[1] Extensive identification and analysis of conserved small ORFs in animals

[2] Role of intestinal anaerobic bacteria in colonization resistance

[3] Characterization of function and regulation of miR-24-1 and miR-31

[4] PPAR gamma is required for the differentiation of adipose tissue in vivo and in vitro

[5] Inflammation-restricted anti-inflammatory activities of a N-acylethanolamine acid amidase (NAAA) inhibitor F215

[6] Application of a mathematical model to prevent in vivo amplification of antibiotic-resistant bacterial populations during therapy

[7] Gene ontology: tool for the unification of biology. The Gene Ontology Consortium

[8] Nerve Growth Factor Protects Against Alcohol-Induced Neurotoxicity in PC12 Cells via PI3K/Akt/mTOR Pathway

[9] Use of hyperbaric oxygen

[10] Immunological responses to monoassociated Bifidobacterium longum and their relation to prevention of bacterial invasion

[11] C/EBPbeta, when expressed from the C/ebpalpha gene locus, can functionally replace C/EBPalpha in liver but not in adipose tissue

[12] CPC: assess the protein-coding potential of transcripts using sequence features and support vector machine

[13] Retroviral expression in embryonic stem cells and hematopoietic stem cells

[14] Reconstitution of insulin-sensitive glucose transport in fibroblasts requires expression of both PPARgamma and C/EBPalpha

[15] Peroxiredoxin II preserves cognitive function against age-linked hippocampal oxidative damage

[16] Respiratory syncytial virus infection in C57BL/6 mice: clearance of virus from the lungs with virus-specific cytotoxic T cells

[17] Stimulation of adipogenesis in fibroblasts by PPAR gamma 2, a lipid-activated transcription factor

[18] Viral subunit vaccines

[19] Fine Particulate Matter (PM 2.5) Promoted the Invasion of Lung Cancer Cells via an ARNT2/PP2A/STAT3/MMP2 Pathway

[20] Acute ethanol administration oxidatively damages and depletes mitochondrial dna in mouse liver, brain, heart, and skeletal muscles: protective effects of antioxidants

[21] UPARANT is an effective antiangiogenic agent in a mouse model of rubeosis iridis

[22] Reinfection of mice with respiratory syncytial virus

[23] In vitro and in vivo inhibition of ortho- and paramyxovirus infections by a new class of sulfonic acid polymers interacting with virus-cell binding and/or fusion

[24] Immunity and immunopathology to respiratory syncytial virus. The mouse model

[25] Analysis of the local and systemic immune responses induced in BALB/c mice by experimental respiratory syncytial virus infection

[26] Virus-specific CD8+ T lymphocytes downregulate T helper cell type 2 cytokine secretion and pulmonary eosinophilia during experimental murine respiratory syncytial virus infection

[27] Recombinant human respiratory syncytial virus (RSV) monoclonal antibody Fab is effective therapeutically when introduced directly into the lungs of RSV-infected mice

[28] Diagnosis of pneumococcal pneumonia by psaA PCR analysis of lung aspirates from adult patients in Kenya

[29] Respiratory syncytial virus (RSV) F, G, M2 (22K), and N proteins each induce resistance to RSV challenge, but resistance induced by M2 and N proteins is relatively short-lived

[30] Peroxiredoxin I deficiency increases LPS‑induced lethal shock in mice

[31] Peroxiredoxin-2 protects against 6-hydroxydopamine-induced dopaminergic neurodegeneration via attenuation of the apoptosis signal-regulating kinase (ASK1) signaling cascade

[32] PPAR gamma mediates high-fat diet-induced adipocyte hypertrophy and insulin resistance

[33] Priming immunization determines T helper cytokine mRNA expression patterns in lungs of mice challenged with respiratory syncytial virus

[34] Protein energy malnutrition impairs homeostatic proliferation of memory CD8 T cells

[35] GIT1 contributes to autophagy in osteoclast through disruption of the binding of Beclin1 and Bcl2 under starvation condition

[36] Ensembl 2012

[37] Tumor induction of VEGF promoter activity in stromal cells

[38] A histone lysine methyltransferase activated by non-canonical Wnt signalling suppresses PPAR-gamma transactivation

[39] Amlexanox Downregulates S100A6 to Sensitize KMT2A/AFF1-Positive Acute Lymphoblastic Leukemia to TNFα Treatment

[40] Resistance to respiratory syncytial virus (RSV) challenge induced by infection with a vaccinia virus recombinant expressing the RSV M2 protein (Vac-M2) is mediated by CD8+ T cells, while that induced by Vac-F or Vac-G recombinants is mediated by antibodies

[41] Regulated expression of three C/EBP isoforms during adipose conversion of 3T3-L1 cells

[42] Persistence of colonization of intestinal mucosa by a probiotic strain, Lactobacillus casei subsp. rhamnosus Lcr35, after oral consumption

[43] A new morphologically characterized cell wall preparation (whole peptidoglycan) from Bifidobacterium infantis with a higher efficacy on the regression of an established tumor in mice

[44] Cytotoxic T cells clear virus but augment lung pathology in mice infected with respiratory syncytial virus

[45] Real-time PCR quantification of spliced X-box binding protein 1 (XBP1) using a universal primer method

[46] Protein energy malnutrition decreases immunity and increases susceptibility to influenza infection in mice

[47] C/EBPalpha is required for differentiation of white, but not brown, adipose tissue

