| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2004PNAS..10114901O |
| P356 | DOI | 10.1073/PNAS.0406196101 |
| P932 | PMC publication ID | 522018 |
| P698 | PubMed publication ID | 15459319 |
| P5875 | ResearchGate publication ID | 8256845 |
| P50 | author | Kay Davies | Q6380176 |
| P2093 | author name string | Emmanuelle Bitoun | |
| Emma L Jones | |||
| Joanne Clark | |||
| Peter L Oliver | |||
| P2860 | cites work | AF5q31, a newly identified AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia with ins(5;11)(q31;q13q23) | Q22010909 |
| Siah-1 facilitates ubiquitination and degradation of synphilin-1 | Q24295130 | ||
| Acute mixed-lineage leukemia t(4;11)(q21;q23) generates an MLL-AF4 fusion product | Q24310468 | ||
| LAF-4 encodes a lymphoid nuclear protein with transactivation potential that is homologous to AF-4, the gene fused to MLL in t(4;11) leukemias | Q24316133 | ||
| Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway | Q24318831 | ||
| Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island | Q24324761 | ||
| p53-inducible human homologue of Drosophila seven in absentia (Siah) inhibits cell growth: suppression by BAG-1. | Q24533238 | ||
| Siah-1 N-terminal RING domain is required for proteolysis function, and C-terminal sequences regulate oligomerization and binding to target proteins | Q24554569 | ||
| Siah ubiquitin ligase is structurally related to TRAF and modulates TNF-alpha signaling | Q27636810 | ||
| A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation | Q28115658 | ||
| Themes and variations on ubiquitylation | Q28206411 | ||
| Regulation of synaptophysin degradation by mammalian homologues of seven in absentia | Q28215219 | ||
| Exon/intron structure of the human AF-4 gene, a member of the AF-4/LAF-4/FMR-2 gene family coding for a nuclear protein with structural alterations in acute leukaemia | Q28244456 | ||
| Interaction of AF4 wild-type and AF4.MLL fusion protein with SIAH proteins: indication for t(4;11) pathobiology? | Q28268824 | ||
| Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice | Q28586975 | ||
| Domains with transcriptional regulatory activity within the ALL1 and AF4 proteins involved in acute leukemia | Q33652400 | ||
| Characterisation and expression of a large, 13.7 kb FMR2 isoform | Q33858233 | ||
| p53 suppresses the c-Myb-induced activation of heat shock transcription factor 3. | Q33896669 | ||
| Insights from mouse models into the molecular basis of neurodegeneration | Q33938799 | ||
| Fragile XE-associated familial mental retardation protein 2 (FMR2) acts as a potent transcription activator | Q33946912 | ||
| Modulation of transforming growth factor beta (TGFbeta)/Smad transcriptional responses through targeted degradation of TGFbeta-inducible early gene-1 by human seven in absentia homologue | Q34134107 | ||
| Identification of the gene FMR2, associated with FRAXE mental retardation | Q34385889 | ||
| Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators | Q34439319 | ||
| Expression of the murine homologue of FMR2 in mouse brain and during development | Q34456606 | ||
| Seven in absentia homolog 1A mediates ubiquitination and degradation of group 1 metabotropic glutamate receptors | Q34513871 | ||
| A binding motif for Siah ubiquitin ligase. | Q34866593 | ||
| Mouse Models of Human CAG Repeat Disorders | Q41527091 | ||
| Neurodegeneration in Lurcher mice caused by mutation in delta2 glutamate receptor gene | Q48045866 | ||
| A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse. | Q48256073 | ||
| Isolation and characterisation of murine homologues of the Drosophila seven in absentia gene (sina). | Q52545500 | ||
| Altered lymphoid development in mice deficient for the mAF4 proto-oncogene | Q73971545 | ||
| P433 | issue | 41 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 14901-14906 | |
| P577 | publication date | 2004-09-30 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Mediation of Af4 protein function in the cerebellum by Siah proteins | |
| P478 | volume | 101 |
| Q33518246 | AF4 is a critical regulator of the IGF-1 signaling pathway during Purkinje cell development. |
| Q84383056 | Animal models of human cerebellar ataxias: a cornerstone for the therapies of the twenty-first century |
| Q33285195 | Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease |
| Q90167898 | DBC1, p300, HDAC3, and Siah1 coordinately regulate ELL stability and function for expression of its target genes |
| Q28076446 | Disorders of Transcriptional Regulation: An Emerging Category of Multiple Malformation Syndromes |
| Q35236310 | Germline gain-of-function mutations in AFF4 cause a developmental syndrome functionally linking the super elongation complex and cohesin |
| Q28513902 | Infertility with defective spermiogenesis in mice lacking AF5q31, the target of chromosomal translocation in human infant leukemia |
| Q35232809 | Laf4/Aff3, a gene involved in intellectual disability, is required for cellular migration in the mouse cerebral cortex |
| Q33383191 | Mecp2-null mice provide new neuronal targets for Rett syndrome. |
| Q38161393 | Molecular and Epigenetic Mechanisms of MLL in Human Leukemogenesis |
| Q30463349 | New insights into behaviour using mouse ENU mutagenesis |
| Q33901300 | Protein network study of human AF4 reveals its central role in RNA Pol II-mediated transcription and in phosphorylation-dependent regulatory mechanisms. |
| Q28590290 | Proteolysis of AKAP121 regulates mitochondrial activity during cellular hypoxia and brain ischaemia |
| Q40147483 | Siah-1S, a novel splice variant of Siah-1 (seven in absentia homolog), counteracts Siah-1-mediated downregulation of beta-catenin |
| Q24313326 | Structural analysis of Siah1-Siah-interacting protein interactions and insights into the assembly of an E3 ligase multiprotein complex |
| Q41352951 | TBP loading by AF4 through SL1 is the major rate-limiting step in MLL fusion-dependent transcription |
| Q40202913 | The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling |
| Q37429914 | The robotic mouse: understanding the role of AF4, a cofactor of transcriptional elongation and chromatin remodelling, in purkinje cell function |
| Q36328456 | The robotic mouse: unravelling the function of AF4 in the cerebellum |
| Q35990164 | The ubiquitin ligase Siah1 controls ELL2 stability and formation of super elongation complexes to modulate gene transcription |
| Q33813039 | The ubiquitin ligase Siah2 and the hypoxia response |
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