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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2016 | 2 |
2017 | 1 |
2018 | 1 |
2021 | 1 |
2023 | 1 |
2024 | 1 |
PubMed for id: 2465536021
6 results
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Page 1
Genetic determinants of micronucleus formation in vivo.
Nature. 2024 Mar;627(8002):130-136. doi: 10.1038/s41586-023-07009-0. Epub 2024 Feb 14.
Nature. 2024.
PMID: 38355793
Free PMC article.
Defects in placental syncytiotrophoblast cells are a common cause of developmental heart disease.
Radford BN, Zhao X, Glazer T, Eaton M, Blackwell D, Mohammad S, Lo Vercio LD, Devine J, Shalom-Barak T, Hallgrimsson B, Cross JC, Sucov HM, Barak Y, Dean W, Hemberger M.
Radford BN, et al.
Nat Commun. 2023 Mar 1;14(1):1174. doi: 10.1038/s41467-023-36740-5.
Nat Commun. 2023.
PMID: 36859534
Free PMC article.
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Accelerating functional gene discovery in osteoarthritis.
Butterfield NC, Curry KF, Steinberg J, Dewhurst H, Komla-Ebri D, Mannan NS, Adoum AT, Leitch VD, Logan JG, Waung JA, Ghirardello E, Southam L, Youlten SE, Wilkinson JM, McAninch EA, Vancollie VE, Kussy F, White JK, Lelliott CJ, Adams DJ, Jacques R, Bianco AC, Boyde A, Zeggini E, Croucher PI, Williams GR, Bassett JHD.
Butterfield NC, et al.
Nat Commun. 2021 Jan 20;12(1):467. doi: 10.1038/s41467-020-20761-5.
Nat Commun. 2021.
PMID: 33473114
Free PMC article.
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Placentation defects are highly prevalent in embryonic lethal mouse mutants.
Perez-Garcia V, Fineberg E, Wilson R, Murray A, Mazzeo CI, Tudor C, Sienerth A, White JK, Tuck E, Ryder EJ, Gleeson D, Siragher E, Wardle-Jones H, Staudt N, Wali N, Collins J, Geyer S, Busch-Nentwich EM, Galli A, Smith JC, Robertson E, Adams DJ, Weninger WJ, Mohun T, Hemberger M.
Perez-Garcia V, et al.
Nature. 2018 Mar 22;555(7697):463-468. doi: 10.1038/nature26002. Epub 2018 Mar 14.
Nature. 2018.
PMID: 29539633
Free PMC article.
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Highly variable penetrance of abnormal phenotypes in embryonic lethal knockout mice.
Wilson R, Geyer SH, Reissig L, Rose J, Szumska D, Hardman E, Prin F, McGuire C, Ramirez-Solis R, White J, Galli A, Tudor C, Tuck E, Mazzeo CI, Smith JC, Robertson E, Adams DJ, Mohun T, Weninger WJ.
Wilson R, et al.
Wellcome Open Res. 2017 Feb 27;1:1. doi: 10.12688/wellcomeopenres.9899.2. eCollection 2016.
Wellcome Open Res. 2017.
PMID: 27996060
Free PMC article.
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Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice.
Shaheen R, Anazi S, Ben-Omran T, Seidahmed MZ, Caddle LB, Palmer K, Ali R, Alshidi T, Hagos S, Goodwin L, Hashem M, Wakil SM, Abouelhoda M, Colak D, Murray SA, Alkuraya FS.
Shaheen R, et al.
Am J Hum Genet. 2016 Apr 7;98(4):643-52. doi: 10.1016/j.ajhg.2016.02.010. Epub 2016 Mar 24.
Am J Hum Genet. 2016.
PMID: 27018474
Free PMC article.
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