Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Richard M, Salmon"'
Autor:
Jingxu Guo, Bin Liu, Midory Thorikay, Minmin Yu, Xiaoyan Li, Zhen Tong, Richard M. Salmon, Randy J. Read, Peter ten Dijke, Nicholas W. Morrell, Wei Li
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-15 (2022)
Mutations in BMPR2 is the major genetic cause for pulmonary arterial hypertension (PAH). Here by solving crystal structures of BMPRII in binary and ternary receptor complexes with BMP10, the authors report the molecular recognition between BMPRII and
Externí odkaz:
https://doaj.org/article/3560786f93824f9e82ae50b7dd42ce97
Autor:
Richard M. Salmon, Jingxu Guo, Jennifer H. Wood, Zhen Tong, John S. Beech, Aleksandra Lawera, Minmin Yu, David J. Grainger, Jill Reckless, Nicholas W. Morrell, Wei Li
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
The molecular basis of activin receptor-like kinase 1 (ALK1)-mediated endothelial bone morphogenetic protein (BMP) signalling is not fully understood. Here, the authors present crystal structures of the BMP10:ALK1 and prodomain-bound BMP9:ALK1 comple
Externí odkaz:
https://doaj.org/article/c95928c8f6c04cf69fb1889c1608aeab
Autor:
Stefan Gräf, Matthias Haimel, Marta Bleda, Charaka Hadinnapola, Laura Southgate, Wei Li, Joshua Hodgson, Bin Liu, Richard M. Salmon, Mark Southwood, Rajiv D. Machado, Jennifer M. Martin, Carmen M. Treacy, Katherine Yates, Louise C. Daugherty, Olga Shamardina, Deborah Whitehorn, Simon Holden, Micheala Aldred, Harm J. Bogaard, Colin Church, Gerry Coghlan, Robin Condliffe, Paul A. Corris, Cesare Danesino, Mélanie Eyries, Henning Gall, Stefano Ghio, Hossein-Ardeschir Ghofrani, J. Simon R. Gibbs, Barbara Girerd, Arjan C. Houweling, Luke Howard, Marc Humbert, David G. Kiely, Gabor Kovacs, Robert V. MacKenzie Ross, Shahin Moledina, David Montani, Michael Newnham, Andrea Olschewski, Horst Olschewski, Andrew J. Peacock, Joanna Pepke-Zaba, Inga Prokopenko, Christopher J. Rhodes, Laura Scelsi, Werner Seeger, Florent Soubrier, Dan F. Stein, Jay Suntharalingam, Emilia M. Swietlik, Mark R. Toshner, David A. van Heel, Anton Vonk Noordegraaf, Quinten Waisfisz, John Wharton, Stephen J. Wort, Willem H. Ouwehand, Nicole Soranzo, Allan Lawrie, Paul D. Upton, Martin R. Wilkins, Richard C. Trembath, Nicholas W. Morrell
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-16 (2018)
Pulmonary arterial hypertension (PAH) is a rare lung disorder characterised by narrowing and obliteration of small pulmonary arteries ultimately leading to right heart failure. Here, the authors sequence whole genomes of over 1000 PAH patients and id
Externí odkaz:
https://doaj.org/article/cb3171b4e79940aa9ab812b5a9ce621a
Autor:
Rebecca M. Baron, Lu Long, Kim Hoenderdos, Charlotte Summers, Paola Caruso, Nicholas W. Morrell, Ross D. King, Ivana Nikolic, Mark Southwood, Xudong Yang, Richard M. Salmon, Paul B. Yu, Geoffrey A. Bocobo, Sussan Nourshargh, Angelica Higuera, Wei Li, Katharine M Lodge, Zhen Tong, Alison M. Condliffe, Paul D. Upton, He Jiang, Edwin R. Chilvers, Peiran Yang
Publikováno v:
American Journal of Respiratory and Critical Care Medicine
Rationale: Pulmonary endothelial permeability contributes to the high-permeability pulmonary edema that characterizes acute respiratory distress syndrome. Circulating BMP9 (bone morphogenetic protein 9) is emerging as an important regulator of pulmon
Autor:
Charlotte Summers, He Jiang, Ivana Nikolic, Alison M. Condliffe, Geoffrey A. Bocobo, Nicholas W. Morrell, Edwin R. Chilvers, Kim Hoenderdos, Peiran Yang, Angelica Higuera, Katharine M Lodge, Richard M. Salmon, Xudong Yang, Mark Southwood, Paul B. Yu, Paola Caruso, Lu Long, Rebecca M. Baron, Wei Li, Paul D. Upton, Zhen Tong
