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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1997 | 1 |
1998 | 2 |
2003 | 1 |
2006 | 1 |
2010 | 1 |
2024 | 0 |
PubMed (cited) for id: 602100
6 results
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Page 1
The absence of Prep1 causes p53-dependent apoptosis of mouse pluripotent epiblast cells.
Development. 2010 Oct;137(20):3393-403. doi: 10.1242/dev.050567. Epub 2010 Sep 8.
Development. 2010.
PMID: 20826531
Free article.
Hypomorphic mutation of the TALE gene Prep1 (pKnox1) causes a major reduction of Pbx and Meis proteins and a pleiotropic embryonic phenotype.
Ferretti E, Villaescusa JC, Di Rosa P, Fernandez-Diaz LC, Longobardi E, Mazzieri R, Miccio A, Micali N, Selleri L, Ferrari G, Blasi F.
Ferretti E, et al.
Mol Cell Biol. 2006 Aug;26(15):5650-62. doi: 10.1128/MCB.00313-06.
Mol Cell Biol. 2006.
PMID: 16847320
Free PMC article.
Item in Clipboard
Overexpression of FABP7 in Down syndrome fetal brains is associated with PKNOX1 gene-dosage imbalance.
Sánchez-Font MF, Bosch-Comas A, Gonzàlez-Duarte R, Marfany G.
Sánchez-Font MF, et al.
Nucleic Acids Res. 2003 Jun 1;31(11):2769-77. doi: 10.1093/nar/gkg396.
Nucleic Acids Res. 2003.
PMID: 12771203
Free PMC article.
Item in Clipboard
Prep1, a novel functional partner of Pbx proteins.
Berthelsen J, Zappavigna V, Mavilio F, Blasi F.
Berthelsen J, et al.
EMBO J. 1998 Mar 2;17(5):1423-33. doi: 10.1093/emboj/17.5.1423.
EMBO J. 1998.
PMID: 9482739
Free PMC article.
Item in Clipboard
PKNOX1, a gene encoding PREP1, a new regulator of Pbx activity, maps on human chromosome 21q22.3 and murine chromosome 17B/C.
Berthelsen J, Viggiano L, Schulz H, Ferretti E, Consalez GG, Rocchi M, Blasi F.
Berthelsen J, et al.
Genomics. 1998 Jan 15;47(2):323-4. doi: 10.1006/geno.1997.5086.
Genomics. 1998.
PMID: 9479508
No abstract available.
Item in Clipboard
Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3.
Chen H, Rossier C, Nakamura Y, Lynn A, Chakravarti A, Antonarakis SE.
Chen H, et al.
Genomics. 1997 Apr 15;41(2):193-200. doi: 10.1006/geno.1997.4632.
Genomics. 1997.
PMID: 9143494
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