[48] Characterization of neural cell types expressing peroxiredoxins in mouse brain

[49] The 22,000-kilodalton protein of respiratory syncytial virus is a major target for Kd-restricted cytotoxic T lymphocytes from mice primed by infection

[50] Prenatal exposure of female rhesus monkeys to testosterone propionate increases serum luteinizing hormone levels in adulthood

[51] Comparison of clindamycin, rifampin, tetracycline, metronidazole, and penicillin for efficacy in prevention of experimental gas gangrene due to Clostridium perfringens

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

[53] Role of T lymphocyte subsets in the pathogenesis of primary infection and rechallenge with respiratory syncytial virus in mice

[54] Antiviral properties of extract of Opuntia streptacantha

[55] Comparison of single and combination antimicrobial agents for prevention of experimental gas gangrene caused by Clostridium perfringens

[56] Insulin signaling displayed a differential tissue-specific response to low-dose dihydrotestosterone in female mice

[57] Recognition of respiratory syncytial virus fusion protein by mouse cytotoxic T cell clones and a human cytotoxic T cell line

[58] Prolactin has a pathogenic role in systemic lupus erythematosus

[59] Diminished primary CD8 T cell response to viral infection during protein energy malnutrition in mice is due to changes in microenvironment and low numbers of viral-specific CD8 T cell precursors

[60] The evolutionary fate and consequences of duplicate genes

[61] Cytotoxic lymphocytes in the lungs of mice infected with respiratory syncytial virus

[62] Esculetin from Fraxinus rhynchophylla attenuates atopic skin inflammation by inhibiting the expression of inflammatory cytokines

[63] Respiratory syncytial virus infection in anti-mu-treated mice

[64] Cytotoxic T cell activity against the 22-kDa protein of human respiratory syncytial virus (RSV) is associated with a significant reduction in pulmonary RSV replication

[65] CD4+ T cells clear virus but augment disease in mice infected with respiratory syncytial virus. Comparison with the effects of CD8+ T cells

[66] Is the BCG vaccine safe for undernourished individuals?

[67] CORUM: the comprehensive resource of mammalian protein complexes

[68] Recombinant respiratory syncytial virus from which the entire SH gene has been deleted grows efficiently in cell culture and exhibits site-specific attenuation in the respiratory tract of the mouse

[69] CCAAT/enhancer binding protein alpha is sufficient to initiate the 3T3-L1 adipocyte differentiation program

[70] Murine cytotoxic T cells specific to respiratory syncytial virus recognize different antigenic subtypes of the virus

[71] Malaria pigment paralyzes dendritic cells

[72] PPAR gamma is required for placental, cardiac, and adipose tissue development

[73] Quantitative studies of the growth of mouse embryo cells in culture and their development into established lines

[74] Cytotoxic T cell specificity for respiratory syncytial virus proteins: fusion protein is an important target antigen

[75] Hepatocyte nuclear factor 4alpha (nuclear receptor 2A1) is essential for maintenance of hepatic gene expression and lipid homeostasis

[76] Differentiation of embryonic stem cells into adipocytes in vitro

[77] Dissemination of mycobacteria to the thymus renders newly generated T cells tolerant to the invading pathogen

[78] 'Self' tolerance in a parent-->F1 radiation chimera

[79] Antigenicity testing of plain and aluminium hydroxide-adsorbed whole-cell cholera vaccines

[80] Vertebrate genomics: More fishy tales about Hox genes

[81] Knockdown of peroxiredoxin V increases glutamate‑induced apoptosis in HT22 hippocampal neuron cells

[82] The uPAR System as a Potential Therapeutic Target in the Diseased Eye

[83] cGAS drives noncanonical-inflammasome activation in age-related macular degeneration

[84] Fecal recovery in humans of viable Bifidobacterium sp ingested in fermented milk

[85] The role of TH1 and TH2 cells in a rodent malaria infection

[86] Cross-regulation of C/EBP alpha and PPAR gamma controls the transcriptional pathway of adipogenesis and insulin sensitivity

[87] Injury factors alter miRNAs profiles of exosomes derived from islets and circulation

[88] An update on approaches to the development of respiratory syncytial virus (RSV) and parainfluenza virus type 3 (PIV3) vaccines

[89] Present and future therapeutic strategies for melioidosis and glanders

[90] Determination of adipocyte size by computer image analysis

[91] Cellular response to respiratory viruses with particular reference to children with disorders of cell-mediated immunity

[92] TCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa

[93] Immunoprophylaxis and immunotherapy of respiratory syncytial virus-infected mice with respiratory syncytial virus-specific immune serum

[94] Neuroendocrine androgen action is a key extraovarian mediator in the development of polycystic ovary syndrome

[95] Human and murine cytotoxic T cells specific to respiratory syncytial virus recognize the viral nucleoprotein (N), but not the major glycoprotein (G), expressed by vaccinia virus recombinants

[96] Humanised monoclonal antibody to respiratory syncytial virus

[97] C/EBPalpha induces adipogenesis through PPARgamma: a unified pathway

[98] Cytolytic T-lymphocyte responses to respiratory syncytial virus: effector cell phenotype and target proteins

[99] Real-time multi-wavelength fluorescence imaging of living cells

[100] Cascade regulation of terminal adipocyte differentiation by three members of the C/EBP family of leucine zipper proteins

[101] Clearance of persistent respiratory syncytial virus infections in immunodeficient mice following transfer of primed T cells