McKeon F - Search Results

1

Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63.

Duijf PH, Vanmolkot KR, Propping P, Friedl W, Krieger E, McKeon F, Dötsch V, Brunner HG, van Bokhoven H. Duijf PH, et al. Among authors: mckeon f. Hum Mol Genet. 2002 Apr 1;11(7):799-804. doi: 10.1093/hmg/11.7.799. Hum Mol Genet. 2002. PMID: 11929852

2

Mutations in the p53 homolog p63: allele-specific developmental syndromes in humans.

van Bokhoven H, McKeon F. van Bokhoven H, et al. Among authors: mckeon f. Trends Mol Med. 2002 Mar;8(3):133-9. doi: 10.1016/s1471-4914(01)02260-2. Trends Mol Med. 2002. PMID: 11879774 Review.

3

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome.

Celli J, Duijf P, Hamel BC, Bamshad M, Kramer B, Smits AP, Newbury-Ecob R, Hennekam RC, Van Buggenhout G, van Haeringen A, Woods CG, van Essen AJ, de Waal R, Vriend G, Haber DA, Yang A, McKeon F, Brunner HG, van Bokhoven H. Celli J, et al. Among authors: mckeon f. Cell. 1999 Oct 15;99(2):143-53. doi: 10.1016/s0092-8674(00)81646-3. Cell. 1999. PMID: 10535733 Free article.

4

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.

McGrath JA, Duijf PH, Doetsch V, Irvine AD, de Waal R, Vanmolkot KR, Wessagowit V, Kelly A, Atherton DJ, Griffiths WA, Orlow SJ, van Haeringen A, Ausems MG, Yang A, McKeon F, Bamshad MA, Brunner HG, Hamel BC, van Bokhoven H. McGrath JA, et al. Among authors: mckeon f. Hum Mol Genet. 2001 Feb 1;10(3):221-9. doi: 10.1093/hmg/10.3.221. Hum Mol Genet. 2001. PMID: 11159940

5

A C-terminal inhibitory domain controls the activity of p63 by an intramolecular mechanism.

Serber Z, Lai HC, Yang A, Ou HD, Sigal MS, Kelly AE, Darimont BD, Duijf PH, Van Bokhoven H, McKeon F, Dötsch V. Serber Z, et al. Among authors: mckeon f. Mol Cell Biol. 2002 Dec;22(24):8601-11. doi: 10.1128/MCB.22.24.8601-8611.2002. Mol Cell Biol. 2002. PMID: 12446779 Free PMC article.

6

p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities.

Yang A, Kaghad M, Wang Y, Gillett E, Fleming MD, Dötsch V, Andrews NC, Caput D, McKeon F. Yang A, et al. Among authors: mckeon f. Mol Cell. 1998 Sep;2(3):305-16. doi: 10.1016/s1097-2765(00)80275-0. Mol Cell. 1998. PMID: 9774969 Free article.

7

International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) syndrome.

Fete M, vanBokhoven H, Clements SE, McKeon F, Roop DR, Koster MI, Missero C, Attardi LD, Lombillo VA, Ratovitski E, Julapalli M, Ruths D, Sybert VP, Siegfried EC, Bree AF. Fete M, et al. Among authors: mckeon f. Am J Med Genet A. 2009 Sep;149A(9):1885-93. doi: 10.1002/ajmg.a.32761. Am J Med Genet A. 2009. PMID: 19353643 Free PMC article.

8

Conformational stability and activity of p73 require a second helix in the tetramerization domain.

Coutandin D, Löhr F, Niesen FH, Ikeya T, Weber TA, Schäfer B, Zielonka EM, Bullock AN, Yang A, Güntert P, Knapp S, McKeon F, Ou HD, Dötsch V. Coutandin D, et al. Among authors: mckeon f. Cell Death Differ. 2009 Dec;16(12):1582-9. doi: 10.1038/cdd.2009.139. Epub 2009 Sep 18. Cell Death Differ. 2009. PMID: 19763140

9

DNA damage in oocytes induces a switch of the quality control factor TAp63α from dimer to tetramer.

Deutsch GB, Zielonka EM, Coutandin D, Weber TA, Schäfer B, Hannewald J, Luh LM, Durst FG, Ibrahim M, Hoffmann J, Niesen FH, Sentürk A, Kunkel H, Brutschy B, Schleiff E, Knapp S, Acker-Palmer A, Grez M, McKeon F, Dötsch V. Deutsch GB, et al. Among authors: mckeon f. Cell. 2011 Feb 18;144(4):566-76. doi: 10.1016/j.cell.2011.01.013. Cell. 2011. PMID: 21335238 Free PMC article.

10

DNA-binding and transactivation activities are essential for TAp63 protein degradation.

Ying H, Chang DL, Zheng H, McKeon F, Xiao ZX. Ying H, et al. Among authors: mckeon f. Mol Cell Biol. 2005 Jul;25(14):6154-64. doi: 10.1128/MCB.25.14.6154-6164.2005. Mol Cell Biol. 2005. PMID: 15988026 Free PMC article.

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