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69 Possible Causes for E2F3, human, protein

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  • Papillomaviridae

    In vitro cleavage of BPV L2 proteins.[] […] increasing the transcription of E2F-responsive genes, such as those encoding cdc6, PCNA, thymidine kinase, minichromosome maintenance proteins, cyclin A, cyclin E1, cdc25A, E2F2, E2F3[] Galloway DOI: 10.1128/JVI.80.10.4664-4672.2006 ABSTRACT The variable surface loops on human papillomavirus (HPV) virions required for type-specific neutralization by human[]

  • Hereditary Hypophosphatemic Rickets with Hypercalciuria

    M137 thus may uncouple sodium-phosphate cotransport, suggesting that this amino acid residue has an important functional role in human NaPi-IIc.[] KCTD1, FGF20, ANLN, EHHADH, TBX18, AGTR1, UPK3A, TRAP1, SGPL1, XPO5, FAT1, NUP205, NUP93, NUP107, ARHGAP24, SIX2, CHD1L, DSTYK, FAN1, FN1, ADCY10, MAGED2, SLC41A1, DACH1, E2F3[] Pages: 1 NPT2C Polyclonal Antibody Gene Names: NPT2C ; SLC34A3; HHRH; NPTIIc Other Names: Sodium-dependent phosphate transport protein 2C; Sodium-phosphate transport protein[]

  • Ewing Family of Tumors

    […] gene by substituting a sequence encoding a putative RNA-binding domain for that of the DNA-binding domain of the human homologue of murine Fli-1 .[] Oncogenic ETS fusions deregulate E2F3 target genes in Ewing sarcoma and prostate cancer. Genome Res. 2013; 23:1797–809. 50.[] We studied the expression of 4 tumor suppressor proteins in the Ewing family of tumors (EFTs).[]

  • Rubinstein-Taybi Syndrome

    Loss of EP300/CBP activity in humans causes a very rare congenital disorder called Rubinstein Taybi Syndrome (RSTS).[] IV Vario us cancers amp(5)(pl3) SKP2 Illa Vario us cancers amp(5)(pl3) SKP2 Illa Vario us cancers amp(6)(p22) E2F3 Illa Vario us cancers del(6q) ?[] Analyses of the entire CBP gene by the protein truncation test showed 4/37 truncating mutations.[]

  • Familial Congenital Mirror Movements 2

    Multiple protein interactions have been demonstrated for the mammalian Rad51 protein.[] EXTL1, FEN1, FHIT, FER, FES, ETV3, ERG, ESRRA, FGF1, FGF7, EZH1, ETV7, ETS2, FBXO11, EREG, ESCO1, ESPL1, FBXO8, FGF6, ETV3L, FGR, FEV, FAT3, EPHA7, PHF1, ELF3, ELF2, DVL2, E2F3[] Human RAD51 shows predominant expression in testis, ovary, and lymphoid tissue.[]

  • Retinoblastoma

    Gelb , Robust identification of mosaic variants in congenital heart disease , Human Genetics , 10.1007/s00439-018-1871-6 , 137 , 2 , (183-193) , (2018) . A. Foster, L.[] […] phosphorylates LIN52, a component of p107- and p130-assembled transcriptionally repressive DREAM complexes that control transcription during the G0/G1 phases, and the Rb-associated E2F3[] A C-terminal LxCxE motif in ORFV119 enabled the protein to interact with the retinoblastoma protein (pRb) a multifunctional protein best known for its tumor suppressor activity[]

  • B-Cell Chronic Lymphocytic Leukemia

    We have developed a protocol to expand Vδ1 and Vδ2 preferentially from human blood. We have characterized these subsets and their specificities for leukemic targets.[] C/EBPα regulated microRNA-34a targets E2F3 during granulopoiesis and is down-regulated in AML with CEBPA mutations. Blood 116(25),5638–5649 ( 2010 ).[] Different pathways were assessed for activation/expression of key signaling proteins. Data obtained were validated by Western blotting and confocal microscopy.[]

  • Congenital Afibrinogenemia

    Author information 1 Department of Genetic Medicine and Development, University of Geneva Faculty of Medicine, Geneva, Switzerland; Abstract Mutations in the human fibrinogen[] KCTD1, FGF20, ANLN, EHHADH, TBX18, AGTR1, UPK3A, TRAP1, SGPL1, XPO5, FAT1, NUP205, NUP93, NUP107, ARHGAP24, SIX2, CHD1L, DSTYK, FAN1, FN1, ADCY10, MAGED2, SLC41A1, DACH1, E2F3[] The diagnosis of hereditary heterozygous type I protein C deficiency was based on the evidence of proportional decreases of activity and antigen of plasma protein C in the[]

  • Chronic Myeloid Leukemia

    RESULT: The mRNA/protein of EphB4 was overexpressed in the DAS-resistant A2-E2 in comparison with the A1-E1 human cell lines.[] ] 5925 RB1; RB transcriptional corepressor 1 [KO: K06618 ] 1869 E2F1; E2F transcription factor 1 [KO: K17454 ] 1870 E2F2; E2F transcription factor 2 [KO: K09389 ] 1871 E2F3[] RESULTS: β-catenin and NFκB-p65 proteins bound to DNA promoter regions of MDR1 in imatinib-sensitive and resistant CML cells, whereas any direct protein-protein interaction[]

  • Autoimmune Polyendocrinopathy

    Our results point to a function of the AIRE1-PHD1 domain in protein-protein interactions, which is impaired in some APECED mutations. [Indexed for MEDLINE] Free full text[] […] cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4) -0.981522 UNC13B unc-13 homolog B (C. elegans) -0.97644 GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1 -0.976156 E2F3[] Murine studies have linked AIRE to thymocyte selection and peripheral deletional tolerance, but the pathogenesis of the human disease remains unclear.[]