Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Alharti, Sameer"'
Autor:
Yang, Chunbo, Yaobo Xu, Yu, Min, Lee, David, Alharti, Sameer, Hellen, Nicola, Ahmad Shaik, Noor, Banaganapalli, Babajan, Sheikh Ali Mohamoud, Hussein, Elango, Ramu, Przyborski, Stefan, Tenin, Gennadiy, Williams, Simon, O’sullivan, John, Al-Radi, Osman O., Atta, Jameel, Harding, Sian E., Keavney, Bernard, Lako, Majlinda, Armstrong, Lyle
Publikováno v:
Human molecular genetics, 2017, Vol.26(16), pp.3031-3045 [Peer Reviewed Journal]
Yang, C, Xu, Y, Yu, M, Lee, D, Alharti, S, Hellen, N, Ahmad Shaik, N, Banaganapalli, B, Sheikh, H A M, Ramu, E, Przyborski, S, Tenin, G, Williams, S, O'Sullivan, J, Al-Radi, O O, Atta, J, Harding, S E, Keavney, B, Lako, M & Armstrong, L 2017, ' Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis ', Human Molecular Genetics . https://doi.org/10.1093/hmg/ddx140
BASE-Bielefeld Academic Search Engine
Yang, C, Xu, Y, Yu, M, Lee, D, Alharti, S, Hellen, N, Ahmad Shaik, N, Banaganapalli, B, Sheikh, H A M, Ramu, E, Przyborski, S, Tenin, G, Williams, S, O'Sullivan, J, Al-Radi, O O, Atta, J, Harding, S E, Keavney, B, Lako, M & Armstrong, L 2017, ' Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis ', Human Molecular Genetics . https://doi.org/10.1093/hmg/ddx140
BASE-Bielefeld Academic Search Engine
Hypoplastic left heart syndrome (HLHS) is among the most severe forms of congenital heart disease. Although the consensus view is that reduced flow through the left heart during development is a key factor in the development of the condition, the mol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b4dc72b29f43c00b28097b5d7a3f2c33
http://dro.dur.ac.uk/22174/2/22174P.pdf
http://dro.dur.ac.uk/22174/2/22174P.pdf
Autor:
Chunbo Yang, Yaobo Xu, Min Yu, Lee, David, Alharti, Sameer, Hellen, Nicola, Shaik, Noor Ahmad, Banaganapalli, Babajan, Ali Mohamoud, Hussein Sheikh, Elango, Ramu, Przyborski, Stefan, Tenin, Gennadiy, Williams, Simon, O'Sullivan, John, Al-Radi, Osman O., Atta, Jameel, Harding, Sian E., Keavney, Bernard, Lako, Majlinda, Armstrong, Lyle
Publikováno v:
Human Molecular Genetics; 8/15/2017, Vol. 26 Issue 16, p3031-3045, 15p
Autor:
Yang C; Institute of Genetic Medicine, Newcastle University, Newcastle, UK., Xu Y; Institute of Genetic Medicine, Newcastle University, Newcastle, UK., Yu M; Institute of Genetic Medicine, Newcastle University, Newcastle, UK., Lee D; Institute of Genetic Medicine, Newcastle University, Newcastle, UK., Alharti S; Princess Al Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Saudi Arabia., Hellen N; NHLI, Faculty of Medicine, Imperial College London, London, UK., Ahmad Shaik N; Princess Al Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Saudi Arabia., Banaganapalli B; Princess Al Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Saudi Arabia., Sheikh Ali Mohamoud H; Princess Al Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Saudi Arabia., Elango R; Princess Al Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Saudi Arabia., Przyborski S; Department of Bioscience, Durham University, Durham, UK., Tenin G; Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK., Williams S; Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK., O'Sullivan J; The Newcastle upon Tyne NHS Hospital, UK., Al-Radi OO; Department of Surgery, King Abdulaziz University, Saudi Arabia., Atta J; Department of Surgery, King Abdulaziz University, Saudi Arabia., Harding SE; NHLI, Faculty of Medicine, Imperial College London, London, UK., Keavney B; Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK., Lako M; Institute of Genetic Medicine, Newcastle University, Newcastle, UK., Armstrong L; Institute of Genetic Medicine, Newcastle University, Newcastle, UK.
Publikováno v:
Human molecular genetics [Hum Mol Genet] 2017 Aug 15; Vol. 26 (16), pp. 3031-3045.