Common JE - Search Results

1

Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high-performance liquid chromatography.

Rugg EL, Common JE, Wilgoss A, Stevens HP, Buchan J, Leigh IM, Kelsell DP. Rugg EL, et al. Among authors: common je. Br J Dermatol. 2002 Jun;146(6):952-7. doi: 10.1046/j.1365-2133.2002.04764.x. Br J Dermatol. 2002. PMID: 12072061

2

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma.

Norgett EE, Hatsell SJ, Carvajal-Huerta L, Cabezas JC, Common J, Purkis PE, Whittock N, Leigh IM, Stevens HP, Kelsell DP. Norgett EE, et al. Hum Mol Genet. 2000 Nov 1;9(18):2761-6. doi: 10.1093/hmg/9.18.2761. Hum Mol Genet. 2000. PMID: 11063735

3

Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations.

Di WL, Monypenny J, Common JE, Kennedy CT, Holland KA, Leigh IM, Rugg EL, Zicha D, Kelsell DP. Di WL, et al. Among authors: common je. Hum Mol Genet. 2002 Aug 15;11(17):2005-14. doi: 10.1093/hmg/11.17.2005. Hum Mol Genet. 2002. PMID: 12165562

4

Functional studies of human skin disease- and deafness-associated connexin 30 mutations.

Common JE, Becker D, Di WL, Leigh IM, O'Toole EA, Kelsell DP. Common JE, et al. Biochem Biophys Res Commun. 2002 Nov 15;298(5):651-6. doi: 10.1016/s0006-291x(02)02517-2. Biochem Biophys Res Commun. 2002. PMID: 12419304

5

Clinical and genetic heterogeneity of erythrokeratoderma variabilis.

Common JE, O'Toole EA, Leigh IM, Thomas A, Griffiths WA, Venning V, Grabczynska S, Peris Z, Kansky A, Kelsell DP. Common JE, et al. J Invest Dermatol. 2005 Nov;125(5):920-7. doi: 10.1111/j.0022-202X.2005.23919.x. J Invest Dermatol. 2005. PMID: 16297190 Free article.

6

Connexin 26 expression and mutation analysis in epidermal disease.

Di WL, Common JE, Kelsell DP. Di WL, et al. Among authors: common je. Cell Commun Adhes. 2001;8(4-6):415-8. doi: 10.3109/15419060109080763. Cell Commun Adhes. 2001. PMID: 12064628 Free article.

7

A case of erythrokeratoderma variabilis without mutations in connexin 31.

Ishida-Yamamoto A, Kelsell D, Common J, Houseman MJ, Hashimoto M, Shibaki H, Asano K, Takahashi H, Hashimoto Y, Senshu T, Leigh IM, Iizuka H. Ishida-Yamamoto A, et al. Br J Dermatol. 2000 Dec;143(6):1283-7. doi: 10.1046/j.1365-2133.2000.03902.x. Br J Dermatol. 2000. PMID: 11122035

8

Cellular mechanisms of mutant connexins in skin disease and hearing loss.

Common JE, Di WL, Davies D, Galvin H, Leigh IM, O'Toole EA, Kelsell DP. Common JE, et al. Cell Commun Adhes. 2003 Jul-Dec;10(4-6):347-51. doi: 10.1080/cac.10.4-6.347.351. Cell Commun Adhes. 2003. PMID: 14681040 Free article.

9

Specific loss of connexin 26 expression in ductal sweat gland epithelium associated with the deletion mutation del(GJB6-D13S1830).

Common JE, Bitner-Glindzicz M, O'Toole EA, Barnes MR, Jenkins L, Forge A, Kelsell DP. Common JE, et al. Clin Exp Dermatol. 2005 Nov;30(6):688-93. doi: 10.1111/j.1365-2230.2005.01878.x. Clin Exp Dermatol. 2005. PMID: 16197390

10

Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysis.

Di WL, Gu Y, Common JE, Aasen T, O'Toole EA, Kelsell DP, Zicha D. Di WL, et al. Among authors: common je. J Cell Sci. 2005 Apr 1;118(Pt 7):1505-14. doi: 10.1242/jcs.01733. Epub 2005 Mar 15. J Cell Sci. 2005. PMID: 15769851 Free article.

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