507 related articles for article (PubMed ID: 12688839)
1. 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]
2. Human keratin diseases: hereditary fragility of specific epithelial tissues.
Corden LD; McLean WH
Exp Dermatol; 1996 Dec; 5(6):297-307. PubMed ID: 9028791
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Keratins and skin disorders.
Lane EB; McLean WH
J Pathol; 2004 Nov; 204(4):355-66. PubMed ID: 15495218
[TBL] [Abstract][Full Text] [Related]
6. Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families.
Shamsher MK; Navsaria HA; Stevens HP; Ratnavel RC; Purkis PE; Kelsell DP; McLean WH; Cook LJ; Griffiths WA; Gschmeissner S
Hum Mol Genet; 1995 Oct; 4(10):1875-81. PubMed ID: 8595410
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Genetic approaches to understanding the keratinopathies.
Bale SJ; DiGiovanna JJ
Adv Dermatol; 1997; 12():99-113; discussion 114. PubMed ID: 8973737
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Mutations in the non-helical linker segment L1-2 of keratin 5 in patients with Weber-Cockayne epidermolysis bullosa simplex.
Chan YM; Yu QC; LeBlanc-Straceski J; Christiano A; Pulkkinen L; Kucherlapati RS; Uitto J; Fuchs E
J Cell Sci; 1994 Apr; 107 ( Pt 4)():765-74. PubMed ID: 7520042
[TBL] [Abstract][Full Text] [Related]
11. [Keratin diseases].
Jensen PK; Sørensen CB; Andresen BS; Brandrup F; Veien NK; Buus SK; Gregersen N; Bolund L
Ugeskr Laeger; 2000 Mar; 162(13):1867-72. PubMed ID: 10765692
[TBL] [Abstract][Full Text] [Related]
12. Insights into genotype-phenotype correlation in pachyonychia congenita from the human intermediate filament mutation database.
McLean WH; Smith FJ; Cassidy AJ
J Investig Dermatol Symp Proc; 2005 Oct; 10(1):31-6. PubMed ID: 16250207
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.
Whittock NV; Ashton GH; Griffiths WA; Eady RA; McGrath JA
Br J Dermatol; 2001 Aug; 145(2):330-5. PubMed ID: 11531804
[TBL] [Abstract][Full Text] [Related]
15. Linkage of the epidermolytic hyperkeratosis phenotype and the region of the type II keratin gene cluster on chromosome 12.
Bonifas JM; Bare JW; Chen MA; Lee MK; Slater CA; Goldsmith LA; Epstein EH
J Invest Dermatol; 1992 Nov; 99(5):524-7. PubMed ID: 1385543
[TBL] [Abstract][Full Text] [Related]
16. The molecular basis for inherited bullous diseases.
Korge BP; Krieg T
J Mol Med (Berl); 1996 Feb; 74(2):59-70. PubMed ID: 8820401
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. How do keratinizing disorders and blistering disorders overlap?
Hamada T; Tsuruta D; Fukuda S; Ishii N; Teye K; Numata S; Dainichi T; Karashima T; Ohata C; Furumura M; Hashimoto T
Exp Dermatol; 2013 Feb; 22(2):83-7. PubMed ID: 23039137
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
