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Year | Number of Results |
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1990 | 1 |
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PubMed (OMIM) for id: 2355
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FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects.
Genet Med. 2022 Dec;24(12):2475-2486. doi: 10.1016/j.gim.2022.09.002. Epub 2022 Oct 4.
Genet Med. 2022.
PMID: 36197437
Free article.
Osteoclast size is controlled by Fra-2 through LIF/LIF-receptor signalling and hypoxia.
Bozec A, Bakiri L, Hoebertz A, Eferl R, Schilling AF, Komnenovic V, Scheuch H, Priemel M, Stewart CL, Amling M, Wagner EF.
Bozec A, et al.
Nature. 2008 Jul 10;454(7201):221-5. doi: 10.1038/nature07019. Epub 2008 Jun 11.
Nature. 2008.
PMID: 18548006
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Chromosomal assignment of the human gene encoding the Fos-related antigen-2 (FRA2) to chromosome 2p22-p23.
Molven A, Houge G, Berger R.
Molven A, et al.
Genomics. 1996 Nov 15;38(1):72-5. doi: 10.1006/geno.1996.0593.
Genomics. 1996.
PMID: 8954781
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Isolation of human fos-related genes and their expression during monocyte-macrophage differentiation.
Matsui M, Tokuhara M, Konuma Y, Nomura N, Ishizaki R.
Matsui M, et al.
Oncogene. 1990 Mar;5(3):249-55.
Oncogene. 1990.
PMID: 2107490
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