134 related articles for article (PubMed ID: 1282526)
21. Extensive acantholysis as the major histological feature of a severe case of Dowling Meara-epidermolysis bullosa simplex: a reappraisal of acantholysis in the newborn.
Darwich E; Vicente A; Bolling MC; González-Enseñat MA; Cusi V; Fortuny C; Bombí JA; Jonkman MF; Mascaró JM
Eur J Dermatol; 2011; 21(6):966-71. PubMed ID: 21856558
[TBL] [Abstract][Full Text] [Related]
22. A premature stop codon mutation in the 2B helix termination peptide of keratin 5 in a German epidermolysis bullosa simplex Dowling-Meara case.
Müller FB; Anton-Lamprecht I; Küster W; Korge BP
J Invest Dermatol; 1999 Jun; 112(6):988-90. PubMed ID: 10383750
[TBL] [Abstract][Full Text] [Related]
23. A keratin K14 gene mutation in a Japanese patient with the Dowling-Meara type of epidermolysis bullosa simplex.
Umeki K; Nomura K; Harada K; Hashimoto I
J Dermatol Sci; 1996 Jan; 11(1):64-9. PubMed ID: 8867769
[TBL] [Abstract][Full Text] [Related]
24. A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein.
Chan Y; Anton-Lamprecht I; Yu QC; Jäckel A; Zabel B; Ernst JP; Fuchs E
Genes Dev; 1994 Nov; 8(21):2574-87. PubMed ID: 7525408
[TBL] [Abstract][Full Text] [Related]
25. Genetic analysis of a severe case of Dowling-Meara epidermolysis bullosa simplex.
Chan YM; Cheng J; Gedde-Dahl T; Niemi KM; Fuchs E
J Invest Dermatol; 1996 Feb; 106(2):327-34. PubMed ID: 8601736
[TBL] [Abstract][Full Text] [Related]
26. [Epidermolysis bullosa simplex Dowling-Meara].
Frangu M; Gedde-Dahl T; Verder H
Ugeskr Laeger; 2006 Nov; 168(48):4222-4. PubMed ID: 17147951
[TBL] [Abstract][Full Text] [Related]
27. Laryngeal involvement in the Dowling-Meara variant of epidermolysis bullosa simplex with keratin mutations of severely disruptive potential.
Shemanko CS; Horn HM; Keohane SG; Hepburn N; Kerr AI; Atherton DJ; Tidman MJ; Lane EB
Br J Dermatol; 2000 Feb; 142(2):315-20. PubMed ID: 10730767
[TBL] [Abstract][Full Text] [Related]
28. Three severe cases of EBS Dowling-Meara caused by missense and frameshift mutations in the keratin 14 gene.
Titeux M; Mazereeuw-Hautier J; Hadj-Rabia S; Prost C; Tonasso L; Fraitag S; de Prost Y; Hovnanian A; Bodemer C
J Invest Dermatol; 2006 Apr; 126(4):773-6. PubMed ID: 16439965
[TBL] [Abstract][Full Text] [Related]
29. Novel mechanism of revertant mosaicism in Dowling-Meara epidermolysis bullosa simplex.
Smith FJ; Morley SM; McLean WH
J Invest Dermatol; 2004 Jan; 122(1):73-7. PubMed ID: 14962092
[TBL] [Abstract][Full Text] [Related]
30. Epidermolysis bullosa simplex with transient erythema circinatum.
Kawana S; Hashimoto I; Nishiyama S
Br J Dermatol; 1994 Oct; 131(4):571-6. PubMed ID: 7947213
[TBL] [Abstract][Full Text] [Related]
31. A recurrent keratin 14 mutation in Dowling-Meara epidermolysis bullosa simplex.
Sasaki Y; Shimizu H; Akiyama M; Hiraoka Y; Takizawa Y; Yamada S; Morishima Y; Yamanishi K; Aiso S; Nishikawa T
Br J Dermatol; 1999 Oct; 141(4):747-8. PubMed ID: 10583131
[No Abstract] [Full Text] [Related]
32. Epidermolysis bullosa nevus arising in a patient with Dowling-Meara type epidermolysis bullosa simplex with a novel K5 mutation.
Sugiyama-Fukamatsu H; Suzuki N; Nakanishi G; Iwatsuki K
J Dermatol; 2009 Aug; 36(8):447-52. PubMed ID: 19691749
[TBL] [Abstract][Full Text] [Related]
33. Temperature sensitivity of the keratin cytoskeleton and delayed spreading of keratinocyte lines derived from EBS patients.
Morley SM; Dundas SR; James JL; Gupta T; Brown RA; Sexton CJ; Navsaria HA; Leigh IM; Lane EB
J Cell Sci; 1995 Nov; 108 ( Pt 11)():3463-71. PubMed ID: 8586658
[TBL] [Abstract][Full Text] [Related]
34. A novel keratin K5 gene mutation in Dowling-Meara epidermolysis bullosa simplex.
Nomura K; Shimizu H; Meng X; Umeki K; Tamai K; Sawamura D; Nagao K; Kawakami T; Nishikawa T; Hashimoto I
J Invest Dermatol; 1996 Aug; 107(2):253-4. PubMed ID: 8757772
[TBL] [Abstract][Full Text] [Related]
35. A function for keratins and a common thread among different types of epidermolysis bullosa simplex diseases.
Coulombe PA; Hutton ME; Vassar R; Fuchs E
J Cell Biol; 1991 Dec; 115(6):1661-74. PubMed ID: 1721910
[TBL] [Abstract][Full Text] [Related]
36. Keratin mutations in patients with epidermolysis bullosa simplex: correlations between phenotype severity and disturbance of intermediate filament molecular structure.
Jerábková B; Marek J; Bucková H; Kopecková L; Veselý K; Valícková J; Fajkus J; Fajkusová L
Br J Dermatol; 2010 May; 162(5):1004-13. PubMed ID: 20030639
[TBL] [Abstract][Full Text] [Related]
37. Epidermolysis bullosa simplex Dowling-Meara: troublesome blistering and pruritus in an adult patient.
McGrath JA; Burrows NP; Russell Jones R; Eady RA
Dermatology; 1993; 186(1):68-71. PubMed ID: 8435522
[TBL] [Abstract][Full Text] [Related]
38. Abnormalities of basal cell keratin in epidermolysis bullosa simplex do not affect the expression patterns of suprabasal keratins and cornified cell envelope proteins.
Sasaki Y; Shimizu H; Akiyama M; Yoneda K; Ishida-Yamamoto A; Watanabe S; Hata J; Nishikawa T
Arch Dermatol Res; 1998 Nov; 290(11):591-7. PubMed ID: 9860278
[TBL] [Abstract][Full Text] [Related]
39. Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutations.
Morley SM; D'Alessandro M; Sexton C; Rugg EL; Navsaria H; Shemanko CS; Huber M; Hohl D; Heagerty AI; Leigh IM; Lane EB
Br J Dermatol; 2003 Jul; 149(1):46-58. PubMed ID: 12890194
[TBL] [Abstract][Full Text] [Related]
40. Novel keratin 14 gene mutations in patients from Hungary with epidermolysis bullosa simplex.
Csikós M; Szalai Z; Becker K; Sebõk B; Schneider I; Horváth A; Kárpáti S
Exp Dermatol; 2004 Mar; 13(3):185-91. PubMed ID: 14987259
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
