| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2014PLoSO...9j5933M |
| P356 | DOI | 10.1371/JOURNAL.PONE.0105933 |
| P932 | PMC publication ID | 4146563 |
| P698 | PubMed publication ID | 25162227 |
| P5875 | ResearchGate publication ID | 265134947 |
| P50 | author | Kay Davies | Q6380176 |
| Tom Lickiss | Q57903314 | ||
| Mattéa J Finelli | Q59684553 | ||
| Zoltán Molnár | Q41787890 | ||
| P2093 | author name string | Sheena Lee | |
| Justin M Moore | |||
| 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 |
| Interaction between LIS1 and doublecortin, two lissencephaly gene products | Q24290295 | ||
| Physical association and coordinate function of the H3 K4 methyltransferase MLL1 and the H4 K16 acetyltransferase MOF | Q24305335 | ||
| Acute mixed-lineage leukemia t(4;11)(q21;q23) generates an MLL-AF4 fusion product | Q24310468 | ||
| Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4 | Q24311907 | ||
| 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 | ||
| Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island | Q24324761 | ||
| BRCA1 is a component of the RNA polymerase II holoenzyme | Q24675704 | ||
| MDGAs interact selectively with neuroligin-2 but not other neuroligins to regulate inhibitory synapse development | Q26269867 | ||
| The AFF4 scaffold binds human P-TEFb adjacent to HIV Tat | Q27676733 | ||
| Loss of FMR2 further emphasizes the link between deregulation of immediate early response genes FOS and JUN and intellectual disability | Q28116032 | ||
| Altered lymphoid development in mice deficient for the mAF4 proto-oncogene | Q73971545 | ||
| Identification of the novel AML1 fusion partner gene, LAF4, a fusion partner of MLL, in childhood T-cell acute lymphoblastic leukemia with t(2;21)(q11;q22) by bubble PCR method for cDNA | Q81516051 | ||
| The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling | Q40202913 | ||
| New insights to the MLL recombinome of acute leukemias | Q44945193 | ||
| Association analysis of schizophrenia on 18 genes involved in neuronal migration: MDGA1 as a new susceptibility gene | Q45138440 | ||
| A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse. | Q48256073 | ||
| The mouse Laf4 gene: exon/intron organization, cDNA sequence, alternative splicing, and expression during central nervous system development. | Q48571316 | ||
| Examining the relationship between early axon growth and transcription factor expression in the developing cerebral cortex | Q48733418 | ||
| Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressing FRAXE. | Q48797273 | ||
| Expression of Leukaemia associated transcription factor Af9/Mllt3 in the cerebral cortex of the mouse | Q48832169 | ||
| The MDGA1 gene confers risk to schizophrenia and bipolar disorder | Q48949086 | ||
| c-Jun N-terminal kinase phosphorylation of MARCKSL1 determines actin stability and migration in neurons and in cancer cells | Q28270073 | ||
| Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism | Q28292730 | ||
| Misguided transcriptional elongation causes mixed lineage leukemia | Q28471927 | ||
| Infertility with defective spermiogenesis in mice lacking AF5q31, the target of chromosomal translocation in human infant leukemia | Q28513902 | ||
| RNAi reveals doublecortin is required for radial migration in rat neocortex | Q28567912 | ||
| Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue | Q28569828 | ||
| Interaction between autism-linked MDGAs and neuroligins suppresses inhibitory synapse development | Q28571273 | ||
| Radial migration of superficial layer cortical neurons controlled by novel Ig cell adhesion molecule MDGA1 | Q28584932 | ||
| IgSF molecule MDGA1 is involved in radial migration and positioning of a subset of cortical upper-layer neurons | Q28585324 | ||
| Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice | Q28586975 | ||
| Neuronal subtype specification in the cerebral cortex | Q29616190 | ||
| Increased LIS1 expression affects human and mouse brain development | Q30639738 | ||
| Fusion of an AF4-related gene, LAF4, to MLL in childhood acute lymphoblastic leukemia with t(2;11)(q11;q23) | Q30792869 | ||
| Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes | Q33474877 | ||
| AF4 is a critical regulator of the IGF-1 signaling pathway during Purkinje cell development. | Q33518246 | ||
| Characterisation and expression of a large, 13.7 kb FMR2 isoform | Q33858233 | ||
| Heterogeneity in ventricular zone neural precursors contributes to neuronal fate diversity in the postnatal neocortex. | Q34019012 | ||
| Functional characterization of the AFF (AF4/FMR2) family of RNA-binding proteins: insights into the molecular pathology of FRAXE intellectual disability | Q34025778 | ||
| Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13. | Q34059516 | ||
| LAF4, an AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia | Q34146868 | ||
| LAF-4 is aberrantly expressed in human breast cancer | Q34392980 | ||
| 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 | ||
| Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1). | Q34468937 | ||
| Rostral growth of commissural axons requires the cell adhesion molecule MDGA2. | Q35040124 | ||
| FRA2A is a CGG repeat expansion associated with silencing of AFF3 | Q35156954 | ||
| Function of leukemogenic mixed lineage leukemia 1 (MLL) fusion proteins through distinct partner protein complexes | Q35229311 | ||
| FMR2 function: insight from a mouse knockout model | Q35550087 | ||
| Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicap. | Q35889234 | ||
| The robotic mouse: unravelling the function of AF4 in the cerebellum | Q36328456 | ||
| A role for the MLL fusion partner ENL in transcriptional elongation and chromatin modification | Q36447915 | ||
| H3K79 methylation profiles define murine and human MLL-AF4 leukemias | Q36991857 | ||
| Mediation of Af4 protein function in the cerebellum by Siah proteins | Q37570724 | ||
| Regulation of the development of tectal neurons and their projections by transcription factors Brn3a and Pax7. | Q38619768 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| ImageQuant | Q112270642 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | disability | Q12131 |
| intellectual disability | Q183560 | ||
| cell migration | Q189092 | ||
| disability affecting intellectual abilities | Q3317827 | ||
| AF4/FMR2 family, member 3 | Q21496854 | ||
| MAM domain containing glycosylphosphatidylinositol anchor 2 | Q21986124 | ||
| P304 | page(s) | e105933 | |
| P577 | publication date | 2014-08-27 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Laf4/Aff3, a gene involved in intellectual disability, is required for cellular migration in the mouse cerebral cortex | |
| P478 | volume | 9 |
| Q37393891 | A sequence variant associating with educational attainment also affects childhood cognition |
| Q35905777 | Combined transcriptome studies identify AFF3 as a mediator of the oncogenic effects of β-catenin in adrenocortical carcinoma |
| Q92461031 | De novo AFF3 variant in a patient with mesomelic dysplasia with foot malformation |
| Q37417813 | FoxO6 affects Plxna4-mediated neuronal migration during mouse cortical development. |
| Q90442613 | Genes regulated by SATB2 during neurodevelopment contribute to schizophrenia and educational attainment |
| Q92352998 | Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis |
| Q26770788 | Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development |
| Q64067342 | Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population |
| Q47904811 | Using Human iPSC-Derived Neurons to Uncover Activity-Dependent Non-Coding RNAs. |
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