Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Lungnasjúkdómar"'
Autor:
Axelsson, Gísli Þór
Introduction: Interstitial lung diseases (ILD), such as idiopathic pulmonary fibrosis (IPF), are diseases of elderly people that are characterised by pulmonary deposition of fibrous tissue and often have a poor prognosis. Interstitial lung abnormalit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3712::b357e691b1946f2e788b17f90e580c98
https://hdl.handle.net/20.500.11815/3492
https://hdl.handle.net/20.500.11815/3492
Autor:
Diane Frankel, Audrey Benoit, Stéphane Robert, Elise Kaspi, Patrice Roll, Philippe Astoul, Nicolas Lévy, Julien Guinde, Kevin Ostacolo
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, MDPI, 2020, 21 (5), pp.1599. ⟨10.3390/ijms21051599⟩
International Journal of Molecular Sciences, 2020, 21 (5), pp.1599. ⟨10.3390/ijms21051599⟩
International Journal of Molecular Sciences, Vol 21, Iss 5, p 1599 (2020)
International Journal of Molecular Sciences, MDPI, 2020, 21 (5), pp.1599. ⟨10.3390/ijms21051599⟩
International Journal of Molecular Sciences, 2020, 21 (5), pp.1599. ⟨10.3390/ijms21051599⟩
International Journal of Molecular Sciences, Vol 21, Iss 5, p 1599 (2020)
Publisher's version (útgefin grein)
In lung adenocarcinoma, low lamin A expression in pleural metastatic cells has been proposed as a pejorative factor. miR-9 physiologically inhibits the expression of lamin A in neural cells and seems to be a
In lung adenocarcinoma, low lamin A expression in pleural metastatic cells has been proposed as a pejorative factor. miR-9 physiologically inhibits the expression of lamin A in neural cells and seems to be a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebe007d4e08cb41d9a5f338fd9d11f83
https://hdl.handle.net/20.500.11815/2429
https://hdl.handle.net/20.500.11815/2429
Autor:
Simon P. Hart, Vilmundur Gudnason, Yingze Zhang, Hiroto Hatabu, Rebecca Braybrooke, R. Gisli Jenkins, Shwu-Fan Ma, Michael Ng, Carlos Flores, George T. O'Connor, Ma'en Obeidat, Nik Hirani, Brian D. Hobbs, Megan L. Paynton, Amy Dressen, Ayodeji Adegunsoye, Helen Booth, Dominic Furniss, Philippe Joubert, Eunice Oballa, Ian Sayers, Martin D. Tobin, Krina T. Zondervan, Richard Hubbard, Xuan Li, Yohan Bossé, John D. Newell, Beatriz Guillen-Guio, Ann B. Millar, Wim Timens, Mary E. Strek, Gunnar Gudmundsson, Philip L. Molyneaux, Gary M. Hunninghake, Ani Manichaikul, Tasha E. Fingerlin, Rachel K. Putman, Richard J. Allen, Vidyia Navaratnam, Maria Molina-Molina, Don D. Sin, Helen Parfrey, Luke M. Kraven, Moira K. B. Whyte, Xuting R. Sheng, Phuwanat Sakornsakolpat, David J. Lederer, David C. Nickle, Ian P. Hall, Brian L. Yaspan, Louise V. Wain, Toby M. Maher, Gauri Saini, Ke Hao, Michael Hill, Naftali Kaminski, Andrew P. Morris, Hanfei Xu, Justin M. Oldham, David A. Schwartz, Robin J. McAnulty, Michael H. Cho, Victor E. Ortega, Margaret Neighbors, Imre Noth, William A. Fahy
Publikováno v:
Allen, R J, Guillen-guio, B, Oldham, J M, Ma, S, Dressen, A, Paynton, M L, Kraven, L M, Obeidat, M, Li, X, Ng, M, Braybrooke, R, Molina-molina, M, Hobbs, B D, Putman, R K, Sakornsakolpat, P, Booth, H L, Fahy, W A, Hart, S P, Hill, M R, Hirani, N, Hubbard, R B, Mcanulty, R J, Millar, A B, Navaratnam, V, Oballa, E, Parfrey, H, Saini, G, Whyte, M K B, Zhang, Y, Kaminski, N, Adegunsoye, A, Strek, M E, Neighbors, M, Sheng, X R, Gudmundsson, G, Gudnason, V, Hatabu, H, Lederer, D J, Manichaikul, A, Newell Jr., J D, O'connor, G T, Ortega, V E, Xu, H, Fingerlin, T E, Bossé, Y, Hao, K, Joubert, P, Nickle, D C, Sin, D D, Timens, W, Furniss, D, Morris, A P, Zondervan, K, Hall, I P, Sayers, I, Tobin, M D, Maher, T M, Cho, M H, Hunninghake, G M, Schwartz, D A, Yaspan, B L, Molyneaux, P L, Flores, C, Noth, I, Jenkins, R G & Wain, L V 2020, ' Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis ', American Journal of Respiratory and Critical Care Medicine, vol. 201, no. 5, pp. 564-574 . https://doi.org/10.1164/rccm.201905-1017OC
