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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2008 | 1 |
2017 | 1 |
2021 | 1 |
2024 | 0 |
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A model for familial exudative vitreoretinopathy caused by LPR5 mutations.
Hum Mol Genet. 2008 Jun 1;17(11):1605-12. doi: 10.1093/hmg/ddn047. Epub 2008 Feb 9.
Hum Mol Genet. 2008.
PMID: 18263894
Free PMC article.
A mutagenesis-derived Lrp5 mouse mutant with abnormal retinal vasculature and low bone mineral density.
Charette JR, Earp SE, Bell BA, Ackert-Bicknell CL, Godfrey DA, Rao S, Anand-Apte B, Nishina PM, Peachey NS.
Charette JR, et al.
Mol Vis. 2017 Mar 18;23:140-148. eCollection 2017.
Mol Vis. 2017.
PMID: 28356706
Free PMC article.
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Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice.
Rios JJ, Denton K, Russell J, Kozlitina J, Ferreira CR, Lewanda AF, Mayfield JE, Moresco E, Ludwig S, Tang M, Li X, Lyon S, Khanshour A, Paria N, Khalid A, Li Y, Xie X, Feng JQ, Xu Q, Lu Y, Hammer RE, Wise CA, Beutler B.
Rios JJ, et al.
J Bone Miner Res. 2021 Aug;36(8):1548-1565. doi: 10.1002/jbmr.4323. Epub 2021 May 10.
J Bone Miner Res. 2021.
PMID: 33905568
Free PMC article.
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