Zobrazeno 1 - 10
of 369
pro vyhledávání: '"Janghra, N."'
Autor:
Zammarchi F; ADC Therapeutics (UK) Ltd, London, United Kingdom., Havenith KE; ADC Therapeutics (UK) Ltd, London, United Kingdom., Sachini N; ADC Therapeutics (UK) Ltd, London, United Kingdom., Janghra N; ADC Therapeutics (UK) Ltd, London, United Kingdom., Chivers S; ADC Therapeutics (UK) Ltd, London, United Kingdom., Idusogie E; ADC Therapeutics America, Inc, Murray Hill, United States., Gaudio E; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland., Tarantelli C; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland., Bertelli F; AstraZeneca (MedImmune/Spirogen), London, United Kingdom., Santos K; AstraZeneca (MedImmune/Spirogen), London, United Kingdom., Tyrer P; AstraZeneca (MedImmune/Spirogen), London, United Kingdom., Corbett S; University College London, London, United Kingdom., Spriano F; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland., Golino G; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland., Cascione L; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland., Bertoni F; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland.; Oncology Institute of Southern Switzerland, Ente Ospedaliero Cantonale, Bellinzona, Switzerland., Hartley JA; University College London, London, United Kingdom., van Berkel PH; ADC Therapeutics (UK) Ltd, London, United Kingdom.
Publikováno v:
Molecular cancer therapeutics [Mol Cancer Ther] 2024 Apr 02; Vol. 23 (4), pp. 520-531.
Akademický článek
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Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0150818 (2016)
PLoS ONE
PLoS ONE
Duchenne muscular dystrophy is a severe and currently incurable progressive neuromuscular condition, caused by mutations in the DMD gene that result in the inability to produce dystrophin. Lack of dystrophin leads to loss of muscle fibres and a reduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ffd1f947413c4d3f66fba41631d4831a
https://ora.ox.ac.uk/objects/uuid:925222c2-e1a6-416b-be5d-a3f3202f1e05
https://ora.ox.ac.uk/objects/uuid:925222c2-e1a6-416b-be5d-a3f3202f1e05
Autor:
Zammarchi F; ADC Therapeutics (UK) Limited, London, United Kingdom., Havenith KE; ADC Therapeutics (UK) Limited, London, United Kingdom., Chivers S; ADC Therapeutics (UK) Limited, London, United Kingdom., Hogg P; ADC Therapeutics (UK) Limited, London, United Kingdom., Bertelli F; AstraZeneca (MedImmune/Spirogen), Cambridge, United Kingdom., Tyrer P; AstraZeneca (MedImmune/Spirogen), Cambridge, United Kingdom., Janghra N; UCL Cancer Institute, London, United Kingdom., Reinert HW; UCL Cancer Institute, London, United Kingdom., Hartley JA; UCL Cancer Institute, London, United Kingdom., van Berkel PH; ADC Therapeutics (UK) Limited, London, United Kingdom.
Publikováno v:
Molecular cancer therapeutics [Mol Cancer Ther] 2022 Apr 01; Vol. 21 (4), pp. 582-593.
Publikováno v:
PloS one.
Duchenne muscular dystrophy is a severe and currently incurable progressive neuromuscular condition, caused by mutations in the DMD gene that result in the inability to produce dystrophin. Lack of dystrophin leads to loss of muscle fibres and a reduc
Autor:
Brambilla, Liliana1 (AUTHOR), Valori, Chiara F.1 (AUTHOR), Guidotti, Giulia1 (AUTHOR), Martorana, Francesca1 (AUTHOR), Sulmona, Claudia1 (AUTHOR), De Martini, Lisa Benedetta1 (AUTHOR), Canciani, Anselmo2 (AUTHOR), Fumagalli, Marco2 (AUTHOR), Talpo, Francesca3 (AUTHOR), Biella, Gerardo3 (AUTHOR), Di Pasquale, Elisa4,5 (AUTHOR), Iacobucci, Claudio6 (AUTHOR), Forneris, Federico2,7 (AUTHOR), Zhou, Haiyan8 (AUTHOR), Rossi, Daniela1 (AUTHOR) daniela.rossi@icsmaugeri.it
Publikováno v:
Translational Neurodegeneration. 12/16/2024, Vol. 13 Issue 1, p1-5. 5p.
Autor:
Rossi, Rachele1,2 (AUTHOR), Torelli, Silvia1,2 (AUTHOR), Moore, Marc1,2,3 (AUTHOR), Ala, Pierpaolo1,2 (AUTHOR), Morgan, Jennifer1,2 (AUTHOR), Malhotra, Jyoti4 (AUTHOR), Muntoni, Francesco1,2 (AUTHOR) f.muntoni@ucl.ac.uk
Publikováno v:
Skeletal Muscle. 11/29/2024, Vol. 14 Issue 1, p1-14. 14p.
Autor:
Caron, Nicholas S.1,2,3 (AUTHOR), Byrne, Lauren M.4 (AUTHOR), Lemarié, Fanny L.1,2,3 (AUTHOR), Bone, Jeffrey N.2,5 (AUTHOR), Aly, Amirah E.-E.1,2,3 (AUTHOR), Ko, Seunghyun1 (AUTHOR), Anderson, Christine1 (AUTHOR), Casal, Lorenzo L.1 (AUTHOR), Hill, Austin M.1 (AUTHOR), Hawellek, David J.6 (AUTHOR), McColgan, Peter7 (AUTHOR), Wild, Edward J.4 (AUTHOR), Leavitt, Blair R.1,2,3 (AUTHOR), Hayden, Michael R.1,2,3 (AUTHOR) mrh@cmmt.ubc.ca
Publikováno v:
Translational Neurodegeneration. 10/8/2024, Vol. 13 Issue 1, p1-22. 22p.
Autor:
Poyatos-García, Javier1,2,3 (AUTHOR) javier.poyatos@uv.es, Soblechero-Martín, Patricia4 (AUTHOR), Liquori, Alessandro5,6 (AUTHOR), López-Martínez, Andrea4 (AUTHOR), Maestre, Pilar1 (AUTHOR), González-Romero, Elisa5 (AUTHOR), Vázquez-Manrique, Rafael P.7,8,9 (AUTHOR), Muelas, Nuria1,10,11 (AUTHOR), García-García, Gema7,8,9 (AUTHOR), Ohana, Jessica12 (AUTHOR), Arechavala-Gomeza, Virginia4,13 (AUTHOR), Vílchez, Juan J.1,3,10,11 (AUTHOR) juan.vilchez@uv.es
Publikováno v:
Skeletal Muscle. 10/1/2024, Vol. 14 Issue 1, p1-14. 14p.
Autor:
Spriano F; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland., Tarantelli C; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland., Cascione L; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland.; SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland., Gaudio E; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland., Golino G; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland., Scalise L; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland., Cacciapuoti MT; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA., Zucca E; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland.; Department of Oncology, Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland., Stathis A; Department of Oncology, Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.; Faculty of Biomedical Sciences, USI, Lugano, Switzerland., Van Berkel PH; ADC Therapeutics (UK) Ltd., London, UK., Inghirami G; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA., Zammarchi F; ADC Therapeutics (UK) Ltd., London, UK., Bertoni F; Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland.; Department of Oncology, Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.
Publikováno v:
British journal of haematology [Br J Haematol] 2024 Nov; Vol. 205 (5), pp. 1873-1882. Date of Electronic Publication: 2024 Jul 30.