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Erwin W. Gelfand

Researcher at University of Colorado Denver

Publications -  679
Citations -  37565

Erwin W. Gelfand is an academic researcher from University of Colorado Denver. The author has contributed to research in topics: Immunoglobulin E & T cell. The author has an hindex of 99, co-authored 675 publications receiving 36059 citations. Previous affiliations of Erwin W. Gelfand include University of Colorado Hospital & University of Virginia.

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Patent

Pifenidone derivatives for treating bronchial asthma

TL;DR: In this article, the authors described a method of treating patients with bronchial asthma with a pirfenidone analog, which they termed as a "miracle" drug.
Book ChapterDOI

Chapter 16 Activation of Sodium—Hydrogen Exchange by Mitogens

TL;DR: The Na + -H + antiport is virtually quiescent at physiological cytosolic pH (pH i ), but is markedly activated when the cytoplasm becomes acidic, suggesting that the antiport plays an important role in the regulation of pH i in resting (nonproliferating) cells.
Journal ArticleDOI

Heterogeneity of non-T, non-B acute lymphocytic leukemia defined by the quantitative expression of Ia and common all antigens

TL;DR: The data indicate that non-T, non-B ALL are heterogeneous with respect to their expression of Ia and CALLA antigens, and suggest a possible correlation between the amount of IA expressed on the leukemic cells and the white blood cell count of the patient at the time of diagnosis.
Book ChapterDOI

Chapter 7 Cytosolic Calcium Changes during T- and B-Lymphocyte Activation: Biological Consequences and Significance

TL;DR: Stimuli of very diverse nature cause increases in [Ca 2+ ] i in both T and B lymphocytes, and these increases presumably give rise to a wide spectrum of cellular effects that are contributory to some and irrelevant to others.
Journal ArticleDOI

Microbial Heat Shock Protein 65 Attenuates Airway Hyperresponsiveness and Inflammation by Modulating the Function of Dendritic Cells

TL;DR: HSP65-induced effects on allergen-induced airway hyperresponsiveness and inflammation were associated with increased Delta1 expression on dendritic cells, modulation of dendrite cell function, and CD4+ Th1 cytokine production.