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Koichiro Asano

Researcher at Brigham and Women's Hospital

Publications -  9
Citations -  1406

Koichiro Asano is an academic researcher from Brigham and Women's Hospital. The author has contributed to research in topics: Epidermal growth factor & Nitric oxide synthase. The author has an hindex of 8, co-authored 9 publications receiving 1394 citations.

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Journal ArticleDOI

Constitutive and inducible nitric oxide synthase gene expression, regulation, and activity in human lung epithelial cells

TL;DR: The coexistence of constitutive and inducible NOS in human alveolar and bronchial epithelium cells is consistent with a complex mechanism evolved by epithelial cells to protect the host from microbial assault at the air/surface interface while shielding thehost from the induction of airway hyperreactivity.
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Nitric oxide produced by human B lymphocytes inhibits apoptosis and Epstein-Barr virus reactivation

TL;DR: Constutive, low level, macrophage-type NO synthase (iNOS) expression in Epstein-Barr virus-transformed human B lymphocytes and Burkitt's lymphoma cell lines suggest that NO plays a physiological role in human B cell biology by inhibiting programmed cell death and maintaining viral latency.
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Diurnal variation of urinary leukotriene E4 and histamine excretion rates in normal subjects and patients with mild-to-moderate asthma.

TL;DR: Although no systematic variation in urinary LTE4 excretion rates over the course of a day was observed in either normal subjects or patients with stable asthma, the presence of a systematic diurnal variation of urinary histamine excretion exists in both groups.
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Prostaglandin G/H synthase-2 is the constitutive and dominant isoform in cultured human lung epithelial cells

TL;DR: It is concluded that PGHS-2 is the dominant PGHS isoform in unstimulated and stimulated lung epithelial cells in culture.
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Acute and chronic effects of allergic airway inflammation on pulmonary nitric oxide production

TL;DR: The hypothesis that endogenous pulmonary NO production, as reflected by expired NO, has an important homeostatic role in acute allergic bronchoconstriction is supported.