Mellerio JE - Search Results

1

Extracellular Vesicles as Biomarkers for the Detection of a Tumor Marker Gene in Epidermolysis Bullosa-Associated Squamous Cell Carcinoma.

Sun Y, Woess K, Kienzl M, Leb-Reichl VM, Feinle A, Wimmer M, Zauner R, Wally V, Luetz-Meindl U, Mellerio JE, Fuentes I, South AP, Bauer JW, Reichelt J, Furihata T, Guttmann-Gruber C, Piñón Hofbauer J. Sun Y, et al. Among authors: mellerio je. J Invest Dermatol. 2018 May;138(5):1197-1200. doi: 10.1016/j.jid.2017.11.022. Epub 2017 Dec 2. J Invest Dermatol. 2018. PMID: 29203361 Free article. No abstract available.

2

A recurrent laminin 5 mutation in British patients with lethal (Herlitz) junctional epidermolysis bullosa: evidence for a mutational hotspot rather than propagation of an ancestral allele.

Ashton GH, Mellerio JE, Dunnill MG, Pulkkinen L, Christiano AM, Uitto J, Eady RA, McGrath JA. Ashton GH, et al. Among authors: mellerio je. Br J Dermatol. 1997 May;136(5):674-7. Br J Dermatol. 1997. PMID: 9205497

3

Recurrent mutations in the type VII collagen gene (COL7A1) in patients with recessive dystrophic epidermolysis bullosa.

Mellerio JE, Dunnill MG, Allison W, Ashton GH, Christiano AM, Uitto J, Eady RA, McGrath JA. Mellerio JE, et al. J Invest Dermatol. 1997 Aug;109(2):246-9. doi: 10.1111/1523-1747.ep12319792. J Invest Dermatol. 1997. PMID: 9242516 Free article.

4

E210K mutation in the gene encoding the beta3 chain of laminin-5 (LAMB3) is predictive of a phenotype of generalized atrophic benign epidermolysis bullosa.

Mellerio JE, Eady RA, Atherton DJ, Lake BD, McGrath JA. Mellerio JE, et al. Br J Dermatol. 1998 Aug;139(2):325-31. doi: 10.1046/j.1365-2133.1998.02377.x. Br J Dermatol. 1998. PMID: 9767254

5

Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14).

Shemanko CS, Mellerio JE, Tidman MJ, Lane EB, Eady RA. Shemanko CS, et al. Among authors: mellerio je. J Invest Dermatol. 1998 Nov;111(5):893-5. doi: 10.1046/j.1523-1747.1998.00388.x. J Invest Dermatol. 1998. PMID: 9804355 Free article.

6

A recurrent glycine substitution mutation, G2043R, in the type VII collagen gene (COL7A1) in dominant dystrophic epidermolysis bullosa.

Mellerio JE, Salas-Alanis JC, Talamantes ML, Horn H, Tidman MJ, Ashton GH, Eady RA, McGrath JA. Mellerio JE, et al. Br J Dermatol. 1998 Oct;139(4):730-7. doi: 10.1046/j.1365-2133.1998.02496.x. Br J Dermatol. 1998. PMID: 9892921

7

A recurrent frameshift mutation in exon 19 of the type VII collagen gene (COL7A1) in Mexican patients with recessive dystrophic epidermolysis bullosa.

Mellerio JE, Salas-Alanis JC, Amaya-Guerra M, Tamez E, Ashton GH, Mohammedi R, Eady RA, McGrath JA. Mellerio JE, et al. Exp Dermatol. 1999 Feb;8(1):22-9. doi: 10.1111/j.1600-0625.1999.tb00344.x. Exp Dermatol. 1999. PMID: 10206718

8

A recurrent COL7A1 mutation, R2814X, in British patients with recessive dystrophic epidermolysis bullosa.

Mohammedi R, Mellerio JE, Ashton GH, Eady RA, McGrath JA. Mohammedi R, et al. Among authors: mellerio je. Clin Exp Dermatol. 1999 Jan;24(1):37-9. doi: 10.1046/j.1365-2230.1999.00404.x. Clin Exp Dermatol. 1999. PMID: 10233647

9

Recurrent molecular abnormalities in type VII collagen in Southern Italian patients with recessive dystrophic epidermolysis bullosa.

Ashton GH, Mellerio JE, Dunnill MG, Milana G, Mayou BJ, Carrera J, McGrath JA, Eady RA. Ashton GH, et al. Among authors: mellerio je. Clin Exp Dermatol. 1999 May;24(3):232-5. doi: 10.1046/j.1365-2230.1999.00461.x. Clin Exp Dermatol. 1999. PMID: 10354186

10

Allelic heterogeneity of dominant and recessive COL7A1 mutations underlying epidermolysis bullosa pruriginosa.

Mellerio JE, Ashton GH, Mohammedi R, Lyon CC, Kirby B, Harman KE, Salas-Alanis JC, Atherton DJ, Harrison PV, Griffiths WA, Black MM, Eady RA, McGrath JA. Mellerio JE, et al. J Invest Dermatol. 1999 Jun;112(6):984-7. doi: 10.1046/j.1523-1747.1999.00614.x. J Invest Dermatol. 1999. PMID: 10383749 Free article.

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