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XBP1 signalling is essential for alleviating mutant protein aggregation in ER-stress related skeletal disease.
Piróg, Katarzyna A; Dennis, Ella P; Hartley, Claire L; Jackson, Robert M; Soul, Jamie; Schwartz, Jean-Marc; Bateman, John F; Boot-Handford, Raymond P; Briggs, Michael D.
Afiliación
  • Piróg KA; Institute of Genetic Medicine, Newcastle University, Newcastle, United Kingdom.
  • Dennis EP; Institute of Genetic Medicine, Newcastle University, Newcastle, United Kingdom.
  • Hartley CL; Wellcome Trust Centre for Cell Matrix Research, University of Manchester, Manchester, United Kingdom.
  • Jackson RM; Institute of Genetic Medicine, Newcastle University, Newcastle, United Kingdom.
  • Soul J; Wellcome Trust Centre for Cell Matrix Research, University of Manchester, Manchester, United Kingdom.
  • Schwartz JM; Wellcome Trust Centre for Cell Matrix Research, University of Manchester, Manchester, United Kingdom.
  • Bateman JF; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Boot-Handford RP; Wellcome Trust Centre for Cell Matrix Research, University of Manchester, Manchester, United Kingdom.
  • Briggs MD; Institute of Genetic Medicine, Newcastle University, Newcastle, United Kingdom.
PLoS Genet ; 15(7): e1008215, 2019 07.
Article en En | MEDLINE | ID: mdl-31260448
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Osteocondrodisplasias / Proteína 1 de Unión a la X-Box / Mutación Límite: Animals / Humans Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Osteocondrodisplasias / Proteína 1 de Unión a la X-Box / Mutación Límite: Animals / Humans Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido