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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

CaM kinase-like vesicle-associated

1G5
Top mentioned proteins: CAN, HAD, V1a, CD4, CYP1A1
Papers on 1G5
Zenker's diverticulum: Rotterdam experience.
New
Baatenburg de Jong et al., Rotterdam, Netherlands. In Eur Arch Otorhinolaryngol, Dec 2015
In the transcervical group 2 complications occurred, 1 G3b and 1 G5.
Endometrial epithelial cell response to semen from HIV-infected men during different stages of infection is distinct and can drive HIV-1-long terminal repeat.
Kaushic et al., Hamilton, Canada. In Aids, 2012
HIV-long terminal repeat (LTR) activation was measured in 1G5 T cells exposed to supernatants from seminal plasma-treated GECs.
Pokeweed antiviral protein increases HIV-1 particle infectivity by activating the cellular mitogen activated protein kinase pathway.
Hudak et al., Toronto, Canada. In Plos One, 2011
However, particles released from PAP-expressing cells were approximately 7-fold more infectious, as determined by single-cycle infection of 1G5 cells and productive infection of MT2 cells.
Epitope reactions can be gauged by relative antibody discriminating specificity (RADS) values supported by deletion, substitution and cysteine bridge formation analyses: potential uses in pathogenesis studies.
Falconar, Barranquilla, Colombia. In Bmc Res Notes, 2011
New xKGSx/xSGKx amino acid motifs were identified on DENV-2 glycoproteins, HIV-1 gp41 and factor IXa. Their potential roles in DENV and HIV-1 antibody-enhanced replication (AER) and auto-immunity were assessed.In this study, a) RADS values were determined for MAbs and PAbs, generated in congeneic (H2: class II) mice against DENV NS1 glycoprotein epitopes, to account for their cross-reaction patterns, and b) MAb 1G5.3 reactions with xKGSx/xSGKx motifs present in the DENV-4 NS1, E and HIV-1 glycoproteins and factor IXa were assessed after the introduction of amino acid substitutions, deletions, or intra-/inter-cysteine (C-C) bridges.
[Preparation of anti-human 4-1BB monoclonal antibody and characterization of its biological activities].
Zhang et al., Wuxi, China. In Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi, 2011
RESULTS: Three hybridoma cell lines 1G5, 4B11 and 9F11 with the property of secreting specific anti-4-1BB monoclonal antibody continuously and steadily were successfully obtained.
Endometrial epithelial cell responses to coinfecting viral and bacterial pathogens in the genital tract can activate the HIV-1 LTR in an NF{kappa}B-and AP-1-dependent manner.
Kaushic et al., Hamilton, Canada. In J Infect Dis, 2011
METHODS: Direct activation of HIV long terminal repeats (LTRs), a proxy measure for HIV-1 replication, was measured after treatment of 1G5 T cells with Toll-like receptor (TLR) ligands, herpes simplex virus type 1 or 2 (HSV-1/2), or Neisseria gonorrhoeae.
Oral bacteria induce a differential activation of human immunodeficiency virus-1 promoter in T cells, macrophages and dendritic cells.
Ebersole et al., Lexington, United States. In Oral Microbiol Immunol, 2009
RESULTS: T cells (1G5) challenged with oral bacteria demonstrated a dose-response of HIV promoter activation with a subset of the bacteria, as well as kinetics that were generally similar irrespective of the stimuli.
Characterisation of two antibodies to oligomeric Abeta and their use in ELISAs on human brain tissue homogenates.
Love et al., Bristol, United Kingdom. In J Neurosci Methods, 2009
We have examined the specificity of two monoclonal antibodies, 7 A1a and 1G5, for synthetic oligomers of Abeta(1-42) and for oligomeric Abeta(1-42) in human brain homogenates, and the utility of these two antibodies for measuring oligomeric Abeta(1-42) by sandwich ELISA.
HI-CHART: a phase I/II study on the feasibility of high-dose continuous hyperfractionated accelerated radiotherapy in patients with inoperable non-small-cell lung cancer.
Lambin et al., Maastricht, Netherlands. In Int J Radiat Oncol Biol Phys, 2008
Maximal toxicity according to the risk groups was as follows: V(20) <25% (n = 35): 1 Grade 4 (G4) lung and 1 G3 reversible esophageal toxicity; V(20) 35-37% (n = 12): 1 G5 lung and 1 G3 reversible esophageal toxicity.
Monoclonal antibodies that bind to common epitopes on the dengue virus type 2 nonstructural-1 and envelope glycoproteins display weak neutralizing activity and differentiated responses to virulent strains: implications for pathogenesis and vaccines.
Falconar, London, United Kingdom. In Clin Vaccine Immunol, 2008
MAb 1G5.3 cross-reacted with the flavivirus-conserved 101-WGNGCGLFG-109 fusion sequence, the 273-SSGNL-277 DENV-2 hinge region sequence, and the 156-GKHGKEIKIT-165 sequence of virulent DENV-2 strains.
Dynamic surface tension and surface dilatational elasticity properties of mixed surfactant/protein systems.
Aramaki et al., Yokohama, Japan. In J Oleo Sci, 2007
We present the study on dynamic surface tension and surface dilatational elasticity properties of dilute aqueous systems of pentaglycerol fatty acid esters (pentaglycerol monostearate, C18G5, and pentaglycerol monooleate, C18:1G5, whey protein, sodium caseinate, and mixed surfactant and protein at room temperature.
[Preparation and characterization of monoclonal antibodies against chicken interferon-gamma].
Liu et al., Yangzhou, China. In Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi, 2006
RESULTS: Two hybridoma cell lines secreting mAbs against ChIFN-gamma named 1G5, 5E3 were obtained.
Generation of monoclonal antibodies and epitope mapping of ApxIVA of Actinobacillus pleuropneumoniae.
Chen et al., Wuhan, China. In Mol Immunol, 2006
Eight monoclonal antibodies were selected, four (designated as 1A8, 1G5, 3E7 and 4H9) against ApxIVAN and another four (named as 1B12, 2E5, 4D8 and 4G2) against ApxIVAC.
Dynamic expression patterns of zebrafish 1G5 (1G5z), a calmodulin kinase-like gene in the developing nervous system.
Rhee et al., South Korea. In Dev Dyn, 2006
1G5 encodes a CaMK like protein, which belongs to a calmodulin (CaM) kinase gene family.
Transactivation of human immunodeficiency virus-1 in T-cells by Mycobacterium tuberculosis-infected mononuclear phagocytes.
Aung et al., Cleveland, United States. In J Lab Clin Med, 2004
In this study we sought to determine whether MTB-infected human primary mononuclear phagocytes-namely, alveolar macrophages (AMs) and their less mature blood precursors, monocytes-activate HIV-1 in a T-cell line stably transfected with an HIV-1 long terminal repeat (LTR) reporter construct (1G5 cells) and induce HIV-1 expression in T-cells from HIV-1-infected subjects.
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