275 related articles for article (PubMed ID: 7678607)
21. A transgenic mouse model that recapitulates the clinical features of both neonatal and adult forms of the skin disease epidermolytic hyperkeratosis.
Bickenbach JR; Longley MA; Bundman DS; Dominey AM; Bowden PE; Rothnagel JA; Roop DR
Differentiation; 1996 Dec; 61(2):129-39. PubMed ID: 8983179
[TBL] [Abstract][Full Text] [Related]
22. Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.
Sybert VP; Francis JS; Corden LD; Smith LT; Weaver M; Stephens K; McLean WH
Am J Hum Genet; 1999 Mar; 64(3):732-8. PubMed ID: 10053007
[TBL] [Abstract][Full Text] [Related]
23. A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythroderma.
Joh GY; Traupe H; Metze D; Nashan D; Huber M; Hohl D; Longley MA; Rothnagel JA; Roop DR
J Invest Dermatol; 1997 Mar; 108(3):357-61. PubMed ID: 9036939
[TBL] [Abstract][Full Text] [Related]
24. An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosis.
Arin MJ; Longley MA; Küster W; Huber M; Hohl D; Rothnagel JA; Roop DR
Exp Dermatol; 1999 Apr; 8(2):124-7. PubMed ID: 10232403
[TBL] [Abstract][Full Text] [Related]
25. Epidermolytic hyperkeratosis type NPS-3: a case report.
Prohić A; Selmanagić A; Bilalović N
Acta Dermatovenerol Croat; 2007; 15(1):20-3. PubMed ID: 17433175
[TBL] [Abstract][Full Text] [Related]
26. Epidermolytic hyperkeratosis type PS-1 caused by aberrant splicing of KRT1.
Tal O; Bergman R; Alcalay J; Indelman M; Sprecher E
Clin Exp Dermatol; 2005 Jan; 30(1):64-7. PubMed ID: 15663507
[TBL] [Abstract][Full Text] [Related]
27. Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma).
Ishida-Yamamoto A; McGrath JA; Judge MR; Leigh IM; Lane EB; Eady RA
J Invest Dermatol; 1992 Jul; 99(1):19-26. PubMed ID: 1376754
[TBL] [Abstract][Full Text] [Related]
28. Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene.
Terron-Kwiatkowski A; Terrinoni A; Didona B; Melino G; Atherton DJ; Irvine AD; McLean WH
Br J Dermatol; 2004 Jun; 150(6):1096-103. PubMed ID: 15214894
[TBL] [Abstract][Full Text] [Related]
29. A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of Siemens.
Arin MJ; Longley MA; Epstein EH; Scott G; Goldsmith LA; Rothnagel JA; Roop DR
J Invest Dermatol; 1999 Mar; 112(3):380-2. PubMed ID: 10084318
[TBL] [Abstract][Full Text] [Related]
30. Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens.
Rothnagel JA; Traupe H; Wojcik S; Huber M; Hohl D; Pittelkow MR; Saeki H; Ishibashi Y; Roop DR
Nat Genet; 1994 Aug; 7(4):485-90. PubMed ID: 7524919
[TBL] [Abstract][Full Text] [Related]
31. A novel substitution in keratin 10 in epidermolytic hyperkeratosis.
Arin MJ; Longley MA; Anton-Lamprecht I; Kurze G; Huber M; Hohl D; Rothnagel JA; Roop DR
J Invest Dermatol; 1999 Apr; 112(4):506-8. PubMed ID: 10201536
[TBL] [Abstract][Full Text] [Related]
32. Keratin 1 and keratin 10 mutations causing epidermolytic hyperkeratosis in Chinese patients.
Sun XK; Ma LL; Xie YQ; Zhu XJ
J Dermatol Sci; 2002 Sep; 29(3):195-200. PubMed ID: 12234709
[TBL] [Abstract][Full Text] [Related]
33. Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE).
McLean WH; Eady RA; Dopping-Hepenstal PJ; McMillan JR; Leigh IM; Navsaria HA; Higgins C; Harper JI; Paige DG; Morley SM
J Invest Dermatol; 1994 Jan; 102(1):24-30. PubMed ID: 7507152
[TBL] [Abstract][Full Text] [Related]
34. A keratin 10 gene mutation (Arg156Cys) in a Japanese patient with bullous congenital ichthyosiform erythroderma.
Saeki H; Hattori N; Mitsui H; Adachi M; Imakado S; Ishibashi Y; Tamaki K
J Dermatol; 2002 Mar; 29(3):168-71. PubMed ID: 11990254
[TBL] [Abstract][Full Text] [Related]
35. Mapping of epidermolysis bullosa simplex mutation to chromosome 12.
Ryynänen M; Knowlton RG; Uitto J
Am J Hum Genet; 1991 Nov; 49(5):978-84. PubMed ID: 1718160
[TBL] [Abstract][Full Text] [Related]
36. A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis.
Rothnagel JA; Fisher MP; Axtell SM; Pittelkow MR; Anton-Lamprecht I; Huber M; Hohl D; Roop DR
Hum Mol Genet; 1993 Dec; 2(12):2147-50. PubMed ID: 7509230
[TBL] [Abstract][Full Text] [Related]
37. Phenotypic heterogeneity in bullous congenital ichthyosiform erythroderma: possible somatic mosaicism for keratin gene mutation in the mildly affected mother of the proband.
Nomura K; Umeki K; Hatayama I; Kuronuma T
Arch Dermatol; 2001 Sep; 137(9):1192-5. PubMed ID: 11559215
[TBL] [Abstract][Full Text] [Related]
38. Epidermolytic Ichthyosis Sine Epidermolysis.
Eskin-Schwartz M; Drozhdina M; Sarig O; Gat A; Jackman T; Isakov O; Shomron N; Samuelov L; Malchin N; Peled A; Vodo D; Hovnanian A; Ruzicka T; Koshkin S; Harmon RM; Koetsier JL; Green KJ; Paller AS; Sprecher E
Am J Dermatopathol; 2017 Jun; 39(6):440-444. PubMed ID: 28121638
[TBL] [Abstract][Full Text] [Related]
39. Use of the frozen section 'jelly-roll' technique to aid in the diagnosis of bullous congenital ichthyosiform erythroderma (epidermolytic hyperkeratosis).
Galler B; Bowen C; Arnold J; Kobayashi T; Dalton SR
J Cutan Pathol; 2016 May; 43(5):434-7. PubMed ID: 26969483
[TBL] [Abstract][Full Text] [Related]
40. Epidermolytic hyperkeratosis.
Kwak J; Maverakis E
Dermatol Online J; 2006 Sep; 12(5):6. PubMed ID: 16962021
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