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
American Journal of Respiratory and Critical Care Medicine, 201(5), 564-574. AMER THORACIC SOC
Allen, R J, Guillen-Guio, B, Oldham, J M, Ma, S-F, Dressen, A, Paynton, M L, Kraven, L M, Obeidat, M, Li, X, Ng, M, Braybrooke, R, Molina-Molina, M, Hobbs, B D, Putman, R K, Sakornsakolpat, P, Booth, H L, Fahy, W A, Hart, S P, Hill, M R, Hirani, N, Hubbard, R B, McAnulty, R J, Millar, A B, Navaratnam, V, Oballa, E, Parfrey, H, Saini, G, Whyte, M K B, Zhang, Y, Kaminski, N, Adegunsoye, A, Strek, M E, Neighbors, M, Sheng, X R, Gudmundsson, G, Gudnason, V, Hatabu, H, Lederer, D J, Manichaikul, A, Newell, J D, O'Connor, G T, Ortega, V E, Xu, H, Fingerlin, T E, Bossé, Y, Hao, K, Joubert, P, Nickle, D C, Sin, D D, Timens, W, Furniss, D, Morris, A P, Zondervan, K, Hall, I P, Sayers, I, Tobin, M D, Maher, T M, Cho, M H, Hunninghake, G M, Schwartz, D A, Yaspan, B L, Molyneaux, P L, Flores, C, Noth, I, Jenkins, R G & Wain, L V 2019, ' Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis ', American Journal of Respiratory and Critical Care Medicine . https://doi.org/10.1164/rccm.201905-1017OC
American Journal of Respiratory and Critical Care Medicine
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
American Journal of Respiratory and Critical Care Medicine, 201(5), 564-574. AMER THORACIC SOC
Allen, R J, Guillen-Guio, B, Oldham, J M, Ma, S-F, Dressen, A, Paynton, M L, Kraven, L M, Obeidat, M, Li, X, Ng, M, Braybrooke, R, Molina-Molina, M, Hobbs, B D, Putman, R K, Sakornsakolpat, P, Booth, H L, Fahy, W A, Hart, S P, Hill, M R, Hirani, N, Hubbard, R B, McAnulty, R J, Millar, A B, Navaratnam, V, Oballa, E, Parfrey, H, Saini, G, Whyte, M K B, Zhang, Y, Kaminski, N, Adegunsoye, A, Strek, M E, Neighbors, M, Sheng, X R, Gudmundsson, G, Gudnason, V, Hatabu, H, Lederer, D J, Manichaikul, A, Newell, J D, O'Connor, G T, Ortega, V E, Xu, H, Fingerlin, T E, Bossé, Y, Hao, K, Joubert, P, Nickle, D C, Sin, D D, Timens, W, Furniss, D, Morris, A P, Zondervan, K, Hall, I P, Sayers, I, Tobin, M D, Maher, T M, Cho, M H, Hunninghake, G M, Schwartz, D A, Yaspan, B L, Molyneaux, P L, Flores, C, Noth, I, Jenkins, R G & Wain, L V 2019, ' Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis ', American Journal of Respiratory and Critical Care Medicine . https://doi.org/10.1164/rccm.201905-1017OC
American Journal of Respiratory and Critical Care Medicine
Publisher's version (útgefin grein)
Rationale: Idiopathic pulmonary fibrosis (IPF) is a complex lung disease characterized by scarring of the lung that is believed to result from an atypical response to injury of the epithelium. Genome-wide ass
Rationale: Idiopathic pulmonary fibrosis (IPF) is a complex lung disease characterized by scarring of the lung that is believed to result from an atypical response to injury of the epithelium. Genome-wide ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f735d247fb5068243ea799597c642afa
https://www.research.manchester.ac.uk/portal/en/publications/genomewide-association-study-of-susceptibility-to-idiopathic-pulmonary-fibrosis(6fbf4813-b9fe-4644-bec4-7b50df3d4de2).html
https://www.research.manchester.ac.uk/portal/en/publications/genomewide-association-study-of-susceptibility-to-idiopathic-pulmonary-fibrosis(6fbf4813-b9fe-4644-bec4-7b50df3d4de2).html
Autor:
John Maret-Ouda, Elsebeth Lynge, Laufey Tryggvadottir, Bright I Nwaru, Giola Santoni, Martti Färkkilä, Jesper Lagergren, My von Euler-Chelpin, Eero Pukkala, Pål Richard Romundstad, Eivind Ness-Jensen, Manar Yanes
