These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. The molecular genetics of keratin disorders. Smith F Am J Clin Dermatol; 2003; 4(5):347-64. PubMed ID: 12688839 [TBL] [Abstract][Full Text] [Related]
5. Keratin gene mutations in disorders of human skin and its appendages. Chamcheu JC; Siddiqui IA; Syed DN; Adhami VM; Liovic M; Mukhtar H Arch Biochem Biophys; 2011 Apr; 508(2):123-37. PubMed ID: 21176769 [TBL] [Abstract][Full Text] [Related]
6. Mutations in the genes for epidermal keratins in epidermolysis bullosa and epidermolytic hyperkeratosis. Leigh IM; Lane EB Arch Dermatol; 1993 Dec; 129(12):1571-7. PubMed ID: 7504434 [TBL] [Abstract][Full Text] [Related]
7. Inducible mouse models for inherited skin diseases: implications for skin gene therapy. Arin MJ; Roop DR Cells Tissues Organs; 2004; 177(3):160-8. PubMed ID: 15388990 [TBL] [Abstract][Full Text] [Related]
9. Complete cytolysis and neonatal lethality in keratin 5 knockout mice reveal its fundamental role in skin integrity and in epidermolysis bullosa simplex. Peters B; Kirfel J; Büssow H; Vidal M; Magin TM Mol Biol Cell; 2001 Jun; 12(6):1775-89. PubMed ID: 11408584 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. The functional diversity of epidermal keratins revealed by the partial rescue of the keratin 14 null phenotype by keratin 16. Paladini RD; Coulombe PA J Cell Biol; 1999 Sep; 146(5):1185-201. PubMed ID: 10477769 [TBL] [Abstract][Full Text] [Related]
12. Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin. Takahashi K; Folmer J; Coulombe PA J Cell Biol; 1994 Oct; 127(2):505-20. PubMed ID: 7523421 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Mutation S233L in the 1B domain of keratin 1 causes epidermolytic palmoplantar keratoderma with "tonotubular" keratin. Terron-Kwiatkowski A; van Steensel MA; van Geel M; Lane EB; McLean WH; Steijlen PM J Invest Dermatol; 2006 Mar; 126(3):607-13. PubMed ID: 16439967 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation. Irvine AD; McLean WH Br J Dermatol; 1999 May; 140(5):815-28. PubMed ID: 10354017 [TBL] [Abstract][Full Text] [Related]
20. A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex. Hovnanian A; Pollack E; Hilal L; Rochat A; Prost C; Barrandon Y; Goossens M Nat Genet; 1993 Apr; 3(4):327-32. PubMed ID: 7526933 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]