Citations for
1FXR1, PKP1, PKP2, PKP3
Plakophilins 1 and 3 bind to FXR1 and thereby influence the mRNA stability of desmosomal proteins.
Fischer-Kešo R, Breuninger S, Hofmann S, Henn M, Röhrig T, Ströbel P, Stoecklin G, Hofmann I.
Mol Cell Biol 34(23):4244-56. doi: 10.1128/MCB.00766-14. Epub 2014 Sep 15. 2014
2EBSPD, PKP1
A plakophilin-1 gene mutation in an egyptian family with ectodermal dysplasia-skin fragility syndrome.
Abdalla EM, Has C.
Mol Syndromol 5(6):304-6. doi: 10.1159/000369267. Epub 2014 Nov 28. 2014
3PKP1
Plakophilin-1 protects keratinocytes from pemphigus vulgaris IgG by forming calcium-independent desmosomes.
Tucker DK, Stahley SN, Kowalczyk AP.
J Invest Dermatol 134(4):1033-43. doi: 10.1038/jid.2013.401. Epub 2013 Sep 20. 2014
4PKP1
Aberrantly methylated PKP1 in the progression of Barrett's esophagus to esophageal adenocarcinoma.
Kaz AM, Luo Y, Dzieciatkowski S, Chak A, Willis JE, Upton MP, Leidner RS, Grady WM.
Genes Chromosomes Cancer 51(4):384-93. doi: 10.1002/gcc.21923. Epub 2011 Dec 14. 2012
5EIF4A1, PKP1
Plakophilin 1 stimulates translation by promoting eIF4A1 activity.
Wolf A, Krause-Gruszczynska M, Birkenmeier O, Ostareck-Lederer A, Hüttelmaier S, Hatzfeld M.
J Cell Biol 188(4):463-71. doi: 10.1083/jcb.200908135. Epub 2010 Feb 15. 2010
6PKP1, PKP2
Plakophilin-1 localizes to the nucleus and interacts with single-stranded DNA.
Sobolik-Delmaire T, Reddy R, Pashaj A, Roberts BJ, Wahl JK 3rd.
J Invest Dermatol 130(11):2638-46. doi: 10.1038/jid.2010.191. Epub 2010 Jul 8. 2010
7PKP1
Ectodermal dysplasia-skin fragility syndrome.
McGrath JA, Mellerio JE.
Dermatol Clin 28(1):125-9. doi: 10.1016/j.det.2009.10.014. Review. 2010
8EBSPD, PKP1
Novel truncating mutations in PKP1 and DSP cause similar skin phenotypes in two Brazilian families.
Tanaka A, Lai-Cheong JE, Café ME, Gontijo B, Salomão PR, Pereira L, McGrath JA.
Br J Dermatol 160(3):692-7. doi: 10.1111/j.1365-2133.2008.08900.x. Epub 2008 Oct 21. 2009
9DSP, PKP1
Carboxyl terminus of Plakophilin-1 recruits it to plasma membrane, whereas amino terminus recruits desmoplakin and promotes desmosome assembly.
Sobolik-Delmaire T, Katafiasz D, Wahl JK 3rd.
J Biol Chem 281(25):16962-70. Epub 2006 Apr 21. 2006
10EBSPD, PKP1
Compound heterozygosity for new splice site mutations in the plakophilin 1 gene (PKP1) in a Chinese case of ectodermal dysplasia-skin fragility syndrome.
Zheng R, Bu DF, Zhu XJ.
Acta Derm Venereol 85(5):394-9. 2005
11EBSPD, PKP1
Clinical and molecular significance of splice site mutations in the plakophilin 1 gene in patients with ectodermal dysplasia-skin fragility syndrome.
Wessagowit V, McGrath JA.
Acta Derm Venereol 85(5):386-8. No abstract available. 2005
12PKP1
Lack of plakophilin 1 increases keratinocyte migration and reduces desmosome stability.
South AP, Wan H, Stone MG, Dopping-Hepenstal PJ, Purkis PE, Marshall JF, Leigh IM, Eady RA, Hart IR, McGrath JA.
J Cell Sci 116(Pt 16):3303-14. Epub 2003 Jul 2. 2003
13EBSPD, PKP1
Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndrome.
Whittock NV, Haftek M, Angoulvant N, Wolf F, Perrot H, Eady RA, McGrath JA.
J Invest Dermatol 115(3):368-74. 2000
14PKP1
Physical characterization of plakophilin 1 reconstituted with and without zinc.
Hofmann I, Mucke N, Reed J, Herrmann H, Langowski J.
Eur J Biochem 267(14):4381-9. 2000
15EBSPD, PKP1
Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1.
McGrath JA, et al.
Br J Dermatol 140(2):297-307. 1999
16EBSPD, PKP1
The head domain of plakophilin-1 binds to desmoplakin and enhances its recruitment to desmosomes. Implications for cutaneous disease.
Kowalczyk AP, et al.
J Biol Chem 274(26):18145-8. 1999
17PKP1, PKP2, PKP3
Plakophilin 3--a novel cell-type-specific desmosomal plaque protein.
Schmidt A, et al.
Differentiation 64(5):291-306 1999
18ARVCF, CTNND1, CTNND2, PKP4, PKP1, PKP2
Chromosomal mapping of human armadillo genes belonging to the p120ctn/plakophilin subfamily.
BonnŽ S, et al.
Genomics 51 : 452-454. 1998
19JUP, PKP1
The plakophilin 1 (PKP1) and plakoglobin (JUP) genes map to human chromosomes 1q and 17, respectively.
Cowley CM, Simrak D, Spurr NK, Arnemann J, Buxton RS.
Hum Genet 100(3-4):486-8. 1997
20EBSPD, PKP1
Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome.
McGrath JA, McMillan JR, Shemanko CS, Runswick SK, Leigh IM, Lane EB, Garrod DR, Eady RA.
Nat Genet 17(2):240-4. 1997
21PKP1
Band 6 protein, a major constituent of desmosomes from stratified epithelia, is a novel member of the armadillo multigene family.
Hatzfeld M, et al.
J Cell Sci 107 : 2259-2270. 1994
22APC, CTNNB1, CTNND1, JUP, KPNA3, ARVCF, CTNND2, KPNA2, PKP4, PKP1, PKP2, SPAG6
A repeating amino acid motif shared by proteins with diverse cellular roles.
Peifer M, et al.
Cell 76(5):789-91. No abstract available 1994