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Modification of an aggressive model of Alport Syndrome reveals early differences in disease pathogenesis due to genetic background.
Falcone, Sara; Wisby, Laura; Nicol, Thomas; Blease, Andrew; Starbuck, Becky; Parker, Andrew; Sanderson, Jeremy; Brown, Steve D M; Scudamore, Cheryl L; Pusey, Charles D; Tam, Frederick W K; Potter, Paul K.
Afiliación
  • Falcone S; Mammalian Genetics Unit, Medical Research Council, Harwell science and innovation campus, Oxford, OX11 0RD, UK.
  • Wisby L; Mammalian Genetics Unit, Medical Research Council, Harwell science and innovation campus, Oxford, OX11 0RD, UK.
  • Nicol T; Mammalian Genetics Unit, Medical Research Council, Harwell science and innovation campus, Oxford, OX11 0RD, UK.
  • Blease A; Mammalian Genetics Unit, Medical Research Council, Harwell science and innovation campus, Oxford, OX11 0RD, UK.
  • Starbuck B; Mammalian Genetics Unit, Medical Research Council, Harwell science and innovation campus, Oxford, OX11 0RD, UK.
  • Parker A; Mammalian Genetics Unit, Medical Research Council, Harwell science and innovation campus, Oxford, OX11 0RD, UK.
  • Sanderson J; Mammalian Genetics Unit, Medical Research Council, Harwell science and innovation campus, Oxford, OX11 0RD, UK.
  • Brown SDM; Mammalian Genetics Unit, Medical Research Council, Harwell science and innovation campus, Oxford, OX11 0RD, UK.
  • Scudamore CL; Mary Lyon Centre, Medical Research Council, Harwell science and innovation campus, Oxford, OX11 0RD, UK.
  • Pusey CD; Renal and Vascular Inflammation Section, Department of Medicine, Imperial College, London, W12 0N, UK.
  • Tam FWK; Renal and Vascular Inflammation Section, Department of Medicine, Imperial College, London, W12 0N, UK.
  • Potter PK; Renal and Vascular Inflammation Section, Department of Medicine, Imperial College, London, W12 0N, UK. ppotter@brookes.ac.uk.
Sci Rep ; 9(1): 20398, 2019 12 31.
Article en En | MEDLINE | ID: mdl-31892712
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Colágeno Tipo IV / Antecedentes Genéticos / Mutación / Nefritis Hereditaria Tipo de estudio: Etiology_studies Límite: Animals Idioma: En Revista: Sci Rep Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
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XML
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Colágeno Tipo IV / Antecedentes Genéticos / Mutación / Nefritis Hereditaria Tipo de estudio: Etiology_studies Límite: Animals Idioma: En Revista: Sci Rep Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido