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Items: 1 to 20 of 81

1.

Analysis of protein-protein interaction between late cornified envelope proteins and corneodesmosin.

Bergboer JG, Dulak MG, van Vlijmen-Willems IM, Jonca N, van Wijk E, Hendriks WJ, Zeeuwen PL, Schalkwijk J.

Exp Dermatol. 2014 Oct;23(10):769-71. doi: 10.1111/exd.12524.

PMID:
25078048
2.

Homozygous deletion of six genes including corneodesmosin on chromosome 6p21.3 is associated with generalized peeling skin disease.

Teye K, Hamada T, Krol RP, Numata S, Ishii N, Matsuda M, Ohata C, Furumura M, Hashimoto T.

J Dermatol Sci. 2014 Jul;75(1):36-42. doi: 10.1016/j.jdermsci.2014.04.003. Epub 2014 Apr 15.

PMID:
24794518
3.

Inflammatory peeling skin syndrome caused by homozygous genomic deletion in the PSORS1 region encompassing the CDSN gene.

Ishida-Yamamoto A, Furio L, Igawa S, Honma M, Tron E, Malan V, Murakami M, Hovnanian A.

Exp Dermatol. 2014 Jan;23(1):60-3. doi: 10.1111/exd.12292.

PMID:
24372652
4.

Alu-mediated large deletion of the CDSN gene as a cause of peeling skin disease.

Wada T, Matsuda Y, Muraoka M, Toma T, Takehara K, Fujimoto M, Yachie A.

Clin Genet. 2014 Oct;86(4):383-6. doi: 10.1111/cge.12294. Epub 2013 Oct 25.

PMID:
24116970
5.

Identification of the first nonsense CDSN mutation with expression of a truncated protein causing peeling skin syndrome type B.

Mallet A, Kypriotou M, George K, Leclerc E, Rivero D, Mazereeuw-Hautier J, Serre G, Huber M, Jonca N, Hohl D.

Br J Dermatol. 2013 Dec;169(6):1322-5. doi: 10.1111/bjd.12593.

PMID:
23957618
6.

A novel nonsense mutation in the CDSN gene underlying hypotrichosis simplex of the scalp in a Chinese family.

Yang SX, Yin JH, Lin ZM, Wang HJ, Ren YL, Zhang J, Li RY, Yang Y.

Clin Exp Dermatol. 2014 Jan;39(1):75-7. doi: 10.1111/ced.12168. Epub 2013 Jun 8. No abstract available.

PMID:
23746069
7.

[Clinical investigation of a Chinese family with hypotrichosis simplex of the scalp and mutational analysis of CDSN gene].

Huang XS, Jiang HO, Quan QL.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):452-4. doi: 10.3760/cma.j.issn.1003-9406.2012.04.016. Chinese.

PMID:
22875505
8.

Inflammatory peeling skin syndrome caused a novel mutation in CDSN.

Telem DF, Israeli S, Sarig O, Sprecher E.

Arch Dermatol Res. 2012 Apr;304(3):251-5. doi: 10.1007/s00403-011-1195-z. Epub 2011 Dec 7.

PMID:
22146835
9.

Association of -619C/T polymorphism in CDSN gene and psoriasis risk: a meta-analysis.

Wu Y, Wang B, Liu JL, Gao XH, Chen HD, Li YH.

Genet Mol Res. 2011 Oct 21;10(4):3632-40. doi: 10.4238/2011.October.21.6.

10.

A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.

Mazereeuw-Hautier J, Leclerc EA, Simon M, Serre G, Jonca N.

Br J Dermatol. 2011 Nov;165(5):1152-5. doi: 10.1111/j.1365-2133.2011.10529.x. No abstract available.

PMID:
21777220
11.

Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses.

Jonca N, Leclerc EA, Caubet C, Simon M, Guerrin M, Serre G.

Eur J Dermatol. 2011 May;21 Suppl 2:35-42. doi: 10.1684/ejd.2011.1264. Review.

PMID:
21628128
12.

Protease sensitivity of corneodesmosin variants encoded by the six more common CDSN haplotypes.

Jonca N, Caubet C, Leclerc EA, Guerrin M, Simon M, Serre G.

J Invest Dermatol. 2011 Jun;131(6):1381-4. doi: 10.1038/jid.2011.7. Epub 2011 Feb 10. No abstract available.

13.

Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin.

Israeli S, Zamir H, Sarig O, Bergman R, Sprecher E.

J Invest Dermatol. 2011 Mar;131(3):779-81. doi: 10.1038/jid.2010.363. Epub 2010 Dec 30. No abstract available.

14.

Detection of corneodesmosin on the surface of stratum corneum using atomic force microscopy.

Rankl C, Zhu R, Luengo GS, Donovan M, Baghdadli N, Hinterdorfer P.

Exp Dermatol. 2010 Nov;19(11):1014-9. doi: 10.1111/j.1600-0625.2010.01179.x.

PMID:
21182673
15.

[Peeling skin disease: the responsibility of corneodesmosin].

Dereure O.

Ann Dermatol Venereol. 2010 Dec;137(12):841. doi: 10.1016/j.annder.2010.09.012. Epub 2010 Oct 20. French. No abstract available.

PMID:
21134591
16.

A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.

Caubet C, Bousset L, Clemmensen O, Sourigues Y, Bygum A, Chavanas S, Coudane F, Hsu CY, Betz RC, Melki R, Simon M, Serre G.

FASEB J. 2010 Sep;24(9):3416-26. doi: 10.1096/fj.10-155622. Epub 2010 May 6.

PMID:
20448140
17.

Alterations in the desquamation-related proteolytic cleavage of corneodesmosin and other corneodesmosomal proteins in psoriatic lesional epidermis.

Simon M, Tazi-Ahnini R, Jonca N, Caubet C, Cork MJ, Serre G.

Br J Dermatol. 2008 Jul;159(1):77-85. doi: 10.1111/j.1365-2133.2008.08578.x. Epub 2008 Jul 1.

PMID:
18460028
18.

A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp.

Dávalos NO, García-Vargas A, Pforr J, Dávalos IP, Picos-Cárdenas VJ, García-Cruz D, Kruse R, Figuera LE, Nöthen MM, Betz RC.

Br J Dermatol. 2005 Dec;153(6):1216-9.

PMID:
16307662
19.

Corneodesmosin polymorphisms in psoriatic arthritis.

Butt C, Rahman P, Siannis F, Farewell VT, Gladman DD.

Rheumatology (Oxford). 2005 May;44(5):684-5. Epub 2005 Feb 16. No abstract available.

PMID:
15716318
20.

Mapping of the major psoriasis-susceptibility locus (PSORS1) in a 70-Kb interval around the corneodesmosin gene (CDSN).

Orrù S, Giuressi E, Carcassi C, Casula M, Contu L.

Am J Hum Genet. 2005 Jan;76(1):164-71. Epub 2004 Nov 4.

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