Publikováno v:
European Journal of Cancer
Yanes, M, Santoni, G, Maret-Ouda, J, Ness-Jensen, E, Farkkila, M, Lynge, E, Nwaru, B, Pukkala, E, Romundstad, P, Tryggvadottir, L, von Euler-Chelpin, M & Lagergren, J 2020, ' Antireflux surgery and risk of lung cancer by histological type in a multinational cohort study ', European Journal of Cancer, vol. 138, pp. 80-88 . https://doi.org/10.1016/j.ejca.2020.07.018
Yanes, M, Santoni, G, Maret-Ouda, J, Ness-Jensen, E, Farkkila, M, Lynge, E, Nwaru, B, Pukkala, E, Romundstad, P, Tryggvadottir, L, von Euler-Chelpin, M & Lagergren, J 2020, ' Antireflux surgery and risk of lung cancer by histological type in a multinational cohort study ', European Journal of Cancer, vol. 138, pp. 80-88 . https://doi.org/10.1016/j.ejca.2020.07.018
Publisher's version (útgefin grein)
Introduction: Airway micro-aspiration might contribute to the proposed associations between gastroesophageal reflux disease (GERD) and some lung diseases, including lung cancer. This study aimed to examine th
Introduction: Airway micro-aspiration might contribute to the proposed associations between gastroesophageal reflux disease (GERD) and some lung diseases, including lung cancer. This study aimed to examine th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79ecb603f626fd868706840f83fec3dd
https://hdl.handle.net/11250/2731436
https://hdl.handle.net/11250/2731436
Autor:
Sigurgeirsdottir, Jonina, Halldorsdottir, Sigridur, Arnardottir, Rangheidur Harpa, Gudmundsson, Gunnar, Bjornsson, Eythor Hreinn
Background: COPD is a common cause of morbidity and mortality. The aim of this study was to explore patients’ experiences, self-reported needs, and needs-driven strategies to cope with self-management of COPD. Patients and methods: In this phenomen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1d9e5ff1c0a4516b83477e772be601d7
https://hdl.handle.net/20.500.11815/1218
https://hdl.handle.net/20.500.11815/1218
Autor:
Armesto Jimenez, Amaranta
Thesis for a doctoral degree at the University of Iceland
Idiopathic pulmonary fibrosis is a severe lung disease with unknown aetiology. The lifespan is approximately 3 to 5 years after diagnosis, and the treatments available such as lung transp
Idiopathic pulmonary fibrosis is a severe lung disease with unknown aetiology. The lifespan is approximately 3 to 5 years after diagnosis, and the treatments available such as lung transp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3712::0bcbb5b45d35703c3794eb214f55880d
https://hdl.handle.net/20.500.11815/764
https://hdl.handle.net/20.500.11815/764
Autor:
Olafur Th Magnusson, Agnar Helgason, Gisli Masson, Adalbjorg Jonasdottir, Gudny A. Arnadottir, Ingileif Jonsdottir, Hakon Jonsson, Jona Saemundsdottir, Aslaug Jonasdottir, Gunnar Gudmundsson, Sif Hansdottir, Reynir Arngrímsson, Asgeir Sigurdsson, Gudmundur A. Thorisson, Ragnar P. Kristjansson, Stefania Benonisdottir, Patrick Sulem, Daniel F. Gudbjartsson, Unnur Thorsteinsdottir, Jon R. Kristinsson, Vigdis Petursdottir, Asmundur Oddsson, Kari Stefansson, Brynjar O. Jensson, Gerald Sulem
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-5 (2017)
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-5 (2017)
Background: Rare missense mutations in the gene encoding coatomer subunit alpha (COPA) have recently been shown to cause autoimmune interstitial lung, joint and kidney disease, also known as COPA syndrome, under a dominant mode of inheritance. Case p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c4c7e96b067cac28a85e16077801262
http://europepmc.org/articles/PMC5686906
http://europepmc.org/articles/PMC5686906
