclear envelope and cytoskeleton , 2008, Journal of Cell Science.
[27] Pat Levitt,et al. Fetal mechanisms in neurodevelopmental disorders. , 2008, Pediatric neurology.
[28] J. Hedreen,et al. TorsinB expression in the developing human brain , 2006, Brain Research.
[29] Beat Lutz,et al. The Endocannabinoid System Controls Key Epileptogenic Circuits in the Hippocampus , 2006, Neuron.
[30] X. Breakefield,et al. Developmental patterns of torsinA and torsinB expression , 2006, Brain Research.
[31] W. Dauer,et al. Loss of the Dystonia-Associated Protein TorsinA Selectively Disrupts the Neuronal Nuclear Envelope , 2005, Neuron.
[32] Gord Fishell,et al. Math1 Is Expressed in Temporally Discrete Pools of Cerebellar Rhombic-Lip Neural Progenitors , 2005, Neuron.
[33] X. Breakefield,et al. TorsinA in the nuclear envelope. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[34] H. Paulson,et al. Aberrant Cellular Behavior of Mutant TorsinA Implicates Nuclear Envelope Dysfunction in DYT1 Dystonia , 2004, The Journal of Neuroscience.
[35] William T Dauer,et al. Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[36] T. Jessell,et al. Coordinate Regulation of Motor Neuron Subtype Identity and Pan-Neuronal Properties by the bHLH Repressor Olig2 , 2001, Neuron.
[37] J. Marth,et al. Ablation of NF1 function in neurons induces abnormal development of cerebral cortex and reactive gliosis in the brain. , 2001, Genes & development.
[38] M. Chesselet,et al. Synaptogenesis and ultrastructural localization of the polysialylated neural cell adhesion molecule in the developing striatum , 1999, The Journal of comparative neurology.
[39] Philippe Soriano. Generalized lacZ expression with the ROSA26 Cre reporter strain , 1999, Nature Genetics.
[40] N. Risch,et al. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein , 1997, Nature Genetics.
[41] R. Schneiter,et al. A yeast acetyl coenzyme A carboxylase mutant links very-long-chain fatty acid synthesis to the structure and function of the nuclear membrane-pore complex , 1996, Molecular and cellular biology.
[42] D. Gottlieb,et al. Retinoic acid promotes neural and represses mesodermal gene expression in mouse embryonic stem cells in culture. , 1996, Biochemical and biophysical research communications.
[43] R. Wepf,et al. Nic96p is required for nuclear pore formation and functionally interacts with a novel nucleoporin, Nup188p , 1996, The Journal of cell biology.
[44] M. Rieger,et al. A Novel Complex of Nucleoporins, Which Includes Sec13p and a Sec13p Homolog, Is Essential for Normal Nuclear Pores , 1996, Cell.
[45] G. Blobel,et al. NUP145 encodes a novel yeast glycine-leucine-phenylalanine-glycine (GLFG) nucleoporin required for nuclear envelope structure , 1994, The Journal of cell biology.
[46] D. Szőllősi,et al. 'Blebbing' of the nuclear envelope of mouse zygotes, early embryos and hybrid cells. , 1988 .
[47] J W Sedat,et al. Three-dimensional organization of Drosophila melanogaster interphase nuclei. II. Chromosome spatial organization and gene regulation , 1987, The Journal of cell biology.
[48] J W Sedat,et al. Three-dimensional organization of Drosophila melanogaster interphase nuclei. I. Tissue-specific aspects of polytene nuclear architecture , 1987, The Journal of cell biology.
[49] R. Burke,et al. Delayed-onset dystonia in patients with "static" encephalopathy. , 1980, Journal of neurology, neurosurgery, and psychiatry.
[50] L. Deaven,et al. Investigation of the determinants of nuclear pore number. , 1980, Cytogenetics and cell genetics.
[51] V. Mareš,et al. Nuclear pore complexes in cells of the developing mouse cerebral cortex. , 1978, Acta histochemica.
[52] D. Szőllősi,et al. EXTRUSION OF NUCLEOLI FROM PRONUCLEI OF THE RAT , 1965, The Journal of cell biology.
[53] H. Swift,et al. NUCLEAR EXTRUSION AND INTRACISTERNAL INCLUSIONS IN THE RABBIT BLASTOCYST , 1962, The Journal of cell biology.
[54] W. Clark. Electron Microscope Studies of Nuclear Extrusions in Pancreatic Acinar Cells of the Rat , 1960, The Journal of biophysical and biochemical cytology.
[55] H. Gay. Nucleocytoplasmic relations in Drosophila. , 1956, Cold Spring Harbor symposia on quantitative biology.