LPS stimulates IgM production in vivo without help from non-B cells.

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Effects of cyanobacteria Oscillatoria sp. lipopolysaccharide on B cell activation and Toll-like receptor 4 signaling.

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P2860

LPS stimulates IgM production in vivo without help from non-B cells.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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LPS stimulates IgM production in vivo without help from non-B cells.

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LPS stimulates IgM production in vivo without help from non-B cells.

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LPS stimulates IgM production in vivo without help from non-B cells.

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P1476

LPS stimulates IgM production in vivo without help from non-B cells.

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Mingfang Lu

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Robert Munford

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P2860

The toll-like receptor protein RP105 regulates lipopolysaccharide signaling in B cells

Adjuvant-enhanced antibody responses in the absence of toll-like receptor signaling

Structural characterization of the lipid A component of pathogenic Neisseria meningitidis

Chapter 2: Kill the bacteria...and also their messengers?

Lipopolysaccharide deacylation by an endogenous lipase controls innate antibody responses to Gram-negative bacteria.

Host inactivation of bacterial lipopolysaccharide prevents prolonged tolerance following gram-negative bacterial infection.

The transport and inactivation kinetics of bacterial lipopolysaccharide influence its immunological potency in vivo.

Genetic control of responses to bacterial lipopolysaccharides in mice. I. Evidence for a single gene that influences mitogenic and immunogenic respones to lipopolysaccharides.

B-cell activation by lipopolysaccharide. Distinct pathways for induction of mitosis and antibody production

Lymph-borne chemokines and other low molecular weight molecules reach high endothelial venules via specialized conduits while a functional barrier limits access to the lymphocyte microenvironments in lymph node cortex.

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307-315

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scholarly article

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10.1177/1753425916644675

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2016-04-25T00:00:00Z

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27189424

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LPS stimulates IgM production in vivo without help from non-B cells.

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P2860

P2860

LPS stimulates IgM production in vivo without help from non-B cells.

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