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Year | Number of Results |
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2000 | 1 |
2002 | 1 |
2005 | 1 |
2013 | 1 |
2024 | 0 |
PubMed (cited) for id: 300286
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Generation of mice deficient in both KLF3/BKLF and KLF8 reveals a genetic interaction and a role for these factors in embryonic globin gene silencing.
Mol Cell Biol. 2013 Aug;33(15):2976-87. doi: 10.1128/MCB.00074-13. Epub 2013 May 28.
Mol Cell Biol. 2013.
PMID: 23716600
Free PMC article.
Mammalian SP/KLF transcription factors: bring in the family.
Suske G, Bruford E, Philipsen S.
Suske G, et al.
Genomics. 2005 May;85(5):551-6. doi: 10.1016/j.ygeno.2005.01.005.
Genomics. 2005.
PMID: 15820306
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Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation.
Lossi AM, Laugier-Anfossi F, Depetris D, Gecz J, Gedeon A, Kooy F, Schwartz C, Mattei MG, Croquette MF, Villard L.
Lossi AM, et al.
J Med Genet. 2002 Feb;39(2):113-7. doi: 10.1136/jmg.39.2.113.
J Med Genet. 2002.
PMID: 11836360
Free PMC article.
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Human Krüppel-like factor 8: a CACCC-box binding protein that associates with CtBP and represses transcription.
van Vliet J, Turner J, Crossley M.
van Vliet J, et al.
Nucleic Acids Res. 2000 May 1;28(9):1955-62. doi: 10.1093/nar/28.9.1955.
Nucleic Acids Res. 2000.
PMID: 10756197
Free PMC article.
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