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Divide and Die: Cell Cycle Events as Triggers of Nerve Cell Death.
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- Journal of Neuroscience, 2004, v. 24, n. 42, p. 9232, doi. 10.1523/JNEUROSCI.3347-04.2004
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- Article
New member of the Snf1/AMPK kinase family, Melk, is expressed in the mouse egg and preimplantation embryo.
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- Molecular Reproduction & Development, 1997, v. 47, n. 2, p. 148, doi. 10.1002/(SICI)1098-2795(199706)47:2<148::AID-MRD4>3.0.CO;2-M
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- Article
Defects in translation-dependent quality control pathways lead to convergent molecular and neurodevelopmental pathology.
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- eLife, 2021, p. 1, doi. 10.7554/eLife.66904
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- Article
GTPBP1 resolves paused ribosomes to maintain neuronal homeostasis.
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- eLife, 2020, p. 1, doi. 10.7554/eLife.62731
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- Article
Activation of GCN2 kinase by ribosome stalling links translation elongation with translation initiation.
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- eLife, 2016, p. 1, doi. 10.7554/eLife.14295
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- Article
Synergistic integration of Netrin and ephrin axon guidance signals by spinal motor neurons.
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- eLife, 2015, p. 1, doi. 10.7554/eLife.10841
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- Article
Endothelial Unc5B controls blood-brain barrier integrity.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28785-9
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- Article
Cholesterol metabolism and Rett syndrome pathogenesis.
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- Nature Genetics, 2013, v. 45, n. 9, p. 965, doi. 10.1038/ng.2738
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- Article
Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP.
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- 2005
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- Letter
Deletion in Catna2, encoding αN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation.
- Published in:
- Nature Genetics, 2002, v. 31, n. 3, p. 279, doi. 10.1038/ng908
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- Article
The cerebellar deficient folia ( cdf ) gene acts intrinsically in Purkinje cell migrations.
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- Genesis: The Journal of Genetics & Development, 2002, v. 32, n. 1, p. 32, doi. 10.1002/gene.10024
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- Article
Notch signaling regulates UNC5B to suppress endothelial proliferation, migration, junction activity, and retinal plexus branching.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-64375-z
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- Article
Loss of Apoptosis-Inducing Factor Results in Cell-Type- Specific Neurogenesis Defects.
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- Journal of Neuroscience, 2008, v. 28, n. 19, p. 4938, doi. 10.1523/JNEUROSCI.0229-08.2008
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- Article
Motor Axon Guidance of the Mammalian Trochlear and Phrenic Nerves: Dependence on the Netrin Receptor Unc5c and Modifier Loci.
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- Journal of Neuroscience, 2006, v. 26, n. 21, p. 5756, doi. 10.1523/JNEUROSCI.0736-06.2006
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- Article
In Vivo Magnetic Resonance Imaging and Semiautomated Image Analysis Extend the Brain Phenotype for cdf/cdf Mice.
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- Journal of Neuroscience, 2006, v. 26, n. 17, p. 4455, doi. 10.1523/JNEUROSCI.5438-05.2006
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- Article
Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration.
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- Nature, 2006, v. 443, n. 7107, p. 50, doi. 10.1038/nature05096
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- Article
Unc5C and DCC act downstream of Ctip2 and Satb2 and contribute to corpus callosum formation.
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- Nature Communications, 2014, v. 5, n. 4, p. 3708, doi. 10.1038/ncomms4708
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- Article
Abnormal dispersion of a purkinje cell subset in the mouse mutant cerebellar deficient folia ( cdf).
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- Journal of Comparative Neurology, 2001, v. 436, n. 1, p. 42, doi. 10.1002/cne.1052
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- Article
The harlequin mouse mutation downregulates apoptosis-inducing factor.
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- Nature, 2002, v. 419, n. 6905, p. 367, doi. 10.1038/nature01034
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- Article
Plexin-A2 and its ligand, Sema6A, control nucleus-centrosome coupling in migrating granule cells.
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- Nature Neuroscience, 2008, v. 11, n. 4, p. 440, doi. 10.1038/nn2064
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- Article
Seryl-tRNA synthetase promotes translational readthrough by mRNA binding and involvement of the selenocysteine incorporation machinery.
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- Nucleic Acids Research, 2023, v. 51, n. 19, p. 10768, doi. 10.1093/nar/gkad773
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- Article
Regulation of ex-translational activities is the primary function of the multi-tRNA synthetase complex.
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- Nucleic Acids Research, 2021, v. 49, n. 7, p. 3603, doi. 10.1093/nar/gkaa1183
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- Article
Netrin 1-mediated chemoattraction regulates the migratory pathway of LHRH neurons.
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- European Journal of Neuroscience, 2004, v. 19, n. 1, p. 11, doi. 10.1111/j.1460-9568.2004.03094.x
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- Article
A Deficiency of Ceramide Biosynthesis Causes Cerebellar Purkinje Cell Neurodegeneration and Lipofuscin Accumulation.
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- PLoS Genetics, 2011, v. 7, n. 5, p. 1, doi. 10.1371/journal.pgen.1002063
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- Article
Alteration of the unfolded protein response modifies neurodegeneration in a mouse model of Marinesco–Sjögren syndrome.
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- Human Molecular Genetics, 2010, v. 19, n. 1, p. 25, doi. 10.1093/hmg/ddp464
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- Article
Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition.
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- Human Molecular Genetics, 2001, v. 10, n. 5, p. 433, doi. 10.1093/hmg/10.5.433
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- Article
Mouse models for the Wolf–Hirschhorn deletion syndrome.
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- Human Molecular Genetics, 2001, v. 10, n. 2, p. 91, doi. 10.1093/hmg/10.2.91
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- Article
Mouse models for the Wolf-Hirschhorn deletion syndrome.
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- Human Molecular Genetics, 2001, v. 10, n. 2, p. 91, doi. 10.1093/hmg/10.2.91
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- Article
Analysis of Expression Pattern and Genetic Deletion of Netrin5 in the Developing Mouse.
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- Frontiers in Molecular Neuroscience, 2016, p. 1, doi. 10.3389/fnmol.2016.00003
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- Article
The mouse rostral cerebellar malformation gene encodes an UNC-5-like protein.
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- Nature, 1997, v. 386, n. 6627, p. 838, doi. 10.1038/386838a0
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- Article
Mutations in the Microtubule-Associated Protein 1A (Map1a) Gene Cause Purkinje Cell Degeneration.
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- Journal of Neuroscience, 2015, v. 35, n. 11, p. 4587, doi. 10.1523/JNEUROSCI.2757-14.2015
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- Article
Loss of Clccl Results in ER Stress, Misfolded Protein Accumulation, and Neurodegeneration.
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- Journal of Neuroscience, 2015, v. 35, n. 7, p. 3001, doi. 10.1523/JNEUROSCI.3678-14.2015
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- Article
Loss of ER Chloride Channel Causes Neurodegeneration.
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- Journal of Neuroscience, 2015, v. 35, n. 7, p. i
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- Article
CHP1-Mediated NHE1 Biosynthetic Maturation Is Required for Purkinje Cell Axon Homeostasis.
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- Journal of Neuroscience, 2013, v. 33, n. 31, p. 12656, doi. 10.1523/JNEUROSCI.0406-13.2013
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- Article
The UNC5C Netrin Receptor Regulates Dorsal Guidance of Mouse Hindbrain Axons.
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- Journal of Neuroscience, 2011, v. 31, n. 6, p. 2167, doi. 10.1523/JNEUROSCI.5254-10.2011
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- Article