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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 2
1996 1
2001 1
2002 2
2003 3
2004 2
2005 1
2006 1
2007 2
2009 1
2011 1
2013 2
2014 2
2015 8
2016 1
2017 3
2018 1
2019 5
2020 7
2021 6
2022 1
2023 1
2024 0

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PubMed for id: 11014

49 results

Results by year

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Page 1
Two novel bi-allelic KDELR2 missense variants cause osteogenesis imperfecta with neurodevelopmental features.
Efthymiou S, Herman I, Rahman F, Anwar N, Maroofian R, Yip J, Mitani T, Calame DG, Hunter JV, Sutton VR, Yilmaz Gulec E, Duan R, Fatih JM, Marafi D, Pehlivan D, Jhangiani SN, Gibbs RA, Posey JE; SYNAPS Study Group; Maqbool S, Lupski JR, Houlden H. Efthymiou S, et al. Am J Med Genet A. 2021 Jul;185(7):2241-2249. doi: 10.1002/ajmg.a.62221. Epub 2021 May 8. Am J Med Genet A. 2021. PMID: 33964184 Free PMC article. No abstract available.
KDEL receptor regulates secretion by lysosome relocation- and autophagy-dependent modulation of lipid-droplet turnover.
Tapia D, Jiménez T, Zamora C, Espinoza J, Rizzo R, González-Cárdenas A, Fuentes D, Hernández S, Cavieres VA, Soza A, Guzmán F, Arriagada G, Yuseff MI, Mardones GA, Burgos PV, Luini A, González A, Cancino J. Tapia D, et al. Nat Commun. 2019 Feb 13;10(1):735. doi: 10.1038/s41467-019-08501-w. Nat Commun. 2019. PMID: 30760704 Free PMC article.
Sequence of a second human KDEL receptor.
Lewis MJ, Pelham HR. Lewis MJ, et al. J Mol Biol. 1992 Aug 20;226(4):913-6. doi: 10.1016/0022-2836(92)91039-r. J Mol Biol. 1992. PMID: 1325562
49 results