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Evolutionarily conserved genetic interactions between nphp-4 and bbs-5 mutations exacerbate ciliopathy phenotypes.
Genetics. 2022 Jan 4;220(1):iyab209. doi: 10.1093/genetics/iyab209.
Genetics. 2022.
PMID: 34850872
Free PMC article.
A mouse model of BBS identifies developmental and homeostatic effects of BBS5 mutation and identifies novel pituitary abnormalities.
Bentley-Ford MR, Engle SE, Clearman KR, Haycraft CJ, Andersen RS, Croyle MJ, Rains AB, Berbari NF, Yoder BK.
Bentley-Ford MR, et al.
Hum Mol Genet. 2021 Apr 26;30(3-4):234-246. doi: 10.1093/hmg/ddab039.
Hum Mol Genet. 2021.
PMID: 33560420
Free PMC article.
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A transgenic Alx4-CreER mouse to analyze anterior limb and nephric duct development.
Rockwell DM, O'Connor AK, Bentley-Ford MR, Haycraft CJ, Croyle MJ, Brewer KM, Berbari NF, Kesterson RA, Yoder BK.
Rockwell DM, et al. Among authors: bentley ford mr.
Dev Dyn. 2022 Sep;251(9):1524-1534. doi: 10.1002/dvdy.328. Epub 2021 Mar 23.
Dev Dyn. 2022.
PMID: 33728725
Free PMC article.
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ATXN10 Is Required for Embryonic Heart Development and Maintenance of Epithelial Cell Phenotypes in the Adult Kidney and Pancreas.
Bentley-Ford MR, Andersen RS, Croyle MJ, Haycraft CJ, Clearman KR, Foote JB, Reiter JF, Yoder BK.
Bentley-Ford MR, et al.
Front Cell Dev Biol. 2021 Dec 14;9:705182. doi: 10.3389/fcell.2021.705182. eCollection 2021.
Front Cell Dev Biol. 2021.
PMID: 34970537
Free PMC article.
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