RationalePulmonary endothelial permeability contributes to the high-permeability pulmonary edema that characterizes acute respiratory distress syndrome (ARDS), which carries a high mortality. Circulating bone morphogeneic protein 9 (BMP9) is emerging
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f39d3085098aa77496ccd8f261c99be
https://doi.org/10.1101/2020.05.12.088880
https://doi.org/10.1101/2020.05.12.088880
Autor:
Christopher J. Rhodes, Allan Lawrie, Robert V. MacKenzie Ross, Mark Toshner, Mélanie Eyries, Werner Seeger, Richard M. Salmon, Stefano Ghio, Laura Scelsi, Stephen J. Wort, Gabor Kovacs, Florent Soubrier, J. Simon R. Gibbs, Richard C. Trembath, Jennifer M. Martin, Nicholas W. Morrell, Matthias Haimel, Gerry Coghlan, Marc Humbert, Jay Suntharalingam, Charaka Hadinnapola, Cesare Danesino, Willem H. Ouwehand, Louise C. Daugherty, Carmen M. Treacy, David G. Kiely, Andrea Olschewski, Joanna Pepke-Zaba, Deborah Whitehorn, Anton Vonk Noordegraaf, Andrew J. Peacock, Robin Condliffe, Horst Olschewski, Paul A. Corris, Joshua Hodgson, Hossein Ardeschir Ghofrani, Arjan C. Houweling, Colin Church, Jingxu Guo, Stefan Gräf, Barbara Girerd, Katherine Yates, Harm Jan Bogaard, Ivana Nikolic, Luke S. Howard, Henning Gall, Laura Southgate, Olga Shamardina, Emilia M. Swietlik, Marta Bleda, Rajiv D. Machado, Inga Prokopenko, John Wharton, James Liley, Simon Holden, Paul B. Yu, Martin R. Wilkins, Shahin Moledina, David Montani, Paul D. Upton, Wei Li
Publikováno v:
American Journal of Respiratory and Critical Care Medicine
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2020, 201 (5), pp.575-585. ⟨10.1164/rccm.201906-1141OC⟩
Hodgson, J, Swietlik, E M, Salmon, R M, Hadinnapola, C, Nikolic, I, Wharton, J, Guo, J, Liley, J, Haimel, M, Bleda, M, Southgate, L, Machado, R D, Martin, J M, Treacy, C M, Yates, K, Daugherty, L C, Shamardina, O, Whitehorn, D, Holden, S, Bogaard, H J, Church, C, Coghlan, G, Condliffe, R, Corris, P A, Danesino, C, Eyries, M, Gall, H, Ghio, S, Ghofrani, H-A, Gibbs, J S R, Girerd, B, Houweling, A C, Howard, L, Humbert, M, Kiely, D G, Kovacs, G, Lawrie, A, MacKenzie Ross, R V, Moledina, S, Montani, D, Olschewski, A, Olschewski, H, Ouwehand, W H, Peacock, A J, Pepke-Zaba, J, Prokopenko, I, Rhodes, C J, Scelsi, L, Seeger, W, Soubrier, F, Suntharalingam, J, Toshner, M R, Trembath, R C, Vonk Noordegraaf, A, Wort, S J, Wilkins, M R, Yu, P B, Li, W, Gräf, S, Upton, P D & Morrell, N W 2020, ' Characterization of GDF2 Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension ', American Journal of Respiratory and Critical Care Medicine, vol. 201, no. 5, pp. 575-585 . https://doi.org/10.1164/rccm.201906-1141OC
American Journal of Respiratory and Critical Care Medicine, 201(5), 575-585. American Thoracic Society
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2020, 201 (5), pp.575-585. ⟨10.1164/rccm.201906-1141OC⟩
Hodgson, J, Swietlik, E M, Salmon, R M, Hadinnapola, C, Nikolic, I, Wharton, J, Guo, J, Liley, J, Haimel, M, Bleda, M, Southgate, L, Machado, R D, Martin, J M, Treacy, C M, Yates, K, Daugherty, L C, Shamardina, O, Whitehorn, D, Holden, S, Bogaard, H J, Church, C, Coghlan, G, Condliffe, R, Corris, P A, Danesino, C, Eyries, M, Gall, H, Ghio, S, Ghofrani, H-A, Gibbs, J S R, Girerd, B, Houweling, A C, Howard, L, Humbert, M, Kiely, D G, Kovacs, G, Lawrie, A, MacKenzie Ross, R V, Moledina, S, Montani, D, Olschewski, A, Olschewski, H, Ouwehand, W H, Peacock, A J, Pepke-Zaba, J, Prokopenko, I, Rhodes, C J, Scelsi, L, Seeger, W, Soubrier, F, Suntharalingam, J, Toshner, M R, Trembath, R C, Vonk Noordegraaf, A, Wort, S J, Wilkins, M R, Yu, P B, Li, W, Gräf, S, Upton, P D & Morrell, N W 2020, ' Characterization of GDF2 Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension ', American Journal of Respiratory and Critical Care Medicine, vol. 201, no. 5, pp. 575-585 . https://doi.org/10.1164/rccm.201906-1141OC
