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PubPharm (11)
1
Mast-cell expressed membrane protein-1 is expressed in classical monocytes and alveolar macrophages in idiopathic pulmonary fibrosis and regulates cell chemotaxis, adhesion, and migration in a TGFβ-dependent manner
enthalten in:
American journal of physiology. Cell physiology
| 2024
von
Perrot, C.
|
Karampitsakos, T.
|
Unterman, A.
| +9
UpdateOf: bioRxiv. 2023 Oct 10;:. - PMID 37873485
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2
A 50-gene high-risk profile predictive of COVID-19 and Idiopathic Pulmonary Fibrosis mortality originates from a genomic imbalance in monocyte and T-cell subsets that reverses in survivors with post-COVID-19 Interstitial Lung Disease
enthalten in:
bioRxiv.org
| 2023
von
Tourki, B.
|
Jia, M.
|
Karampitsakos, T.
| +17
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3
Mast-Cell Expressed Membrane Protein-1 (MCEMP1) is expressed in classical monocytes and alveolar macrophages in Idiopathic Pulmonary Fibrosis and regulates cell chemotaxis, adhesion, and migration in a TGFβ dependent manner
enthalten in:
bioRxiv.org
| 2023
von
Perrot, C.
|
Karampitsakos, T.
|
Unterman, A.
| +9
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4
Mast-Cell Expressed Membrane Protein-1 (MCEMP1) is expressed in classical monocytes and alveolar macrophages in Idiopathic Pulmonary Fibrosis and regulates cell chemotaxis, adhesion, and migration in a TGFβ dependent manner
enthalten in:
bioRxiv : the preprint server for biology
| 2023
von
Perrot, C.
|
Karampitsakos, T.
|
Unterman, A.
| +9
UpdateIn: Am J Physiol Cell Physiol. 2024 Jan 8;:. - PMID 38189137
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5
Successful Treatment of a Patient With Severe COVID-19 Using an Integrated Approach Addressing Mast Cells and Their Mediators
enthalten in:
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
| 2022
von
Theoharides, T.
|
Guerra, L.
|
Patel, K.
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6
Aberrant Expression of ACO1 in Vasculatures Parallels Progression of Idiopathic Pulmonary Fibrosis
enthalten in:
Frontiers in pharmacology
| 2022
von
Fukumoto, J.
|
Lin, M.
|
Banday, M.
| +12
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7
Long-term safety and efficacy of tezacaftor-ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND) : an open-label extension study
enthalten in:
The Lancet. Respiratory medicine
| 2021
von
Flume, P.
|
Biner, R.
|
Downey, D.
| +118
ErratumIn: Lancet Respir Med. 2021 Apr;9(4):e38. - PMID 33636124
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8
Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation : a double-blind, randomised, phase 3 trial
enthalten in:
Lancet (London, England)
| 2019
von
Heijerman, H.
|
McKone, E.
|
Downey, D.
| +63
CommentIn: Lancet. 2019 Nov 23;394(10212):1886-1888. - PMID 31679947
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9
VX-445-Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles
enthalten in:
The New England journal of medicine
| 2018
von
Keating, D.
|
Marigowda, G.
|
Burr, L.
| +54
CommentIn: Nat Med. 2019 Jan;25(1):19. - PMID 30617328
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10
Addressing inherited predisposition for breast cancer in transplant recipients
enthalten in:
Journal of surgical oncology
| 2016
von
Yang, R.
|
Kurian, A.
|
Winton, L.
| +4
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