Functional divergence of the two Elongator subcomplexes during neurodevelopment
暂无分享,去创建一个
Melissa J. Davis | E. Eichler | D. Nickerson | V. Chau | M. Bellingham | B. Wainwright | Marija Kojic | S. Glatt | M. Piper | A. Biela | S. Mercimek-Andrews | A. Ünalp | S. Cingöz | P. Indyka | Handan Güleryüz | A. Kościelniak | M. Gaik | M. Rawski | Sazia Sharmin | Alun Jones | Megan R Stegeman | Tülay Öncü-Öner | Ahmed Mohamed | P. Y. S. Chau | A. Chramiec-Głąbik | Dominika Dobosz | Amanda Millar | N. Abbassi | Konrad Jazgar | Handan Güleryüz | Monika Gaik
[1] A. Brazma,et al. The PRIDE database resources in 2022: a hub for mass spectrometry-based proteomics evidences , 2021, Nucleic Acids Res..
[2] L. Vissers,et al. Genetic convergence of developmental and epileptic encephalopathies and intellectual disability , 2021, Developmental medicine and child neurology.
[3] Melissa J. Davis,et al. Elp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotype , 2021, Nature Communications.
[4] Wenjun Tan,et al. The Correlation of ELP4-PAX6 With Rolandic Spike Sources in Idiopathic Rolandic Epilepsy Syndromes , 2021, Frontiers in Neurology.
[5] Jacqueline Peng,et al. Multiplex gene and phenotype network to characterize shared genetic pathways of epilepsy and autism , 2021, Scientific reports.
[6] P. Jin,et al. The Emerging Neuroepitranscriptome , 2021, Epitranscriptomics.
[7] S. Cuevas-Covarrubias,et al. Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case report , 2020, World journal of clinical cases.
[8] Conrad C. Huang,et al. UCSF ChimeraX: Structure visualization for researchers, educators, and developers , 2020, Protein science : a publication of the Protein Society.
[9] Melissa J. Davis,et al. MSImpute: Imputation of label-free mass spectrometry peptides by low-rank approximation , 2020, bioRxiv.
[10] S. Gräf,et al. Eukaryotic life without tQCUG: the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum , 2020, Nucleic acids research.
[11] G. Novarino,et al. Neurodevelopmental Disorders: From Genetics to Functional Pathways , 2020, Trends in Neurosciences.
[12] F. Hormozdiari,et al. Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders , 2019, Genome Medicine.
[13] Gennady Korotkevich,et al. Fast gene set enrichment analysis , 2019, bioRxiv.
[14] J. Sled,et al. Aged hind-limb clasping experimental autoimmune encephalomyelitis models aspects of the neurodegenerative process seen in multiple sclerosis , 2019, Proceedings of the National Academy of Sciences.
[15] C. Müller,et al. Molecular basis of tRNA recognition by the Elongator complex , 2019, Science Advances.
[16] J. P. Clement,et al. Understanding intellectual disability and autism spectrum disorders from common mouse models: synapses to behaviour , 2019, Open Biology.
[17] S. Glatt,et al. The Elongator subunit Elp3 is a non-canonical tRNA acetyltransferase , 2019, Nature Communications.
[18] S. Glatt,et al. Roles of Elongator Dependent tRNA Modification Pathways in Neurodegeneration and Cancer , 2018, Genes.
[19] P. Sah,et al. Elongator mutation in mice induces neurodegeneration and ataxia-like behavior , 2018, Nature Communications.
[20] Whole Exome Sequencing Reveals A Mutation in ELP2 Gene in Iranian Family Suffering from Autosomal Recessive Mental Retardation , 2018 .
[21] K. Becker,et al. Elongator and codon bias regulate protein levels in mammalian peripheral neurons , 2018, Nature Communications.
[22] L. Nguyen,et al. Elongator subunit 3 (ELP3) modifies ALS through tRNA modification , 2018, Human molecular genetics.
[23] Conrad C. Huang,et al. UCSF ChimeraX: Meeting modern challenges in visualization and analysis , 2018, Protein science : a publication of the Protein Society.
[24] T. Schwede,et al. Modeling protein quaternary structure of homo- and hetero-oligomers beyond binary interactions by homology , 2017, Scientific Reports.
[25] G. Carlson,et al. The familial dysautonomia disease gene IKBKAP is required in the developing and adult mouse central nervous system , 2017, Disease Models & Mechanisms.
[26] B. Séraphin,et al. Architecture of the yeast Elongator complex , 2016, EMBO reports.
[27] B. Wainwright,et al. The Many Faces of Elongator in Neurodevelopment and Disease , 2016, Front. Mol. Neurosci..
[28] L. Nguyen,et al. Elongator controls cortical interneuron migration by regulating actomyosin dynamics , 2016, Cell Research.
[29] E. Wirrell,et al. A microRNA‐328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy , 2016, Annals of clinical and translational neurology.
[30] J. Peters,et al. biGBac enables rapid gene assembly for the expression of large multisubunit protein complexes , 2016, Proceedings of the National Academy of Sciences.
[31] Sebastian A. Leidel,et al. A Dynamic Unfolded Protein Response Contributes to the Control of Cortical Neurogenesis. , 2015, Developmental cell.
[32] D. Pinto,et al. Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation , 2015, Human mutation.
[33] Sebastian A. Leidel,et al. Optimization of Codon Translation Rates via tRNA Modifications Maintains Proteome Integrity , 2015, Cell.
[34] A. Fatemi,et al. ELP2 is a novel gene implicated in neurodevelopmental disabilities , 2015, American journal of medical genetics. Part A.
[35] Matthew E. Ritchie,et al. limma powers differential expression analyses for RNA-sequencing and microarray studies , 2015, Nucleic acids research.
[36] S. E. Dougherty,et al. Cerebellar transcriptional alterations with Purkinje cell dysfunction and loss in mice lacking PGC-1α , 2014, Front. Cell. Neurosci..
[37] Elhanan Borenstein,et al. The discovery of integrated gene networks for autism and related disorders , 2015, Genome research.
[38] A. Byström,et al. Familial dysautonomia (FD) patients have reduced levels of the modified wobble nucleoside mcm(5)s(2)U in tRNA. , 2014, Biochemical and biophysical research communications.
[39] H. Lerche,et al. Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy , 2014, Epilepsia.
[40] J. Cendelin. From mice to men: lessons from mutant ataxic mice , 2014, Cerebellum & Ataxias.
[41] Clement T Y Chan,et al. Quantitative analysis of ribonucleoside modifications in tRNA by HPLC-coupled mass spectrometry , 2014, Nature Protocols.
[42] K. Anand,et al. Hippocampus in health and disease: An overview , 2012, Annals of Indian Academy of Neurology.
[43] L. Nguyen,et al. DERP6 (ELP5) and C3ORF75 (ELP6) Regulate Tumorigenicity and Migration of Melanoma Cells as Subunits of Elongator* , 2012, The Journal of Biological Chemistry.
[44] R. Pocock,et al. Neuronal Responses to Physiological Stress , 2012, Front. Gene..
[45] Kevin W Eliceiri,et al. NIH Image to ImageJ: 25 years of image analysis , 2012, Nature Methods.
[46] P. Kind,et al. Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome. , 2012, Human molecular genetics.
[47] C. Tanner,et al. A High-Density Genome-Wide Association Screen of Sporadic ALS in US Veterans , 2012, PloS one.
[48] D. Turner,et al. Cellular Links between Neuronal Activity and Energy Homeostasis , 2012, Front. Pharmacol..
[49] B. Séraphin,et al. The Elongator subcomplex Elp456 is a hexameric RecA-like ATPase , 2012, Nature Structural &Molecular Biology.
[50] Wei Chen,et al. Deep sequencing reveals 50 novel genes for recessive cognitive disorders , 2011, Nature.
[51] J. Douglas Armstrong,et al. Bioinformatics Applications Note Systems Biology Simple Neurite Tracer: Open Source Software for Reconstruction, Visualization and Analysis of Neuronal Processes , 2022 .
[52] Robert Lalonde,et al. Brain regions and genes affecting limb-clasping responses , 2011, Brain Research Reviews.
[53] Helga Thorvaldsdóttir,et al. Molecular signatures database (MSigDB) 3.0 , 2011, Bioinform..
[54] G. Garden,et al. A Simple Composite Phenotype Scoring System for Evaluating Mouse Models of Cerebellar Ataxia , 2010, Journal of visualized experiments : JoVE.
[55] L. Nguyen,et al. Elongator Controls the Migration and Differentiation of Cortical Neurons through Acetylation of α-Tubulin , 2009, Cell.
[56] Jingyue Ju,et al. Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4) , 2009, European Journal of Human Genetics.
[57] R. Ophoff,et al. Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration , 2008, Human molecular genetics.
[58] M. Hims,et al. Loss of Mouse Ikbkap, a Subunit of Elongator, Leads to Transcriptional Deficits and Embryonic Lethality That Can Be Rescued by Human IKBKAP , 2008, Molecular and Cellular Biology.
[59] Bo Huang,et al. Elevated levels of two tRNA species bypass the requirement for elongator complex in transcription and exocytosis. , 2006, Molecular cell.
[60] Jonathan R. Whitlock,et al. Learning Induces Long-Term Potentiation in the Hippocampus , 2006, Science.
[61] Agnès Gruart,et al. Involvement of the CA3–CA1 Synapse in the Acquisition of Associative Learning in Behaving Mice , 2006, The Journal of Neuroscience.
[62] Bo Huang,et al. An early step in wobble uridine tRNA modification requires the Elongator complex. , 2005, RNA.
[63] D. Ferriero,et al. Differential vulnerability of immature murine neurons to oxygen-glucose deprivation , 2004, Experimental Neurology.
[64] W. Delano. The PyMOL Molecular Graphics System , 2002 .
[65] C Maayan,et al. Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia. , 2001, American journal of human genetics.
[66] B. Rubin,et al. Familial dysautonomia is caused by mutations of the IKAP gene. , 2001, American journal of human genetics.
[67] E. Fisher,et al. Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment , 1997, Mammalian Genome.