281 related articles for article (PubMed ID: 7504434)
21. A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis.
Müller FB; Huber M; Kinaciyan T; Hausser I; Schaffrath C; Krieg T; Hohl D; Korge BP; Arin MJ
Hum Mol Genet; 2006 Apr; 15(7):1133-41. PubMed ID: 16505000
[TBL] [Abstract][Full Text] [Related]
22. The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes.
Cheng J; Syder AJ; Yu QC; Letai A; Paller AS; Fuchs E
Cell; 1992 Sep; 70(5):811-9. PubMed ID: 1381287
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Ultrastructural findings in epidermolysis bullosa.
Smith LT
Arch Dermatol; 1993 Dec; 129(12):1578-84. PubMed ID: 7504435
[TBL] [Abstract][Full Text] [Related]
25. Genomic organization and amplification of the human epidermal type II keratin genes K1 and K5.
Whittock NV; Eady RA; McGrath JA
Biochem Biophys Res Commun; 2000 Jul; 274(1):149-52. PubMed ID: 10903910
[TBL] [Abstract][Full Text] [Related]
26. The keratins and their disorders.
Rugg EL; Leigh IM
Am J Med Genet C Semin Med Genet; 2004 Nov; 131C(1):4-11. PubMed ID: 15452838
[TBL] [Abstract][Full Text] [Related]
27. Epidermolysis bullosa simplex in Israel: clinical and genetic features.
Ciubotaru D; Bergman R; Baty D; Indelman M; Pfendner E; Petronius D; Moualem H; Kanaan M; Ben Amitai D; McLean WH; Uitto J; Sprecher E
Arch Dermatol; 2003 Apr; 139(4):498-505. PubMed ID: 12707098
[TBL] [Abstract][Full Text] [Related]
28. Epidermolytic hyperkeratosis: a keratin 1 or 10 mutational event.
Lacz NL; Schwartz RA; Kihiczak G
Int J Dermatol; 2005 Jan; 44(1):1-6. PubMed ID: 15663649
[TBL] [Abstract][Full Text] [Related]
29. Novel keratin 5 and 14 gene mutations in patients with epidermolysis bullosa simplex from Poland.
Hamada T; Kawano Y; Szczecinska W; Wozniak K; Yasumoto S; Kowalewski C; Hashimoto T
Arch Dermatol Res; 2005 Jun; 296(12):577-9. PubMed ID: 15827748
[TBL] [Abstract][Full Text] [Related]
30. Epidermolytic hyperkeratosis and epidermolysis bullosa simplex caused by frameshift mutations altering the v2 tail domains of keratin 1 and keratin 5.
Sprecher E; Yosipovitch G; Bergman R; Ciubutaro D; Indelman M; Pfendner E; Goh LC; Miller CJ; Uitto J; Richard G
J Invest Dermatol; 2003 Apr; 120(4):623-6. PubMed ID: 12648226
[TBL] [Abstract][Full Text] [Related]
31. [Epidermolysis bullosa simplex: genotype-phenotype correlation in Danish patients].
Sørensen CB; Ladekjaer-Mikkelsen AS; Andresen BS; Brandrup F; Veien NK; Buus SK; Anton-Lamprecht I; Kruse T; Jensen PK; Eiberg H; Bolund L; Gregersen N
Ugeskr Laeger; 2000 Mar; 162(13):1873-6. PubMed ID: 10765693
[TBL] [Abstract][Full Text] [Related]
32. Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis.
Arin MJ; Oji V; Emmert S; Hausser I; Traupe H; Krieg T; Grimberg G
Br J Dermatol; 2011 Feb; 164(2):442-7. PubMed ID: 21271994
[TBL] [Abstract][Full Text] [Related]
33. Keratins and skin disorders.
Lane EB; McLean WH
J Pathol; 2004 Nov; 204(4):355-66. PubMed ID: 15495218
[TBL] [Abstract][Full Text] [Related]
34. Disruption of the suprabasal keratin network by mutation M150T in the helix initiation motif of keratin 10 does not affect cornified cell envelope formation in human epidermis.
Akiyama M; Takizawa Y; Sawamura D; Matsuo I; Shimizu H
Exp Dermatol; 2003 Oct; 12(5):638-45. PubMed ID: 14705805
[TBL] [Abstract][Full Text] [Related]
35. Genetic bases of epidermolysis bullosa simplex and epidermolytic hyperkeratosis.
Fuchs E; Coulombe P; Cheng J; Chan YM; Hutton E; Syder A; Degenstein L; Yu QC; Letai A; Vassar R
J Invest Dermatol; 1994 Nov; 103(5 Suppl):25S-30S. PubMed ID: 7525738
[TBL] [Abstract][Full Text] [Related]
36. Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q.
Compton JG; DiGiovanna JJ; Santucci SK; Kearns KS; Amos CI; Abangan DL; Korge BP; McBride OW; Steinert PM; Bale SJ
Nat Genet; 1992 Jul; 1(4):301-5. PubMed ID: 1284546
[TBL] [Abstract][Full Text] [Related]
37. Characterization of immortalized human epidermolysis bullosa simplex (KRT5) cell lines: trimethylamine N-oxide protects the keratin cytoskeleton against disruptive stress condition.
Chamcheu JC; Lorié EP; Akgul B; Bannbers E; Virtanen M; Gammon L; Moustakas A; Navsaria H; Vahlquist A; Törmä H
J Dermatol Sci; 2009 Mar; 53(3):198-206. PubMed ID: 19157792
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Epidermolysis bullosa: hereditary skin fragility diseases as paradigms in cell biology.
Eady RA; Dunnill MG
Arch Dermatol Res; 1994; 287(1):2-9. PubMed ID: 7537032
[TBL] [Abstract][Full Text] [Related]
40. Genetic mutations in the K1 and K10 genes of patients with epidermolytic hyperkeratosis. Correlation between location and disease severity.
Syder AJ; Yu QC; Paller AS; Giudice G; Pearson R; Fuchs E
J Clin Invest; 1994 Apr; 93(4):1533-42. PubMed ID: 7512983
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
