187 related articles for article (PubMed ID: 21628128)
1. 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. PubMed ID: 21628128
[TBL] [Abstract][Full Text] [Related]
2. 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; 122(Pt 15):2699-709. PubMed ID: 19596793
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 12754508
[TBL] [Abstract][Full Text] [Related]
4. 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; 105(18):6720-4. PubMed ID: 18436651
[TBL] [Abstract][Full Text] [Related]
5. Order and disorder in corneocyte adhesion.
Ishida-Yamamoto A; Igawa S; Kishibe M
J Dermatol; 2011 Jul; 38(7):645-54. PubMed ID: 21545505
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 20448140
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 22146835
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 23957618
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 18460028
[TBL] [Abstract][Full Text] [Related]
10. Mutations in the CDSN gene cause peeling skin disease and hypotrichosis simplex of the scalp.
van der Velden JJAJ; van Geel M; Engelhart JJ; Jonkman MF; Steijlen PM
J Dermatol; 2020 Jan; 47(1):3-7. PubMed ID: 31663161
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 24116970
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 15086560
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 11454986
[TBL] [Abstract][Full Text] [Related]
14. Peeling Skin Disorders: A Paradigm for Skin Desquamation.
Has C
J Invest Dermatol; 2018 Aug; 138(8):1689-1691. PubMed ID: 30032785
[TBL] [Abstract][Full Text] [Related]
15. Refined Immunochemical Characterization in Healthy Dog Skin of the Epidermal Cornification Proteins, Filaggrin, and Corneodesmosin.
Pin D; Pendaries V; Keita Alassane S; Froment C; Amalric N; Cadiergues MC; Serre G; Haftek M; Vidémont E; Simon M
J Histochem Cytochem; 2019 Feb; 67(2):85-97. PubMed ID: 30199656
[TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 16307662
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 24794518
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 15086562
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 24372652
[TBL] [Abstract][Full Text] [Related]
20. [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. PubMed ID: 22875505
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]