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Substrate-biased activity-based probes identify proteases that cleave receptor CDCP1.
Kryza, Thomas; Khan, Tashbib; Lovell, Scott; Harrington, Brittney S; Yin, Julia; Porazinski, Sean; Pajic, Marina; Koistinen, Hannu; Rantala, Juha K; Dreyer, Tobias; Magdolen, Viktor; Reuning, Ute; He, Yaowu; Tate, Edward W; Hooper, John D.
Afiliación
  • Kryza T; Mater Research Institute, The University of Queensland, Translational Research Institute, Woolloongabba, Queensland, Australia.
  • Khan T; Mater Research Institute, The University of Queensland, Translational Research Institute, Woolloongabba, Queensland, Australia.
  • Lovell S; Department of Chemistry, Molecular Sciences Research Hub, Imperial College London, White City Campus, London, UK.
  • Harrington BS; Department of Pathology, Stanford University, Stanford, CA, USA.
  • Yin J; Mater Research Institute, The University of Queensland, Translational Research Institute, Woolloongabba, Queensland, Australia.
  • Porazinski S; The Kinghorn Cancer Centre, The Garvan Institute of Medical Research, Sydney, New South Wales, Australia.
  • Pajic M; St Vincent's Clinical School, Faculty of Medicine, University of NSW Sydney, Sydney, New South Wales, Australia.
  • Koistinen H; The Kinghorn Cancer Centre, The Garvan Institute of Medical Research, Sydney, New South Wales, Australia.
  • Rantala JK; St Vincent's Clinical School, Faculty of Medicine, University of NSW Sydney, Sydney, New South Wales, Australia.
  • Dreyer T; The Kinghorn Cancer Centre, The Garvan Institute of Medical Research, Sydney, New South Wales, Australia.
  • Magdolen V; St Vincent's Clinical School, Faculty of Medicine, University of NSW Sydney, Sydney, New South Wales, Australia.
  • Reuning U; Department of Clinical Chemistry, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • He Y; Misvik Biology, Turku, Finland.
  • Tate EW; Clinical Research Unit, Department of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
  • Hooper JD; Clinical Research Unit, Department of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Nat Chem Biol ; 17(7): 776-783, 2021 07.
Article en En | MEDLINE | ID: mdl-33859413
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Péptido Hidrolasas / Moléculas de Adhesión Celular / Antígenos de Neoplasias Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Nat Chem Biol Asunto de la revista: BIOLOGIA / QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Australia
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Péptido Hidrolasas / Moléculas de Adhesión Celular / Antígenos de Neoplasias Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Nat Chem Biol Asunto de la revista: BIOLOGIA / QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Australia