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Items: 1 to 20 of 88

1.

Homo-oligomerization of human corneodesmosin is mediated by its N-terminal glycine loop domain.

Caubet C, Jonca N, Lopez F, Estève JP, Simon M, Serre G.

J Invest Dermatol. 2004 Mar;122(3):747-54.

2.

Corneodesmosin, a component of epidermal corneocyte desmosomes, displays homophilic adhesive properties.

Jonca N, Guerrin M, Hadjiolova K, Caubet C, Gallinaro H, Simon M, Serre G.

J Biol Chem. 2002 Feb 15;277(7):5024-9. Epub 2001 Dec 5.

3.

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
4.

Refined characterization of corneodesmosin proteolysis during terminal differentiation of human epidermis and its relationship to desquamation.

Simon M, Jonca N, Guerrin M, Haftek M, Bernard D, Caubet C, Egelrud T, Schmidt R, Serre G.

J Biol Chem. 2001 Jun 8;276(23):20292-9. Epub 2001 Feb 16. Erratum in: J Biol Chem 2001 Dec 14;276(50):47742-3.

5.

Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction.

Leclerc EA, Huchenq A, Mattiuzzo NR, Metzger D, Chambon P, Ghyselinck NB, Serre G, Jonca N, Guerrin M.

J Cell Sci. 2009 Aug 1;122(Pt 15):2699-709. doi: 10.1242/jcs.050302. Epub 2009 Jul 13.

6.

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
8.

Degradation of corneodesmosome proteins by two serine proteases of the kallikrein family, SCTE/KLK5/hK5 and SCCE/KLK7/hK7.

Caubet C, Jonca N, Brattsand M, Guerrin M, Bernard D, Schmidt R, Egelrud T, Simon M, Serre G.

J Invest Dermatol. 2004 May;122(5):1235-44.

9.

Corneodesmosin expression in psoriasis vulgaris differs from normal skin and other inflammatory skin disorders.

Allen M, Ishida-Yamamoto A, McGrath J, Davison S, Iizuka H, Simon M, Guerrin M, Hayday A, Vaughan R, Serre G, Trembath R, Barker J.

Lab Invest. 2001 Jul;81(7):969-76.

PMID:
11454986
10.

Targeted deletion of the murine corneodesmosin gene delineates its essential role in skin and hair physiology.

Matsumoto M, Zhou Y, Matsuo S, Nakanishi H, Hirose K, Oura H, Arase S, Ishida-Yamamoto A, Bando Y, Izumi K, Kiyonari H, Oshima N, Nakayama R, Matsushima A, Hirota F, Mouri Y, Kuroda N, Sano S, Chaplin DD.

Proc Natl Acad Sci U S A. 2008 May 6;105(18):6720-4. doi: 10.1073/pnas.0709345105. Epub 2008 Apr 24.

11.

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
12.

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.

Levy-Nissenbaum E, Betz RC, Frydman M, Simon M, Lahat H, Bakhan T, Goldman B, Bygum A, Pierick M, Hillmer AM, Jonca N, Toribio J, Kruse R, Dewald G, Cichon S, Kubisch C, Guerrin M, Serre G, Nöthen MM, Pras E.

Nat Genet. 2003 Jun;34(2):151-3.

PMID:
12754508
13.
14.

Emerging issues of connexin channels: biophysics fills the gap.

Harris AL.

Q Rev Biophys. 2001 Aug;34(3):325-472. Review. Erratum in: Q Rev Biophys 2002 Feb;35(1):109.

PMID:
11838236
15.

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
16.

Characterization of the putative type III secretion ATPase CdsN (Cpn0707) of Chlamydophila pneumoniae.

Stone CB, Johnson DL, Bulir DC, Gilchrist JD, Mahony JB.

J Bacteriol. 2008 Oct;190(20):6580-8. doi: 10.1128/JB.00761-08. Epub 2008 Aug 15.

17.

The importance of TM3-4 loop subdomains for functional reconstitution of glycine receptors by independent domains.

Unterer B, Becker CM, Villmann C.

J Biol Chem. 2012 Nov 9;287(46):39205-15. doi: 10.1074/jbc.M112.376053. Epub 2012 Sep 20.

18.

A 4.2 kb upstream region of the human corneodesmosin gene directs site-specific expression in hair follicles and hyperkeratotic epidermis of transgenic mice.

Gallinaro H, Jonca N, Langbein L, Vincent C, Simon M, Serre G, Guerrin M.

J Invest Dermatol. 2004 Mar;122(3):730-8.

20.

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

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