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Heterogeneity in the progression of retinal pathologies in mice harboring patient mimicking Impg2 mutations.
Williams, Brittany N; Draper, Adam; Lang, Patrick F; Lewis, Tylor R; Smith, Audrey L; Mayerl, Steven J; Rougié, Marie; Simon, Jeremy M; Arshavsky, Vadim Y; Greenwald, Scott H; Gamm, David M; Pinilla, Isabel; Philpot, Benjamin D.
Afiliación
  • Williams BN; Neuroscience Center, University of North Carolina, Chapel Hill, NC 27599, United States.
  • Draper A; Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, United States.
  • Lang PF; Carolina Institute for Developmental Disabilities, University of North Carolina, Chapel Hill, NC 27599, United States.
  • Lewis TR; Neuroscience Center, University of North Carolina, Chapel Hill, NC 27599, United States.
  • Smith AL; Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, United States.
  • Mayerl SJ; Neuroscience Center, University of North Carolina, Chapel Hill, NC 27599, United States.
  • Rougié M; Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, United States.
  • Simon JM; Department of Ophthalmology, Duke University, Durham, NC 27705, United States.
  • Arshavsky VY; Neuroscience Center, University of North Carolina, Chapel Hill, NC 27599, United States.
  • Greenwald SH; Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, United States.
  • Gamm DM; Department of Ophthalmology and Visual Sciences, McPherson Eye Research Institute, University of Wisconsin-Madison, Madison, WI 53705, United States.
  • Pinilla I; Neuroscience Center, University of North Carolina, Chapel Hill, NC 27599, United States.
  • Philpot BD; Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, United States.
Hum Mol Genet ; 33(5): 448-464, 2024 Feb 18.
Article en En | MEDLINE | ID: mdl-37975905
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteoglicanos / Retinitis Pigmentosa Límite: Adult / Animals / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteoglicanos / Retinitis Pigmentosa Límite: Adult / Animals / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido