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Norway

PMID:28356706  

A mutagenesis-derived Lrp5 mouse mutant with abnormal retinal vasculature and low bone mineral density.

Jeremy R Charette | Sarah E Earp | Brent A Bell | Cheryl L Ackert-Bicknell | Dana A Godfrey | Sujata Rao | Bela Anand-Apte | Patsy M Nishina | Neal S Peachey
Molecular vision | 2017

Familial exudative vitreoretinopathy (FEVR) is caused by mutations in the genes encoding low-density lipoprotein receptor-related protein (LRP5) or its interacting partners, namely frizzled class receptor 4 (FZD4) and norrin cystine knot growth factor (NDP). Mouse models for Lrp5, Fzd4, and Ndp have proven to be important for understanding the retinal pathophysiology underlying FEVR and systemic abnormalities related to defective Wnt signaling. Here, we report a new mouse mutant, tvrm111B, which was identified by electroretinogram (ERG) screening of mice generated in the Jackson Laboratory Translational Vision Research Models (TVRM) mutagenesis program.

Pubmed ID: 28356706

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Associated grants

  • Agency: NEI NIH HHS, United States
    Id: R01 EY027077
  • Agency: NEI NIH HHS, United States
    Id: R01 EY016490
  • Agency: NEI NIH HHS, United States
    Id: R01 EY020861
  • Agency: BLRD VA, United States
    Id: IK6 BX005233
  • Agency: NCI NIH HHS, United States
    Id: P30 CA034196
  • Agency: NEI NIH HHS, United States
    Id: R01 EY026181
  • Agency: NEI NIH HHS, United States
    Id: R01 EY011996
  • Agency: NEI NIH HHS, United States
    Id: R01 EY016501

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C57BL/6J (tool)

RRID:IMSR_JAX:000664

Mus musculus with name C57BL/6J from IMSR.

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DBA/2J (tool)

RRID:IMSR_JAX:000671

Mus musculus with name DBA/2J from IMSR.

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