| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2012PLoSO...733786L |
| P356 | DOI | 10.1371/JOURNAL.PONE.0033786 |
| P932 | PMC publication ID | 3307762 |
| P698 | PubMed publication ID | 22442722 |
| P5875 | ResearchGate publication ID | 221971484 |
| P50 | author | Françoise Muscatelli | Q52097093 |
| Shalev Itzkovitz | Q88129198 | ||
| Mike Fainzilber | Q37828795 | ||
| P2093 | author name string | Marianna Tcherpakov | |
| Zehava Levy | |||
| Anat Lavi-Itzkovitz | |||
| P2860 | cites work | Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons | Q51953730 |
| Definition of a consensus transportin-specific nucleocytoplasmic transport signal | Q74638201 | ||
| Two motifs essential for nuclear import of the hnRNP A1 nucleocytoplasmic shuttling sequence M9 core | Q82456478 | ||
| Transportin-mediated Nuclear Import of Heterogeneous Nuclear RNP Proteins | Q24312051 | ||
| The Prader-Willi syndrome protein necdin interacts with the E1A-like inhibitor of differentiation EID-1 and promotes myoblast differentiation | Q24321957 | ||
| Rules for nuclear localization sequence recognition by karyopherin beta 2 | Q24600321 | ||
| Separate necdin domains bind ARNT2 and HIF1alpha and repress transcription | Q24674557 | ||
| The use of edge-betweenness clustering to investigate biological function in protein interaction networks | Q24806078 | ||
| VisANT: data-integrating visual framework for biological networks and modules | Q24812791 | ||
| Fast algorithm for detecting community structure in networks | Q27348772 | ||
| Network biology: understanding the cell's functional organization | Q27861027 | ||
| The postmitotic growth suppressor necdin interacts with a calcium-binding protein (NEFA) in neuronal cytoplasm | Q28142122 | ||
| Physical and functional interactions of neuronal growth suppressor necdin with p53 | Q28144785 | ||
| Ligand-induced internalization of the p75 neurotrophin receptor: a slow route to the signaling endosome | Q28201387 | ||
| The p75 neurotrophin receptor interacts with multiple MAGE proteins | Q28213040 | ||
| Necdin interacts with the ribonucleoprotein hnRNP U in the nuclear matrix | Q28216773 | ||
| The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse | Q28249408 | ||
| The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region | Q28253418 | ||
| The ras recruitment system, a novel approach to the study of protein-protein interactions | Q28285841 | ||
| Necdin, a Negative Growth Regulator, Is a Novel STAT3 Target Gene Down-Regulated in Human Cancer | Q28477663 | ||
| Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth | Q28508700 | ||
| Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival | Q28508839 | ||
| Nogo-A inhibits necdin-accelerated neurite outgrowth by retaining necdin in the cytoplasm | Q28584001 | ||
| Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules | Q28590634 | ||
| IntAct--open source resource for molecular interaction data | Q29617575 | ||
| Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death | Q33264123 | ||
| A novel brain-specific mRNA encoding nuclear protein (necdin) expressed in neurally differentiated embryonal carcinoma cells | Q33652807 | ||
| Keap1 regulates the oxidation-sensitive shuttling of Nrf2 into and out of the nucleus via a Crm1-dependent nuclear export mechanism | Q33836992 | ||
| Necdin protects embryonic motoneurons from programmed cell death | Q34017758 | ||
| Efficient sampling algorithm for estimating subgraph concentrations and detecting network motifs | Q34303213 | ||
| A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome | Q34326210 | ||
| The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease | Q34561533 | ||
| Multi-tasking by the p75 neurotrophin receptor: sortilin things out? | Q35911455 | ||
| Huntingtin as an essential integrator of intracellular vesicular trafficking | Q37408730 | ||
| Evolution of biomolecular networks: lessons from metabolic and protein interactions | Q37620156 | ||
| The powerful law of the power law and other myths in network biology | Q37659825 | ||
| On the death Trk. | Q37699051 | ||
| g:Profiler--a web-based toolset for functional profiling of gene lists from large-scale experiments | Q38302104 | ||
| GraphWeb: mining heterogeneous biological networks for gene modules with functional significance | Q38513822 | ||
| CCM2 mediates death signaling by the TrkA receptor tyrosine kinase | Q39799566 | ||
| EBNA3C can modulate the activities of the transcription factor Necdin in association with metastasis suppressor protein Nm23-H1. | Q39900063 | ||
| Functional domains of necdin for protein-protein interaction, nuclear matrix targeting, and cell growth suppression | Q40485094 | ||
| Ras signaling pathway for analysis of protein-protein interactions in yeast and mammalian cells | Q40593776 | ||
| Axonal transcription factors signal retrogradely in lesioned peripheral nerve | Q42554579 | ||
| Necdin regulates p53 acetylation via Sirtuin1 to modulate DNA damage response in cortical neurons | Q46407035 | ||
| Detection of functional modules from protein interaction networks. | Q47285412 | ||
| Necdin downregulates CDC2 expression to attenuate neuronal apoptosis. | Q48368860 | ||
| Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome. | Q49155367 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | e33786 | |
| P577 | publication date | 2012-03-19 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Functional consequences of necdin nucleocytoplasmic localization | |
| P478 | volume | 7 |
| Q47105992 | Characterization of MAGEG2 with testis-specific expression in mice |
| Q50892653 | Necdin Controls Proliferation and Apoptosis of Embryonic Neural Stem Cells in an Oxygen Tension-Dependent Manner |
| Q35009426 | Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders |
| Q47706180 | The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin receptor cell surface abundance through ubiquitination pathways |
| Q28078294 | The neurobiology of the Prader-Willi phenotype of fragile X syndrome |
Search more.