KMT2A and KMT2B Mediate Memory Function by Affecting Distinct Genomic Regions - ScienceDirect
Genes | Free Full-Text | KMT2A: Umbrella Gene for Multiple Diseases
KMT2A (myeloid/lymphoid or mixed lineage leukemia)
XL MLL plus - Break Apart Probe | MetaSystems Probes
GATA3 (GATA-Binding Protein 3)/KMT2A (Lysine-Methyltransferase-2A) Complex by Increasing H3K4-3me (Trimethylated Lysine-4 of Histone-3) Upregulates NCX3 (Na+-Ca2+ Exchanger 3) Transcription and Contributes to Ischemic Preconditioning Neuroprotection ...
KMT2A rearranged acute lymphoblastic leukaemia: Unravelling the genomic complexity and heterogeneity of this high-risk disease - ScienceDirect
LSP KMT2A 3' FISH Probe - CytoTest
Biomedicines | Free Full-Text | BTK, NUTM2A, and PRPF19 Are Novel KMT2A Partner Genes in Childhood Acute Leukemia
A cryptic KMT2A-rearranged AML. The figure shows an AML with a... | Download Scientific Diagram
A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia | BMC Medical Genetics | Full Text
Family A with KMT2A-associated Wiedemann-Steiner syndrome (WSS). (a)... | Download Scientific Diagram
RUO - KMT2A / MLLT3 - ISH Probes - Molecular Pathology
Gene: KMT2A (ENSBTAG00000018093) - Summary - Bos_taurus - Ensembl genome browser 109
Genes | Free Full-Text | KMT2A: Umbrella Gene for Multiple Diseases
Acute leukemias harboring KMT2A/MLLT10 fusion: a 10‐year experience from a single genomics laboratory - Peterson - 2019 - Genes, Chromosomes and Cancer - Wiley Online Library
Protein kinase Msk1 physically and functionally interacts with the KMT2A/MLL1 methyltransferase complex and contributes to the regulation of multiple target genes | Epigenetics & Chromatin | Full Text
Genes | Free Full-Text | KMT2A: Umbrella Gene for Multiple Diseases
CytoCell MLL/MLLT3 Translocation, Dual Fusion FISH Probe | OGT
Human MLL/KMT2A gene exhibits a second breakpoint cluster region for recurrent MLL–USP2 fusions | Leukemia
KMT2A-MLLT3 Dual Fusion/Translocation FISH Probe Kit - CytoTest
XL KMT2A BA - Break Apart Probe | MetaSystems Probes
Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndrome | European Journal of Human Genetics
