Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hebah A. Sindi"'
Publikováno v:
Polymers, Vol 16, Iss 14, p 2065 (2024)
Cancer is a threatening disease that needs strong therapy with fewer side effects. A lot of different types of chemotherapy or chemo-drugs are used in cancer treatments but have many side effects. The increasing number of antibiotic-resistant microor
Externí odkaz:
https://doaj.org/article/7cbb1aa7a3a443dc87f31ff0c30c0513
Autor:
Hebah A. Sindi, Giusy Russomanno, Sandro Satta, Vahitha B. Abdul-Salam, Kyeong Beom Jo, Basma Qazi-Chaudhry, Alexander J. Ainscough, Robert Szulcek, Harm Jan Bogaard, Claire C. Morgan, Soni S. Pullamsetti, Mai M. Alzaydi, Christopher J. Rhodes, Roberto Piva, Christina A. Eichstaedt, Ekkehard Grünig, Martin R. Wilkins, Beata Wojciak-Stothard
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-17 (2020)
Pulmonary arterial hypertension is a severe lung disease characterised by progressive vascular remodelling. Here, the authors show that reduced signalling of flow-activated transcription factor KLF2 is a common feature of human PAH and that KLF2-regu
Externí odkaz:
https://doaj.org/article/4eebb969beec4b25a1d7906be6c74e47
Autor:
Hebah A. Sindi, Giusy Russomanno, Sandro Satta, Vahitha B. Abdul-Salam, Kyeong Beom Jo, Basma Qazi-Chaudhry, Alexander J. Ainscough, Robert Szulcek, Harm Jan Bogaard, Claire C. Morgan, Soni S. Pullamsetti, Mai M. Alzaydi, Christopher J. Rhodes, Roberto Piva, Christina A. Eichstaedt, Ekkehard Grünig, Martin R. Wilkins, Beata Wojciak-Stothard
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-1 (2020)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/fa8a888d88b04f9885e436a2355e805e
Autor:
Sandro Satta, Christopher J. Rhodes, Kyeong Beom Jo, Hebah A. Sindi, Martin R. Wilkins, Mai M. Alzaydi, Alexander J. Ainscough, Basma Qazi-Chaudhry, Harm Jan Bogaard, Giusy Russomanno, Beata Wojciak-Stothard, Soni Savai Pullamsetti, Robert Szulcek, Claire Morgan, Roberto Piva, Christina A. Eichstaedt, Ekkehard Grünig, Vahitha B. Abdul-Salam
Publikováno v:
Nature Communications, 11(1):1185. Nature Publishing Group UK
Nature Communications, Vol 11, Iss 1, Pp 1-17 (2020)
NATURE COMMUNICATIONS
Sindi, H A, Russomanno, G, Satta, S, Abdul-Salam, V B, Jo, K B, Qazi-Chaudhry, B, Ainscough, A J, Szulcek, R, Jan Bogaard, H, Morgan, C C, Pullamsetti, S S, Alzaydi, M M, Rhodes, C J, Piva, R, Eichstaedt, C A, Grünig, E, Wilkins, M R & Wojciak-Stothard, B 2020, ' Therapeutic potential of KLF2-induced exosomal microRNAs in pulmonary hypertension ', Nature Communications, vol. 11, no. 1, 1185 . https://doi.org/10.1038/s41467-020-14966-x
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-17 (2020)
NATURE COMMUNICATIONS
Sindi, H A, Russomanno, G, Satta, S, Abdul-Salam, V B, Jo, K B, Qazi-Chaudhry, B, Ainscough, A J, Szulcek, R, Jan Bogaard, H, Morgan, C C, Pullamsetti, S S, Alzaydi, M M, Rhodes, C J, Piva, R, Eichstaedt, C A, Grünig, E, Wilkins, M R & Wojciak-Stothard, B 2020, ' Therapeutic potential of KLF2-induced exosomal microRNAs in pulmonary hypertension ', Nature Communications, vol. 11, no. 1, 1185 . https://doi.org/10.1038/s41467-020-14966-x
Nature Communications
Pulmonary arterial hypertension (PAH) is a severe disorder of lung vasculature that causes right heart failure. Homoeostatic effects of flow-activated transcription factor Krüppel-like factor 2 (KLF2) are compromised in PAH. Here, we show that KLF2-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff2d0f7a264a7a3a9a16f23e72f3402b
https://research.vumc.nl/en/publications/049dd2cd-5692-4828-b334-1f78c2e52991
https://research.vumc.nl/en/publications/049dd2cd-5692-4828-b334-1f78c2e52991
Autor:
Robert Szulcek, Soni Savai Pullamsetti, Basma Qazi-Chaudhry, Christopher J. Rhodes, Hebah A. Sindi, Martin R. Wilkins, Vahitha B. Abdul-Salam, Mai M. Alzaydi, Claire Morgan, Giusy Russomanno, Harm Jan Bogaard, Christina A. Eichstaedt, Ekkehard Grünig, Kyeong Beom Jo, Beata Wojciak-Stothard, Roberto Piva, Alexander J. Ainscough, Sandro Satta
Publikováno v:
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-1 (2020)
Nature Communications, Vol 11, Iss 1, Pp 1-1 (2020)
Pulmonary arterial hypertension (PAH) is a severe disorder of lung vasculature that causes right heart failure. Homoeostatic effects of flow-activated transcription factor Krüppel-like factor 2 (KLF2) are compromised in PAH. Here, we show that KLF2-