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231224s2014 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2013.11.009
|2 doi
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|a pubmed24n0778.xml
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|a (DE-627)NLM233616713
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|a (NLM)24333536
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|a (PII)S1521-6616(13)00301-X
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Esnault, Stephane
|e verfasserin
|4 aut
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|a Semaphorin 7A is expressed on airway eosinophils and upregulated by IL-5 family cytokines
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|c 2014
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 11.03.2014
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|a Date Revised 21.10.2021
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2013 Elsevier Inc. All rights reserved.
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|a Semaphorin 7A (sema7a) plays a major role in TGF-β1-induced lung fibrosis. Based on the accumulating evidence that eosinophils contribute to fibrosis/remodeling in the airway, we hypothesized that airway eosinophils may be a significant source of sema7a. In vivo, sema7a was expressed on the surface of circulating eosinophils and upregulated on bronchoalveolar lavage eosinophils obtained after segmental bronchoprovocation with allergen. Based on mRNA levels in unfractionated and isolated bronchoalveolar cells, eosinophils are the predominant source of sema7a. In vitro, among the members of the IL-5-family cytokines, sema7a protein on the surface of blood eosinophils was increased more by IL-3 than by GM-CSF or IL-5. Cytokine-induced expression of cell surface sema7a required translation of newly synthesized protein. Finally, a recombinant sema7a induced alpha-smooth muscle actin production in human bronchial fibroblasts. semaphorin 7A is a potentially important modulator of eosinophil profibrotic functions in the airway remodeling of patients with chronic asthma
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|a Journal Article
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|a Research Support, N.I.H., Extramural
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|a BAL
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|a EOS
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|a Eosinophil
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|a Fibrosis
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|a IL-3
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|a RT-qPCR
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|a SBP-Ag
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|a Sema7a
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|a Semaphorin 7A
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|a Translation
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|a bronchoalveolar lavage
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|a eosinophils
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|a real-time quantitative PCR
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|a segmental bronchoprovocation with allergen
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|a semaphorin 7A.
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|a ACTA2 protein, human
|2 NLM
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|a Actins
|2 NLM
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|a Allergens
|2 NLM
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|a Antigens, CD
|2 NLM
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|a GPI-Linked Proteins
|2 NLM
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|a IL5 protein, human
|2 NLM
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|a Interleukin-5
|2 NLM
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|a SEMA7A protein, human
|2 NLM
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|a Semaphorins
|2 NLM
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|a Kelly, Elizabeth A
|e verfasserin
|4 aut
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|a Johansson, Mats W
|e verfasserin
|4 aut
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|a Liu, Lin Ying
|e verfasserin
|4 aut
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|a Han, Shih-Tsung
|e verfasserin
|4 aut
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|a Akhtar, Moneeb
|e verfasserin
|4 aut
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|a Sandbo, Nathan
|e verfasserin
|4 aut
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|a Mosher, Deane F
|e verfasserin
|4 aut
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|a Denlinger, Loren C
|e verfasserin
|4 aut
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|a Mathur, Sameer K
|e verfasserin
|4 aut
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|a Malter, James S
|e verfasserin
|4 aut
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|a Jarjour, Nizar N
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 150(2014), 1 vom: 01. Jan., Seite 90-100
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:150
|g year:2014
|g number:1
|g day:01
|g month:01
|g pages:90-100
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|u http://dx.doi.org/10.1016/j.clim.2013.11.009
|3 Volltext
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|a GBV_USEFLAG_A
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|a SYSFLAG_A
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|a GBV_NLM
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|a GBV_ILN_11
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|a GBV_ILN_24
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|a GBV_ILN_350
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|a AR
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|d 150
|j 2014
|e 1
|b 01
|c 01
|h 90-100
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