[1] Cytoplasmic inclusions of respiratory syncytial virus-infected cells: formation of inclusion bodies in transfected cells that coexpress the nucleoprotein, the phosphoprotein, and the 22K protein

[2] Analysis of respiratory syncytial virus F, G, and SH proteins in cell fusion

[3] Modulation of the murine peroxisome proliferator-activated receptor gamma 2 promoter activity by CCAAT/enhancer-binding proteins

[4] RNA replication by respiratory syncytial virus (RSV) is directed by the N, P, and L proteins; transcription also occurs under these conditions but requires RSV superinfection for efficient synthesis of full-length mRNA

[5] Increased expression of the N protein of respiratory syncytial virus stimulates minigenome replication but does not alter the balance between the synthesis of mRNA and antigenome

[6] Sterol-dependent repression of low density lipoprotein receptor promoter mediated by 16-base pair sequence adjacent to binding site for transcription factor Sp1

[7] A signature motif in transcriptional co-activators mediates binding to nuclear receptors

[8] Functional interactions of peroxisome proliferator-activated receptor, retinoid-X receptor, and Sp1 in the transcriptional regulation of the acyl-coenzyme-A oxidase promoter

[9] CBP-induced stimulation of c-Fos activity is abrogated by E1A

[10] Virus induction of human IFN beta gene expression requires the assembly of an enhanceosome

[11] Cutting edge: repurification of lipopolysaccharide eliminates signaling through both human and murine toll-like receptor 2

[12] Regulation of NF-kappaB by cyclin-dependent kinases associated with the p300 coactivator

[13] Isoform 1c of sterol regulatory element binding protein is less active than isoform 1a in livers of transgenic mice and in cultured cells

[14] SREBP-2, a second basic-helix-loop-helix-leucine zipper protein that stimulates transcription by binding to a sterol regulatory element

[15] Different activation domains of Sp1 govern formation of multimers and mediate transcriptional synergism

[16] Regulation of p53 stability by Mdm2

[17] A role for the cytoplasmic polyadenylation element in NMDA receptor-regulated mRNA translation in neurons

[18] Extracellular matrix production regulation by TGF-beta in corneal endothelial cells

[19] STAT3 activation of miR-21 and miR-181b-1 via PTEN and CYLD are part of the epigenetic switch linking inflammation to cancer

[20] Senescence bypass screen identifies TBX2, which represses Cdkn2a (p19(ARF)) and is amplified in a subset of human breast cancers

[21] Mdm2 promotes the rapid degradation of p53

[22] Murine NK cell allospecificity-1 is defined by inhibitory ligands

[23] Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus

[24] Induction of ARF tumor suppressor gene expression and cell cycle arrest by transcription factor DMP1

[25] Acquisition of HLA-DR and costimulatory molecules by T cells from allogeneic antigen presenting cells

[26] On the frequency of protein glycosylation, as deduced from analysis of the SWISS-PROT database

[27] Nuclear protein that binds sterol regulatory element of low density lipoprotein receptor promoter. I. Identification of the protein and delineation of its target nucleotide sequence

[28] Enforced c-KIT expression renders highly metastatic human melanoma cells susceptible to stem cell factor-induced apoptosis and inhibits their tumorigenic and metastatic potential

[29] Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin

[30] Reconstitution of mitotic chromatids with a minimum set of purified factors

[31] FZD4 as a mediator of ERG oncogene-induced WNT signaling and epithelial-to-mesenchymal transition in human prostate cancer cells

[32] Interaction of D-type cyclins with a novel myb-like transcription factor, DMP1

[33] A Universal Design of Betacoronavirus Vaccines against COVID-19, MERS, and SARS

[34] Liposome-based transfection enhances RNAi and CRISPR-mediated mutagenesis in non-model nematode systems

[35] Ultrasound-assisted Cu(I)-catalyzed azide-alkyne click cycloaddition as polymer-analogous transformation in chitosan chemistry. High antibacterial and transfection activity of novel triazol betaine chitosan derivatives and their nanoparticles

[36] the mechanism of high transfection efficiency of human serum albumin conjugated polyethylenimine in a549 cells

[37] a simple and efficient in vivo non-viral rna transfection method for labeling the whole axonal tree of individual adult long-range projection neurons

[38] systematic screening of commonly used commercial transfection reagents towards efficient transfection of single-stranded oligonucleotides

[39] the effect of cationic charge density change on transfection efficiency of polyethylenimine

[40] optimization of transfection of green fluorescent protein in pursuing mesenchymal stem cells in vivo

[41] induction of dental epithelial cell differentiation marker gene expression in non-odontogenic human keratinocytes by transfection with thymosin beta 4

[42] highly branched poly(5-amino-1-pentanol-co-1,4-butanediol diacrylate) for high performance gene transfection

[43] bioreducible pei-sirna nanocomplex for liver cancer therapy: transfection, biodistribution, and tumor growth inhibition in vivo

[44] factors influencing transfection efficiency of pidua/nanoemulsion complexes in a mucopolysaccharidosis type i murine model

[45] cellular injury of cardiomyocytes during hepatocyte growth factor gene transfection with ultrasound-triggered bubble liposome destruction

[46] Stable transfection of Eimeria intestinalis and investigation of its life cycle, reproduction and immunogenicity