| P50 | author | Pietro Lo Riso | Q57058932 |
| P2093 | author name string | Vania Broccoli | |
| | Robert Jech | |
| | Sylvia Boesch | |
| | Juliane Winkelmann | |
| | Giuseppe Testa | |
| | Bernhard Haslinger | |
| | Massimiliano Caiazzo | |
| | Michael Zech | |
| | Sina Atashpaz | |
| | Pierre-Luc Germain | |
| | Erika Tenderini | |
| | Agnieszka D'Antonio-Chronowska | |
| | Giulia Barbagiovanni | |
| | Adrian Francis Stewart | |
| P2860 | cites work | YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction | Q38432867 |
| | Cooperative Binding of Transcription Factors Orchestrates Reprogramming | Q39006802 |
| | An improved Flp deleter mouse in C57Bl/6 based on Flpo recombinase | Q39699570 |
| | H3K4 Methylation-Dependent Memory of Somatic Cell Identity Inhibits Reprogramming and Development of Nuclear Transfer Embryos | Q40985261 |
| | Rapid Chromatin Switch in the Direct Reprogramming of Fibroblasts to Neurons | Q42379954 |
| | KMT2A and KMT2B Mediate Memory Function by Affecting Distinct Genomic Regions. | Q42777129 |
| | Definitive hematopoiesis requires the mixed-lineage leukemia gene | Q44805187 |
| | The epigenetic factor Kmt2a/Mll1 regulates neural progenitor proliferation and neuronal and glial differentiation | Q47074146 |
| | Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. | Q47849142 |
| | A reliable lacZ expression reporter cassette for multipurpose, knockout-first alleles | Q47867233 |
| | The histone methyltransferase Wbp7 controls macrophage function through GPI glycolipid anchor synthesis | Q47932561 |
| | Histone-methyltransferase MLL2 (KMT2B) is required for memory formation in mice. | Q48155491 |
| | Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up | Q48788624 |
| | Not All H3K4 Methylations Are Created Equal: Mll2/COMPASS Dependency in Primordial Germ Cell Specification. | Q50217919 |
| | Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations | Q50335666 |
| | Mll2 is required for H3K4 trimethylation on bivalent promoters in embryonic stem cells, whereas Mll1 is redundant. | Q50695883 |
| | A de novo paradigm for mental retardation. | Q51828800 |
| | Coactivator as a target gene specificity determinant for histone H3 lysine 4 methyltransferases | Q24305587 |
| | Menin associates with a trithorax family histone methyltransferase complex and with the hoxc8 locus | Q24313196 |
| | Direct conversion of fibroblasts to functional neurons by defined factors | Q24641912 |
| | Analysis of protein-coding genetic variation in 60,706 humans | Q26831376 |
| | Multiple epigenetic maintenance factors implicated by the loss of Mll2 in mouse development | Q28587425 |
| | Hierarchical mechanisms for direct reprogramming of fibroblasts to neurons | Q29871108 |
| | Myt1l safeguards neuronal identity by actively repressing many non-neuronal fates | Q29871111 |
| | Myogenic lineage determination and differentiation: evidence for a regulatory gene pathway | Q30462236 |
| | Increased apoptosis and skewed differentiation in mouse embryonic stem cells lacking the histone methyltransferase Mll2. | Q30479488 |
| | De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing | Q33812098 |
| | Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patients | Q34414345 |
| | Integrative Analyses of Human Reprogramming Reveal Dynamic Nature of Induced Pluripotency | Q35880090 |
| | Familial cortical myoclonus with a mutation in NOL3. | Q36200469 |
| | Dissecting direct reprogramming from fibroblast to neuron using single-cell RNA-seq | Q37056065 |
| | Chromatin remodelling factor Mll1 is essential for neurogenesis from postnatal neural stem cells | Q37238475 |
| | Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia | Q37480675 |
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 988-1001 | |
| P577 | publication date | 2018-10-01 | |
| P1433 | published in | Cell Reports | Q5058165 |
| P1476 | title | KMT2B Is Selectively Required for Neuronal Transdifferentiation, and Its Loss Exposes Dystonia Candidate Genes | |
| P478 | volume | 25 | |