• 224 Hits
  • Search Condition : Filter (MeSH = DNA-Binding Proteins / genetics*)
Species Resource Title
Human and Animal Cells CGM1(RCB0566) A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese.
Zebrafish HGj4A Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction.
Zebrafish hspGFF53A , UAS:GFP Delaying Gal4-driven gene expression in the zebrafish with morpholinos and Gal80.
C.intestinalis / (O.japonicus) Wild C. int The maternal genes Ci-p53/p73-a and Ci-p53/p73-b regulate zygotic ZicL expression and notochord differentiation in Ciona intestinalis embryos.
Yeast Condensin controls cellular RNA levels through the accurate segregation of chromosomes instead of directly regulating transcription.
Human and Animal Cells HBL-100(RCB0460) Genomic binding-site cloning reveals an estrogen-responsive gene that encodes a RING finger protein.
Mice RBRCGD000108 , RBRCGD000110 Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis.
General Microbes JCM7685 Unique Properties of the Alpha-Helical DNA-Binding Protein KfrA Encoded by the IncU Incompatibility Group Plasmid RA3 and Its Host-Dependent Role in Plasmid Maintenance.
Drosophila DGRC#114255 Paths and pathways that generate cell-type heterogeneity and developmental progression in hematopoiesis.
Drosophila DGRC#140993 TSG101 negatively regulates mitochondrial biogenesis in axons.
Drosophila GL00030 Cell competition is driven by Xrp1-mediated phosphorylation of eukaryotic initiation factor 2α.
Human and Animal Cells M10(RCB0136) Functional analysis of XRCC4 mutations in reported microcephaly and growth defect patients in terms of radiosensitivity.
Human and Animal Cells HeLa.S3 Canonical non-homologous end joining in mitosis induces genome instability and is suppressed by M-phase-specific phosphorylation of XRCC4.
Human and Animal Cells U251(RCB0461) , GI-1(RCB0763) Identification of an epigenetically silenced gene, RFX1, in human glioma cells using restriction landmark genomic scanning.
Human and Animal Cells THP-1(RCB1189) An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis.
Human and Animal Cells C2C12(RCB0987) Dietary isoflavone daidzein promotes Tfam expression that increases mitochondrial biogenesis in C2C12 muscle cells.
Human and Animal Cells HCT116(RCB2979) , HCT116-XRCC4(-/-)(RCB2981) XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency.
Zebrafish RIKEN WT A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis.
Human and Animal Cells HuH-7 Loss of FBP1 facilitates aggressive features of hepatocellular carcinoma cells through the Warburg effect.
Human and Animal Cells MG6(RCB2403) Progranulin regulates lysosomal function and biogenesis through acidification of lysosomes.