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Disease Info Card
Alpha-thalassemia/mental Retardation Syndrome, Nondeletion Type, X-linked
Information about Alpha-thalassemia/mental Retardation Syndrome, Nondeletion Type, X-linked: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Alpha-thalassemia/mental Retardation Syndrome, Nondeletion Type, X-linked
Most recent studies have shown that Alpha-thalassemia/mental Retardation Syndrome, Nondeletion Type, X-linked shares some biological mechanisms with acute-promyelocytic-leukemia, alpha-thalassemia, anemia, congenital-anomaly-of-face, dwarfism, dysmyelopoietic-syndromes, embryonic-mosaic, epilepsy, juberg-marsidi-syndrome, leukemia, microcephaly, muscle-hypotonia, severe-mental-retardation, thalassemia, urogenital-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Alpha-thalassemia/mental Retardation Syndrome, Nondeletion Type, X-linked, and have been seen in publications frequently: Atp-dependent Chromatin Remodeling, Brain Development, Cell Cycle, Cell Division, Chromatin Remodeling, Chromosome Breakage, Chromosome Segregation, Dna Recombination, Dna Repair, Histone Methylation, Interphase, Localization, M Phase, Meiosis, Methylation, Mitosis, Pathogenesis, Primary Follicle Stage, Regulation Of Gene Expression, Spermatogenesis
Quite a number of genes have been found to play important roles in Alpha-thalassemia/mental Retardation Syndrome, Nondeletion Type, X-linked, such as AR, ARHGAP26, ATR, ATRX, CHD3, DNMT3B, GRIA1, HBA1, HNF1A, MTSS1, NPRL3, NSD1, OPN1LW, PAG1, PML, SMARCA1, SMARCA2, SMARCA4, TMEFF2. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.