BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 1281858)

  • 1. Genetic skin disorders of keratin.
    Fuchs E
    J Invest Dermatol; 1992 Dec; 99(6):671-4. PubMed ID: 1281858
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Epidermal disease: faulty keratin filaments take their toll.
    Compton JG
    Nat Genet; 1994 Jan; 6(1):6-7. PubMed ID: 7511022
    [No Abstract]   [Full Text] [Related]  

  • 6. Lessons from keratin transgenic and knockout mice.
    Magin TM
    Subcell Biochem; 1998; 31():141-72. PubMed ID: 9932492
    [No Abstract]   [Full Text] [Related]  

  • 7. [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]  

  • 8. Keratins and skin disorders.
    Lane EB; McLean WH
    J Pathol; 2004 Nov; 204(4):355-66. PubMed ID: 15495218
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Use of laser capture microscopy in the analysis of mouse models of human diseases.
    Arin MJ; Roop DR
    Methods Enzymol; 2002; 356():207-15. PubMed ID: 12418199
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Expression of a truncated keratin 5 may contribute to severe palmar--plantar hyperkeratosis in epidermolysis bullosa simplex patients.
    Livingston RJ; Sybert VP; Smith LT; Dale BA; Presland RB; Stephens K
    J Invest Dermatol; 2001 Jun; 116(6):970-4. PubMed ID: 11407989
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Blistering skin disorders in the neonate.
    Rimoin L; Graham JM
    Clin Pediatr (Phila); 2012 Jul; 51(7):685-8. PubMed ID: 22231587
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Keratins and the skin.
    Fuchs E
    Annu Rev Cell Dev Biol; 1995; 11():123-53. PubMed ID: 8689554
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A novel deletion mutation in keratin 5 causing the removal of 5 amino acids and elevated mutant mRNA levels in Dowling-Meara epidermolysis bullosa simplex.
    Kemp MW; Klingberg S; Lloyd L; Molloy TJ; Marr P; Wang Y; Murrell GA; Murrell DF
    J Invest Dermatol; 2005 May; 124(5):1083-5. PubMed ID: 15854057
    [No Abstract]   [Full Text] [Related]  

  • 18. A keratin K5 mutation (Leu 463-->Pro) in a family with the Weber-Cockayne type of epidermolysis bullosa simplex.
    Nomura K; Umeki K; Meng X; Tamai K; Sawamura D; Hosokawa M; Miyazawa T; Funayama M; Hashimoto I
    Arch Dermatol Res; 1997 Jul; 289(8):493-5. PubMed ID: 9266030
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. A novel mutation in the helix termination peptide of keratin 5 causing epidermolysis bullosa simplex Dowling-Meara.
    Irvine AD; McKenna KE; Bingham A; Nevin NC; Hughes AE
    J Invest Dermatol; 1997 Dec; 109(6):815-6. PubMed ID: 9406827
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.