American Journal of Respiratory and Critical Care Medicine, 201(5), 575-585. American Thoracic Society
International audience; Rationale: Recently, rare heterozygous mutations in GDF2 were identified in patients with pulmonary arterial hypertension (PAH). GDF2 encodes the circulating BMP (bone morphogenetic protein) type 9, which is a ligand for the B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7057d541ab94be4cf6a3450d45c90e47
https://hal.sorbonne-universite.fr/hal-02967807
https://hal.sorbonne-universite.fr/hal-02967807
Autor:
Joshua, Hodgson, Emilia M, Swietlik, Richard M, Salmon, Charaka, Hadinnapola, Ivana, Nikolic, John, Wharton, Jingxu, Guo, James, Liley, Matthias, Haimel, Marta, Bleda, Laura, Southgate, Rajiv D, Machado, Jennifer M, Martin, Carmen M, Treacy, Katherine, Yates, Louise C, Daugherty, Olga, Shamardina, Deborah, Whitehorn, Simon, Holden, Harm J, Bogaard, Colin, Church, Gerry, Coghlan, Robin, Condliffe, Paul A, Corris, Cesare, Danesino, Mélanie, Eyries, Henning, Gall, Stefano, Ghio, Hossein-Ardeschir, Ghofrani, J Simon R, Gibbs, Barbara, Girerd, Arjan C, Houweling, Luke, Howard, Marc, Humbert, David G, Kiely, Gabor, Kovacs, Allan, Lawrie, Robert V, MacKenzie Ross, Shahin, Moledina, David, Montani, Andrea, Olschewski, Horst, Olschewski, Willem H, Ouwehand, Andrew J, Peacock, Joanna, Pepke-Zaba, Inga, Prokopenko, Christopher J, Rhodes, Laura, Scelsi, Werner, Seeger, Florent, Soubrier, Jay, Suntharalingam, Mark R, Toshner, Richard C, Trembath, Anton, Vonk Noordegraaf, Stephen J, Wort, Martin R, Wilkins, Paul B, Yu, Wei, Li, Stefan, Gräf, Paul D, Upton, Nicholas W, Morrell
Publikováno v:
Am J Respir Crit Care Med
Rationale: Recently, rare heterozygous mutations in GDF2 were identified in patients with pulmonary arterial hypertension (PAH). GDF2 encodes the circulating BMP (bone morphogenetic protein) type 9, which is a ligand for the BMP2 receptor. Objectives
Publikováno v:
Biochemical Society Transactions. 44:1135-1141
Bone morphogenetic protein (BMP)9 and BMP10 are high affinity ligands for activin receptor-like kinase 1 (ALK1), a type I BMP receptor mainly expressed on vascular endothelial cells (ECs). ALK1-mediated BMP9/BMP10 signalling pathways have emerged as
Autor:
Ross D. King, Paola Caruso, Mark Southwood, Paul D. Upton, Nicholas W. Morrell, Sussan Nourshargh, Wei Li, Edwin R. Chilvers, Lu Long, Xudong Yang, Richard M. Salmon, Zhen Tong, Alison M. Condliffe
Publikováno v:
Fundamental mechanisms of pulmonary arterial hypertension.
Introduction and objective Heightened endothelial cell permeability is a feature of life-threatening conditions such as sepsis and acute respiratory distress syndrome. However, there is a lack of pharmacological therapies targeting this pathological
Autor:
Nicholas W. Morrell, John Wharton, Richard M. Salmon, Matthias Haimel, Joshua Hodgson, Wei Li, Stefan Gräf, Aleksandra Lawera, Martin R. Wilkins, Charaka Hadinnapola, Marta Bleda, Emilia M. Swietlik, Paul D. Upton
Publikováno v:
Fundamental mechanisms of pulmonary arterial hypertension.
Most heritable cases of pulmonary arterial hypertension (PAH) are explained by mutations in BMPR2, which encodes the bone morphogenetic protein type 2 receptor (BMPR-II). Additionally, mutations in the endothelial type 1 receptor, ALK1, can cause PAH